S.B.&#39;s PhD grant is funded by Region Bretagne (ARED grant Number COH20020) and Sorbonne Universit&#233;. I.T.is PhD grant is funded by Region Bretagne (ARED grant Number COH18020) and the Norvegian NMBU University. This project has received financial support from the CNRS through the MITI interdisciplinary programs.&#160;MRic is member of the national infrastructure France-BioImaging supported by the French National Research Agency (ANR-10-INBS-04).

1. Production of Saccharina latissima gametophytes
<ol>
	<li>Collect mature sporophytes of S. latissima from the wild as previously described20,21. Ensure that the selected sporophytes are devoid of epiphytes (small organisms visible on the blade&#39;s surface) or internal parasites (found in the bleached areas or spots on the blade). </li>
	<li>Using a scalpel, cut the darkest part in the center of the blade (fertile spore-producing tissue22) into 1-5 square pieces (1 cm&#178;), avoiding any bleached spots, if present.</li>
	<li>Remove any remaining epiphytes by gently cleaning the cut pieces with the back of a scalpel and some absorbent paper.</li>
	<li>Place the cleaned pieces in a glass dish filled with sterile natural seawater (see Table of Materials) for 45 min to release spores following previously published report22.</li>
	<li>Remove the blade pieces and filter the seawater through a 40 &#181;m cell strainer to remove debris or unwanted organisms.</li>
	<li>Dilute the spores in the filtrate to a 20-40 spores/mL concentration in plastic Petri dishes22.</li>
	<li>Place the spore solution in a culture cabinet (see Table of Materials) configured with the optimal culture conditions (13 &#176;C, 24 &#181;E.m-2.s-1, photoperiod 16:8 L:D).</li>
	<li>Allow the spores to germinate and develop into gametophytes. 
	NOTE: Spore germination is visible after 2 days in the cabinet, and the first cell division of the gametophytic cells usually occurs within the following 48 h.</li>
	<li>Replace the growth medium after 5 days with micro-filtered natural seawater enriched with a 0.5x Provasoli solution (NSW1/2) (see Table of Materials). 
	NOTE: To avoid repeating these steps, specific male and female gametophytes can be selected and vegetatively propagated for several months. The gametophytes remain vegetative when grown under red light (4 &#181;E.m-2.s-1 with a wavelength of at least 580 nm)23 in the same culture conditions described above (step 1.7).</li>
</ol>
2. Fragmentation and induction of oogenesis
<ol>
	<li>Harvest gametophytes with a cell scraper.</li>
	<li>Using a small plastic pestle, crush the collected gametophytes in a 1.5 mL tube into 4-5-celled pieces.</li>
	<li>Fill the tube with 1 mL NSW1/2 (step 1.9).</li>
	<li>Add 2.5 &#181;L of the crushed gametophyte solution into 3 mL of natural seawater enriched with 1x Provasoli solution (NSW) and place them in a Petri dish. 
	NOTE: A 25 mm, glass-bottomed Petri dish is recommended for easier handling.</li>
	<li>Place the prepared dishes in a culture cabinet and induce gametogenesis at 13 &#176;C under white light with an intensity of 24 &#181;E.m-2.s-1&#160;(dim light, photoperiod 16:8 L:D). 
	NOTE: The first gametangia (female oogonia and male archegonia) can be observed after 5 days. The male is hyper-branched with small cells, and the female is composed of larger cells forming long filaments15,22. The first eggs are observed ~10 days later, and the first division of zygotes usually occurs within the following 2 days.</li>
	<li>Six days after observing the first eggs, transfer the dishes to brighter white light conditions: 50 &#181;E.m-2.s-1, photoperiod 16:8 L:D, still at 13 &#176;C.</li>
</ol>
3. Image acquisition for selecting embryos for ablation and monitoring subsequent growth
<ol>
	<li>Image the entire Petri dish to (re)locate the embryos selected during the ablation step (no need to return the dish to the ocular microscope) and monitor the subsequent development of the selected embryos. 
	NOTE: Use an inverted laser scanning confocal microscope (see Table of Materials) for imaging (Figure 1), and the laser ablation is described in step 5.</li>
	<li>Place the Petri dish on the stage and orientate it with a visual mark (e.g., draw a line with a permanent marker).</li>
	<li>Use the 10x/0.45 objective to focus on an embryo. Record the position of the four cardinal points of the Petri dish.</li>
	<li>Start the tile scan. Acquire transmitted/fluorescent images of the whole Petri dish at low resolution: 256 x 256 pixels, a pixel dwell time of 1.54 &#181;s with bidirectional scanning, and a digital zoom of 0.6x using a 561 nm laser at 1.2% transmission. 
	NOTE: The scan time for a whole 2.5 cm Petri dish is ~6 min for 225 tiles (Figure 2). Here, the 561 nm laser was used for transmission and fluorescence imaging.&#160;The fluorescence signal was collected between 580&#8211;720 nm on the confocal photomultipliers (PMT) and the transmitted light was collected on the transmitted PMT. The 561 nm laser can also monitor chlorophyll at this step, but it is unnecessary because it only helps distinguish the signal noise and the organisms correctly.</li>
	<li>Save the tile scan image and keep it open in the image acquisition software (see Table of Materials) window.</li>
	<li>Change the objective, do not remove the Petri dish. 
	NOTE: The 40x/1.2 water objective was moved to the side of the stage so that the immersion medium (water) could be added to the objective without moving the Petri dish from its initial position.</li>
