Bu prosedür, Bill Jeffrey laboratuar tarafından mağara balıkları için geliştirilmiş nakli tekniği büyük ölçüde izler.

Bölüm 1: embriyoların hazırlanması Bu protokol, varsayımsal bir zebrafish objektif mutant göstermek için jj xy sembolü kullanabilirsiniz. <ol><li> Zebra balığı suşları 14h light/10h karanlık döngüsü 28.5 C&#39;de standart balık tesisi şartlarda muhafaza edilir. </li><li> Akşam, erkek ve zebrafish gerginlik jj xy kadınların yer: AB / TU, birbirinden ayırmak için bölücü ile bir tank tg (mGFP). Bu haç döl tüm dokularda GFP transgen ifade edecek ve bağışçılar olarak kullanılacaktır. Buna paralel olarak, transgenik olmayan yabani tip hayvanlar arasındaki haçlar kurmak için aynı prosedürü kullanın. Bu deneyin amacı bağlı olarak, bir bağışçılar veya ana gibi jj xy lokustaki yabani tip hayvanlar geçebilir. </li><li> Sabah ışık yanar sonra bir saat içinde balık, çiftleşmek için izin vermek için bölücüler çıkarın. </li><li> 15-30 dakika 100 x 15 mm Petri kapları embriyolar topladıktan sonra, onlara temiz ve orta (yumurta su) değiştirmek. </li><li> 28.5 C inkübatörde embriyolar istenilen zaman kadar tutun. </li><li> Transplantasyon için hazır, iki çift keskin forseps ile koryon el kaldırmak ve embriyoların% 0.2 EDTA kalsiyum ZFR 30 dakika inkübe edin. </li></ol> Bölüm 2: diseksiyon iğneleri Hazırlık <ol><li> Ve donör objektif hareket ve ev sahibi içine girmek için kullanılan bir künt bir iğne, lens çevre dokulara kesmek koryon kaldırmak ve agaroz serbest embriyolar kullanılır bilenmiş biri: nakli prosedürü iki tür iğneler gerektirir. İşte biz bu iğneler nasıl yapılacağını göstereceğim. </li><li> Birincisi, bir elmas bıçak kullanarak Pasteur pipet ucu kesilmiş olmalıdır. Sonra bir cam kapiller uzunluğu yaklaşık yarısı içinde böylece Pasteur pipet içine yerleştirin. Bu kolay bir sonraki adım cam içine eriterek tungsten tel hareketsiz hale getirecektir. </li><li> Sonra ince kılcal açık ucunu bir tungsten tel yerleştirin. Bunsen beki ile tel üzerinden cam eritin. Elinizle iğnenin diğer ucunu büküm forseps kullanarak, metal tel ile sabit cam sonunda tutun. Yumuşatılmış cam, metal çevresinde sarmal yerde sürükleyici olmalıdır. </li><li> Künt bir ucu iğne yapıyorsanız, o zaman bu prosedürün sonuna. Bilenmiş bir iğne oluşturmak için, çok ince uçlu oluşturulur böylece metal yakarak, Bunsen beki üzerinden 1-1.5 dakika tungsten tel tutun. Microscropy.It ucu kalite nakli hemen önce birkaç saniye için alev hem de iğneler sterilize etmek için iyi bir fikir olup olmadığını kontrol edin. </li></ol> Bölüm 3: reaktiflerin hazırlanması <ol><li> Kalsiyum-Zebra balığı Ringer (ZFR) Çözümleri (116 mM NaCl, 2.9 mM KCl, 5 mM HEPES, pH 7.2) </li><li> Kalsiyum Zebra balığı Ringer Çözümleri (pH 7,2)% 0.2 EDTA </li><li> Kalsiyum ücretsiz ZFR% 1.2 agaroz (düşük erime noktası) </li><li> Kalsiyum ücretsiz ZFR% 0.2 agaroz (düşük erime noktası) </li><li> Embriyo orta (pH 7.0, litre başına içerir: 10 ml Hanks Çözüm # 1, 1 ml Hanks Çözüm # 2, 10ml Hanks Çözüm # 4, 10ml Hanks Çözüm # 5, 0.35 g sodyum bikarbonat, 300 uL 2M HCl, penisilin-streptomisin 500.000 U) Zebra balığı Kitap (Oregon Üniversitesi Press, 2000) gibi. </li><li> Tungsten tel, altın kaplama, 0.1mm çap, Alfa Aesar </li><li> Kapiler tüp, 