This work was made possible by a Pilot Grant from the Alliance for Regenerative Rehabilitation Research and Training (AR3T) and a Faculty Startup Package from Wayne State University to JAR. AR3T is supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institute of Neurological Disorders and Stroke (NINDS), and National Institute of Biomedical Imaging and Bioengineering (NIBIB) of the National Institutes of Health under Award Number P2CHD086843. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

All studies involving live animals are approved by the Institution Animal Care and Use Committee (IACUC) at Wayne State University, Detroit, Michigan, USA, and are in accordance with the Guide for the Care and Use of Laboratory Animals (8th Edition, 2011, published by National Academies Press, 500 Fifth Street, NW, Lockbox 285, Washington, DC 20055, USA). As per the approved IACUC protocols, procedures involving pain and/or distress were performed under general anesthesia, which is induced and maintained by isoflurane inhalation (1.5 - 5% to effect). Anesthesia was verified by lack of withdrawal to toe pinch, and lack of palpebral or vibrissae responses (the percentage of isoflurane was increased as needed to maintain effect). Due to the minimally invasive nature of the protocols, a &#34;sterile tips&#34; technique was followed. While animals were under anesthesia, petroleum jelly was applied to the eyes to prevent dryness. No special treatments were required; however, diet gel was provided to the animals for 24 h following procedures that involved general anesthesia.&#160;The investigator is approved by the IACUC to withhold analgesia following MIME, since the procedure does not involve surgically exposing the host muscle, because it is confined to one hindlimb and does not affect normal function, and because many common analgesic drugs are known to affect normal muscle regeneration. &#160;
1. Animal Models
<ol>
	<li>Host mice for MIME
	<ol>
		<li>Use NSG-GFP mice (8 - 10 week, male) as hosts for the muscle grafts studies. 
		NOTE: These mice are ideal hosts for allogeneic muscle grafts because they lack mature T and B lymphocytes and functional natural killer cells, are deficient in cytokine signaling, and have been used by others for allografting or xenografting non-muscle cells14. Ubiquitous GFP expression allows for easy identification of host (GFP+) and donor-cell-derived (GFP-) muscle fibers.</li>
	</ol>
	</li>
	<li>Donor mice for MIME
	<ol>
		<li>Use C57BL/6J mice (12 - 16 week) as donor mice. 
		NOTE: These mice are suitable donor mice because they have a fully mapped genome, are not known to have any skeletal muscle pathology, are easily available and economical, and do not express GFP.</li>
	</ol>
	</li>
</ol>
2. Preparing Donor Muscle Tissue
<ol>
	<li>Tying Guiding Sutures and Harvesting donor EDL muscles
	<ol>
		<li>Euthanize the donor mice by cervical dislocation and thoracotomy performed under general anesthesia administered by a tabletop isoflurane vaporizer driven by medical oxygen (inhaled isoflurane; 2 - 5% to effect).</li>
		<li>To access the EDL muscles, use a pair of surgical scissors to open the skin over the anterior surface of the leg. Locate the TA muscle in the anterior leg and remove it to visualize the EDL muscle that is situated behind the TA muscle. Slide the tip of a pair of forceps behind the EDL muscle and apply gentle traction to see if the toes extend (this confirms that the muscle is the EDL).&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160; &#160; &#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160; &#160; &#160; &#160; &#160; &#160; &#160; &#160; &#160; &#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160;&#160; 
		NOTE: Donor tissue area should be surgically, aseptically prepped prior to harvest.</li>
		<li>Use ~ 10 cm segments of 4-0 silk, braided, non-absorbable, sterile suture, and make two double knots to apply the guiding sutures to the proximal and distal tendons of the EDL muscle. (Figure 1A).</li>
		<li>Cut the distal EDL tendon, reflect the EDL muscle and cut the proximal tendon.</li>
		<li>Place the donor EDL muscles in a Petri dish filled with mouse Ringer solution.</li>
	</ol>
	</li>
</ol>
3. Preparing Host Mice for MIME
<ol>
	<li>Anesthesia
	<ol>
		<li>Place the host mouse under general anesthesia (inhaled isoflurane; 1.5 - 5% to effect) administered by a tabletop isoflurane vaporizer driven by medical oxygen.</li>
		<li>Induce anesthesia in an induction chamber and then transfer the mouse to a nose-cone to maintain the anesthesia while performing other procedures on the animal. Provide thermal support with an isothermal gel heating pad while the animal is under anesthesia.</li>
	</ol>
	</li>
	<li>Skin preparation
	<ol>
		<li>To remove the animal&#39;s fur, apply a depilatory cream over the anterior aspect of the left hind leg. The right leg serves as a control leg for subsequent procedures.</li>
		<li>Leave the depilatory cream on for 2 min. Clean off the depilatory cream along with the detached fur with wipes soaked in phosphate buffered saline (PBS). After fur removal, scrub the skin with three alternating wipes of povidone-iodine scrubbing solution and 70 % ethanol.</li>
	</ol>
	</li>
	<li>Creating a needle track in the host TA muscle
	<ol>
		<li>Pass an 18-gauge (1 in long) surgical needle through the center of the host TA muscle along the muscle&#39;s long axis (Figure 1B). Pass the needle in a cephalo-caudal direction, along the length of the TA muscle, and through the center of the muscle belly (Figure 1B). 
		NOTE: The purpose of this step is to create a needle track, into which a piece of donor muscle may be embedded. Embedding the donor tissue in the center of the TA muscle would potentially allow the SCs from the donor tissue to migrate and facilitate myogenesis across the entire host TA muscle.</li>
	</ol>
	</li>
	<li>Embedding donor tissue in the needle track of host TA muscle
	<ol>
		<li>Once the surgical needle is within the host TA muscle, pass the guiding sutures at one end of the donor tissue through the lumen of surgical needle in a caudo-cephalic direction (Figure 1C).</li>
		<li>Draw the donor tissue through the needle track as the needle is withdrawn from the host TA muscle in a caudo-cephalic direction.</li>
		<li>Use the guiding sutures at the caudal and cephalic ends of the donor tissue to adjust the placement of the donor tissue. Ensure that the donor tissue is ensconced within the host TA muscle (Figure 1D).</li>
		<li>Once the donor tissue placement is optimized, cut off the guiding sutures, make any final adjustments to the donor tissue placement with fine-tipped forceps.</li>
		<li>Seal cutaneous needle wounds (Figure 1E - F) by approximating the wound edge with forceps and applying veterinary tissue adhesive with the tip of a 27-gauge surgical needle.</li>
	</ol>
	</li>
</ol>
4. Intramuscular Myotoxin Injection to Induce Concerted Muscle Degeneration and Regeneration
<ol>
	<li>After MIME, inject 50 - 60 &#181;L of 1.2% BaCl2 (myotoxin) into the host TA muscle to induce extensive muscle fiber damage in the host muscle and the donor tissue embedded within it15.
	<ol>
		<li>Inject BaCl2 at 3 sites along the length of the host TA muscle (proximal, middle and distal one-third of the muscle belly). 
		NOTE: Injecting myotoxins like BaCl2, cardiotoxins and notexin into skeletal muscle induces concerted muscle fiber damage followed by regeneration16.</li>
	</ol>
	</li>
</ol>
5. Post-procedural Animal Care
<ol>
	<li>After MIME and BaCl2 injection, clean the host mouse&#39;s left hind leg with ethanol and apply a thin layer of petroleum jelly to protect the skin.</li>
	<li>After post-procedural skin care, remove the host mouse from the nose cone.</li>