	<li>Navigate through the previously acquired tile scan image to select the appropriate embryo. Once an embryo has been identified on this image, move the stage to the exact position of the embryo and acquire transmitted/fluorescent images of that embryo at high resolution. 
	NOTE: High-resolution settings: 512 x 512 pixels, 0.130 &#181;m/pixel, 0.208 &#181;s pixel dwell time with mono-directional scanning and 2x digital zoom using a 561 nm laser at 0.9% transmission.</li>
	<li>Annotate the tile scan image for each embryo candidate for laser ablation (Figure 2B) and proceed to the laser ablation step.</li>
</ol>
4. Laser calibration
<ol>
	<li>Calibrate the laser and synchronize the image acquisition software with the laser-driver software in the &#34;Click &#38; Fire mode&#34; and a pulsed 355 nm laser. 
	NOTE: This step is crucial to ensure perfect synchronization between the mouse cursor&#39;s position in the laser-driver software (see Table of Materials) with the position in the live image of the acquisition software.</li>
	<li>Open the laser-driver software package and click on Live in the image acquisition software package.</li>
	<li>Synchronize both software packages by clicking on Start acquisition in the laser-driver software package. The live image is now also recorded in the UV laser-driver software.</li>
	<li>Define an area of interest (AOI) by clicking on Choose AOI button and clicking on the edges of the image (right, left, top and bottom) in the UV laser-driver software package. 
	NOTE: After this calibration step, the settings for pixel size, image format, and zoom in the acquisition software package must remain constant.</li>
	<li>Select an empty area on the dish and lower the level of the stage to 20 &#181;m below the sample focal plane to focus on the glass bottom.</li>
	<li>Set the ablation laser and imaging laser trajectories by clicking on Start calibration and choose Manual calibration.</li>
	<li>Select a laser power high enough to see a black dot in the center of the live image corresponding to the hole in the glass coverslip (all the shutters must be open).</li>
	<li>Click on this central black dot with the mouse cursor and click on 18 additional dots proposed by the software to complete the alignment procedure.</li>
	<li>Check the calibration in the &#34;Click &#38; Fire mode&#34; on the same coverslip. 
	NOTE: Laser calibration depends on the imaging parameters. Once the laser has been calibrated, ensure that the imaging parameters (i.e., 512 x 512 pixels, 0.130 &#181;m/pixel, 0.208 &#181;s pixel dwell time with mono-directional scanning and 2x digital zoom) have not changed.</li>
</ol>
5. Laser ablation
<ol>
	<li>Select an embryo of interest. Start a time-lapse recording in the image-acquisition software.</li>
	<li>Acquire transmitted/fluorescence images with a 40x/1.2 W objective at high resolution (i.e., 512 x 512 pixels, 0.130 &#181;m/pixel, 1.54 &#181;s pixel dwell time with mono-directional scanning and 2x digital zoom using a 561 nm laser at 0.9% transmission). Acquire the time-lapse recording at maximum speed.</li>
	<li>Zoom out of the area at the beginning of the time-lapse recording. Zoom in on the AOI.</li>
	<li>Use the &#34;Click &#38; Fire&#34; function of the laser-driver software to apply the damaging irradiation on the cell of interest in the embryo. Use the following parameters: 45% laser transmission (corresponding to a maximum of 40 &#181;W) and 1 ms pulse time duration (step 4). 
	NOTE: Video recording during the laser shooting is recommended.</li>
	<li>Under 688 nm, monitor the ejection of autofluorescent chloroplasts from the cytoplasm.</li>
	<li>If cell contents remain in the cell, use the &#34;Click &#38; Fire&#34; function once more to increase the size of the breach in the cell. Repeat, keeping the number of shots to a minimum until most of the cell contents have been released.</li>
	<li>Stop the time-lapse recording after the embryo has stabilized (i.e., no further intracellular movement can be detected (~1-5 min).</li>
	<li>Update the annotation on the tile scan image, if necessary.</li>
</ol>
6. Monitoring the growth of irradiated embryos
NOTE: Monitoring is carried out over several days.
<ol>
	<li>Determine the survival rate by monitoring the number of embryos that develop after laser ablation and compare them to those that die. 
	NOTE: Some embryos die immediately after ablation for various reasons. A high and rapid mortality rate is usually a sign of inappropriate laser parameters or higher/longer exposure to stress during the experiment or subsequent transport.</li>
	<li>Determine the growth delay by measuring the length of the laser-shot embryos every day and comparing it to intact embryos. 
	NOTE: The growth rate of laser-shot organisms is generally slower than that of untreated organisms. However, some (inappropriate) laser settings can inhibit growth for more than a week, with growth resuming after that.</li>
	<li>Find out the adjacent damage by monitoring the reaction of cells adjacent to the ablated cells. In some cases, post-burst depressurization may cause neighboring cells to burst.</li>
	<li>Check for microbe contaminations. Monitor the growth of microalgae and bacteria in the medium. If an unusual level of microbes are present in the dish, then discard it and repeat the protocol from step 2 or step 3. 
	NOTE: After laser ablation, damaged S. latissima embryos are already highly stressed, and additional external stress can cause increased mortality. Bacterial or viral outbreaks are possible because the treated embryos cannot grow in axenic conditions.</li>
	<li>Check the global development of the shot organisms by studying the phenotype and understanding the role in the development of the targeted region.</li>
</ol>