1.0mm çap, Dünya Hassas Aletler </li></ol> Bölüm 4: Transplantasyon prosedürü <ol><li> Plastik bir santrifüj tüpüne, bir su banyosunda 40 ° C önceden ısıtılmış kalsiyum ücretsiz ZFR% 1.2 düşük erime noktası agaroz hazırlamak. </li><li> Istenilen evre (30 hpf, örneğin), bir Pasteur pipeti embriyoların sürebilir santrifüj tüpü içine yavaş yavaş onları kovmak ve santrifüj tüpü içine yavaş yavaş onları kovmak ve yaklaşık 5 saniye boyunca inkübe edin. Donörler ve bilgisayarlara ayrı inkübe edilmelidir. </li><li> Bir pipet ile,% 1.2 agaroz santrifüj tüpüne embriyoların kadar sürebilir ve 100mm polistiren Petri kabındaki iki paralel sıralar halinde düzenlemek, host ve donörlerin ayrı tutulması. Yavaş ve dikkatli bir şekilde onları pipetleme, en embriyolar agaroz onların yüzüne yalan. Agaroz katılaşır önce göz yukarı bakacak şekilde künt bir iğne kullanılarak bu pozisyonda yalan olmadığını reorient gerekecektir. </li><li> Sağlamlaştırmak için% 1.2 agaroz için bekleyin ve daha sonra% 0.2 düşük erime noktası agaroz çözümü ile kaplaması. </li><li> Bilenmiş bir iğne yardımıyla, göz çevresi herhangi bir agaroz kaldırmak ve çok dikkatli bir şekilde küçük bir vuruş kullanan ev sahibi ve donör embriyoları mercek kesip. Lensin yeterince yakın şekilde gözyaşı kesmek için emin olun, ancak bu nedenle ev sahibi göz geri kalanından çok fazla doku çıkarmayın. </li><li> Bir kez ücretsiz, lensler orta float. Künt iğne kullanarak, dikkatli bir şekilde donör itinobjektif sadece normal ev sahibi objektif olacağını yerini yukarıda ve daha sonra göz içine künt iğne ile aşağı doğru itin. Ev sahibi objektif atılabilir. </li><li> 30-60 dakika süreyle% 1.2 agaroz donör ve host embriyolar bırakın, sonra keskin bir iğne kullanılarak agaroz onları serbest bırakın ve embriyo orta ile 24 plaka içine aktarabilirsiniz. Her embriyo ayrı bir iyi kurulmalıdır. Bu yüzden düzgün bir şekilde ev sahibi olan donör tekabül eden net olduğunu kuyuların etiket emin olun. </li><li> 28.5 C inkübe donör elde edilen objektif, aynı hayvanın GFP floresan dayalı unoperated tarafta ev sahibi objektif ayırt edilebilir. Bölümleri de objektif boyutunu ölçmek için ve düzgün bir şekilde ayıran olup olmadığını belirlemek için yapılabilir. </li></ol><img src="/files/ftp_upload/1258/1258fig1.jpg" alt="Şekil 1" /> Şekil 1 objektif nakli için kullanılan bir bilenmiş iğne Düşük büyütme görüntü. Kılcal bir cam Pasteur pipeti (A) (B) eklenir ve kılcal açık ucuna ince bir tungsten teli (C) eklenir. Tel üzerinden cam bir Bunsen beki ile yumuşatılmış. Pasteur pipetin diğer ucunu elinizle büküm forseps kullanarak, metal tel ile sabit cam sonunda tutun. Yumuşatılmış cam bir yere sürükleyici, metal etrafında sarmal. <img src="/files/ftp_upload/1258/fig2 1258.png" alt="" width="600" height="204" /> Şekil 2 objektif nakli için kullanılan iki çeşit iğne uçları. <img src="/files/ftp_upload/1258/1258fig3.jpg" alt="Şekil 3" /> Şekil 3 Embriyolar 30hpf objektif nakli yapıldı. Gösterilen bir donör embriyo (A, B), nakledilen lens (C, D) ile bir host göz ve ev sahibi embriyo kontrol tarafı (E, F). Belirtildiği gibi her bir göz iletilen ışık ve UV aydınlatma hem de gösterilmiştir. Fotoğraflar 48 hpf alınmıştır. Q01 [9] transgenik hattı bu deneyde kullanıldı.

