Biz Dan Carlin kafesli floresein yapımında yardım için teşekkür etmek istiyorum. Buna ek olarak aşağıdaki finansman kaynakları teşekkür etmek istiyorum: JAC Gelişimsel Biyoloji Eğitimi Hibe Vanderbilt Üniversitesi Tıp Fakültesi Program ve NIH HD054534to JTG.

1. Kafesli Floresein Dextran&#39;ın Sentezi <ol><li> 3.5 Tedbir - aminodextran 4 mg ve 1 mg CMNB-kafesli floresein GD içeren Invitrogen sağlanan renkli bir tüp içine ekleyin. Bizim ellerde bu oran ortalama bir yükleme ~ dekstran ortalama 2.5 boya molekülleri verir. </li><li> Tüp 0,1 M Na 2 B 4 O 7 (sodyum borat) tampon 500 mcL ekleyin. </li><li> Cap ve aminodextran ve kafesli floresein çözmek için 30 saniye karıştırın. </li><li> Vorteks karıştırıcı gecede tepki olsun. </li><li> Zeba spin kolon alt kapatma Twist ve kapağı gevşetin. Bir keçeli kalem ile sütun üzerinde bir nokta işaretleyin. 15 ml konik tüp yerleştirin sütun. </li><li> Rotor merkezi karşılaştığı nokta ile 2 dakika süreyle 1000 xg&#39;de santrifüjleyin. Hemen sıkıştırma sonra sütunu kullanın. </li><li> Yeni bir 15-ml konik tüp sıkıştırılmış sütunu yerleştirin. </li><li> Havuzu reaksiyon karışımı ve sıkıştırılmış sütun reçine yatak merkezine transfer. Kapağını takın. </li><li> Rotor merkezi karşılaştığı nokta ile 2 dakika süreyle 1000 xg&#39;de santrifüjleyin. Spin sonra Eluent ve sütunun üst kabaca aynı renk sarı gölge olacaktır. </li><li> Sarı Eluent (~ 350 mcL) 1.5 mL mikrosantrifüj tüpüne aktarın. </li><li> Bir speedvac kuruluk Lyophilize. Speedvac folyo ile örtün. </li><li> % 1 w / v nihai konsantrasyonu, su, soluk sarı köpük, yeniden askıya çıkan ~ 2-3 mg </li><li> Bu çözüm folyo kaplı tüplerde -20 ° C&#39;de saklayın. Bu kısım tekrarlayan donma-çözülme önlemek için dekstran çözüm iyi bir fikirdir. </li></ol> 2. Zebra balığı Embriyolar içine Kafesli Floresein Dextran&#39;ın Enjeksiyon <ol><li> 0,2 M KCl kafesli floresein dekstran 1:5 veya 1:10% 1 w / v hisse senedi sulandırınız. </li><li> 0.5 enjekte basıncı enjektör kullanarak bir hücre dönem embriyoların yumurta sarısı içine kafesli floresein çözüm, 1.0nL. Bir kez enjekte edilen embriyolar, kavramalar ° C, non-spesifik uncaging azaltmak için 28.5 karanlıkta muhafaza edilmelidir. </li><li> El embriyolardan chorions çıkarın. </li><li> 4% tricaine embriyolar anestezisi. </li><li> Embriyolar 35mmx10mm petri sonra yumurta su ile kaplı,% 0.8 agaroz monte olacak. </li><li> En az 15 dakika süreyle 50 ° C ısı bloğu içinde erimiş agaroz dengelenmesi. </li><li> Cam bir pipet kullanarak, az miktarda su, tek bir embriyo çizmek ve agaroz Not içine bırakın. Önlemek için embriyo tüp içine koyarak, yaklaşık 30 saniye önce elinizde agaroz tüp soğutmak için önemlidir . embriyonun öldürülmesi. </li><li> Agaroz, yaklaşık 50μL ile birlikte, embriyo tüp Pipet ve petri merkezi üzerine içeriğini çıkarmak. </li><li> Hızla şark yukarı bakacak Uncaged hücreleri ile plastik bir iş parçacığı kullanarak embriyo Not: serin hızlı embriyo yönlendirilmesi ile acele agaroz. Agaroz katı olduktan sonra manipüle eğer Embriyolar zarar görebilir. </li><li> Agaroz tamamen katılaşmaya (bu birkaç dakika sürer) ve% 4 ve% 0.003 tricaine PTU içeren yumurta su ile dolu çanak üçte ikisi doldurmak için izin verin. </li></ol> 3. Lazer Uncaging Floresein Dextran&#39;ın <ol><li> Uncaging için kullanılan mikroskop, 40X suya daldırma hedefi sahip olması gerekir. </li><li> Biz, 365 nm boya hücre ve% 70 /% 30 split dikroik ayna ile bir Fotonik Instruments lazer kullanır. </li><li> Önce uncaging, lazer, objektif ve uygun güç için zayıflatılmış parfocal yapılmalıdır. </li><li> Lazer odaklanmak için, aynalı cam slayt hedefi altında bir yerde ve slayt çizikler görülebilir kadar objektif odak. </li><li> Lazer, tek bir darbe ile ayna açıkça görünür bir çizik üretebilecek hale gelene kadar lazer zayıflatıcı ayarlayın. </li><li> Objektif odak yukarı ve aşağı doğru ayarlayın. Objektif odak dışında olduğunda lazer bir çizik üretebilir, lazer odağı ayarlamak ¼ açmak veya aşağı yukarı. Lazer ayna sadece amaç odaklı çizebilir kadar tekrarlayın. </li><li> Place Uncaged alan amaç ve odak altında embriyo monte edilebilir. </li><li> Uncage için, bir hücre ilgi odağı ve 2-3 Hz&#39;de 10-20 kez darbe. </li><li> Forseps ile agaroz soyma ve yumurta su koyarak% 0.003 PTU içeren uncaging sonra, embriyo. Sabit oluncaya kadar embriyolar bir ışık geçirmez kutu gelişir. </li></ol> 4. Antikor Etiketleme ve Uncaged Floresein Dextran&#39;ın Algılama <ol><li> Ab fiksatif embriyolar Fix 4 2-4 saat oda sıcaklığında (RT) ya da gecelik (O / N) ° C (% 4 paraformaldehid, 0.3mm CaCl 2,% 8 sakaroz, 1X Fosfat Tuzlu, pH 7,3 Tamponlu ) Etiketleme tüm adımlar için, ışık geçirmez bir kutu veya folyo sarılmış tüp embriyolar tutun. </li><li> Fiksatif çıkarın ve% 100 MeOH ile değiştirin, oda sıcaklığında 10 dakika bekletin, MeOH ve Repla kaldırmak% 100 taze MeOH ile ce. </li><li> -20 ° C&#39;de en az 30 dakika süreyle MeOH Mağaza Not: epitoplar düşmeye başlamadan önce, iki hafta kadar için MeOH saklayabilirsiniz . </li><li> % 75 MeOH/1X Fosfat RT 5 dakika yıkar embriyo rehidrate tamponlu tuzlu su ile% 0.1 Tween 20 (1X PBSTw), daha sonra% 50% MeOH/50 1XPBTw, daha sonra% 25 MeOH/75% 1X PBSTw. </li><li> 1XPBSTw 5 dakika için üç kez yıkayın. </li><li> Eğer embriyolar&gt; 24 saat, 10 mikrogram / mL proteinaz K 1XPBSTw embriyo permiabilize. Permiabilization zaman sahnede bağlıdır. Embriyolar, 24 ve 48 saat sonrası fertilizasyon (hpf) arasında olup olmadığını proteinaz K Beş dakika yeterlidir. Eğer eski larvaları için daha fazla zaman gerekebilir. RT 20 dakika Ab fiksatif Re-fix </li><li> RT 1XPBSTw 5 dakika süreyle beş kez yıkayın. </li><li> Oda sıcaklığında 1-2 saat (1XPBS,% 0.1 Triton x100,% 10 koyunu serum,% 10 Bovine serum albümin,% 1 Dimetil sülfoksit) blok çözüm inkübe edin. </li><li> Çözümü engelleme primer antikorları (anti-floresein artı hücre türüne özgü belirteçler karşı antikorlar) sulandırınız. </li><li> 4 inkübe embriyolar O / N ° C primer antikorları içeren bir çözüm. </li><li> 1XPhosphate 20 dakika boyunca dört kez yıkayın RT% 0,1 Triton x100 (PBSTx) Tuzlu Tamponlu. </li><li> Çözümü engelleme floresan etiketli sekonder antikor (genellikle 1:300) sulandırınız. </li><li> 4 inkübe O / N ° C sekonder antikorlar içeren bir çözüm. </li><li> RT 1XPBSTx 20 dakika boyunca dört kez yıkayın. </li><li> RT en az iki saat için 50% glycerol/50% 1XPBS net embriyolar, daha sonra kaldırmak gliserol / PBS karışımı ve% 100 gliserol ekleyin ve bekletin 4 O / N ° C </li></ol> 5. Temsilcisi Sonuçlar: Immunolabeling sonra, (Şekil.1) Uncaged hücrelerinde boyanma zengin bir alan olmalıdır. Floresein spontan uncaging nedeniyle, nispeten yüksek bir sinyal gürültü oranı&gt; 48 saat eski Zebra balığı görmek için alışılmadık bir durum değildir. <img src="/files/ftp_upload/2672/2672fig1.jpg" alt="Şekil 1" /> Şekil 1 zebrafish epifiz kompleks Lineage etiketleme. Hpf foxd3 tarafından belirtilen ön epifiz anlage bir kısmı, 24 yaşında GFP ifade, UV lazer darbeleri kullanarak Uncaged A) 48hpf olarak, hücrelerin sol taraflı bir küme parapineal (kırmızı daire) Uncaged ortaya çıkmıştır etki alanı (beyaz daire). B), parapineal (kırmızı daire içinde Uncaged floresein sinyali zenginleştirilmiş) ve pineal organ (beyaz daire) .