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The authors have nothing to disclose.

Local cellular laser ablation allows for temporal and spatial ablation with a high level of precision. However, its efficiency can be hampered by the non-accessibility of target cells; for example, all the cells are of a three-dimensional embryo. This protocol was developed on the embryo of the alga Saccharina latissima, which develops a monolayered lamina in which all cells can be easily distinguished and destroyed individually with a laser beam.
Laser power and wavelength</s...

Laser ablation has been used for decades to study embryo development. Irradiating embryo cells with a laser beam makes it possible to monitor the regenerative potential and the modification of the cell lineage during embryogenesis and investigate the impact of targeted ablation on cell division and cell fate. The model organisms used in laser ablation methods are typically animals, such as insects1,2, nematodes3,4, vertebrates5,6, and occasionally plants7,8. In addition, a laser micro-ablation approach was used on the brown alga Fucus in 1994 and 1998 to demonstrate the role of the cell wall in the photopolarization of the early embryo9,10.
Brown algae belong to the group Stramenopiles, diverged at the root of the eukaryotic tree 1.6 billion years ago. As a result, they are phylogenetically independent of other multicellular organisms, such as animals and plants11. Saccharina latissima belongs to the order Laminariales, more commonly known as kelps, and they are among the largest organisms on earth, reaching sizes of over 30 m. Saccharina sp.&#160;is a large seaweed used for many applications such as food and feed, and its polysaccharides are extracted for use in the agricultural, pharmacological and cosmetic industries worldwide12,13. Its cultivation, mainly in Asia and more recently in Europe, requires the preparation of embryos in hatcheries before releasing juveniles in the open sea. Like all kelps, it&#160;has a biphasic life cycle composed of a microscopic gametophytic phase, during which a haploid gametophyte grows and produces gametes for fertilization, and a diploid macroscopic sporophytic phase, where a large planar blade develops from its holdfast attached to the seafloor or rocks. The sporophyte releases haploid spores at maturity, thereby completing the life cycle14,15,16.
S. latissima presents some interesting&#160;morphological features17. Its embryo develops as a monolayered planar sheet15,18,19&#160;before acquiring a multilayered structure coinciding with the emergence of different tissue types. In addition, Laminariales is one of the only taxa of brown algae whose embryos remain attached to their maternal gametophytic tissue (Desmarestiales and Sporochnales do too15). This feature offers the opportunity to study the role of maternal tissue in this developmental process and compare maternal control mechanisms in brown algae with those in animals and plants.
This article presents the first complete protocol for laser ablation in an early kelp embryo. This protocol involving UV ns-pulsed technique results in the specific destruction of individual embryo cells to study their respective roles during embryogenesis. The procedure offers a reliable approach for investigating cell interactions and cell fate during embryogenesis in Laminariales.