<ol>
	<li>Thut, C. J., Rountree, R. B., Hwa, M., Kingsley, D. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+large-scale+in+situ+screen+provides+molecular+evidence+for+the+induction+of+eye+anterior+segment+structures+by+the+developing+lens.">A large-scale in situ screen provides molecular evidence for the induction of eye anterior segment structures by the developing lens.</a> Dev Biol. 231, 63-76 (2001).</li><li>Yamamoto, Y., Jeffery, W. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Central+role+for+the+lens+in+cave+fish+eye+degeneration.">Central role for the lens in cave fish eye degeneration.</a> Science. 289, 631-633 (2000).</li><li>Easter, S. S., Nicola, G. N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+development+of+vision+in+the+zebrafish(Danio+rerio).">The development of vision in the zebrafish(Danio rerio).</a> Dev Biol. 180, 646-663 (1996).</li><li>Schmitt, E., Dowling, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Early+eye+morphogenesis+in+the+zebrafish.+Brachydanio+rerio.">Early eye morphogenesis in the zebrafish. Brachydanio rerio.</a> J.comp. Neuro. 344 (4), 532-542 (1994).</li><li>Malicki, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Harnessing+the+power+of+forward+genetics--analysis+of+neuronal+diversity+and+patterning+in+the+zebrafish+retina.">Harnessing the power of forward genetics--analysis of neuronal diversity and patterning in the zebrafish retina.</a> Trends Neurosci. 23 (11), 531-541 (2000).</li><li>Malicki, J., Pujic, Z., Thisse, C., Thisse, B., Wei, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Forward+and+reverse+genetic+approaches+to+the+analysis+of+eye+development+in+zebrafish.">Forward and reverse genetic approaches to the analysis of eye development in zebrafish.</a> Vision Res. 42 (4), 527-533 (2002).</li><li>Avanesov, A., Malicki, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Approaches+to+study+neurogenesis+in+the+zebrafish+retina.">Approaches to study neurogenesis in the zebrafish retina.</a> Methods Cell Biol. 76, 333-384 (2004).</li><li>Vihtelic, T. S., Hyde, D. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Zebrafish+mutagenesis+yields+eye+morphological+mutants+with+retinal+and+lens+defects.">Zebrafish mutagenesis yields eye morphological mutants with retinal and lens defects.</a> Vision Res. 42, 535-540 (2002).</li><li>Godinho, L., Mumm, J. S., Williams, P. R., Schroeter, E. H., Koerber, A., Park, S. W., Leach, S. D., Wong, R. O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Targeting+of+amacrine+cell+neurites+to+appropriate+synaptic+laminae+in+the+developing+zebrafish+retina.">Targeting of amacrine cell neurites to appropriate synaptic laminae in the developing zebrafish retina.</a> Development. Nov 132, 5069-5079 (2005).</li></ol>

Birkaç adım objektif transplantasyon sırasında özel dikkat gerektirir. <ol><li> Bilenmiş iğneler: objektif nakli yapılmadan önce birkaç iğne hazırlamak için daha iyi ve iğne ucu mümkün olduğunca ince olmalıdır. Kalın iğne gözü iyileşmek için bir başarısızlık neden daha geniş çapı nedeniyle daha fazla doku gözyaşı. </li><li> Embriyoların Düzenleme: onlar, yan yatarken, böylece sağ nakli önce size embriyoların pozisyon gerekir. Yerleştirirken,% 1.2 agaroz sertleşerek çok hı...