	<li>Place the mouse in a solitary recovery cage without bedding. Provide thermal support to the recovering animal through an isothermal gel heating pad placed under half of the recovery cage. 
	NOTE: One half is not heated so that animal may move away from the heating pad if needed.</li>
	<li>After the host mouse has completely recovered from anesthesia, return the animal to its original cage. Place the animal back in the animal facility until follow-up experiments are performed. Monitor the host mouse daily until it is ready for follow-up&#160;&#8211; example: at 3 or 14 days post-MIME. Following MIME, animals are monitored by laboratory personnel as well by veterinary staff &#8211; this mainly involves assessing if animals are bright, alert and responsive; and also assessing if animals are showing overt signs of pain or are having difficulty moving, feeding, drinking and grooming.</li>
</ol>
6. Tissue Collection
<ol>
	<li>Harvesting host muscle
	<ol>
		<li>Euthanize the host mice by cervical dislocation and thoracotomy performed under general anesthesia administered by a tabletop isoflurane vaporizer driven by medical oxygen (inhaled isoflurane; 2 - 5% to effect).&#160;The investigator also has IACUC approval to harvest TA muscles under general anesthesia prior to euthanasia.&#160;</li>
		<li>To access the host TA muscles, use a pair of surgical scissors to open the skin over the anterior surface of the leg. Locate the TA muscle in the anterior leg, cut the distal tendon, reflect the muscle and cut the proximal muscle attachments (see section 2.1).</li>
		<li>Collect both left (experimental) and right (control) TA muscles.</li>
	</ol>
	</li>
	<li>&#160;Snap freezing harvested muscles
	<ol>
		<li>Weigh the harvested muscles by placing on weigh paper and weighing scale.</li>
		<li>Briefly dip the muscles in mineral oil for cryoprotection. Blot off the excess oil.</li>
		<li>Place muscles on aluminum foil, and snap freeze the muscles by rapidly immersing them in liquid nitrogen filled in a Dewar. Transfer the samples to labeled cryovials and store the samples in a -80 &#176;C freezer for later studies.</li>
	</ol>
	</li>
</ol>
7. Histological Studies
<ol>
	<li>Cryosectioning muscle tissue to collect serial cross sections
	<ol>
		<li>Transfer the samples from the -80 &#176;C freezer to a cryostat by placing them in a Dewar containing liquid nitrogen.</li>
		<li>In the cryostat, handle one sample at a time. With a cold razor blade (blade stored in cryostat), cut the sample twice at the mid-belly of the TA muscle to produce a segment of muscle that is about 1 - 2 mm thick. Keep this segment for making the cryostat sections and return the remaining portions of muscle to its cryovial.</li>
		<li>With the optimum cutting temperature (OCT) freezing compound, secure the thick segment of tissue onto a cryostat specimen disc. Place the specimen disc on the specimen holder.</li>
		<li>Rough-face the sample by cutting 20 &#181;m sections. Collect a few 20 &#181;m sections on glass slides for the cryostat sections.</li>
		<li>If the quality of the 20 &#181;m sections is satisfactory, change the cutting thickness to 5 &#181;m and collect a few sections to assess the quality. If the 5 &#181;m sections are satisfactory in quality, collect serial sections. Collect 2 - 3 sections per slide and collect enough sections for 3 slides.</li>
		<li>Collect sections from both the experimental (left) and control (right) TA muscles of each animal.</li>
	</ol>
	</li>
	<li>Studying GFP expression 
	NOTE: Designate one set of the prepared slides (section 7.1) to study GFP expression in the muscle fibers.
	<ol>
		<li>Apply ~50 &#181;L of anti-fade medium on the sections and apply a glass coverslip. Seal the coverslip edges with clear nail polish.</li>
		<li>Using the light and fluorescent microscope (see Table of Materials), study the sections with a 10X objective and an appropriate filter for visualizing GFP.
		<ol>
			<li>Collect digital images (~15) of overlapping visual fields to cover the entire cross section of the TA muscle. Collect the phase contrast images for each of the visual fields by switching from fluorescence to phase contrast mode on the microscope.</li>
		</ol>
		</li>
		<li>Open images with a suitable imaging software that can tile individual images to produce a single composite image; e.g., use the &#34;photomerge&#34; option under File Menu in the imaging software listed in the Table of Materials.</li>
		<li>Open the GFP fluorescence images with a suitable image analysis software (e.g., ImageJ). Circle individual muscle fibers using the &#34;ROI tool&#34; and record the Mean Fluorescence Intensity for each fiber.
		<ol>
			<li>Calculate the Maximum GFP (Fluorescence) Intensity by taking the average of the Mean Fluorescence Intensity of 10 fibers that show high GFP expression and have normal morphology. Calculate the % Maximum GFP Intensity for each fiber by dividing the Mean Florescence Intensity for each fiber by the Maximum GFP Intensity and multiplying by 100. Tabulate the results of the GFP analysis for each TA muscle as shown in Figure 3E.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Studying muscle fiber integrity and myonuclear location by Immunofluorescent labeling of desmin and 4&#39;,6-diamidino-2-phenylindole (DAPI), respectively. 
	NOTE: Designate one set of the slides prepared, as above, to study the desmin labeling in the muscle fibers.
	<ol>
		<li>Fix sections with 2% paraformaldehyde in PBS for 10 min. Wash the sections three times with PBS. 
		CAUTION: Wear appropriate personal protective equipment (PPE) when handling when handling paraformaldehyde.</li>
		<li>Block sections with 3% bovine serum albumin diluted in PBS containing 0.01% Triton-X100 for 30 min. This blocking solution is referred to hereafter as the primary diluent.</li>
		<li>Dilute the rabbit anti-desmin immunoglobulin G (IgG) in the primary diluent (1:200).</li>
		<li>After the blocking is complete, apply the diluted primary antibodies on sections and incubate overnight in a refrigerator at ~4 &#176;C. Wash the sections once (5 min) with PBS containing 0.1% Triton X-100. This solution is referred to hereafter as the first wash buffer.</li>
		<li>Wash the sections 3 times (5 min per wash) with PBS.</li>
		<li>Prepare the secondary antibody by diluting goat anti rabbit IgG (conjugated to red fluorescent dye) in PBS containing 0.01% Triton X-100.</li>
		<li>Apply the diluted secondary antibody on the sections and incubate at room temperature (~23 &#176;C) for 60 min.</li>
		<li>Wash the sections once (5 min) with the first wash buffer. Wash the sections 3 times (5 min per wash) with PBS.</li>
		<li>Apply DAPI for 3 min. Wash the sections 3 times (1 min per wash) with PBS. Apply ~ 50 &#181;L of the anti-fade medium on the sections and apply glass coverslip. Seal the coverslip edges with clear nail polish.</li>
		<li>Using the light and fluorescent microscope (see Table of Materials), study the serial sections with a 10X objective and an appropriate filter for visualizing red fluorescent dye.</li>
		<li>Collect the digital images (~15) of the overlapping visual fields to cover the entire cross section of the TA muscle. Collect the fluorescence images of DAPI labeling for each of the visual fields by switching to the appropriate filter setting.</li>
		<li>Open and analyze the images using a suitable imaging software as described in steps 7.2.3 - 7.2.4. 
		NOTE: Study images to identify, which muscle fibers are damaged (desmin negative), which muscle fibers have central nucleation (desmin positive fibers that have DAPI-labeled nuclei located internally rather than peripherally), and, which areas of the section have inflammation and/or fibrosis (areas that have many DAPI-labeled nuclei clustered together, but are devoid of muscle fibers).</li>
	</ol>
	</li>
</ol>