<table><tbody><tr><td>25 mm glass bottom petri dish</td><td>NEST</td><td>801001</td><td></td></tr><tr><td>Autoclaved sea water</td><td>-</td><td></td><td>Collected offshore near the Astan buoy (48&amp;deg;44.934 N 003&amp;deg;57.702 W) close to Roscoff, France, at a depth of 20 m.</td></tr><tr><td>Cell scraper</td><td>MED 2</td><td>83.3951</td><td></td></tr><tr><td>Cell strainer 40 &amp;micro;m</td><td>Corning / Falcon</td><td>352340</td><td></td></tr><tr><td>Culture cabinets</td><td>Snijders Scientific Plant Growth Cabinet ECD01</td><td></td><td>Any other brand is suitable provided that the light intensity, the photoperiod and the temperature can be controlled.</td></tr><tr><td>LSM 880 Zeiss confocal microscope</td><td>Carl Zeiss microscopy, Jena, Germany</td><td></td><td>Ablation and imaging were performed using a 40x/1.2 water objective</td></tr><tr><td>Pellet pestles</td><td>Sigma Aldrich</td><td>Z359947</td><td>Blue polypropylene (autoclavable)</td></tr><tr><td>Provasoli supplement</td><td>-</td><td></td><td>Recipe is available here: http://www.sb-roscoff.fr/sites/www.sb-roscoff.fr/files/documents/station-biologique-roscoff-preparation-du-provasoli-2040.pdf</td></tr><tr><td>Pulsed 355 laser (UGA-42 Caliburn 355/25)</td><td>Rapp OptoElectronic, Wedel, Germany</td><td></td><td></td></tr><tr><td>Scalpel</td><td>Paramount</td><td>PDSS 11</td><td></td></tr><tr><td>SysCon software</td><td>Rapp OptoElectronic, Wedel, Germany</td><td></td><td>Laser-driver software</td></tr><tr><td>ZEN software</td><td>Carl Zeiss microscopy, Jena, Germany</td><td></td><td>Imaging software, used together with the SysCon software; Black 2.3 version</td></tr></tbody></table>

targeted laser ablation in the embryo of saccharina latissima

In Saccharina latissima, the embryo&#160;develops as a monolayered cell sheet called the lamina or the blade. Each embryo cell is easy to observe, readily distinguishable from its neighbors, and can be individually targeted. For decades, laser ablation has been used to study embryo development. Here, a protocol for cell-specific laser ablation was developed for early embryos of the brown alga S. latissima. The presented work includes: (1) the preparation of Saccharina embryos, with a description of the critical parameters, including culture conditions, (2) the laser ablation settings, and (3) the monitoring of the subsequent growth of the irradiated embryo using time-lapse microscopy. In addition, details are provided on the optimal conditions for transporting the embryos from the imaging platform back to the lab, which can profoundly affect subsequent embryo development. Algae belonging to the order Laminariales display embryogenesis patterns similar to Saccharina; this protocol can thus be easily transferred to other species in this taxon.

Gametophytes of S. latissima were grown, and gametogenesis was induced to produce zygotes and embryos. Twelve days after the induction of gametogenesis, the embryos underwent laser ablation. Here, the experiment aimed to assess the role of specific cells in the overall development of S. latissima embryos. The most apical cell, the most basal cell, and the median cells were targeted. After tile scanning, the entire Petri dish (Figure 2A), an embryo of interest, was identifie...

Watch this Scientific Journal Video about Targeted Laser Ablation in the Embryo of Saccharina latissima at JoVE.com

Targeted Laser Ablation in the Embryo of Saccharina latissima

The destruction of specific cells in the embryo is a powerful tool for studying cellular interactions involved in cell fate. The present protocol describes techniques for the laser ablation of targeted cells in the early embryo of the brown alga Saccharina latissima.

Targeted Laser Ablation in the Embryo of Saccharina latissima

In Saccharina latissima, the embryo&#160;develops as a monolayered cell sheet called the lamina or the blade. Each embryo cell is easy to observe, readily ...

targeted-laser-ablation-in-the-embryo-of-saccharina-latissima

Universidad de Cartagena UDEC

Research

JoVE Journal

Developmental Biology

1.6K Views.  UMR8227, CNRS / Sorbonne University. The destruction of specific cells in the embryo is a powerful tool for studying cellular interactions involved in cell fate. The present protocol describes techniques for the laser ablation of targeted cells in the early embryo of the brown alga Saccharina latissima.