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<td>0.1mm diameter tungsten wire</td>
<td>&nbsp;</td>
<td>A Johnson Matthey</td>
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<td>Agarose(low melting point)</td>
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<td>Dumont #5</td>
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lens transplantation in zebrafish and its application in the analysis of eye mutants

Objektifi, optik fincan [1,2] gelişiminde önemli bir rol oynar. Bir model organizma olarak zebrafish kullanılması, objektif gelişimi ile ilgili sorular ele alınabilir. Zebrafish dahil olmak üzere birçok avantajlı özellikleri, küçük boyutu, yüksek fekondite, kısa bir yaşam döngüsü, ve bakım kolaylığı nedeniyle genetik çalışmalar için yararlıdır. Lens geliştirme zebrafish hızla oluşur. 72 hpf, zebrafish objektif fonksiyonel olgun [3]. Bol ve moleküler genetik kaynakları zebrafish araştırmaları desteklemek için kullanılabilir. Buna ek olarak, diğer omurgalıların zebrafish göz benzerlik, insan kusurları mükemmel bir hayvan modeli [4-7] olarak kullanımı için temel sağlar . Birkaç zebrafish mutantlar, bazı durumlarda objektif dokularda tam bir dejenerasyon hücre ölümüne yol açan yüksek seviyede, [8]. Da dahil olmak üzere, lens anormallikler de sergileyebilirler Lens anormallikleri içsel nedenler ya da çevre dokulara arızalı etkileşimleri nedeniyle olup olmadığını belirlemek için, bir mutant yabani tip bir göz içine lens nakli yapılır. Dikkatli bir şekilde kullanılması yangına cilalanmış metal iğneler, mutant ya da yabani tip lensler donör hayvan disseke ve sahibi aktarılır. Yabani tip ve mutant dokuların ayırt etmek için, bir transgenik çizgi donör olarak kullanılır. Bu satır, lens dahil olmak üzere tüm dokularda membran-bağlı GFP ifade eder. Bu nakli tekniği zebrafish lens mutantlar çalışmalarda önemli bir araçtır.

Watch this Scientific Journal Video about Lens Transplantation in Zebrafish and its Application in the Analysis of Eye Mutants at JoVE.com

Lens Transplantation in Zebrafish and its Application in the Analysis of Eye Mutants

Lens geliştirme, diğer dokuları ile etkileşimleri içerir. Çeşitli zebrafish göz mutantlar anormal küçük bir lens boyutuna göre karakterize edilir. İşte biz bu fenotip içsel nedenler veya objektif çevreleyen dokuların arızalı etkileşimler nedeniyle olup olmadığını belirlemek için bir lens nakli deney göstermektedir.

Zebra balığı Lens Nakli ve Göz Mutants Analizi Uygulaması

The lens plays an important role in the development of the optic cup[1,2]. Using the zebrafish as a model organism, questions regarding lens development ...

lens-transplantation-zebrafish-its-application-analysis-eye

Universidad de Cartagena UDEC

Research

JoVE Journal

Biology

11.0K Görüntüleme.  The Second Teaching Hospital of Jilin University. Lens geliştirme, diğer dokuları ile etkileşimleri içerir. Çeşitli zebrafish göz mutantlar anormal küçük bir lens boyutuna göre karakterize edilir. İşte biz bu fenotip içsel nedenler veya objektif çevreleyen dokuların arızalı etkileşimler nedeniyle olup olmadığını belirlemek için bir lens nakli deney göstermektedir.

Video: Lens Transplantation in Zebrafish and its Application in the Analysis of Eye Mutants

Transplantation of Whole Kidney Marrow in Adult Zebrafish

Hematopoietic stem cells (HSC) are a rare population of pluripotent cells that maintain all the differentiated blood lineages throughout the life of an organism. The functional definition of a HSC is a transplanted cell that has the ability to reconstitute all the blood lineages of an irradiated recipient long term. This designation was established by decades of seminal work in mammalian systems. Using hematopoietic cell transplantation (HCT) and reverse genetic manipulations in the mouse, the underlying regulatory factors of HSC biology are beginning to be unveiled, but are still largely under-explored. Recently, the zebrafish has emerged as a powerful genetic model to study vertebrate hematopoiesis. Establishing HCT in zebrafish will allow scientists to utilize the large-scale genetic and chemical screening methodologies available in zebrafish to reveal novel mechanisms underlying HSC regulation. In this article, we demonstrate a method to perform HCT in adult zebrafish. We show the dissection and preparation of zebrafish whole kidney marrow, the site of adult hematopoiesis in the zebrafish, and the introduction of these donor cells into the circulation of irradiated recipient fish via intracardiac injection. Additionally, we describe the post-transplant care of fish in an "ICU" to increase their long-term health. In general, gentle care of the fish before, during, and after the transplant is critical to increase the number of fish that will survive more than one month following the procedure, which is essential for assessment of long term (&lt;3 month) engraftment. The experimental data used to establish this protocol will be published elsewhere. The establishment of this protocol will allow for the merger of large-scale zebrafish genetics and transplant biology.