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The authors have no competing financial interests.

Here, we present a detailed protocol for the novel experimental technique known as MIME, developed in our laboratory, to implant donor muscle tissue into host muscle tissue. This is an adaptation of an open muscle grafting technique that has already proven to be effective in promoting donor-cell-mediated myogenesis in a host muscle9,10,17.
The goal of MIME is not to enable engraftment of the donor muscle tissue itself into the host muscle (we currently do not know if this occurs), but rather to provide a source of donor SCs that can contribute to myogenesis in the host muscle under conditions that stimulate muscle regeneration. Our hope is that after MIME has been optimized and tested in basic and preclinical studies, it could provide valuable insights to guide clinical therapies aimed at increasing muscle regeneration in skeletal muscles that have undergone myogenic muscle loss.
There are numerous questions that have yet to be answered regarding how MIME could be translated into a clinical therapy, for example: How would we control the quality of donor tissue? How would we control immune rejection of donor tissue and cells? Is the donor tissue cleared after providing cells for myogenesis or does it leave behind a fibrotic scar? Does the fiber type of donor and/or host muscle affect the donor-cell-mediated myogenesis? Which muscles can practically benefit from MIME?&#160;We are currently expanding our studies to assess if MIME is safe and effective, identify adjunctive treatments that can augment donor-derived myogenesis, and answer many of the questions, listed above.&#160;
After completing our tests of mouse-to-mouse allogeneic transplantation with MIME, our next step is to perform human-to-mouse MIME with cadaveric human tissue to evaluate the myogenic potential of cadaveric muscle tissue. We anticipate that these experiments will lead to a new line of basic and translational research, which involves muscle tissue from donors, who are registered in initiatives such as the Body Bequest Program for education and the Gift of Life program for organ donation.
The representative data presented in this manuscript suggest that at 14 days after MIME, there are several viable myofibers that either lack GFP or have low levels of GFP. Our interpretation of these data is that GFP- donor satellite cells contributed to the myogenesis in the host muscle. We performed this experiment in preparation for implantation of human cadaveric tissue into a host mouse muscle. To demonstrate unequivocally that the donor satellite cells contribute to myogenesis in the host muscle following MIME, it would be useful to implant donor tissue that expresses a fluorescent reporter, which can be easily distinguished from GFP (e.g., red fluorescent protein expressing donor tissue implanted into GFP+ host muscle).
This technique is mainly limited by the nature of the SCs present in the donor tissue. If the SCs in the donor tissue are viable, the technique is likely to facilitate donor-cell-mediated myogenesis, while if they are not viable,&#160;myogenesis cannot occur. However, since&#160;SCs are very resilient and are viable for about 2 weeks post-mortem, it is highly likely that for experimental purposes, the donor tissue that is implanted within a few minutes after harvest will facilitate donor-cell-mediated myogenesis13. Additionally, as alluded to above, it is possible that since the whole muscle tissue (that contains SCs, mature muscle fibers, as well as muscle-resident fibroblasts) is embedded into the host muscle, fibrosis could occur. However, this assumption needs to be empirically examined. The literature on muscle damage arising from injurious contractions, cryoinjury, and experimental myotoxins, suggests that immune cells (mainly macrophages) are capable of effectively clearing cellular debris from damaged fibers and remodeling the extracellular matrix18. Therefore, it is possible that after MIME and BaCl2 injection, as long as the host immune cells have access to degenerating donor muscle fibers, they could clear debris, leaving behind just the donor SCs. Finally, the extent of the donor-derived myogenesis is dependent on the amount of donor muscle tissue that is embedded in the host muscle. In order for the host muscle compartment to be completely repopulated by donor-cell-derived myofibers, it would require a method like X- or gamma-irradiation to ablate host muscle SCs and also require repeated MIME procedures.
It has been demonstrated that surgically exposing a host muscle and suturing a piece of donor tissue onto the host muscle can facilitate donor-cell-mediated myogenesis9,10,17. This open surgical approach has been used in the past to track the progression of myogenesis and to generate mouse models of human muscle diseases. The innovative aspect of the MIME technique is that it is minimally invasive and does not involve surgically exposing the host muscle. This reduces the risk of iatrogenic infection and the degree of discomfort in the host animal, therefore making it more feasible to perform MIME repeatedly on the same host muscle if needed.
We anticipate that the MIME technique might be a suitable refinement to the open surgical approach that is currently followed to implant donor muscle tissue into a host mouse. This could expedite the generation of humanized mouse models, by embedding biopsied human muscle in the host mouse muscle. Additionally, based on our preliminary data from mouse-to-mouse grafting, we anticipate that MIME will be effective in achieving donor-cell-mediated myogenesis from human cadaveric donor tissue as long as donor SCs are viable. Finally, with additional testing and validation, we hope that the MIME technique will help develop new therapies to facilitate donor-cell-mediated myogenesis in humans with muscle diseases.
The success of the MIME technique is critically dependent upon precisely embedding the donor tissue within the fascial compartment (epimysium) of the host muscle. Only if the donor tissue is placed within the host muscle compartment, will it be able to provide SCs to the host muscle in a precise manner. If the donor tissue is placed outside of the host muscle, it is unclear as to what would be its fate. In our experimental model for MIME, we use the TA muscle as the host muscle, since it is prominent and superficially placed in the anterolateral aspect of the leg. The size, orientation and anatomical position of the TA muscle, makes it easy to confirm that the donor tissue is placed correctly within the host TA muscle after MIME. In this paper, we have provided experimental evidence that the donor tissue remains embedded within the host TA muscle at 3 days post-MIME, and that there is donor-cell-mediated myogenesis in the host muscle at 14 days post-MIME.