Video: Targeted Laser Ablation in the Embryo of Saccharina latissima

Laser-assisted Cytoplasmic Microinjection in Livestock Zygotes

Cytoplasmic microinjection into one-cell embryos is a very powerful technique. As an example, it enables the delivery of genome editing tools that can create genetic modifications that will be present in every cell of an adult organism. It can also be used to deliver siRNA, mRNAs or blocking antibodies to study gene function in preimplantation embryos. The conventional technique for microinjecting embryos used in rodents consists of a very thin micropipette that directly penetrates the plasma membrane when advanced into the embryo. When this technique is applied to livestock animals it usually results in low efficiency. This is mainly because in contrast to mice and rats, bovine, ovine, and porcine zygotes have a very dark cytoplasm and a highly elastic plasma membrane that makes visualization during injection and penetration of the plasma membrane hard to achieve. In this protocol, we describe a suitable microinjection method for the delivery of solutions into the cytoplasm of cattle zygotes that has proved to be successful for sheep and pig embryos as well. First, a laser is used to create a hole in the zona pellucida. Then a blunt-end glass micropipette is introduced through the hole and advanced until the tip of the needle reaches about 3/4 into the embryo. Then, the plasma membrane is broken by aspiration of cytoplasmic content inside the needle. Finally, the aspirated cytoplasmic content followed by the solution of interest is injected back into the embryonic cytoplasm. This protocol has been successfully used for the delivery of different solutions into bovine and ovine zygotes with 100% efficiency, minimal lysis, and normal blastocysts development rates.

This protocol shows how to perform cytoplasmic microinjection in farm animal zygotes. This technique can be used to deliver any solution into the one-cell embryo such as genome editing tools to generate knockout animals.

Cytoplasmic microinjection into one-cell embryos is a very powerful technique. As an example, it enables the delivery of genome editing tools that can ...

Genetics

Confocal Microscope-Based Laser Ablation and Regeneration Assay in Zebrafish Interneuromast Cells

Hair cells are mechanosensory cells that mediate the sense of hearing. These cells do not regenerate after damage in humans, but they are naturally replenished in non-mammalian vertebrates such as zebrafish. The zebrafish lateral line system is a useful model for characterizing sensory hair cell regeneration. The lateral line is comprised of hair cell-containing organs called neuromasts, which are linked together by a string of interneuromast cells (INMCs). INMCs act as progenitor cells that give rise to new neuromasts during development. INMCs can repair gaps in the lateral line system created by&#160;cell death. A method is described here for selective INMC ablation using a conventional laser-scanning confocal microscope and transgenic fish that express green fluorescent protein in INMCs. Time-lapse microscopy is then used to monitor INMC regeneration and determine the rate of gap closure. This represents an accessible protocol for cell ablation that does not require specialized equipment, such as a high-powered pulsed ultraviolet laser. The ablation protocol may serve broader interests, as it could be useful for the ablation of additional cell types, employing a tool set that is already available to many users. This technique will further enable the characterization of INMC regeneration under different conditions and from different genetic backgrounds, which will advance the understanding of sensory progenitor cell regeneration.

Laser ablation is a widely applicable technology for studying regeneration in biological systems. The presented protocol describes use of a standard laser-scanning confocal microscope for laser ablation and subsequent time-lapse imaging of regenerating interneuromast cells in the zebrafish lateral line.

Hair cells are mechanosensory cells that mediate the sense of hearing. These cells do not regenerate after damage in humans, but they are naturally ...

Deep and Spatially Controlled Volume Ablations using a Two-Photon Microscope in the Zebrafish Gastrula

Morphogenesis involves many cell movements to organize cells into tissues and organs. For proper development, all these movements need to be tightly coordinated, and accumulating evidence suggests this is achieved, at least in part, through mechanical interactions. Testing this in the embryo requires direct physical perturbations. Laser ablations are an increasingly used option that allows relieving mechanical constraints or physically isolating two cell populations from each other. However, many ablations are performed with an ultraviolet (UV) laser, which offers limited axial resolution and tissue penetration. A method is described here to ablate deep, significant, and spatially well-defined volumes using a two-photon microscope. Ablations are demonstrated in a transgenic zebrafish line expressing the green fluorescent protein in the axial mesendoderm and used to sever the axial mesendoderm without affecting the overlying ectoderm or the underlying yolk cell. Cell behavior is monitored by live imaging before and after the ablation. The ablation protocol can be used at different developmental stages, on any cell type or tissue, at scales ranging from a few microns to more than a hundred microns.

