L. Rinaldi, S. Schäffer, D. Reitz, H. Thomas ve A. Weber&#39;in teknik desteği minnettarlıkla kabul edilmektedir. Yazarlar, el yazmalarının derin kanıtı okuma ve dil düzenlemesi için Dr. E. Martinson&#39;a teşekkür etmek istiyorlar. Çalışma, M. Aslam ve D. Gündüz&#39;e verilen Giessen Anschubsfinanzierung Üniversitesi tarafından desteklendi.

<ol>
	<li>Zaragoza, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Animal+models+of+cardiovascular+diseases.">Animal models of cardiovascular diseases.</a> J Biomed Biotechnol. 2011, 497841 (2011).</li><li>Claycomb, W. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=HL-1+cells:+a+cardiac+muscle+cell+line+that+contracts+and+retains+phenotypic+characteristics+of+the+adult+cardiomyocyte.">HL-1 cells: a cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte.</a> Proc Natl Acad Sci U S A. 95 (6), 2979-2984 (1998).</li><li>Barbieri, S. S., Weksler, B. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tobacco+smoke+cooperates+with+interleukin-1beta+to+alter+beta-catenin+trafficking+in+vascular+endothelium+resulting+in+increased+permeability+and+induction+of+cyclooxygenase-2+expression+in+vitro+and+in+vivo.">Tobacco smoke cooperates with interleukin-1beta to alter beta-catenin trafficking in vascular endothelium resulting in increased permeability and induction of cyclooxygenase-2 expression in vitro and in vivo.</a> FASEB J. 21 (8), 1831-1843 (2007).</li><li>Piper, H. M., Probst, I., Schwartz, P., Hutter, F. J., Spieckermann, P. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Culturing+of+calcium+stable+adult+cardiac+myocytes.">Culturing of calcium stable adult cardiac myocytes.</a> J Mol Cell Cardiol. 14 (7), 397-412 (1982).</li><li>Xu, X., Colecraft, H. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Primary+culture+of+adult+rat+heart+myocytes.">Primary culture of adult rat heart myocytes.</a> J Vis Exp. (28), (2009).</li><li>G&#252;nd&#252;z, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Accumulation+of+extracellular+ATP+protects+against+acute+reperfusion+injury+in+rat+heart+endothelial+cells.">Accumulation of extracellular ATP protects against acute reperfusion injury in rat heart endothelial cells.</a> Cardiovasc.Res. 71 (4), 764-773 (2006).</li><li>Brilla, C. G., Zhou, G., Matsubara, L., Weber, K. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Collagen+metabolism+in+cultured+adult+rat+cardiac+fibroblasts:+response+to+angiotensin+II+and+aldosterone.">Collagen metabolism in cultured adult rat cardiac fibroblasts: response to angiotensin II and aldosterone.</a> J Mol Cell Cardiol. 26 (7), 809-820 (1994).</li><li>Shahzad, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mechanisms+involved+in+postconditioning+protection+of+cardiomyocytes+against+acute+reperfusion+injury.">Mechanisms involved in postconditioning protection of cardiomyocytes against acute reperfusion injury.</a> J Mol Cell Cardiol. 58, 209-216 (2013).</li><li>G&#252;nd&#252;z, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Insulin+Stabilizes+Microvascular+Endothelial+Barrier+Function+via+Phosphatidylinositol+3-Kinase/Akt-Mediated+Rac1+Activation.">Insulin Stabilizes Microvascular Endothelial Barrier Function via Phosphatidylinositol 3-Kinase/Akt-Mediated Rac1 Activation.</a> Arterioscler.Thromb.Vasc.Biol. 30, 1237-1245 (2010).</li><li>Lipps, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=N-terminal+fragment+of+cardiac+myosin+binding+protein-C+triggers+pro-inflammatory+responses+in+vitro.">N-terminal fragment of cardiac myosin binding protein-C triggers pro-inflammatory responses in vitro.</a> J Mol Cell Cardiol. 99, 47-56 (2016).</li><li>Abdallah, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Interplay+between+Ca2++cycling+and+mitochondrial+permeability+transition+pores+promotes+reperfusion-induced+injury+of+cardiac+myocytes.">Interplay between Ca2+ cycling and mitochondrial permeability transition pores promotes reperfusion-induced injury of cardiac myocytes.</a> J Cell Mol Med. 15 (11), 2478-2485 (2011).</li><li>G&#252;nd&#252;z, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effect+of+ticagrelor+on+endothelial+calcium+signalling+and+barrier+function.">Effect of ticagrelor on endothelial calcium signalling and barrier function.</a> Thromb Haemost. , (2016).</li><li>G&#252;nd&#252;z, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Opposing+effects+of+ATP+and+adenosine+on+barrier+function+of+rat+coronary+microvasculature.">Opposing effects of ATP and adenosine on barrier function of rat coronary microvasculature.</a> J Mol.Cell Cardiol. , (2012).</li></ol>

Yazarlar beyanda bulunacak bir şeyleri yok.