Healthy skeletal muscle, even though post-mitotic, possesses excellent regenerative capacity due to the presence of tissue-resident myogenic cells known as satellite cells (SCs)1,2; and reviewed in3,4. However, under pathological conditions caused by muscular dystrophies, trauma or accelerated aging, the muscle regeneration might not keep up with muscle breakdown, and thus, progressive muscle fiber loss occurs5. Although effective methods have been developed to isolate SCs from muscle and expand them in culture to generate large numbers of myoblasts (and subsequently myotubes), attempts to generate physiologically relevant numbers of muscle fibers in host muscle have yielded only minimal success6. As with many other cell types, when myoblasts are injected alone into host tissue, most of the cells do not engraft7,8. We have shown that neuromuscular electrical stimulation (NMES) facilitates donor-cell-derived myogenesis in regeneration-deficient host mouse muscle that was injected with human myoblasts8. Others have demonstrated that surgically grafting biopsied muscle or single muscle fibers with attached SCs, facilitate moderate myogenesis even without NMES, suggesting that implanting whole muscle fibers with SCs might be more advantageous than implanting myogenic cells alone9,10. Since donor or engineered muscle tissue grafted into host muscle produces better results than transplanting cells alone, it is possible that tissue or tissue-like structures might provide crucial cues for donor-cell engraftment; a concept which is becoming increasingly evident in cell-therapy studies involving various cell types10,11,12.
Recent data suggest that SCs obtained from humans more than 2 weeks post mortem generate myotubes in culture13. We therefore intend to assess if implantation of muscle tissue harvested post-mortem into a living host will reverse muscle fiber loss. We have developed a novel technique called MIME to implant donor muscle tissue into skeletal muscle tissue of a living host in order to promote donor-cell-derived myogenesis. MIME involves passing a surgical needle through the host muscle to create a needle track; drawing a small segment of donor muscle tissue through the needle track; leaving the donor tissue embedded in the host muscle; and closing the needle holes with tissue adhesive. After practicing the technique in euthanized mice studied in other experiments, we have now performed MIME in live mice that are immunodeficient and ubiquitously express a green fluorescent protein (GFP), and follow-up at 3 and 14 days post-MIME. At 3 days post-MIME, we confirm that donor mouse (GFP-) EDL muscle implanted into host mouse (GFP+) TA muscle, remains embedded in the host muscle. At 14 days post-MIME, after BaCl2 myotoxin injury to induce damage and myogenesis, we confirm that approximately 5%, 26%, 26% and 43% of the fibers in a single host TA muscle show no host contribution, minimal host contribution, moderate host contribution, and maximal host contribution, respectively. Central nucleation (a marker of degeneration and subsequent regeneration) is seen in approximately 95% of TA muscle fibers after MIME and myotoxin injection.
We study TA muscles 14 days after MIME+BaCl2 because this time point captures the intermediate stage of regeneration, when a majority of the regenerated fibers are centrally nucleated. We study GFP+ mice as hosts for MIME, so that when we eventually transplant human cadaveric muscle into host mice, we will be able to easily distinguish muscle fibers of host and donor origin. We use the mouse EDL muscle as the experimental donor tissue, since single fibers from this muscle have shown greater myogenic potential than TA muscles9. The EDL muscle is also synergistic to the TA muscle and has similar fiber-type composition. Our preliminary data suggest that MIME is capable of facilitating donor-cell-derived myogenesis in the host muscle.

<table><tbody><tr><td>NSG-GFP mice</td><td>The Jackson Laboratory (Bar Harbor, ME)</td><td>Stock #021937</td><td>Immunodeficient host mice that ubiquitously express green fluorescent protein</td></tr><tr><td>C57BL/6J mice</td><td>The Jackson Laboratory (Bar Harbor, ME)&amp;nbsp;</td><td>Stock #000664</td><td>Control donor mice</td></tr><tr><td>Tabletop isoflurane vaporizer&amp;nbsp;</td><td>VetEquip (Livermore, CA)</td><td>Item #901801</td><td>Inhaled anesthesia system</td></tr><tr><td>Magic depilatory crea</td><td>Softsheen Carson (New York, NY)</td><td>N/A</td><td>Razorless hair removal cream</td></tr><tr><td>4-0 Silk, black, braided, non-absorbable sutures</td><td>Roboz Surgical Instrument Co, Inc. (Gaithersburg, MD)</td><td>SUT106631</td><td>Guiding sutures for donor tissue</td></tr><tr><td>VetBond veterinary tissue adhesive</td><td>3M (Maplewood, MN)</td><td>Catalog #1469Sb</td><td>Veterinary tissue adhesive for sutureless skin closure</td></tr><tr><td>Barium chloride&amp;nbsp;</td><td>Ricca Chemical Company (Arlington, TX)</td><td>Product #R0854000-500A 854-16&amp;nbsp;</td><td>Myotoxin to induce muscle damage and stimulate regeneration</td></tr><tr><td>Deltaphase isothermal gel heating pad&amp;nbsp;</td><td>Braintree Scientific (Braintree, MA)</td><td>&amp;nbsp;Item #39DP</td><td>Heating pad to provide thermal support to animals while under anesthesia</td></tr><tr><td>HM525NX cryostat&amp;nbsp;&amp;nbsp;</td><td>ThermoFisher (Waltham, MA)</td><td>Catalog #HM525NX&amp;nbsp;</td><td>Cryostat to make frozen sections of muscle</td></tr><tr><td>Vectashield Antifade Medium</td><td>Vector Laboratories, Inc. (Burlingame, CA)</td><td>Catalog Number: H-1000</td><td>Antifade medium to preserve fluorescence in immunofluorescently labeled samples</td></tr><tr><td>Rabbit anti Desmin Antibody</td><td>Labvision Thermo Scientific (Fremont, CA)</td><td>RB9014P</td><td>Rabbit anti desmin antibody for desmin immunofluorescent labeling</td></tr><tr><td>Goat anti Rabbit Alexa 568 Antibody</td><td>ThermoFisher (Waltham, MA)</td><td>Catalog#: A-21069</td><td>Goat anti rabbit secondary antibody for desmin immunofluorescent labeling</td></tr><tr><td>4&#039;,6-diamidino-2-phenylindole (DAPI)&amp;nbsp;</td><td>Seracare (Milford, MA)</td><td>Catalog #5930-0006 or 71-03-01</td><td>Reagent for fluorescent labeling of nuclei</td></tr><tr><td>Axio Scope.A1 microscope</td><td>Carl Zeiss (Peabody, MA)&amp;nbsp;</td><td>Product #Axio Scope.A1</td><td>Light and fluorescence microscope</td></tr><tr><td>Photoshop CS4</td><td>Adobe Systems (San Jose, CA)</td><td>Photoshop CS4</td><td>Imaging Software for perform image tiling</td></tr><tr><td>Image J</td><td>National Institutes of Health (Bethesda, MD)</td><td>Image J for Windows 64-bit Operating System</td><td>Imaging Software for quantitative fluorescence analysis</td></tr></tbody></table>

minimally invasive muscle embedding (mime) - a novel experimental technique to facilitate donor-cell-mediated myogenesis