Embryonic development requires large-scale coordination of cell motion. Two-photon excitation mediated laser ablation allows the spatially controlled 3-dimensional ablation of large groups of deep cells. In addition, this technique can probe the reaction of collectively migrating cells in vivo to perturbations in their mechanical environment.

Morphogenesis involves many cell movements to organize cells into tissues and organs. For proper development, all these movements need to be tightly ...

Laser Ablation Method to Study Bone Regeneration in Zebrafish Larvae

Two-Photon Laser-Mediated Ablation of Osteoblasts in Developing Zebrafish Larvae

Zebrafish (Danio rerio) have an outstanding capacity to regenerate different organs and appendages. Bone regeneration in zebrafish has been studied using different methods such as fin amputation, scale plucking, skull trepanation, and microscopic approaches. Using a confocal laser scanning setup equipped with a two-photon laser, a laser ablation method was developed as a lesion paradigm to ablate bone-forming cells (osteoblasts) in the developing opercle of zebrafish larvae. The method described here allows the ablation of cells in a precise manner, as the area, shape, and depth can be finely adjusted. In addition, this method allows imaging of the area before and just after the ablation, so that short-term effects of the injury can be analyzed. In this experimental setup, the immune response after ablation of osteoblasts in the injured area was studied. An increase in the recruitment of macrophages was observed after ablation, indicating the relevance of their presence during bone regeneration.

Author Spotlight: Immune-Mediated Bone Regeneration &#8212; The Critical Role of Macrophages and Controlled Immunomodulation in Restorative Processes

This protocol describes a two-photon laser ablation approach carried out in zebrafish larvae, which serves as a model to study bone regeneration and the effects of the immune response to ablation.

Zebrafish (Danio rerio) have an outstanding capacity to regenerate different organs and appendages. Bone regeneration in zebrafish has been studied using ...

Single Cell Fate Mapping in Zebrafish

The ability to differentially label single cells has important implications in developmental biology. For instance, determining how hematopoietic, lymphatic, and blood vessel lineages arise in developing embryos requires fate mapping and lineage tracing of undifferentiated precursor cells. Recently, photoactivatable proteins which include: Eos1, 2, PAmCherry3, Kaede4-7, pKindling8, and KikGR9, 10 have received wide interest as cell tracing probes. The fluorescence spectrum of these photosensitive proteins can be easily converted with UV excitation, allowing a population of cells to be distinguished from adjacent ones. However, the photoefficiency of the activated protein may limit long-term cell tracking11. As an alternative to photoactivatable proteins, caged fluorescein-dextran has been widely used in embryo model systems7, 12-14. Traditionally, to uncage fluorescein-dextran, UV excitation from a fluorescence lamp house or a single photon UV laser has been used; however, such sources limit the spatial resolution of photoactivation. Here we report a protocol to fate map, lineage trace, and detect single labeled cells. Single cells in embryos injected with caged fluorescein-dextran are photoactivated with near-infrared laser pulses produced from a titanium sapphire femtosecond laser. This laser is customary in all two-photon confocal microscopes such as the LSM 510 META NLO microscope used in this paper. Since biological tissue is transparent to near-infrared irradiation15, the laser pulses can be focused deep within the embryo without uncaging cells above or below the selected focal plane. Therefore, non-linear two-photon absorption is induced only at the geometric focus to uncage fluorescein-dextran in a single cell. To detect the cell containing uncaged fluorescein-dextran, we describe a simple immunohistochemistry protocol16 to rapidly visualize the activated cell. The activation and detection protocol presented in this paper is versatile and can be applied to any model system. 
Note: The reagents used in this protocol can be found in the table appended at the end of the article.

A method is described to photoactivate single cells containing a caged fluorescent protein using two-photon absorption from a Ti:Sapphire femtosecond laser oscillator. To fate map the photoactivated cell, immunohistochemistry is used. This technique can be applied to any cell type.

The ability to differentially label single cells has important implications in developmental biology. For instance, determining how hematopoietic, ...