Bu makalede, kardiyak miyositlerin, endotel hücrelerinin ve fibroblastların izolasyonu ve kültürü için tekrarlanabilir bir protokol anlatılmıştır. Bu protokol, sadece bir hücre türünün aksine, kardiyomiyosit, endotel hücreleri ve fibroblastlar gibi kardiyak doku majör hücre tiplerinin eşzamanlı ve yüksek kalitede izolasyonunu tanımlar. İzolasyon prosedüründe kritik bir adım, kalp dokusunun doğru sindirilmesidir. Sindirim tamamlanmazsa, çok sayıda miyosit elde edilebilir ancak kalitesi çok zayıftır ve çoğunlukla hiperkontrakt ve yuvarlaktır ( Şekil 2B ) ve deneylerde değeri yoktur. Üstelik, endotel hücreleri ve fibroblastın verimi de azalacaktır. Bu problem sindirim süresini kontrol ederek çözülebilir. Kalbi perfüzyon sisteminden çıkarmadan önce kalbin yumuşaklığı forseps ve parmak ucu yardımıyla kontrol edilebilir. Doku hala belirgin değilseOft, kalp 5-10 dakika daha perfüze edilebilir. Sağlıklı kardiyomiyosit izolasyonunda ikinci bir kritik adım, izolasyon tamponlarında Ca 2+ &#39;nin artan restorasyonudur. Medyada yüksek Ca2 + konsantrasyonlarının hızlı şekilde restorasyonu yuvarlak kardiyomiyositlere neden olacaktır. Tamponların hazırlanması için kullanılan suyun kalitesi kardiyomiyositlerin kalitesini etkileyen önemli bir faktördür. Bu nedenle, kaliteli su kullanılması önerilir. Endotel hücrelerinin saflığı yıkama adımlarına oldukça bağlıdır. Endotel hücrelerinin non-spesifik olarak manyetik boncuklara bağlanmasını önlemek için yıkama tamponunda EDTA bulunması gerekir. Hücre süspansiyonunda kan hücrelerinin varlığı, endotel hücrelerinin verimini büyük ölçüde düşürecektir; Dolayısıyla, kalbi perfüzyon sistemine monte ettikten ve kollajenaz ilavesinden önce kalbe uygun şekilde yıkamak çok önemlidir. Artık kan bileşenleri ayrıca tO kollajenaz faaliyeti ve dolayısıyla kalbin sindirimini engellemektedir. Fibroblast hücre kültüründe en yaygın bulaşma, epitel hücrelerinin uydu kolonilerinin ortaya çıkmasıdır ( Şekil 4C ). Bu kirlenme, fibroblastların iki aşamalı kültürlenmesi ile önlenebilir. İlk aşamada, fibroblast hücre kültürü ortamındaki FCS konsantrasyonu% 5&#39;e düşürülür ve hücre süspansiyonu inkübatöre 30 dakika boyunca hücre kültürü çanağına yapışmaya bırakılır. Epitelyal hücreler hızla yapışır, ancak fibroblast hücre yapışma zamanı düşük bir serum konsantrasyonunun varlığında arttırılır. 30 dakika inkübasyondan sonra, yapışkan olmayan fibroblastları ihtiva eden hücre süspansiyonu yeni bir hücre kültürü çanağına dikkatlice çıkarılır. Bu şekilde fibroblastların verimi azaltılabilir, ancak saflıkları büyük ölçüde arttırılmıştır.