<ol>
	<li>Hatada, Y., Stern, C. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+fate+map+of+the+epiblast+of+the+early+chick+embryo.">A fate map of the epiblast of the early chick embryo.</a> Development. 120, 2879-2889 (1994).</li><li>Moody, S. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fates+of+the+blastomeres+of+the+32-cell-stage+Xenopus+embryo.">Fates of the blastomeres of the 32-cell-stage Xenopus embryo.</a> Dev Biol. 122, 300-319 (1987).</li><li>Wetts, R., Fraser, S. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Multipotent+Precursors+Can+Give+Rise+to+All+Major+Cell-Types+of+the+Frog+Retina.">Multipotent Precursors Can Give Rise to All Major Cell-Types of the Frog Retina.</a> Science. 239, 1142-1145 (1988).</li><li>Wetts, R., Fraser, S. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microinjection+of+fluorescent+tracers+to+study+neural+cell+lineages.">Microinjection of fluorescent tracers to study neural cell lineages.</a> Development. , 1-8 (1991).</li><li>Woo, K., Fraser, S. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Order+and+coherence+in+the+fate+map+of+the+zebrafish+nervous+system.">Order and coherence in the fate map of the zebrafish nervous system.</a> Development. 121, 2595-2609 (1995).</li><li>Ando, R., Hama, H., Yamamoto-Hino, M., Mizuno, H., Miyawaki, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+optical+marker+based+on+the+UV-induced+green-to-red+photoconversion+of+a+fluorescent+protein.">An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein.</a> Proc Natl Acad Sci U S A. 99, 12651-12656 (2002).</li><li>Sato, T., Takahoko, M., Okamoto, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=HuC:Kaede,+a+useful+tool+to+label+neural+morphologies+in+networks+in+vivo.">HuC:Kaede, a useful tool to label neural morphologies in networks in vivo.</a> Genesis. 44, 136-142 (2006).</li><li>Wiedenmann, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=EosFP,+a+fluorescent+marker+protein+with+UV-inducible+green-to-red+fluorescence+conversion.">EosFP, a fluorescent marker protein with UV-inducible green-to-red fluorescence conversion.</a> Proc Natl Acad Sci U S A. 101, 15905-15910 (2004).</li><li>Haugland, R. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Handbook of Fluorescent Probes and Research Chemicals. , 707-711 (2002).</li><li>Kozlowski, D. J., Murakami, T., Ho, R. K., Weinberg, E. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regional+cell+movement+and+tissue+patterning+in+the+zebrafish+embryo+revealed+by+fate+mapping+with+caged+fluorescein.">Regional cell movement and tissue patterning in the zebrafish embryo revealed by fate mapping with caged fluorescein.</a> Biochem Cell Biol. 75, 551-562 (1997).</li><li>Kozlowski, D. J., Weinberg, E. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Photoactivatable+(caged)+fluorescein+as+a+cell+tracer+for+fate+mapping+in+the+zebrafish+embryo.">Photoactivatable (caged) fluorescein as a cell tracer for fate mapping in the zebrafish embryo.</a> Methods Mol Biol. 135, 349-355 (2000).</li><li>Russek-Blum, N., Nabel-Rosen, H., Levkowitz, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High+resolution+fate+map+of+the+zebrafish+diencephalon.">High resolution fate map of the zebrafish diencephalon.</a> Dev Dyn. 238, 1827-1835 (2009).</li><li>Summers, R. G., Piston, D. W., Harris, K. M., Morrill, J. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+orientation+of+first+cleavage+in+the+sea+urchin+embryo,+Lytechinus+variegatus,+does+not+specify+the+axes+of+bilateral+symmetry.">The orientation of first cleavage in the sea urchin embryo, Lytechinus variegatus, does not specify the axes of bilateral symmetry.</a> Dev Biol. 175, 177-183 (1996).</li></ol>