Biology

Ablation of a Neuronal Population Using a Two-photon Laser and Its Assessment Using Calcium Imaging and Behavioral Recording in Zebrafish Larvae

To identify the role of a subpopulation of neurons in behavior, it is essential to test the consequences of blocking its activity in living animals. Laser ablation of neurons is an effective method for this purpose when neurons are selectively labeled with fluorescent probes. In the present study, protocols for laser ablating a subpopulation of neurons using a two-photon microscope and testing of its functional and behavioral consequences are described. In this study, prey capture behavior in zebrafish larvae is used as a study model. The pretecto-hypothalamic circuit is known to underlie this visually-driven prey catching behavior. Zebrafish pretectum were laser-ablated, and neuronal activity in the inferior lobe of the hypothalamus (ILH; the target of the pretectal projection) was examined. Prey capture behavior after pretectal ablation was also tested.

Here, we present a protocol to ablate a genetically labeled subpopulation of neurons by a two-photon laser from Zebrafish larvae.

To identify the role of a subpopulation of neurons in behavior, it is essential to test the consequences of blocking its activity in living animals. Laser ...

Neuroscience

Controlled Semi-Automated Laser-Induced Injuries for Studying Spinal Cord Regeneration in Zebrafish Larvae

Zebrafish larvae possess a fully functional central nervous system (CNS) with a high regenerative capacity only a few days after fertilization. This makes this animal model very useful for studying spinal cord injury and regeneration. The standard protocol for inducing such lesions is to transect the dorsal part of the trunk manually. However, this technique requires extensive training and damages additional tissues. A protocol was developed for laser-induced lesions to circumvent these limitations, allowing for high reproducibility and completeness of spinal cord transection over many animals and between different sessions, even for an untrained operator. Furthermore, tissue damage is mainly limited to the spinal cord itself, reducing confounding effects from injuring different tissues, e.g., skin, muscle, and CNS. Moreover, hemi-lesions of the spinal cord are possible. Improved preservation of tissue integrity after laser injury facilitates further dissections needed for additional analyses, such as electrophysiology. Hence, this method offers precise control of the injury extent that is unachievable manually. This allows for new experimental paradigms in this powerful model in the future.

The present protocol describes a method to induce tissue-specific and highly reproducible injuries in zebrafish larvae using a laser lesion system combined with an automated microfluidic platform for larvae handling.

Zebrafish larvae possess a fully functional central nervous system (CNS) with a high regenerative capacity only a few days after fertilization. This makes ...

Medicine

Single-Neuron Ablation in Drosophila for Studying Nervous System Adaptation

Laser Cell Ablation in Intact Drosophila Larvae Reveals Synaptic Competition

The protocol describes single-neuron ablation with a 2-photon laser system in the central nervous system (CNS) of intact Drosophila melanogaster larvae. Using this non-invasive method, the developing nervous system can be manipulated in a cell-specific manner. Disrupting the development of individual neurons in a network can be used to study how the nervous system can compensate for the loss of synaptic input. Individual neurons were specifically ablated in the giant fiber system of Drosophila, with a focus on two neurons: the presynaptic giant fiber (GF) and the postsynaptic tergotrochanteral motor neuron (TTMn). The GF synapses with the ipsilateral TTMn, which is crucial to the escape response. Ablating one of the GFs in the 3rd instar brain, just after the GF starts axonal growth, permanently removes the cell during the development of the CNS. The remaining GF reacts to the absent neighbor and forms an ectopic synaptic terminal to the contralateral TTMn. This atypical, bilaterally symmetric terminal innervates both TTMns, as demonstrated by dye coupling, and drives both motor neurons, as demonstrated by electrophysiological assays. In summary, the ablation of a single interneuron demonstrates synaptic competition between a bilateral pair of neurons that can compensate for the loss of one neuron and restore normal responses to the escape circuit.

Author Spotlight: Investigating the Mechanisms of Neural Circuit Assembly and Synapse Formation in Drosophila

This protocol demonstrates the laser cell ablation of individual neurons in intact Drosophila larvae. The method enables the study of the effect of reducing competition between neurons in the developing nervous system.

The protocol describes single-neuron ablation with a 2-photon laser system in the central nervous system (CNS) of intact Drosophila melanogaster larvae. ...