In this article, we demonstrate a method to perform HCT in adult zebrafish.

Yetişkin Zebra balığı Tüm Böbrek İliği Nakli

Hematopoietic stem cells (HSC) are a rare population of pluripotent cells that maintain all the differentiated blood lineages throughout the life of an ...

Biyoloji

The Ladder Rung Walking Task: A Scoring System and its Practical Application.

Progress in the development of animal models for/stroke, spinal cord injury, and other neurodegenerative disease requires tests of high sensitivity to elaborate distinct aspects of motor function and to determine even subtle loss of movement capacity. To enhance efficacy and resolution of testing, tests should permit qualitative and quantitative measures of motor function and be sensitive to changes in performance during recovery periods. The present study describes a new task to assess skilled walking in the rat to measure both forelimb and hindlimb function at the same time. Animals are required to walk along a horizontal ladder on which the spacing of the rungs is variable and is periodically changed. Changes in rung spacing prevent animals from learning the absolute and relative location of the rungs and so minimize the ability of the animals to compensate for impairments through learning. In addition, changing the spacing between the rungs allows the test to be used repeatedly in long-term studies. Methods are described for both quantitative and qualitative description of both fore- and hindlimb performance, including limb placing, stepping, co-ordination. Furthermore, use of compensatory strategies is indicated by missteps or compensatory steps in response to another limb&#x2019;s misplacement. 

The ladder rung walking task is a new test to assess skilled walking and measure both forelimb and hindlimb placing, stepping, and inter-limb co-ordination.

Görev Yürüyüş Merdiven Basamak: Puanlama Sistemi ve Pratik Uygulama.

Progress in the development of animal models for/stroke, spinal cord injury, and other neurodegenerative disease requires tests of high sensitivity to ...

Preparation and Culture of Rat Lens Epithelial Explants for Studying Terminal Differentiation

The anterior surface of the ocular lens is covered by a monolayer of epithelial cells, which proliferate in an annular zone underlying the ciliary body.  Following division, these cells migrate posteriorly, where FGF diffusing from the retina induces them to differentiate into a posterior array of elongated lens fiber cells, which compose the bulk of the lens.  Differentiation of lens epithelial cells into lens fibers can be induced in vitro by culturing explants of the central region of the anterior epithelium in the presence of FGF-2.  Explants are prepared from lenses of neonatal rats by removing the lens from the eye and grasping the lens capsule on the posterior side with dissecting tweezers.  The posterior capsule is then gently torn open and pressed down into the plastic bottom of a tissue culture dish. The peripheral regions of the explant are removed with a scalpel and the central area is then cultured in the presence of 100ng/ml FGF-2 for as long as 2-3 weeks, depending on the parameters to be studied.  Since epithelial cells in cultured explants differentiate in approximate synchrony over a period of days to weeks, the time course of signaling and gene expression can be determined using molecular, biochemical, and pharmacological techniques.  Immunofluorescence microscopy is a powerful adjunct to these methods as it demonstrates the subcellular localization of proteins of interest and can reveal the physiological consequences of experimental manipulations of signaling pathways.

Explants of the central region of rat lens epithelia differentiate synchronously when cultured in the presence of FGF-2. Immunofluorescence microscopy of such cultures can provides novel information about gene expression and signaling events associated with terminal differentiation.

Terminal Farklılaşma incelenmesi için hazırlanması ve Rat Lens Epitel eksplantlar Kültür

The anterior surface of the ocular lens is covered by a monolayer of epithelial cells, which proliferate in an annular zone underlying the ciliary body.  ...

Primary Culture and Plasmid Electroporation of the Murine Organ of Corti. 