Açıklandığı gibi, bu protokol, mikroenjeksiyon, mikroskopi ve immünofloresan sık kullanılan teknikler üzerine inşa edilmiştir zebrafish nispeten hızlı bir soy etiketleme yöntemi sağlar. Biz lazer yerelleştirilmiş bir moda flöresein uncage için en verimli ve maliyet etkin yolu olarak uncaging olduğunu bulduk. Bu yöntem 4 dpf&#39;e gibi geç olarak deneysel uç noktaları ile soy etiket olabilir. Ancak, hücre bölünmeleri gibi, hücre başına kafesli-floresein toplama sonunda saptanabilir düzeylerde ötesinde azalır. Buna ek olarak, zebrafish larvaları 11 flöresein spontan, non-spesifik uncaging bildirilmiştir. Uncaged floresein gibi, algılama, en erken larva aşamasında etkili (48-72 hpf) veya daha önceki gibi. Bizim tercih uncaging yöntemi darbeli azot lazer kullanımı. Bunlar genel olarak, hücre ablasyonların deneyleri için kullanılan ve singe hücre veya hücreleri küçük gruplar 11-12 uncage yeterince doğru vardır . Ancak, aynı zamanda uncaging konfokal mikroskop kullanılarak elde edilebilir; iki foton konfokal mikroskoplar çok hassas uncaging 12 elde etmek için kullanılmaktadır. Hassas gerekli değilse Yelpazenin diğer ucunda, daha sonra lazer vazgeçilebilir. 11 üzerinden küçük bir iğne deliği uncage DAPI filtre seti ile donatılmış bir epifluorescent mikroskop kullanılabilir. Biz bu algılama, kırmızı ya da uzak-kırmızı dalga boyu (örneğin Alexa 633) bizim ihtiyaçlarımıza en uygun yayan bir birincil antikor ve floresan ikincil antikor kullanarak Uncaged flöresein bulduk. Bu bize, transgen (Şekil 1) tarafından ifade GFP Uncaged floresein ayırt etmek için izin verir.

A correction was made to <a href="https://www-jove-com.remotexs.ntu.edu.sg/details.php?id=2672">Lineage Labeling of Zebrafish Cells with Laser Uncagable Fluorescein Dextran</a>. There was an error in the authors, Ilya A. Shestopalov and James K. Chen, names. The author's names have been corrected to: Ilya A. Shestopalov and James K. Chen instead of: Ilya Shestopalov and James Chen

A correction to the article Lineage Labeling of Zebrafish Cells with Laser Uncagable Fluorescein Dextran was made.