Kemirgen modelleri, sağlık ve hastalıkta kardiyovasküler fizyoloji konusundaki anlayışımızı genişletmek için uzun zamandır araç olarak kullanılmıştır. 1 Bu hayvan modelleri, bir hastalığın organ seviyesinde patofizyolojisini anlamamıza ve kardiyovasküler hastalıkların tedavisinde kullanılan çeşitli farmakolojik ajanların farmakokinetik ve farmakodinamiklerini analiz etmemize, kardiyovasküler hastalık gelişiminin moleküler mekanizmalarının anlaşılmasına ve belirli bir hastalığa katkıda bulunmamıza izin vermesine rağmen Hücre tipi, in vitro hücre kültürü modellerinin kullanılmasını gerektirir. Bu amaçla kardiyovasküler sistemden farklı ölümsüzleştirilmiş hücre hatları geliştirilmiştir; Bununla birlikte, yeni izole edilen primer hücreler, canlı dokular ve organizmalar için fizyolojik ve fonksiyonel açıdan daha alakalıdır. Kalp, kardiyovasküler sistemin tüm önemli hücrelerini içeren çok yönlü bir organtır.Ystem ve sıçan kalbi halen kardiyovasküler fizyolojinin anlaşılması için yaygın olarak kullanılan bir model. Son birkaç on yıl boyunca, tek tek hücre tiplerinin kalp dokusunda izole edilmesi için farklı yöntemler tanımlanmıştır; Bununla birlikte, bu yöntemler yalnızca belirli bir hücre türünün izolasyonuna odaklanır, bu nedenle artık hücresel analiz için kullanılmayan diğer hücrelerin kaybına neden olur. Burada, kardiyak doku, yani kardiyomiyositler, endotel hücreleri ve fibroblastların majör hücre tiplerinin eşzamanlı ve yüksek kalitede izolasyonunu sağlayan optimize edilmiş bir protokol anlatılmıştır. Bu hücre tiplerinin hepsi farklı deneysel kurulumlarda 8 , 9 , 10 ve aynı hayvantan hücre-hücre etkileşimlerinin analizi için kullanılabilir.

<table border="0" cellpadding="0" cellspacing="0" width="717">
	<tbody>
		<tr height="42">
			<td height="42" style="height:42px;width:299px;">anti-vWF</td>
			<td style="width:133px;">Santa Cruz Biotech.</td>
			<td style="width:119px;">SC-14014</td>
			<td style="width:167px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Calcium chloride</td>
			<td style="width:133px;">Merck</td>
			<td style="width:119px;">102378</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Carnitin</td>
			<td style="width:133px;">Sigma-Aldrich</td>
			<td style="width:119px;">C0283</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Collagenase type II</td>
			<td style="width:133px;">Worthington</td>
			<td style="width:119px;">LS004176</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Creatin</td>
			<td style="width:133px;">Sigma-Aldrich</td>
			<td style="width:119px;">C0780</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">D-Glucose</td>
			<td style="width:133px;">Merck</td>
			<td style="width:119px;">108342</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Dil-Ac-LDL</td>
			<td style="width:133px;">Thermo Scientific</td>
			<td style="width:119px;">L3484</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">EDTA Solution (0.2 M)</td>
			<td style="width:133px;">Biochrome AG</td>
			<td style="width:119px;">L2113</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Embeding solution</td>
			<td style="width:133px;">Citiflour</td>
			<td style="width:119px;">AF1-25</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Endothelial cell medium MV2</td>
			<td style="width:133px;">PromoCell</td>
			<td style="width:119px;">C-22022</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Foetal calf serum (FCS)</td>
			<td style="width:133px;">Biochrome AG</td>
			<td style="width:119px;">S0615</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Gentamicin</td>
			<td style="width:133px;">Serva Chemicals</td>
			<td style="width:119px;">47991</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">HEPES</td>
			<td style="width:133px;">Sigma-Aldrich</td>
			<td style="width:119px;">H0887</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Isoflurane</td>
			<td style="width:133px;">Abbott</td>
			<td style="width:119px;">TU 061219</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Laminin&#160;</td>
			<td style="width:133px;">Roche/Sigma</td>
			<td style="width:119px;">11243217001</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">M199 medium</td>
			<td style="width:133px;">Thermo Scientific</td>
			<td style="width:119px;">11150059</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">M199 medium (Powder)</td>
			<td style="width:133px;">Biochrome AG</td>
			<td style="width:119px;">T061</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Magnesium sulphate</td>
			<td style="width:133px;">Sigma-Aldrich</td>
			<td style="width:119px;">63138</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Mouse anti-rat CD31 antibody (TLD-3A12)</td>
			<td style="width:133px;">Thermo Scientific</td>
			<td style="width:119px;">MA1-81051</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">NaCl solution (0.9%), Sterile</td>
			<td style="width:133px;">B. Braun</td>
			<td style="width:119px;">30820080</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Pan mouse IgG beads (Dynabeads)</td>
			<td style="width:133px;">Thermo Scientific</td>
			<td style="width:119px;">11041</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:299px;">Paraformaldehyde (PFA) 4% Solution</td>
			<td style="width:133px;">Santa Cruz Biotech.</td>
			<td>sc-281692</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Penicillin-Streptomycin</td>
			<td style="width:133px;">Thermo Scientific</td>
			<td style="width:119px;">15070-063</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Phosphate buffer saline (PBS) 1x&#160;</td>
			<td style="width:133px;">PAN-Biotech</td>
			<td style="width:119px;">P04-36500</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Plastic consumables</td>
			<td style="width:133px;">Greiner Bio-One</td>
			<td style="width:119px;"></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Potassium Chloride</td>
			<td style="width:133px;">Merck</td>
			<td style="width:119px;">4933</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Potassium dihydrogen phosphate</td>
			<td style="width:133px;">Merck</td>
			<td style="width:119px;">7873</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Sodium Chloride</td>
			<td style="width:133px;">Merck</td>
			<td style="width:119px;">6404</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Sodium Hydroxide Solution (2 N)</td>
			<td style="width:133px;">Merck</td>
			<td style="width:119px;">109136</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Sterile filtration system</td>
			<td style="width:133px;">Thermo Scientific</td>
			<td style="width:119px;">5660020</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Taurine</td>
			<td style="width:133px;">Sigma-Aldrich</td>
			<td style="width:119px;">T8691</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">TO-PRO</td>
			<td style="width:133px;">Thermo Scientific</td>
			<td style="width:119px;">T3605</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Trypsin-EDTA Solution (10X)</td>
			<td style="width:133px;">Sigma-Aldrich</td>
			<td style="width:119px;">T4174</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:299px;">Water, Sterile</td>
			<td style="width:133px;">B. Braun</td>
			<td style="width:119px;"></td>
			<td></td>
		</tr>
	</tbody>
</table>