In all mammals, the sensory epithelium for audition is located along the spiraling organ of Corti that resides within the conch shaped cochlea of the inner ear (fig 1). Hair cells in the developing cochlea, which are the mechanosensory cells of the auditory system, are aligned in one row of inner hair cells and three (in the base and mid-turns) to four (in the apical turn) rows of outer hair cells that span the length of the organ of Corti. Hair cells transduce sound-induced mechanical vibrations of the basilar membrane into neural impulses that the brain can interpret. Most cases of sensorineural hearing loss are caused by death or dysfunction of cochlear hair cells.
An increasingly essential tool in auditory research is the isolation and in vitro culture of the organ explant 1,2,9. Once isolated, the explants may be utilized in several ways to provide information regarding normative, anomalous, or therapeutic physiology. Gene expression, stereocilia motility, cell and molecular biology, as well as biological approaches for hair cell regeneration are examples of experimental applications of organ of Corti explants.
This protocol describes a method for the isolation and culture of the organ of Corti from neonatal mice. The accompanying video includes stepwise directions for the isolation of the temporal bone from mouse pups, and subsequent isolation of the cochlea, spiral ligament, and organ of Corti. Once isolated, the sensory epithelium can be plated and cultured in vitro in its entirety, or as a further dissected micro-isolate that lacks the spiral limbus and spiral ganglion neurons. Using this method, primary explants can be maintained for 7-10 days. As an example of the utility of this procedure, organ of Corti explants will be electroporated with an exogenous DsRed reporter gene. This method provides an improvement over other published methods because it provides reproducible, unambiguous, and stepwise directions for the isolation, microdissection, and primary culture of the organ of Corti.

Primary Culture and Plasmid Electroporation of the Murine Organ of Corti.

This procedure describes a method for the isolation and culture of the murine organ of Corti with or without the spiral limbus and spiral ganglion neurons. We also demonstrate a method for the expression of an exogenous reporter gene in the organ of Corti explant by electroporation.

İlköğretim Kültür ve Corti murin Organ Plazmid Elektroporasyon.

In all mammals, the sensory epithelium for audition is located along the spiraling organ of Corti that resides within the conch shaped cochlea of the ...

Gavaging Adult Zebrafish

The zebrafish has become an important in vivo model in biomedical research. Effective methods must be developed and utilized to deliver compounds or agents in solutions for scientific research. Current methods for administering compounds orally to adult zebrafish are inaccurate due to variability in voluntary consumption by the fish. A gavage procedure was developed to deliver precise quantities of infectious agents to zebrafish for study in biomedical research. Adult zebrafish over 6 months of age were anesthetized with 150 mg/L of buffered MS-222 and gavaged with 5 &mu;l of solution using flexible catheter implantation tubing attached to a cut 22-G needle tip. The flexible tubing was lowered into the oral cavity of the zebrafish until the tip of the tubing extended past the gills (approximately 1 cm). The solution was then injected slowly into the intestinal tract. This method was effective 88% of the time, with fish recovering uneventfully. This procedure is also efficient as one person can gavage 20-30 fish in one hour. This method can be used to precisely administer agents for infectious diseases studies, or studies of other compounds in adult zebrafish.

The increasing use of zebrafish as an animal model requires the development of effective methods for the delivery of known quantities of compounds and solutions. The gavage procedure described below allows for the oral delivery of precise volumes of solution reliably, safely and efficiently to adult zebrafish.

Yetişkin Zebra balığı Gavaging

The zebrafish has become an important in vivo model in biomedical research. Effective methods must be developed and utilized to deliver compounds or ...

Design and Analysis of Temperature Preference Behavior and its Circadian Rhythm in Drosophila