Skeletal muscle possesses regenerative capacity due to tissue-resident, muscle-fiber-generating (myogenic) satellite cells (SCs), which can form new muscle fibers under the right conditions. Although SCs can be harvested from muscle tissue and cultured in vitro, the resulting myoblast cells are not very effective in promoting myogenesis when transplanted into host muscle. Surgically exposing the host muscle and grafting segments of donor muscle tissue, or the isolated muscle fibers with their SCs onto host muscle, promotes better myogenesis compared to myoblast transplantation. We have developed a novel technique that we call Minimally Invasive Muscle Embedding (MIME). MIME involves passing a surgical needle through the host muscle, drawing a piece of donor muscle tissue through the needle track, and then leaving the donor tissue embedded in the host muscle so that it may act as a source of SCs for the host muscle. Here we describe in detail the steps involved in performing MIME in an immunodeficient mouse model that expresses a green fluorescent protein (GFP) in all of its cells. Immunodeficiency in the host mouse reduces the risk of immune rejection of the donor tissue, and GFP expression enables easy identification of the host muscle fibers (GFP+) and donor-cell-derived muscle fibers (GFP-). Our pilot data suggest that MIME can be used to implant an extensor digitorum longus (EDL) muscle from a donor mouse into the tibialis anterior (TA) muscle of a host mouse. Our data also suggest that when a myotoxin (barium chloride, BaCl2) is injected into the host muscle after MIME, there is evidence of donor-cell-derived myogenesis in the host muscle, with approximately 5%, 26%, 26% and 43% of the fibers in a single host TA muscle showing no host contribution, minimal host contribution, moderate host contribution, and maximal host contribution, respectively.

At 3 days post-MIME, the donor EDL that is implanted by MIME is contained within the host TA muscle compartment (Figure 2A-C). As expected, the cross sections of the TA muscle from donor mice, studied under fluorescence optics, do not show green fluorescence because they do not express GFP (Figure 2D). In contrast, the cross sections of the TA muscle from host mice that are not implanted with donor tissue, show uniform green fluorescence in the TA muscle fibers, as the fibers express GFP (Figure 2E). In the cross sections of muscles implanted by MIME with donor muscle tissue, there is a line of demarcation between the host muscle fibers (GFP+) and donor muscle fibers (GFP-). The phase contrast images of the visual fields shown in Figure 2D-F are presented in Figure 2E&#39;-F&#39; and suggest that there are indeed muscle fibers present in the regions where there is no GFP signal.
At 14 days post-MIME and BaCl2 injection, by studying serial cross sections of the TA muscle that are left unlabeled or are labeled with antibodies to desmin (Figure 3), we learn that the GFP signal is expressed by all the muscle fibers in the untreated muscle from host mice, but not in the MIME-treated muscle (red desmin labeling detects viable muscle fibers). In the host TA muscle treated with MIME and BaCl2 injection, the donor-cell-derived myogenesis is evident from the presence of many desmin(+) muscle fibers that show no detectable GFP signal (Figure 3C-D, 3 C&#39;-D&#39;). Chimeric muscle fibers arising from the likely fusion of the host and donor myogenic cells can be detected by the low to moderate levels of GFP fluorescence exhibited by these fibers. Numerous chimeric fibers appear across the entire diameter of the TA muscle suggesting that the donor SCs are capable of migrating several hundreds of microns within the epimysium of the host muscle. Quantitation of GFP+ fibers is shown in Figure 3E. Figure 4 shows high magnification images of serial cross sections of an entire MIME+BaCl2 treated TA muscle.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/55731/55731fig1.jpg" /> 
Figure 1. Steps involved in Minimally Invasive Muscle Embedding (MIME). 
MIME is performed under general anesthesia. It involves placing ~10 mg of donor muscle (donor mouse EDL) in Ringer solution and tying the guiding sutures to its ends (A). An 18-gauge needle is passed through the long axis of the host muscle (B) and the donor tissue is drawn through the needle track (C). The donor tissue is left embedded in the host muscle (D), the guiding sutures are cut, and the needle holes are sealed with tissue adhesive (E). The sealed needle wounds are indicated with arrows (F). <a href="http://cloudflare.jove.com/files/ftp_upload/55731/55731fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/55731/55731fig2.jpg" /> 
Figure 2. Studies of the TA Muscle 3 Days After MIME. 
Host muscle collected 3 days after MIME; note needle marks on host TA (arrows; A-B). Data further confirm that the embedded donor mouse EDL is ensconced within the TA muscle compartment (B-C). Fluorescence images of TA muscle cross sections show no green fluorescence in&#160;wild-type TA muscle (D), bright green fluorescence in NSG-GFP TA muscle (E), and a distinction between host and donor muscle in NSG-GFP TA muscle at 3 days post-MIME (F). The phase contrast images of the visual fields in D-F are shown in D&#39;-F&#39;, respectively. The red line in panels F and F&#39; shows the line of demarcation between the host and donor tissue. Scale bar = 50 &#181;m. <a href="http://cloudflare.jove.com/files/ftp_upload/55731/55731fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/55731/55731fig3.jpg" /> 
Figure 3. Studies of TA Muscle 14 Days after MIME. 
Data collected 14 days post-MIME are presented. The red signal is from immunofluorescent labeling of desmin (a positive signal for desmin denotes that myofibers are viable), the blue signal is from DAPI (stains nuclei), and the green signal is from GFP. In Control TA muscle (right hindlimb) harvested from the host mouse, as expected, nearly all myofibers are positive for desmin, suggesting that these myofibers are viable (A; red signal). Additionally, based on DAPI staining, it is evident that myonuclei of nearly all myofibers are peripherally located, as would be expected in healthy muscle (A; blue signal). Serial sections of the Control TA muscle show that, nearly all muscle fibers are bright green, implying that they are positive for GFP. In MIME+BaCl2 -treated TA muscle (left hindlimb), donor-cell-mediated myogenesis is evident from the presence of many desmin(+) muscle fibers that show no detectable GFP fluorescence (C-D, C&#39;-D&#39;). Desmin(+) muscle fibers with low to moderate GFP fluorescence (chimeric muscle fibers) are present across the diameter of the entire TA muscle, suggesting that, MIME provides donor SCs that can migrate within the epimysium of the TA muscle and promote donor-cell-derived myogenesis. A&#39;-D&#39; are high-magnification images of the regions within the blue boxes in A-D. Quantitation of GFP(+) fibers and centrally nucleated fibers are shown in E. Scale bars = 100 &#181;m (A-D) and 50 &#181;m (A&#39;-D&#39;). <a href="http://cloudflare.jove.com/files/ftp_upload/55731/55731fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/55731/55731fig4.jpg" /> 
Figure 4. Evidence of Widespread Damage and Regeneration 14 Days after MIME and BaCl2 Injection. 
High magnification, serial cross sections of an entire MIME+BaCl2 treated TA muscle are presented. The data show that many muscle fibers, which are moderately or strongly GFP+ have centrally located nuclei (A-B; red signal in A is from desmin, blue signal in A is from DAPI, and green signal in B is from GFP). These data suggest that degeneration and regeneration after BaCl2 injection does not affect GFP expression. In this context, the presence of centrally nucleated muscle fibers in MIME+BaCl2 treated TA muscle, with little-to-no GFP expression, suggests that these fibers are the likely result of myogenesis (or regeneration) with significant contribution from GFP- myogenic cells. These observations can be further verified in high magnification images of selected fields (C-F; C and D, and E and F, respectively, are overlapping regions from serial cross sections; color coding of image borders denote the location of those regions in A and B). Scale bars = 100 &#181;m (A-B) and 50 &#181;m (C-F). <a href="http://cloudflare.jove.com/files/ftp_upload/55731/55731fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Minimally Invasive Muscle Embedding MIME - A Novel Experimental Technique to Facilitate Donor-Cell-Mediated Myogenesis at JoVE.com