simultaneous isolation of high quality cardiomyocytes, endothelial cells, and fibroblasts from an adult rat heart

Sıçan, kardiyovasküler araştırmalarda kullanılan önemli bir hayvan modelidir ve fare kalp hücreleri, kalp hipertrofisi, fibroz ve ateroskleroz gibi kardiyovasküler hastalık ilerlemesinin moleküler mekanizmalarının in vitro analizi için rutin olarak kullanılmaktadır. Bu hücresel mekanizmaları anlamak için kardiyovasküler sistemden ölümsüzleştirilmiş hücre hatları geliştirmek için değişken başarı ile çeşitli girişimler yapılmış olsa da, primer hücreler bu çalışmalar için daha doğal ve canlı ortamda çevreye yakınlık sağlar. Bu nedenle, belirli bir hücre tipinde çalışan farklı laboratuvarlar, ilgili fare kalp hücrelerinin bireysel tiplerini izole etmek için protokoller geliştirmiştir. Bununla birlikte, birden fazla hücre türünün izolasyonunu sağlayan bir protokol eksiktir. Burada, yüksek kalitede büyük kardiyak hücre tiplerinin (kardiyomiyosit, endotel hücreleri ve fibroblastların) tek bir preparasyondan izole edilmesini sağlayan ve bir preparasyondanH hücresel analizler için kullanın. Bu, kullanılabilir kaynaklardan en verimli şekilde yararlanılmasına izin verir; bu da zaman kazandırabilir ve araştırma maliyetlerini düşürebilir.