The circadian clock regulates many aspects of life, including sleep, locomotor activity, and body temperature (BTR) rhythms1,2. We recently identified a novel Drosophila circadian output, called the temperature preference rhythm (TPR), in which the preferred temperature in flies rises during the day and falls during the night 3. Surprisingly, the TPR and locomotor activity are controlled through distinct circadian neurons3. Drosophila locomotor activity is a well&#160;known circadian behavioral output and has provided strong contributions to the discovery of many conserved mammalian circadian clock genes and mechanisms4. Therefore, understanding TPR will lead to the identification of hitherto unknown molecular and cellular circadian mechanisms. Here, we describe how to perform and analyze the TPR assay. This technique not only allows for dissecting the molecular and neural mechanisms of TPR, but also provides new insights into the fundamental mechanisms of the brain functions that integrate different environmental signals and regulate animal behaviors. Furthermore, our recently published data suggest that the fly TPR shares features with the mammalian BTR3. Drosophila are ectotherms, in which the body temperature is typically behaviorally regulated. Therefore, TPR is a strategy used to generate a rhythmic body temperature in these flies5-8. We believe that further exploration of Drosophila TPR will facilitate the characterization of the mechanisms underlying body temperature control in animals.

Design and Analysis of Temperature Preference Behavior and its Circadian Rhythm in Drosophila

We recently identified a novel Drosophila circadian output, temperature preference rhythm (TPR), in which the preferred temperature in flies rises during the day and falls during the night. TPR is regulated independently from another circadian output, locomotor activity. Here&#160;we describe the design and analysis of TPR in Drosophila.

Drosophila'da Sıcaklık Tercih Davranışının ve Sirkadiyen Ritminin Tasarımı ve Analizi

The circadian clock regulates many aspects of life, including sleep, locomotor activity, and body temperature (BTR) rhythms1,2. We recently identified a ...

Analysis of Oxidative Stress in Zebrafish Embryos

High levels of reactive oxygen species (ROS) may cause a change of cellular redox state towards oxidative stress condition. This situation causes oxidation of molecules (lipid, DNA, protein) and leads to cell death. Oxidative stress also impacts the progression of several pathological conditions such as diabetes, retinopathies, neurodegeneration, and cancer. Thus, it is important to define tools to investigate oxidative stress conditions not only at the level of single cells but also in the context of whole organisms. Here, we consider the zebrafish embryo as a useful in vivo system to perform such studies and present a protocol to measure in vivo oxidative stress. Taking advantage of fluorescent ROS probes and zebrafish transgenic fluorescent lines, we develop two different methods to measure oxidative stress in vivo: i) a &#8220;whole embryo ROS-detection method&#8221; for qualitative measurement of oxidative stress and ii) a &#8220;single-cell&#160;ROS detection method&#8221; for quantitative measurements of oxidative stress. Herein, we demonstrate the efficacy of these procedures by increasing oxidative stress in tissues by oxidant agents and physiological or genetic methods. This protocol is amenable for forward genetic screens and it will help address cause-effect relationships of ROS in animal models of oxidative stress-related pathologies such as neurological disorders and cancer.

Here we report a protocol to measure oxidative stress in living zebrafish embryos. This procedure allows reactive oxygen species (ROS) detection in both whole embryo tissues and single-cell populations. This protocol will accomplish both qualitative and quantitative analyses.

Zebra balığı Embriyolar Oksidatif Stres Analizi

High levels of reactive oxygen species (ROS) may cause a change of cellular redox state towards oxidative stress condition. This situation causes ...

Sequential Application of Glass Coverslips to Assess the Compressive Stiffness of the Mouse Lens: Strain and Morphometric Analyses

The eye lens is a transparent organ that refracts and focuses light to form a clear image on the retina. In humans, ciliary muscles contract to deform the lens, leading to an increase in the lens&#39; optical power to focus on nearby objects, a process known as accommodation. Age-related changes in lens stiffness have been linked to presbyopia, a reduction in the lens&#39; ability to accommodate, and, by extension, the need for reading glasses. Even though mouse lenses do not accommodate or develop presbyopia, mouse models can provide an invaluable genetic tool for understanding lens pathologies, and the accelerated aging observed in mice enables the study of age-related changes in the lens. This protocol demonstrates a simple, precise, and cost-effective method for determining mouse lens stiffness, using glass coverslips to apply sequentially increasing compressive loads onto the lens. Representative data confirm that mouse lenses become stiffer with age, like human lenses. This method is highly reproducible and can potentially be scaled up to mechanically test lenses from larger animals.

Age-related increases in eye lens stiffness are linked to presbyopia. This protocol describes a simple, cost-effective method for measuring mouse lens stiffness. Mouse lenses, like human lenses, become stiffer with age. This method is precise and can be adapted for lenses from larger animals.