Laser-assisted Lentiviral Gene Delivery to Mouse Fertilized Eggs

Lentiviruses are efficient vectors for gene delivery to mammalian cells. Following transduction, the lentiviral genome is stably incorporated into the host chromosome and is passed on to progeny. Thus, they are ideal vectors for creation of stable cell lines, in vivo delivery of indicators, and transduction of single cell fertilized eggs to create transgenic animals. However, mouse fertilized eggs and early stage embryos are protected by the zona pellucida, a glycoprotein matrix that forms a barrier against lentiviral gene delivery. Lentiviruses are too large to penetrate the zona and are typically delivered by microinjection of viral particles into the perivitelline cavity, the space between the zona and the embryonic cells. The requirement for highly skilled technologists and specialized equipment has minimized the use of lentiviruses for gene delivery to mouse embryos. This article describes a protocol for permeabilizing the mouse fertilized eggs by perforating the zona with a laser. Laser-perforation does not result in any damage to embryos and allows lentiviruses to gain access to embryonic cells for gene delivery. Transduced embryos can develop into blastocyst in vitro, and if implanted in pseudopregnant mice, develop into transgenic pups. The laser used in this protocol is effective and easy to use. Genes delivered by lentiviruses stably incorporate into mouse embryonic cells and are germline transmittable. This is an alternative method for creation of transgenic mice that requires no micromanipulation and microinjection of fertilized eggs.

Mouse fertilized eggs and early stage embryos are protected by the zona pellucida, a glycoprotein matrix that forms a barrier against gene delivery. This article describes a protocol for perforating the zona with a laser to transduce embryonic cells with lentiviral vectors and to create transgenic mice.

Lentiviruses are efficient vectors for gene delivery to mammalian cells. Following transduction, the lentiviral genome is stably incorporated into the ...

Selective Single-Neuron Laser Ablation in a Zebrafish Larva Using a Confocal Microscope

Source:&#160;<a style='text-decoration:none;' href='https://appjove.unicartagenaproxy.elogim.com/v/54983/triggering-cell-stress-and-death-using-conventional-uv-laser-confocal-microscopy'><span style='-webkit-text-decoration-skip:none;font-family:Arial,sans-serif;font-size:12pt;font-style:normal;font-variant:normal;font-weight:400;text-decoration-skip-ink:none;vertical-align:baseline;white-space:pre-wrap;'>Morsch, M.,&#160;<span style='-webkit-text-decoration-skip:none;font-family:Arial,sans-serif;font-size:12pt;font-style:normal;font-variant:normal;font-weight:400;text-decoration-skip-ink:none;vertical-align:baseline;white-space:pre-wrap;'>&#160;et. al.<span style='-webkit-text-decoration-skip:none;font-family:Arial,sans-serif;font-size:12pt;font-style:normal;font-variant:normal;font-weight:400;text-decoration-skip-ink:none;vertical-align:baseline;white-space:pre-wrap;'>,&#160;<span style='-webkit-text-decoration-skip:none;font-family:Arial,sans-serif;font-size:12pt;font-style:normal;font-variant:normal;font-weight:400;text-decoration-skip-ink:none;vertical-align:baseline;white-space:pre-wrap;'>Triggering Cell Stress and Death Using Conventional UV Laser Confocal Microscopy.&#160;J. Vis. Exp.<span style='-webkit-text-decoration-skip:none;font-family:Arial,sans-serif;font-size:12pt;font-style:normal;font-variant:normal;font-weight:400;text-decoration-skip-ink:none;vertical-align:baseline;white-space:pre-wrap;'> (2017)</a> &#160;In this video, we explore the technique of high-intensity UV laser ablation for precisely targeting and studying individual neurons in transgenic zebrafish. We demonstrate how to prepare, immobilize, and visualize neuronal responses, highlighting the cellular dynamics of injury and recovery.

Source:&#160;Morsch, M.,&#160;&#160;et. al.,&#160;Triggering Cell Stress and Death Using Conventional UV Laser Confocal Microscopy.&#160;J. Vis. Exp. ...

Targeted Laser Ablation in the Embryo of Saccharina latissima

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Przeglądaj więcej filmów

Laser-assisted Cytoplasmic Microinjection in Livestock Zygotes

Confocal Microscope-Based Laser Ablation and Regeneration Assay in Zebrafish Interneuromast Cells

Deep and Spatially Controlled Volume Ablations using a Two-Photon Microscope in the Zebrafish Gastrula

Two-Photon Laser-Mediated Ablation of Osteoblasts in Developing Zebrafish Larvae

Single Cell Fate Mapping in Zebrafish

Ablation of a Neuronal Population Using a Two-photon Laser and Its Assessment Using Calcium Imaging and Behavioral Recording in Zebrafish Larvae

Controlled Semi-Automated Laser-Induced Injuries for Studying Spinal Cord Regeneration in Zebrafish Larvae

Laser Cell Ablation in Intact Drosophila Larvae Reveals Synaptic Competition

Laser-assisted Lentiviral Gene Delivery to Mouse Fertilized Eggs

Selective Single-Neuron Laser Ablation in a Zebrafish Larva Using a Confocal Microscope