<html> İzolasyon prosedürü, planlanan deneyler için kullanılabilir% 70 - 80 canlı, çubuk şeklinde, çizgili kardiyomiyositlerin ( Şekil 2A ve 2C ) bir verimiyle sonuçlanır. Laboratuarımızda kardiyomiyositler Ca 2+ sinyalizasyonunun analizi için rutin olarak kullanılırlar. Şekil 5A , Fura-AM (5 uM) yüklü kardiyomiyositlerde iskemi / reperfüzyona yanıt olarak hücre içi kalsiyum [Ca 2+ ] i salınımlarını göstermektedir. Şekil 5B , ATP&#39;nin (100 uM) eklenmesinden sonra endotel hücrelerinde ve fibroblastlarda [Ca2 + ] i&#39;deki değişiklikleri göstermektedir. Farklı kardiyak hücre tiplerinde [Ca 2+ ] i&#39;deki değişiklikler daha önce tarif edildiği gibi analiz edildi. 6 , 11 , 12 Re 1 &quot;src =&quot; / dosyalar / ftp_upload / 55601 / 55601fig1.jpg &quot;/&gt; Şekil 1: Modifiye Langendorf Perfüzyon Sistemi. ( A ) Kalp hücrelerinin izolasyonu için kullanılan tüm Langendorff perfüzyon sistemi ( B ) &quot;kalp bölmesindeki&quot; asılı kalp görüntüsü, devridaim için perfüzyon tamponunun toplanması için de kullanılır. <a href="https://ecsource-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/55601/55601fig1large.jpg" target="_blank">Bu rakamın daha büyük bir versiyonunu görmek için lütfen tıklayınız.</a> <img alt="şekil 2" src="/files/ftp_upload/55601/55601fig2.jpg" /> Şekil 2: Erişkin Sıçan Kardiyomiyositleri. ( A ) Laminin kaplı hücre kültürü kaplarında kaplamadan 2 saat sonra tipik çubuk şekilli, sağlıklı kardiyomiyosit ( B ) Tamamlanmamış doku sindirimine bağlı olarak zayıf bir preparatın tipik bir örneği. Laminin kaplı hücre kültürü kaplarında kaplandıktan 2 saat sonra, moHücrelerin steri köprü daralıyor ve yuvarlak görünüyor; çubuk şeklindeki birkaç kardiyomiyosit var. Ölçek çubuğu = 10 μm ( C ) Tek kardiyomiyositin konfokal mikrografı daha önce tarif edildiği gibi aktin görselleştirilmesi için boyandı. 13 Ölçek çubuğu = 50 μm. <a href="https://ecsource-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/55601/55601fig2large.jpg" target="_blank">Bu rakamın daha büyük bir versiyonunu görmek için lütfen tıklayınız.</a> <img alt="Şekil 3" src="/files/ftp_upload/55601/55601fig3.jpg" /> Şekil 3: Sıçan Kardiyak Endotel Hücreleri. ( A ) İzolasyondan 3 gün sonra konfluent olmayan endotel hücre monolayerının faz kontrastlı mikrografı. Koyu lekeler, ana endotel hücrelerine hala bağlı manyetik boncuklardır. Ölçek çubuğu = 10 μm ( B ) İzolasyondan 7 gün sonra konfluent endotel hücresi tek katmanının faz kontrast mikrografı ( C) Endotel hücrelerinin immüno-boyanması, Dil-Ac-LDL alımını (Kırmızı) ve nükleer boyayı ( M ) gösteren ( D ) vWF (Kırmızı) ve boyanmayı gösteren endotel hücrelerinin immün boyaması (Mavi) ( E ) Sekonder antikorla inkübe edilen hücreler Ve nükleer leke (Mavi) (Scale bar = 50 μm) <a href="https://ecsource-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/55601/55601fig3large.jpg" target="_blank">Bu şekli daha geniş bir sürümünü görmek için buraya tıklayın.</a> <img alt="Şekil 4" src="/files/ftp_upload/55601/55601fig4.jpg" /> Şekil 4: Sıçan Kardiyak Fibroblastları. ( A ) İzolasyonun ikinci gününde tipik iğ şekilli kardiyak fibroblastlar. ( B ) 7 günlük kültürden sonra konfluent, saf fibroblastlar. ( C ) Epitel hücrelerle kontamine olmuş zayıf bir preparatın tipik bir örneği. Ok uçları ile gösterilen hücreler, kalp epitel hücreleri<html> . Ölçek çubuğu = 10 μm. <a href="https://ecsource-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/55601/55601fig4large.jpg" target="_blank">Bu rakamın daha büyük bir versiyonunu görmek için lütfen tıklayınız.</a> <img alt="Şekil 5" src="/files/ftp_upload/55601/55601fig5.jpg" /> Şekil 5: Kardiyak Hücrelerdeki [Ca 2+ ] i&#39;deki değişiklikler. ( A ) Kemik iskemisine (Na-siyanat; 2 mM) maruz kalan sıçan kardiyomiyositlerinde Fura-2 oranı ile ölçülen hücre içi kalsiyum [Ca 2+ ] i değişiminin temsili izlemesi, ardından reperfüzyon ( B ) İntraselüler kalsiyum değişikliklerinin temsili izleri [Ca 2+ ] i , belirtilen şekilde ATP (100 uM) ile muamele edilmiş sıçan kalp endotel hücreleri ve fibroblastlarında Fura-2 oranı ile ölçülmüştür. &gt; Bu rakamın daha büyük bir versiyonunu görmek için lütfen tıklayınız.