Erratum: Lineage Labeling of Zebrafish Cells with Laser Uncagable Fluorescein Dextran

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<tr>
<td>CMNB-caged fluorescein SE</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>C20050</td>
<td>&nbsp;</td>
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<td>Aminodextran, 10kDa</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>D1860</td>
<td>&nbsp;</td>
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<td>Zeba desalt spin columns</td>
<td>&nbsp;</td>
<td>Pierce</td>
<td>89889</td>
<td>&nbsp;</td>
<tr>
<td>goat anti-fluorescein antibody</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>A11095</td>
<td>&nbsp;</td>
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<td>Alexa Fluor 633 Donkey anti-goat antibody</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>A21082</td>
<td>&nbsp;</td>
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<td>35mmx10mm petri dishes</td>
<td>&nbsp;</td>
<td>Becton-Dickinson</td>
<td>351008</td>
<td>&nbsp;</td>
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<td>Upright compound microscope with 40x water immersion objective</td>
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<td>Leica</td>
<td>DM6000B</td>
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<td>MicroPoint Manual Laser Illumination System</td>
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<td>&nbsp;</td>
<td>&nbsp;</td>
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<td>Phenylthiourea (PTU)</td>
<td>&nbsp;</td>
<td>Alfa Aesar</td>
<td>L06690</td>
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<td>Tricaine</td>
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<td>E10521</td>
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<td>&nbsp;</td>
<td>Roche</td>
<td>03115836991</td>
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<td>Plastic thread</td>
<td>&nbsp;</td>
<td>Any sewing supply store</td>
<td>&nbsp;</td>
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<td>Agarose</td>
<td>&nbsp;</td>
<td>Research Products International</td>
<td>A20090</td>
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<td>SpeedVac</td>
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<td>Pressure injector</td>
<td>&nbsp;</td>
<td>Applied Scientific Instrumentation</td>
<td>MPPI-3</td>
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lineage labeling of zebrafish cells with laser uncagable fluorescein dextran

Gelişimsel biyoloji merkezi bir sorun farklılaşmamış öncüleri olarak ortaya çıkan omurgalıların bulunan sayısız hücre tiplerinin kökenini anlamak için. Araştırmacılar DII etiketleme 1 ve model sistemler geliştirme sonraki aşamalarında tespit hücre kaderinin izlenebilir enzimlerin basınçlı enjeksiyon 2 gibi soy etiketleme çeşitli yöntemleri, istihdam var. Zebra balığı (Danio rerio) ilk kaderi haritalar rodamin dekstran gibi floresan boyalar, iyontoforez enjeksiyon yoluyla embriyo ayrık bölgelerinde tek hücrelerin içine monte edilmiş ve üzerinden etiketli hücrenin kaderini izleme süresi 3-5. Etkili olsa da, bu yöntemlerin teknik olarak zor ve yaygın zebrafish laboratuarları bulunan olmayan özel ekipman gerektirmez. Son zamanlarda, ultraviyole ışığa maruz kaldığında yeşil kırmızı floresan geri dönüşümsüz geçiş Eos ve Kaede photoconvertable floresan proteinleri, zebrafish 6-8 artış görüyoruz. Zebrafish embriyo ve transgenesis göreli kolaylığı optik netlik soy etiketlenmesi için bu özellikle çekici araçlar yapmış ve in vivo 7 hücrelerin göç gözlemlemek için. Onların yardımcı programı olmasına rağmen, bu proteinlerin, boya-aracılı soy etiketleme yöntemleri, bazı dezavantajları karşılaştırıldığında var. En önemli zorluk biz Fotoçevrim sırasında bu proteinlerin 3 boyutlu yüksek çözünürlük elde bulduk. Bu ışık, belki de çözünürlüğü ve kullanım kolaylığı zebrafish soy etiketleme için en iyi kombinasyonu kafesli floresein dekstran kullanımı, su verme grubuna bağlı bir floresan boya yapar, maskeler, floresan 9 . Sonra boya, floresan veya İmmuno görselleştirme sağlayan bir lazer veya cıva lambası, UV ışık kullanarak belirli bir hücre içinde (su verme grubu serbest) &quot;Uncaged&quot; olabilir. Iyontoforez yöntemlerinin aksine, kafesli floresein standart enjeksiyon aparatları ile enjekte edilir ve bir iğne deliği 10 ile donatılmış bir Epifloresans mikroskop ile Uncaged. Buna ek olarak, floresein karşı antikor sadece Uncaged formu tespit ve epitop fiksasyonu iyi 11 hayatta. Son olarak, kafesli floresein iki foton mikroskopi 12,13 istihdam, özellikle çok yüksek 3-D çözünürlük ile aktive olabilir. Bu protokol, kafesli floresein ve lazer uncaging soy etiketleme bir yöntem açıklanır. Subsequenctly, Uncaged floresein antikorlar ile etiketleme gibi GFP gibi diğer epitopları ile eş zamanlı olarak algılanır.

Watch this Scientific Journal Video about Lineage Labeling of Zebrafish Cells with Laser Uncagable Fluorescein Dextran at JoVE.com

Lineage Labeling of Zebrafish Cells with Laser Uncagable Fluorescein Dextran

Bu protokol, Uncaged floresein gelen sinyali yükseltmek için immunolabeling tüm montaj takip kafesli flöresein UV uncaging kullanarak hücrelerin zebrafish embriyoların küçük gruplar kaderi etiket ve takip etmek için bir yol çizer.

Lazer Uncagable Floresein Dextran&#39;ın Zebra balığı Hücre Lineage Etiketleme

A central problem in developmental biology is to deduce the origin of the myriad cell types present in vertebrates as they arise from undifferentiated ...

lineage-labeling-zebrafish-cells-with-laser-uncagable-fluorescein

Nanyang Technological University

Research

JoVE Journal

Biology

13.8K Görüntüleme.  Vanderbilt University. Bu protokol, Uncaged floresein gelen sinyali yükseltmek için immunolabeling tüm montaj takip kafesli flöresein UV uncaging kullanarak hücrelerin zebrafish embriyoların küçük gruplar kaderi etiket ve takip etmek için bir yol çizer.