Minimally Invasive Muscle Embedding MIME - A Novel Experimental Technique to Facilitate Donor-Cell-Mediated Myogenesis

We describe a novel experimental technique that we call Minimally Invasive Muscle Embedding (MIME), which is based on the evidence that skeletal muscle tissue contains viable myogenic cells that can facilitate donor-cell-mediated myogenesis when implanted into a host muscle.

Minimally Invasive Muscle Embedding (MIME) - A Novel Experimental Technique to Facilitate Donor-Cell-Mediated Myogenesis

Skeletal muscle possesses regenerative capacity due to tissue-resident, muscle-fiber-generating (myogenic) satellite cells (SCs), which can form new ...

minimally-invasive-muscle-embedding-mime-novel-experimental-technique

Universidad de Cartagena UDEC

Research

JoVE Journal

Medicine

7.7K Views.  Wayne State University. We describe a novel experimental technique that we call Minimally Invasive Muscle Embedding (MIME), which is based on the evidence that skeletal muscle tissue contains viable myogenic cells that can facilitate donor-cell-mediated myogenesis when implanted into a host muscle.

Video: Minimally Invasive Muscle Embedding MIME - A Novel Experimental Technique to Facilitate Donor-Cell-Mediated Myogenesis

Transplantation of Induced Pluripotent Stem Cell-derived Mesoangioblast-like Myogenic Progenitors in Mouse Models of Muscle Regeneration

Patient-derived iPSCs could be an invaluable source of cells for future autologous cell therapy protocols. iPSC-derived myogenic stem/progenitor cells similar to pericyte-derived mesoangioblasts (iPSC-derived mesoangioblast-like stem/progenitor cells: IDEMs) can be established from iPSCs generated from patients affected by different forms of muscular dystrophy. Patient-specific IDEMs can be genetically corrected with different strategies (e.g. lentiviral vectors, human artificial chromosomes) and enhanced in their myogenic differentiation potential upon overexpression of the myogenesis regulator MyoD. This myogenic potential is then assessed in vitro with specific differentiation assays and analyzed by immunofluorescence. The regenerative potential of IDEMs is further evaluated in vivo, upon intramuscular and intra-arterial transplantation in two representative mouse models displaying acute and chronic muscle regeneration. The contribution of IDEMs to the host skeletal muscle is then confirmed by different functional tests in transplanted mice. In particular, the amelioration of the motor capacity of the animals is studied with treadmill tests. Cell engraftment and differentiation are then assessed by a number of histological and immunofluorescence assays on transplanted muscles. Overall, this paper describes the assays and tools currently utilized to evaluate the differentiation capacity of IDEMs, focusing on the transplantation methods and subsequent outcome measures to analyze the efficacy of cell transplantation.

Induced pluripotent stem cell (iPSC)-derived myogenic progenitors are promising candidates for cell therapy strategies to treat muscular dystrophies. This protocol describes transplantation and functional measurements required to evaluate the engraftment and differentiation of iPSC-derived mesoangioblasts (a type of muscle progenitors) in mouse models of acute and chronic muscle regeneration.

Patient-derived iPSCs could be an invaluable source of cells for future autologous cell therapy protocols. iPSC-derived myogenic stem/progenitor cells ...

Bioengineering

In Vitro Differentiation of Mature Myofibers for Live Imaging

Skeletal muscles are composed of myofibers, the biggest cells in the mammalian body and one of the few syncytia. How the complex and evolutionarily conserved structures that compose it are assembled remains under investigation. Their size and physiological features often constrain manipulation and imaging applications. The culture of immortalized cell lines is widely used, but it can only replicate the early steps of differentiation.
Here, we describe a protocol that enables easy genetic manipulation of myofibers originating from primary mouse myoblasts. After one week of differentiation, the myofibers display contractility, aligned sarcomeres and triads, as well as peripheral nuclei. The entire differentiation process can be followed by live imaging or immunofluorescence. This system combines the advantages of the existing ex vivo and in vitro protocols. The possibility of easy and efficient transfection as well as the ease of access to all differentiation stages broadens the potential applications. Myofibers can subsequently be used not only to address relevant developmental and cell biology questions, but also to reproduce muscle disease phenotypes for clinical applications.

In Vitro Differentiation of Mature Myofibers for Live Imaging

Muscle cells are among the most complex eukaryotic cells. We present a protocol for the in vitro differentiation of highly mature myofibers that allows for genetic manipulation and clear imaging during all developmental stages.

Skeletal muscles are composed of myofibers, the biggest cells in the mammalian body and one of the few syncytia. How the complex and evolutionarily ...

Developmental Biology

Molecular Imaging to Target Transplanted Muscle Progenitor Cells

Duchenne muscular dystrophy (DMD) is a severe genetic neuromuscular disorder that affects 1 in 3,500 boys, and is characterized by progressive muscle degeneration1, 2. In patients, the ability of resident muscle satellite cells (SCs) to regenerate damaged myofibers becomes increasingly inefficient4. Therefore, transplantation of muscle progenitor cells (MPCs)/myoblasts from healthy subjects is a promising therapeutic approach to DMD. A major limitation to the use of stem cell therapy, however, is a lack of reliable imaging technologies for long-term monitoring of implanted cells, and for evaluating its effectiveness. Here, we describe a non-invasive, real-time approach to evaluate the success of myoblast transplantation. This method takes advantage of a unified fusion reporter gene composed of genes (firefly luciferase [fluc], monomeric red fluorescent protein [mrfp] and sr39 thymidine kinase [sr39tk]) whose expression can be imaged with different imaging modalities9, 10. A variety of imaging modalities, including positron emission tomography (PET), single-photon emission computed tomography (SPECT), magnetic resonance imaging (MRI), optical imaging, and high frequency 3D-ultrasound are now available, each with unique advantages and limitations11. Bioluminescence imaging (BLI) studies, for example, have the advantage of being relatively low cost and high-throughput. It is for this reason that, in this study, we make use of the firefly luciferase (fluc) reporter gene sequence contained within the fusion gene and bioluminescence imaging (BLI) for the short-term localization of viable C2C12 myoblasts following implantation into a mouse model of DMD (muscular dystrophy on the X chromosome [mdx] mouse)12-14. Importantly, BLI provides us with a means to examine the kinetics of labeled MPCs post-implantation, and will be useful to track cells repeatedly over time and following migration. Our reporter gene approach further allows us to merge multiple imaging modalities in a single living subject; given the tomographic nature, fine spatial resolution and ability to scale up to larger animals and humans10,11, PET will form the basis of future work that we suggest may facilitate rapid translation of methods developed in cells to preclinical models and to clinical applications.