Watch this Scientific Journal Video about Simultaneous Isolation of High Quality Cardiomyocytes, Endothelial Cells, and Fibroblasts from an Adult Rat Heart at JoVE.com

Simultaneous Isolation of High Quality Cardiomyocytes, Endothelial Cells, and Fibroblasts from an Adult Rat Heart

Bir fare kalpten farklı kardiyak hücre tiplerinin izolasyonu için çeşitli protokoller geliştirilmiş ve açıklanmıştır. Burada, yüksek kaliteli ana kardiyak hücre tiplerinin (kardiyomiyosit, endotel hücreleri ve fibroblastların) tek bir preparasyondan izole edilmesini sağlayan deneysel maliyetleri düşüren optimize edilmiş bir protokol tarif edilmiştir.

Bir Yetişkin Sıçan Kalpten Yüksek Kalitede Kardiyomiyosit, Endotel Hücresi ve Fibroblastların Eşzamanlı İzolasyonu

The rat is an important animal model used in cardiovascular research, and rat cardiac cells are used routinely for in vitro analysis of the molecular ...

simultaneous-isolation-high-quality-cardiomyocytes-endothelial-cells

Nanyang Technological University

Research

JoVE Journal

Biology

13.2K Görüntüleme.  University Hospital Giessen.  Bir fare kalpten farklı kardiyak hücre tiplerinin izolasyonu için çeşitli protokoller geliştirilmiş ve açıklanmıştır. Burada, yüksek kaliteli ana kardiyak hücre tiplerinin (kardiyomiyosit, endotel hücreleri ve fibroblastların) tek bir preparasyondan izole edilmesini sağlayan deneysel maliyetleri düşüren optimize edilmiş bir protokol tarif edilmiştir. 

Video: Simultaneous Isolation of High Quality Cardiomyocytes, Endothelial Cells, and Fibroblasts from an Adult Rat Heart

Primary Culture of Adult Rat Heart Myocytes

Cultured primary adult rodent heart cells are an important model system for cardiovascular research. Nevertheless, establishment of robust, viable cultured adult myocytes can be a technically challenging, rate-limiting step for many researchers. Here we described a protocol to obtain a high yield of adult rat heart myocytes that remain viable in culture for several days. The heart is isolated and perfused with collagenase and protease under low Ca2+ conditions to recover single myocytes. Ca2+-tolerant cells are obtained by stepwise increases in extracellular Ca2+ concentration in three subsequent wash steps. Cells are filtered, resuspended in culture medium, and plated on laminin coated slips. Cultured myocytes obtained using this protocol are viable for up to four days and are suitable for most experiments including electrophysiology, biochemistry, imaging and molecular biology.

In this paper, we described a typical way to isolate and culture adult rat heart myocytes. Collagenase and protease are used to digest and isolate single myocytes. Myocytes cultured follow this protocol meet most experiment requirements.

Yetişkin Sıçan Kalp miyositler İlköğretim Kültür

Cultured primary adult rodent heart cells are an important model system for cardiovascular research.  Nevertheless, establishment of robust, viable ...

Biyoloji

Isolation and Large Scale Expansion of Adult Human Endothelial Colony Forming Progenitor Cells

This paper introduces a novel recovery strategy for endothelial colony forming progenitor cells (ECFCs) from heparinized but otherwise unmanipulated adult human peripheral blood within a mean of 12 days. After large scale expansion &gt;1x108 ECFCs can be obtained for further tests. Advantageously by using pHPL the contact of human cells with bovine serum antigens can be excluded. By flow cytometry and immunohistochemistry the isolated cells can be characterized as ECFC and their in vitro functionality to form vascular like structures can be tested in a matrigel assay. Further these cells can be subcutaneously injected in a mouse model to form functional, perfused vessels in vivo. After long term expansion and cryopreservation proliferation, function and genomic stability appear to be preserved. 3,4
This animal-protein free isolation and expansion method is easily applicable to generate a large quantity of ECFCs.