Fare Lens Basınç Sertliği değerlendirin Cam lameller Sıralı Uygulama: Gerilme ve Morfometrik Analizleri

The eye lens is a transparent organ that refracts and focuses light to form a clear image on the retina. In humans, ciliary muscles contract to deform the ...

High-resolution Time-lapse Imaging and Automated Analysis of Microtubule Dynamics in Living Human Umbilical Vein Endothelial Cells

The physiological process by which new vasculature forms from existing vasculature requires specific signaling events that trigger morphological changes within individual endothelial cells (ECs). These processes are critical for homeostatic maintenance such as wound healing, and are also crucial in promoting tumor growth and metastasis. EC morphology is defined by the organization of the cytoskeleton, a tightly regulated system of actin and microtubule (MT) dynamics that is known to control EC branching, polarity and directional migration, essential components of angiogenesis. To study MT dynamics, we used high-resolution fluorescence microscopy coupled with computational image analysis of fluorescently-labeled MT plus-ends to investigate MT growth dynamics and the regulation of EC branching morphology and directional migration. Time-lapse imaging of living Human Umbilical Vein Endothelial Cells (HUVECs) was performed following transfection with fluorescently-labeled MT End Binding protein 3 (EB3) and Mitotic Centromere Associated Kinesin (MCAK)-specific cDNA constructs to evaluate effects on MT dynamics. PlusTipTracker software was used to track EB3-labeled MT plus ends in order to measure MT growth speeds and MT growth lifetimes in time-lapse images. This methodology allows for the study of MT dynamics and the identification of how localized regulation of MT dynamics within sub-cellular regions contributes to the angiogenic processes of EC branching and migration.

Protocols for Human Umbilical Vein Endothelial Cell (HUVEC) culture, transient transfection of fluorescently-labeled markers of microtubule growth, live-cell imaging and automated analysis of interphase microtubule growth dynamics are detailed.

Yüksek çözünürlüklü Time-lapse Görüntüleme ve Yaşayan İnsan Umbilikal Ven Endotelyal Hücrelerinde Mikrotubul Dinamiği Otomatik Analizi

The physiological process by which new vasculature forms from existing vasculature requires specific signaling events that trigger morphological changes ...

The Assembly and Application of 'Shear Rings': A Novel Endothelial Model for Orbital, Unidirectional and Periodic Fluid Flow and Shear Stress

Deviations from normal levels and patterns of vascular fluid shear play important roles in vascular physiology and pathophysiology by inducing adaptive as well as pathological changes in endothelial phenotype and gene expression. In particular, maladaptive effects of periodic, unidirectional flow induced shear stress can trigger a variety of effects on several vascular cell types, particularly endothelial cells. While by now endothelial cells from diverse anatomic origins have been cultured, in-depth analyses of their responses to fluid shear have been hampered by the relative complexity of shear models (e.g., parallel plate flow chamber, cone and plate flow model). While these all represent excellent approaches, such models are technically complicated and suffer from drawbacks including relatively lengthy and complex setup time, low surface areas, requirements for pumps and pressurization often requiring sealants and gaskets, creating challenges to both maintenance of sterility and an inability to run multiple experiments. However, if higher throughput models of flow and shear were available, greater progress on vascular endothelial shear responses, particularly periodic shear research at the molecular level, might be more rapidly advanced. Here, we describe the construction and use of shear rings: a novel, simple-to-assemble, and inexpensive tissue culture model with a relatively large surface area that easily allows for a high number of experimental replicates in unidirectional, periodic shear stress studies on endothelial cells.

Different levels and patterns of fluid shear are known to modulate endothelial gene expression, phenotype and susceptibility to disease. We discuss the assembly and use of 'shear rings': a model that produces unidirectional, periodic shear stress patterns. Shear rings are simple to assemble, economical and can produce high cell yields.

Montaj ve &#39;Kayma Rings&#39; Uygulama: Orbital tek yönlü ve Periyodik Akışkan Akışının ve Kayma Stres için Yeni Bir Endotel Modeli

Deviations from normal levels and patterns of vascular fluid shear play important roles in vascular physiology and pathophysiology by inducing adaptive as ...