A non-invasive means to evaluate the success of myoblast transplantation is described. The method takes advantage of a unified fusion reporter gene composed of genes whose expression can be imaged with different imaging modalities. Here, we make use of a fluc reporter gene sequence to target cells via bioluminescence imaging.

Duchenne muscular dystrophy (DMD) is a severe genetic neuromuscular disorder that affects 1 in 3,500 boys, and is characterized by progressive muscle ...

Direct Reprogramming of Human Fibroblasts into Myoblasts to Investigate Therapies for Neuromuscular Disorders

Investigations into both the pathophysiology and therapeutic targets in muscular dystrophies have been hampered by the limited proliferative capacity of human myoblasts. Several mouse models have been created but they either do not truly represent the human physiopathology of the disease or are not representative of the broad spectrum of mutations found in humans. The immortalization of human primary myoblasts is an alternative to this limitation; however, it is still dependent on muscle biopsies, which are invasive and not easily available. In contrast, skin biopsies are easier to obtain and less invasive to patients. Fibroblasts derived from skin biopsies can be immortalized and transdifferentiated into myoblasts, providing a source of cells with excellent myogenic potential. Here, we describe a fast and direct reprogramming method of fibroblast into a myogenic lineage. Fibroblasts are transduced with two lentiviruses: hTERT to immortalize the primary culture and a tet-inducible MYOD, which upon the addition of doxycycline, induces the conversion of fibroblasts into myoblasts and then mature myotubes, which express late differentiation markers. This quick transdifferentiation protocol represents a powerful tool to investigate pathological mechanisms and to investigate innovative gene-based or pharmacological biotherapies for neuromuscular disorders.

This protocol describes the conversion of skin fibroblasts into myoblasts and their differentiation into myotubes. The cell lines are derived from patients with neuromuscular disorders and can be used to investigate pathological mechanisms and to test therapeutic strategies.

Investigations into both the pathophysiology and therapeutic targets in muscular dystrophies have been hampered by the limited proliferative capacity of ...

Genetics

Tracking Dynamics of Muscle Engraftment in Small Animals by In Vivo Fluorescent Imaging

Muscular dystrophies are a group of degenerative muscle diseases characterized by progressive loss of contractile muscle cells. Currently, there is no curative treatment available. Recent advances in stem cell biology have generated new hopes for the development of effective cell based therapies to treat these diseases. Transplantation of various types of stem cells labeled with fluorescent proteins into muscles of dystrophic animal models has been used broadly in the field. A non-invasive technique with the capability to track the transplanted cell fate longitudinally can further our ability to evaluate muscle engraftment by transplanted cells more accurately and efficiently.
In the present study, we demonstrate that in vivo fluorescence imaging is a sensitive and reliable method for tracking transplanted GFP (Green Fluorescent Protein)-labeled cells in mouse skeletal muscles. Despite the concern about background due to the use of an external light necessary for excitation of fluorescent protein, we found that by using either nude mouse or eliminating hair with hair removal reagents much of this problem is eliminated. Using a CCD camera, the fluorescent signal can be detected in the tibialis anterior (TA) muscle after injection of 5 x 105 cells from either GFP transgenic mice or eGFP transduced myoblast culture. For more superficial muscles such as the extensor digitorum longus (EDL), injection of fewer cells produces a detectable signal. Signal intensity can be measured and quantified as the number of emitted photons per second in a region of interest (ROI). Since the acquired images show clear boundaries demarcating the engrafted area, the size of the ROI can be measured as well. If the legs are positioned consistently every time, the changes in total number of photons per second per muscle and the size of the ROI reflect the changes in the number of engrafted cells and the size of the engrafted area. Therefore the changes in the same muscle over time are quantifiable. In vivo fluorescent imaging technique has been used primarily to track the growth of tumorogenic cells, our study shows that it is a powerful tool that enables us to track the fate of transplanted stem cells.

Tracking Dynamics of Muscle Engraftment in Small Animals by In Vivo Fluorescent Imaging

We describe an in vivo fluorescence imaging protocol to monitor muscle regeneration by GFP-labeled myoblasts after transplantation into skeletal muscles of both healthy and dystrophic mice. This protocol can be adapted to study muscle regeneration by transplantation of other types of cells and in other muscular conditions as well.

Muscular dystrophies are a group of degenerative muscle diseases characterized by progressive loss of contractile muscle cells. Currently, there is no ...

Biology

Performing Human Skeletal Muscle Xenografts in Immunodeficient Mice

Treatment effects observed in animal studies often fail to be recapitulated in clinical trials. While this problem is multifaceted, one reason for this failure is the use of inadequate laboratory models. It is challenging to model complex human diseases in traditional laboratory organisms, but this issue can be circumvented through the study of human xenografts. The surgical method we describe here allows for the creation of human skeletal muscle xenografts, which can be used to model muscle disease and to carry out preclinical therapeutic testing. Under an Institutional Review Board (IRB)-approved protocol, skeletal muscle specimens are acquired from patients and then transplanted into NOD-Rag1null IL2r&gamma;null (NRG) host mice. These mice are ideal hosts for transplantation studies due to their inability to make mature lymphocytes and are thus unable to develop cell-mediated and humoral adaptive immune responses. Host mice are anaesthetized with isoflurane, and the mouse tibialis anterior and extensor digitorum longus muscles are removed. A piece of human muscle is then placed in the empty tibial compartment and sutured to the proximal and distal tendons of the peroneus longus muscle. The xenografted muscle is spontaneously vascularized and innervated by the mouse host, resulting in robustly regenerated human muscle that can serve as a model for preclinical studies.

Complex human diseases can be challenging to model in traditional laboratory model systems. Here, we describe a surgical approach to model human muscle disease through the transplantation of human skeletal muscle biopsies into immunodeficient mice.

Treatment effects observed in animal studies often fail to be recapitulated in clinical trials. While this problem is multifaceted, one reason for this ...

Isolation and Immortalization of Patient-derived Cell Lines from Muscle Biopsy for Disease Modeling

The generation of patient-specific cell lines represents an invaluable tool for diagnostic or translational research, and these cells can be collected from skin or muscle biopsy tissue available during the patient&#8217;s diagnostic workup. In this protocol, we describe a technique for live cell isolation from small amounts of muscle or skin tissue for primary cell culture. Additionally, we provide a technique for the immortalization of myogenic cell lines and fibroblast cell lines from primary cells. Once cell lines are immortalized, substantial expansion of patient-derived cells can be achieved. Immortalized cells are amenable to many downstream applications, including drug screening and in vitro correction of the genetic mutation. Altogether, these protocols provide a reliable tool to generate and preserve patient-derived cells for downstream applications.