Endothelial colony forming progenitor cells (ECFCs) are a promising tool to study vascular homeostasis and repair.1,2 This paper introduces a novel animal-serum free method for isolation and expansion of ECFC from heparinised adult human peripheral blood with pooled human platelet lysate (pHPL) diminishing the risk of anti-bovine immunisation.

İzolasyon ve Büyük Ölçekli Genişleme Yetişkin İnsan Endotel Koloni Oluşturan Progenitör Hücreler

This paper introduces a novel recovery strategy for endothelial colony forming progenitor cells (ECFCs) from heparinized but otherwise unmanipulated adult ...

Isolation and Culture of Pulmonary Endothelial Cells from Neonatal Mice

Endothelial cells provide a useful research model in many areas of vascular biology. Since its first isolation 1, human umbilical vein endothelial cells (HUVECs) have shown to be convenient, easy to obtain and culture, and thus are the most widely studied endothelial cells. However, for research focused on processes like angiogenesis, permeability or many others, microvascular endothelial cells (ECs) are a much more physiologically relevant model to study 2. Furthermore, ECs isolated from knockout mice provide a useful tool for analysis of protein function ex vivo. Several approaches to isolate and culture microvascular ECs of different origin have been reported to date 3-7, but consistent isolation and culture of pure ECs is still a major technical problem in many laboratories. Here, we provide a step-by-step protocol on a reliable and relatively simple method of isolating and culturing mouse lung endothelial cells (MLECs). In this approach, lung tissue obtained from 6- to 8-day old pups is first cut into pieces, digested with collagenase/dispase (C/D) solution and dispersed mechanically into single-cell suspension. MLECS are purified from cell suspension using positive selection with anti-PECAM-1 antibody conjugated to Dynabeads using a Magnetic Particle Concentrator (MPC). Such purified cells are cultured on gelatin-coated tissue culture (TC) dishes until they become confluent. At that point, cells are further purified using Dynabeads coupled to anti-ICAM-2 antibody. MLECs obtained with this protocol exhibit a cobblestone phenotype, as visualized by phase-contrast light microscopy, and their endothelial phenotype has been confirmed using FACS analysis with anti-VE-cadherin 8 and anti-VEGFR2 9 antibodies and immunofluorescent staining of VE-cadherin. In our hands, this two-step isolation procedure consistently and reliably yields a pure population of MLECs, which can be further cultured. This method will enable researchers to take advantage of the growing number of knockout and transgenic mice to directly correlate in vivo studies with results of in vitro experiments performed on isolated MLECs and thus help to reveal molecular mechanisms of vascular phenotypes observed in vivo.

Here, we describe a protocol for isolation and culture of murine pulmonary endothelial cells. This method comprises mechanic and enzymatic lung tissue dissociation as well as a 2-step purification process using anti-PECAM-1 and anti-ICAM-2 antibodies conjugated to magnetic beads, which produces a pure endothelial cell population of mostly microvascular origin.

Yenidoğan Fareler Pulmoner Endotel Hücreleri İzolasyon ve Kültür

Endothelial cells provide a useful research model in many areas of vascular biology. Since its first isolation 1, human umbilical vein endothelial cells ...

Selecting and Isolating Colonies of Human Induced Pluripotent Stem Cells Reprogrammed from Adult Fibroblasts

Herein we present a protocol of reprogramming human adult fibroblasts into human induced pluripotent stem cells (hiPSC) using retroviral vectors encoding Oct3/4, Sox2, Klf4 and c-myc (OSKM) in the presence of sodium butyrate 1-3. We used this method to reprogram late passage (&gt;p10) human adult fibroblasts derived from Friedreich's ataxia patient (GM03665, Coriell Repository). The reprogramming approach includes highly efficient transduction protocol using repetitive centrifugation of fibroblasts in the presence of virus-containing media. The reprogrammed hiPSC colonies were identified using live immunostaining for Tra-1-81, a surface marker of pluripotent cells, separated from non-reprogrammed fibroblasts and manually passaged 4,5. These hiPSC were then transferred to Matrigel plates and grown in feeder-free conditions, directly from the reprogramming plate. Starting from the first passage, hiPSC colonies demonstrate characteristic hES-like morphology. Using this protocol more than 70% of selected colonies can be successfully expanded and established into cell lines. The established hiPSC lines displayed characteristic pluripotency markers including surface markers TRA-1-60 and SSEA-4, as well as nuclear markers Oct3/4, Sox2 and Nanog. 
The protocol presented here has been established and tested using adult fibroblasts obtained from Friedreich's ataxia patients and control individuals 6, human newborn fibroblasts, as well as human keratinocytes.