Video: Lineage Labeling of Zebrafish Cells with Laser Uncagable Fluorescein Dextran

Labeling Stem Cells with Fluorescent Dyes for non-invasive Detection with Optical Imaging

Optical imaging (OI) is an easy, fast and inexpensive tool for in vivo monitoring of new stem cell based therapies. The technique is based on ex vivo labeling of stem cells with a fluorescent dye, subsequent intravenous injection of the labeled cells and visualization of their accumulation in specific target organs or pathologies. The presented technique demonstrates how we label human mesenchymal stem cells (hMSC) by simple incubation with the lipophilic fluorescent dye DiD (C67H103CIN2O3S) and how we label human embryonic stem cells (hESC) with the FDA approved fluorescent dye Indocyanine Green (ICG). The uptake mechanism is via adherence and diffusion of the lypophilic dye across the phospholipid cell membrane bilayer. The labeling efficiency is usually improved if the cells are incubated with the dye in serum-free media as opposed to incubation in serum-containing media. Furthermore, the addition of the transfection agent Protamine Sulfate significantly improves contrast agent uptake.

This video shows techniques for labeling of human embryonic stem cells and mesenchymal stem cells with fluorescent dyes. This technique can be used for an in vivo tracking of transplanted stem cells with optical imaging and for histopathological correlations with fluorescence microscopy.

Optik Görüntüleme ile non-invaziv Algılama için Floresan Boyalar Kök Hücreler Etiketleme

Optical imaging (OI) is an easy, fast and inexpensive tool for in vivo monitoring of new stem cell based therapies. The technique is based on ex vivo ...

Biyoloji

Imaging Glycans in Zebrafish Embryos by Metabolic Labeling and Bioorthogonal Click Chemistry

Imaging glycans in vivo has recently been enabled using a bioorthogonal chemical reporter strategy by treating cells or organisms with azide- or alkyne-tagged monosaccharides1, 2. The modified monosaccharides, processed by the glycan biosynthetic machinery, are incorporated into cell surface glycoconjugates. The bioorthogonal azide or alkyne tags then allow covalent conjugation with fluorescent probes for visualization, or with affinity probes for enrichment and glycoproteomic analysis. This protocol describes the procedures typically used for noninvasive imaging of fucosylated glycans in zebrafish embryos, including: 1) microinjection of one-cell stage embryos with GDP-5-alkynylfucose (GDP-FucAl), 2) labeling fucosylated glycans in the enveloping layer of zebrafish embryos with azide-conjugated fluorophores via biocompatible Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC), and 3) imaging by confocal microscopy3. The method described here can be readily extended to visualize other classes of glycans, e.g. glycans containing sialic acid4 and N-acetylgalactosamine5, 6, in developing zebrafish and in other living organisms.

A click-chemistry based method that allows for the rapid, noninvasive, and robust labeling of alkyne-tagged glycans in zebrafish embryos is described. Fucosylated glycans in the enveloping layer of zebrafish embryos in the late gastrulation stage were imaged in this study.

Metabolik Etiketleme ve Bioorthogonal tıklayın Kimya Zebra balığı Embriyolar Görüntüleme glukanlardır

Imaging glycans in vivo has recently been enabled using a bioorthogonal chemical reporter strategy by treating cells or organisms with azide- or ...

Laser Ablation of the Zebrafish Pronephros to Study Renal Epithelial Regeneration

Acute kidney injury (AKI) is characterized by high mortality rates from deterioration of renal function over a period of hours or days that culminates in renal failure1. AKI can be caused by a number of factors including ischemia, drug-based toxicity, or obstructive injury1. This results in an inability to maintain fluid and electrolyte homeostasis. While AKI has been observed for decades, effective clinical therapies have yet to be developed. Intriguingly, some patients with AKI recover renal functions over time, a mysterious phenomenon that has been only rudimentally characterized1,2. Research using mammalian models of AKI has shown that ischemic or nephrotoxin-injured kidneys experience epithelial cell death in nephron tubules1,2, the functional units of the kidney that are made up of a series of specialized regions (segments) of epithelial cell types3. Within nephrons, epithelial cell death is highest in proximal tubule cells. There is evidence that suggests cell destruction is followed by dedifferentiation, proliferation, and migration of surrounding epithelial cells, which can regenerate the nephron entirely1,2. However, there are many unanswered questions about the mechanisms of renal epithelial regeneration, ranging from the signals that modulate these events to reasons for the wide variation of abilities among humans to regenerate injured kidneys.
The larval zebrafish provides an excellent model to study kidney epithelial regeneration as its pronephric kidney is comprised of nephrons that are conserved with higher vertebrates including mammals4,5. The nephrons of zebrafish larvae can be visualized with fluorescence techniques because of the relative transparency of the young zebrafish6. This provides a unique opportunity to image cell and molecular changes in real-time, in contrast to mammalian models where nephrons are inaccessible because the kidneys are structurally complex systems internalized within the animal. Recent studies have employed the aminoglycoside gentamicin as a toxic causative agent for study of AKI and subsequent renal failure: gentamicin and other antibiotics have been shown to cause AKI in humans, and researchers have formulated methods to use this agent to trigger kidney damage in zebrafish7,8. However, the effects of aminoglycoside toxicity in zebrafish larvae are catastrophic and lethal, which presents a difficulty when studying epithelial regeneration and function over time. Our method presents the use of targeted cell ablation as a novel tool for the study of epithelial injury in zebrafish. Laser ablation gives researchers the ability to induce cell death in a limited population of cells. Varying areas of cells can be targeted based on morphological location, function, or even expression of a particular cellular phenotype. Thus, laser ablation will increase the specificity of what researchers can study, and can be a powerful new approach to shed light on the mechanisms of renal epithelial regeneration. This protocol can be broadly applied to target cell populations in other organs in the zebrafish embryo to study injury and regeneration in any number of contexts of interest.