This protocol describes techniques for live cell isolation and primary culture of myogenic and fibroblast cell lines from muscle or skin tissue. A technique for the immortalization of these cell lines is also described. Altogether, these protocols provide a reliable tool to generate and preserve patient-derived cells for downstream applications.

The generation of patient-specific cell lines represents an invaluable tool for diagnostic or translational research, and these cells can be collected ...

Isolation, Culture, and Transplantation of Muscle Satellite Cells

Muscle satellite cells are a stem cell population required for postnatal skeletal muscle development and regeneration, accounting for 2-5% of sublaminal nuclei in muscle fibers. In adult muscle, satellite cells are normally mitotically quiescent. Following injury, however, satellite cells initiate cellular proliferation to produce myoblasts, their progenies, to mediate the regeneration of muscle. Transplantation of satellite cell-derived myoblasts has been widely studied as a possible therapy for several regenerative diseases including muscular dystrophy, heart failure, and urological dysfunction. Myoblast transplantation into dystrophic skeletal muscle, infarcted heart, and dysfunctioning urinary ducts has shown that engrafted myoblasts can differentiate into muscle fibers in the host tissues and display partial functional improvement in these diseases. Therefore, the development of efficient purification methods of quiescent satellite cells from skeletal muscle, as well as the establishment of satellite cell-derived myoblast cultures and transplantation methods for myoblasts, are essential for understanding the molecular mechanisms behind satellite cell self-renewal, activation, and differentiation. Additionally, the development of cell-based therapies for muscular dystrophy and other regenerative diseases are also dependent upon these factors.

However, current prospective purification methods of quiescent satellite cells require the use of expensive fluorescence-activated cell sorting (FACS) machines. Here, we present a new method for the rapid, economical, and reliable purification of quiescent satellite cells from adult mouse skeletal muscle by enzymatic dissociation followed by magnetic-activated cell sorting (MACS). Following isolation of pure quiescent satellite cells, these cells can be cultured to obtain large numbers of myoblasts after several passages. These freshly isolated quiescent satellite cells or ex vivo expanded myoblasts can be transplanted into cardiotoxin (CTX)-induced regenerating mouse skeletal muscle to examine the contribution of donor-derived cells to regenerating muscle fibers, as well as to satellite cell compartments for the examination of self-renewal activities.

The isolation and culture of a pure population of quiescent satellite cells, a muscle stem cell population, is essential to the understanding of muscle stem cell biology and regeneration, as well as stem cell transplantation for therapies in muscular dystrophy and other degenerative diseases.&#160;

Muscle satellite cells are a stem cell population required for postnatal skeletal muscle development and regeneration, accounting for 2-5% of sublaminal ...

Single Myofiber Isolation and Culture from a Murine Model of Emery-Dreifuss Muscular Dystrophy in Early Post-Natal Development

Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) is caused by mutations in the LMNA gene, which encodes the A-type nuclear lamins, intermediate filament proteins that sustain the nuclear envelope and the components of the nucleoplasm. We recently reported that muscle wasting in EDMD can be ascribed to intrinsic epigenetic dysfunctions affecting muscle (satellite) stem cells regenerative capacity. Isolation and culture of single myofibers is one of the most physiological ex-vivo approaches to monitor satellite cells behavior within their niche, as they remain between the basal lamina surrounding the fiber and the sarcolemma. Therefore, it represents an invaluable experimental paradigm to study satellite cells from a variety of murine models. Here, we describe a re-adapted method to isolate intact and viable single myofibers from post-natal hindlimb muscles (Tibialis Anterior, Extensor Digitorum Longus, Gastrocnemius and Soleus). Following this protocol, we were able to study satellite cells from Lamin &#916;8-11 -/- mice, a severe EDMD murine model, at only 19 days after birth.
We detail the isolation procedure, as well as the culture conditions for obtaining a good amount of myofibers and their associated satellite-cells-derived progeny. When cultured in growth-factors rich medium, satellite cells derived from wild type mice activate, proliferate, and eventually differentiate or undergo self-renewal. In homozygous Lamin &#916;8-11 -/- mutant mice these capabilities are severely impaired.
This technique, if strictly followed, allows to study all processes linked to the myofiber-associated satellite cell even in early post-natal developmental stages and in fragile muscles.

Here, we propose a method to efficiently obtain single muscle fibers at early post-natal developmental stages from homozygous mutant Lamin &#916;8-11 mouse model, a very severe model for Emery-Dreifuss muscular dystrophy (EDMD).

Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) is caused by mutations in the LMNA gene, which encodes the A-type nuclear lamins, intermediate ...

DNA Electroporation, Isolation and Imaging of Myofibers

Mature muscle has a unique structure that is amenable to live cell imaging. Herein, we describe the experimental protocol for expressing fluorescently labeled proteins in the flexor digitorum brevis (FDB) muscle. Conditions have been optimized to provide a large number of high quality myofibers expressing the electroporated plasmid while minimizing muscle damage. The method employs fluorescent tags on various proteins. Combining this expression method with high resolution confocal microscopy permits live cell imaging, including imaging after laser-induced damage. Fluorescent dyes combined with imaging of fluorescently-tagged proteins provides information regarding the basic structure of muscle and its response to stimuli.

This protocol utilizes electroporation to introduce and express fluorescently labeled proteins in mouse muscle fibers. Following recovery after electroporation, fibers are isolated. Individual fibers are then imaged using high resolution confocal microscopy to visualize muscle structure.

Mature muscle has a unique structure that is amenable to live cell imaging. Herein, we describe the experimental protocol for expressing fluorescently ...

Minimally Invasive Muscle Embedding (MIME) - A Novel Experimental Technique to Facilitate Donor-Cell-Mediated Myogenesis

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Transplantation of Induced Pluripotent Stem Cell-derived Mesoangioblast-like Myogenic Progenitors in Mouse Models of Muscle Regeneration

In Vitro Differentiation of Mature Myofibers for Live Imaging

Molecular Imaging to Target Transplanted Muscle Progenitor Cells

Direct Reprogramming of Human Fibroblasts into Myoblasts to Investigate Therapies for Neuromuscular Disorders

Tracking Dynamics of Muscle Engraftment in Small Animals by In Vivo Fluorescent Imaging

Performing Human Skeletal Muscle Xenografts in Immunodeficient Mice

Isolation and Immortalization of Patient-derived Cell Lines from Muscle Biopsy for Disease Modeling

Isolation, Culture, and Transplantation of Muscle Satellite Cells

Single Myofiber Isolation and Culture from a Murine Model of Emery-Dreifuss Muscular Dystrophy in Early Post-Natal Development

DNA Electroporation, Isolation and Imaging of Myofibers