Acute kidney injury (AKI) in humans is a common clinical problem caused by damage to the epithelial cells that comprise kidney nephrons, and AKI is associated with high mortality rates of 50-70%1. Following epithelial cell destruction, nephrons have a limited ability to regenerate, though the mechanisms and limitations that guide this phenomenon remain poorly understood. In this video article, we describe our technique for targeted laser ablation of kidney nephron cells in the zebrafish embryo kidney, or pronephros. Our new method can be used to complement nephrotoxicity-induced models of AKI and gain a high-resolution understanding of the cell and molecular alterations that are associated with epithelial regeneration in the kidney nephron.

Zebra balığı Pronephros Lazer Ablasyon Böbrek Epitel Rejenerasyon Eğitim

Acute kidney injury (AKI) is characterized by high mortality rates from deterioration of renal function over a period of hours or days that culminates in ...

Determination of Lipid Raft Partitioning of Fluorescently-tagged Probes in Living Cells by Fluorescence Correlation Spectroscopy (FCS)

In the past fifteen years the notion that cell membranes are not homogenous and rely on microdomains to exert their functions has become widely accepted. Lipid rafts are membrane microdomains enriched in cholesterol and sphingolipids. They play a role in cellular physiological processes such as signalling, and trafficking1,2 but are also thought to be key players in several diseases including viral or bacterial infections and neurodegenerative diseases3.
Yet their existence is still a matter of controversy4,5. Indeed, lipid raft size has been estimated to be around 20 nm6, far under the resolution limit of conventional microscopy (around 200 nm), thus precluding their direct imaging. Up to now, the main techniques used to assess the partition of proteins of interest inside lipid rafts were Detergent Resistant Membranes (DRMs) isolation and co-patching with antibodies. Though widely used because of their rather easy implementation, these techniques were prone to artefacts and thus criticized7,8. Technical improvements were therefore necessary to overcome these artefacts and to be able to probe lipid rafts partition in living cells.
Here we present a method for the sensitive analysis of lipid rafts partition of fluorescently-tagged proteins or lipids in the plasma membrane of living cells. This method, termed Fluorescence Correlation Spectroscopy (FCS), relies on the disparity in diffusion times of fluorescent probes located inside or outside of lipid rafts. In fact, as evidenced in both artificial membranes and cell cultures, probes would diffuse much faster outside than inside dense lipid rafts9,10. To determine diffusion times, minute fluorescence fluctuations are measured as a function of time in a focal volume (approximately 1 femtoliter), located at the plasma membrane of cells with a confocal microscope (Fig. 1). The auto-correlation curves can then be drawn from these fluctuations and fitted with appropriate mathematical diffusion models11.
FCS can be used to determine the lipid raft partitioning of various probes, as long as they are fluorescently tagged. Fluorescent tagging can be achieved by expression of fluorescent fusion proteins or by binding of fluorescent ligands. Moreover, FCS can be used not only in artificial membranes and cell lines but also in primary cultures, as described recently12. It can also be used to follow the dynamics of lipid raft partitioning after drug addition or membrane lipid composition change12.

Determination of Lipid Raft Partitioning of Fluorescently-tagged Probes in Living Cells by Fluorescence Correlation Spectroscopy FCS

A technique to probe the lipid raft partitioning of fluorescent proteins at the plasma membrane of living cells is described. It takes advantage of the disparity in diffusion times of proteins located inside or outside of lipid rafts. Acquisition can be performed dynamically in control conditions or after drug addition.

Lipid Raft belirlenmesi Flüoresan Korelasyon Spektroskopisi (FCS) tarafından Yaşayan hücreler içinde floresan etiketli Soruşturmasının Bölümleme

In the past fifteen years the notion that cell membranes are not homogenous and rely on microdomains to exert their functions has become widely accepted. ...

Phenotypic Analysis and Isolation of Murine Hematopoietic Stem Cells and Lineage-committed Progenitors

The bone marrow is the principal site where HSCs and more mature blood cells lineage progenitors reside and differentiate in an adult organism. HSCs constitute a minute cell population of pluripotent cells capable of generating all blood cell lineages for a life-time1. The molecular dissection of HSCs homeostasis in the bone marrow has important implications in hematopoiesis, oncology and regenerative medicine. We describe the labeling protocol with fluorescent antibodies and the electronic gating procedure in flow cytometry to score hematopoietic progenitor subsets and HSCs distribution in individual mice (Fig. 1). In addition, we describe a method to extensively enrich hematopoietic progenitors as well as long-term (LT) and short term (ST) reconstituting HSCs from pooled bone marrow cell suspensions by magnetic enrichment of cells expressing c-Kit. The resulting cell preparation can be used to sort selected subsets for in vitro and in vivo functional studies (Fig. 2).
Both trabecular osteoblasts2,3 and sinusoidal endothelium4 constitute functional niches supporting HSCs in the bone marrow. Several mechanisms in the osteoblastic niche, including a subset of N-cadherin+ osteoblasts3 and interaction of the receptor tyrosine kinase Tie2 expressed in HSCs with its ligand angiopoietin-15 concur in determining HSCs quiescence. "Hibernation" in the bone marrow is crucial to protect HSCs from replication and eventual exhaustion upon excessive cycling activity6. Exogenous stimuli acting on cells of the innate immune system such as Toll-like receptor ligands7 and interferon-&alpha;6 can also induce proliferation and differentiation of HSCs into lineage committed progenitors. Recently, a population of dormant mouse HSCs within the lin- c-Kit+ Sca-1+ CD150+ CD48- CD34- population has been described8. Sorting of cells based on CD34 expression from the hematopoietic progenitors-enriched cell suspension as described here allows the isolation of both quiescent self-renewing LT-HSCs and ST-HSCs9. A similar procedure based on depletion of lineage positive cells and sorting of LT-HSC with CD48 and Flk2 antibodies has been previously described10. In the present report we provide a protocol for the phenotypic characterization and ex vivo cell cycle analysis of hematopoietic progenitors, which can be useful for monitoring hematopoiesis in different physiological and pathological conditions. Moreover, we describe a FACS sorting procedure for HSCs, which can be used to define factors and mechanisms regulating their self-renewal, expansion and differentiation in cell biology and signal transduction assays as well as for transplantation.

A method to analyse the distribution of bone marrow hematopoietic progenitors in flow cytometry as well as to efficiently isolate highly purified hematopoietic stem cells (HSCs) is described. The isolation procedure is essentially based on magnetic enrichment of c-Kit+ cells and cell sorting to purify HSCs for cellular and molecular studies.

Mürin Hematopoetik Kök Hücreler ve Lineage-kararlı progenitörlerin Fenotipik Analizi ve İzolasyon

The bone marrow is the principal site where HSCs and more mature blood cells lineage progenitors reside and differentiate in an adult organism. HSCs ...

Laser-inflicted Injury of Zebrafish Embryonic Skeletal Muscle

Various experimental approaches have been used in mouse to induce muscle injury with the aim to study muscle regeneration, including myotoxin injections (bupivacaine, cardiotoxin or notexin), muscle transplantations (denervation-devascularization induced regeneration), intensive exercise, but also murine muscular dystrophy models such as the mdx mouse (for a review of these approaches see 1). In zebrafish, genetic approaches include mutants that exhibit muscular dystrophy phenotypes (such as runzel2 or sapje3) and antisense oligonucleotide morpholinos that block the expression of dystrophy-associated genes4. Besides, chemical approaches are also possible, e.g. with Galanthamine, a chemical compound inhibiting acetylcholinesterase, thereby resulting in hypercontraction, which eventually leads to muscular dystrophy5. However, genetic and pharmacological approaches generally affect all muscles within an individual, whereas the extent of physically inflicted injuries are more easily controlled spatially and temporally1. Localized physical injury allows the assessment of contralateral muscle as an internal control. Indeed, we recently used laser-mediated cell ablation to study skeletal muscle regeneration in the zebrafish embryo6, while another group recently reported the use of a two-photon laser (822 nm) to damage very locally the plasma membrane of individual embryonic zebrafish muscle cells7.
Here, we report a method for using the micropoint laser (Andor Technology) for skeletal muscle cell injury in the zebrafish embryo. The micropoint laser is a high energy laser which is suitable for targeted cell ablation at a wavelength of 435 nm. The laser is connected to a microscope (in our setup, an optical microscope from Zeiss) in such a way that the microscope can be used at the same time for focusing the laser light onto the sample and for visualizing the effects of the wounding (brightfield or fluorescence). The parameters for controlling laser pulses include wavelength, intensity, and number of pulses.
Due to its transparency and external embryonic development, the zebrafish embryo is highly amenable for both laser-induced injury and for studying the subsequent recovery. Between 1 and 2 days post-fertilization, somitic skeletal muscle cells progressively undergo maturation from anterior to posterior due to the progression of somitogenesis from the trunk to the tail8, 9. At these stages, embryos spontaneously twitch and initiate swimming. The zebrafish has recently been recognized as an important vertebrate model organism for the study of tissue regeneration, as many types of tissues (cardiac, neuronal, vascular etc.) can be regenerated after injury in the adult zebrafish10, 11.

The method presented here comprises the precise injury of live zebrafish embryos with high-energy laser pulses and the subsequent analysis of these injuries and their recovery with time. We also show how genetically labeled single or groups of skeletal muscle cells can be tracked during and after laser light induced damage.

Zebra balığı Embriyonik İskelet Kası Lazer-yaralama

Various experimental approaches have been used in mouse to induce muscle injury with the aim to study muscle regeneration, including myotoxin injections ...

Fluorescence Imaging with One-nanometer Accuracy (FIONA)

Fluorescence imaging with one-nanometer accuracy (FIONA) is a simple but useful technique for localizing single fluorophores with nanometer precision in the x-y plane. Here a summary of the FIONA technique is reported and examples of research that have been performed using FIONA are briefly described. First, how to set up the required equipment for FIONA experiments, i.e., a total internal reflection fluorescence microscopy (TIRFM), with details on aligning the optics, is described. Then how to carry out a simple FIONA experiment on localizing immobilized Cy3-DNA single molecules using appropriate protocols, followed by the use of FIONA to measure the 36 nm step size of a single truncated myosin Va motor labeled with a quantum dot, is illustrated. Lastly, recent effort to extend the application of FIONA to thick samples is reported. It is shown that, using a water immersion objective and quantum dots soaked deep in sol-gels and rabbit eye corneas (&#62;200 &#181;m), localization precision of 2-3 nm can be achieved.

Fluorescence Imaging with One-nanometer Accuracy FIONA

Single fluorophores can be localized with nanometer precision using FIONA. Here a summary of the FIONA technique is reported, and how to carry out FIONA experiments is described.

Bir nanometre Hassasiyet Floresans Görüntüleme (Fiona)

Fluorescence imaging with one-nanometer accuracy (FIONA) is a simple but useful technique for localizing single fluorophores with nanometer precision in ...

Nephrotoxin Microinjection in Zebrafish to Model Acute Kidney Injury

The kidneys are susceptible to harm from exposure to chemicals they filter from the bloodstream. This can lead to organ injury associated with a rapid decline in renal function and development of the clinical syndrome known as acute kidney injury (AKI). Pharmacological agents used to treat medical circumstances ranging from bacterial infection to cancer, when administered individually or in combination with other drugs, can initiate AKI. Zebrafish are a useful animal model to study the chemical effects on renal function in vivo, as they form an embryonic kidney comprised of nephron functional units that are conserved with higher vertebrates, including humans. Further, zebrafish can be utilized to perform genetic and chemical screens, which provide opportunities to elucidate the cellular and molecular facets of AKI and develop therapeutic strategies such as the identification of nephroprotective molecules. Here, we demonstrate how microinjection into the zebrafish embryo can be utilized as a paradigm for nephrotoxin studies.

Renal injuries incurred from nephrotoxins, which include drugs ranging from antibiotics to chemotherapeutics, can result in complex disorders whose pathogenesis remains incompletely understood. This protocol demonstrates how zebrafish can be used for disease modeling of these conditions, which can be applied to the identification of renoprotective measures.

Zebra balığı Nephrotoxin Mikroenjeksiyon Akut Böbrek Yaralanması Model

The kidneys are susceptible to harm from exposure to chemicals they filter from the bloodstream. This can lead to organ injury associated with a rapid ...

Visualization and Quantification of Mesenchymal Cell Adipogenic Differentiation Potential with a Lineage Specific Marker

Several dyes are currently available for use in detecting differentiation of mesenchymal cells into adipocytes. Dyes, such as Oil Red O, are cheap, easy to use and widely utilized by laboratories analyzing the adipogenic potential of mesenchymal cells. However, they are not specific to changes in gene transcription. We have developed a gene-specific differentiation assay to analyze when a mesenchymal cell has switched its fate to an adipogenic lineage. Immuno-labelling against fatty acid binding protein-4 (FABP4), a lineage-specific marker of adipogenic differentiation, enabled visualization and quantification of differentiated cells. The ability to quantify adipogenic differentiation potential of mesenchymal cells in a 96 well microplate format has promising implications for a number of applications. Hundreds of clinical trials involve the use of adult mesenchymal stromal cells and it is currently difficult to correlate therapeutic outcomes within and especially between such clinical trials. This simple high-throughput FABP4 assay provides a quantitative assay for assessing the differentiation potential of patient-derived cells and is a robust tool for comparing different isolation and expansion methods. This is particularly important given the increasing recognition of the heterogeneity of the cells being administered to patients in mesenchymal cell products. The assay also has potential utility in high throughput drug screening, particularly in obesity and pre-diabetes research.

Traditional methods of assessing adipogenic differentiation are cheap and easy to use, but are not specific to changes in gene expression. We have developed an assay to quantify mesenchymal cell differentiation into mature adipocytes using a lineage specific marker. This assay has diverse applications across basic research and clinical medicine.

Görselleştirme ve miktar Mezenkimal hücre Adipojenik farklılaşma potansiyeli bir Lineage belirli Marker ile

Several dyes are currently available for use in detecting differentiation of mesenchymal cells into adipocytes. Dyes, such as Oil Red O, are cheap, easy ...

Lineage Tracing and Clonal Analysis in Developing Cerebral Cortex Using Mosaic Analysis with Double Markers (MADM)

Beginning from a limited pool of progenitors, the mammalian cerebral cortex forms highly organized functional neural circuits. However, the underlying cellular and molecular mechanisms regulating lineage transitions of neural stem cells (NSCs) and eventual production of neurons and glia in the developing neuroepithelium remains unclear. Methods to trace NSC division patterns and map the lineage of clonally related cells have advanced dramatically. However, many contemporary lineage tracing techniques suffer from the lack of cellular resolution of progeny cell fate, which is essential for deciphering progenitor cell division patterns. Presented is a protocol using mosaic analysis with double markers (MADM) to perform in vivo clonal analysis. MADM concomitantly manipulates individual progenitor cells and visualizes precise division patterns and lineage progression at unprecedented single cell resolution. MADM-based interchromosomal recombination events during the G2-X phase of mitosis, together with temporally inducible CreERT2, provide exact information on the birth dates of clones and their division patterns. Thus, MADM lineage tracing provides unprecedented qualitative and quantitative optical readouts of the proliferation mode of stem cell progenitors at the single cell level. MADM also allows for examination of the mechanisms and functional requirements of candidate genes in NSC lineage progression. This method is unique in that comparative analysis of control and mutant subclones can be performed in the same tissue environment in vivo. Here, the protocol is described in detail, and experimental paradigms to employ MADM for clonal analysis and lineage tracing in the developing cerebral cortex are demonstrated. Importantly, this protocol can be adapted to perform MADM clonal analysis in any murine stem cell niche, as long as the CreERT2 driver is present.

Lineage Tracing and Clonal Analysis in Developing Cerebral Cortex Using Mosaic Analysis with Double Markers MADM

A protocol to perform lineage tracing and functional genetic analysis of candidate genes at a single cell level using mosaic analysis with double markers (MADM) is presented. MADM clonal analysis provides a quantitative framework to measure the proliferative behavior, cellular output, and lineage relationship of individual progenitors and their daughter cells.

Çift Marker (MADM) ile Mozaik Analizi Kullanarak Serebral Korteks Geliştirilmesinde Soy İzleme ve Klonal Analizi

Beginning from a limited pool of progenitors, the mammalian cerebral cortex forms highly organized functional neural circuits. However, the underlying ...