We present a protocol for efficient reprogramming of human somatic cells into human induced pluripotent stem cells (hiPSC) using retroviral vectors encoding Oct3/4, Sox2, Klf4 and c-myc (OSKM) and identification of correctly reprogrammed hiPSC by live staining with Tra-1-81 antibody.

İnsan İsteyerek Pluripotent Kök Hücre seçme ve ayırma Kolonileri Yetişkin Fibroblastlar gelen reprogrammed

Herein we present a protocol of reprogramming human adult fibroblasts into human induced pluripotent stem cells (hiPSC) using retroviral vectors encoding ...

Isolation of Embryonic Ventricular Endothelial Cells

Cell culture has greatly enhanced our ability to assess individual populations of cells under myriad culture conditions. While immortalized cell lines offer significant advantages for their ease of use, these cell lines are unavailable for all potential cell types. By isolating primary cells from a specific region of interest, particularly from a transgenic mouse, more nuanced studies can be performed. The basic technique involves dissecting the organ or partial organ of interest (e.g. the heart or a specific region of the heart) and dissociating the organ to single cells. These cells are then incubated with magnetic beads conjugated to an antibody that recognizes the cell type of interest. The cells of interest can then be isolated with the use of a magnet, with a short trypsin incubation dissociating the cells from the beads. These isolated cells can then be cultured and analyzed as desired. This technique was originally designed for adult mouse organs but can be easily scaled down for use with embryonic organs, as demonstrated herein. Because our interest is in the developing coronary vasculature, we wanted to study this population of cells during specific embryonic stages. Thus, the original protocol had to be modified to be compatible with the small size of the embryonic ventricles and the low potential yield of endothelial cells at these developmental stages. Utilizing this scaled-down approach, we have assessed coronary plexus remodeling in transgenic embryonic ventricular endothelial cells.

Primary cell culture is a useful technique for analyzing specific populations of cells, particularly from transgenic mouse embryos at specific developmental stages. Herein, embryonic ventricles are dissected and dissociated, and antibody-conjugated beads recognize and separate out the endothelial cells for further analysis.

Embriyonik Ventriküler Endotel Hücre İzolasyonu

Cell culture has greatly enhanced our ability to assess individual populations of cells under myriad culture conditions. While immortalized cell lines ...

Isolation of Murine Valve Endothelial Cells

Normal valve structures consist of stratified layers of specialized extracellular matrix (ECM) interspersed with valve interstitial cells (VICs) and surrounded by a monolayer of valve endothelial cells (VECs). VECs play essential roles in establishing the valve structures during embryonic development, and are important for maintaining life-long valve integrity and function. In contrast to a continuous endothelium over the surface of healthy valve leaflets, VEC disruption is commonly observed in malfunctioning valves and is associated with pathological processes that promote valve disease and dysfunction. Despite the clinical relevance, focused studies determining the contribution of VECs to development and disease processes are limited. The isolation of VECs from animal models would allow for cell-specific experimentation. VECs have been isolated from large animal adult models but due to their small population size, fragileness, and lack of specific markers, no reports of VEC isolations in embryos or adult small animal models have been reported. Here we describe a novel method that allows for the direct isolation of VECs from mice at embryonic and adult stages. Utilizing the Tie2-GFP reporter model that labels all endothelial cells with Green Fluorescent Protein (GFP), we have been successful in isolating GFP-positive (and negative) cells from the semilunar and atrioventricular valve regions using fluorescence activated cell sorting (FACS). Isolated GFP-positive VECs are enriched for endothelial markers, including CD31 and von Willebrand Factor (vWF), and retain endothelial cell expression when cultured; while, GFP-negative cells exhibit molecular profiles and cell shapes consistent with VIC phenotypes. The ability to isolate embryonic and adult murine VECs allows for previously unattainable molecular and functional studies to be carried out on a specific valve cell population, which will greatly improve our understanding of valve development and disease mechanisms.

The ability to isolate heart valve endothelial cells (VECs) is critical for understanding mechanisms of valve development, maintenance, and disease. Here we describe the isolation of VECs from embryonic and adult Tie2-GFP mice using FACS that will allow for studies determining the contribution of VECs in developmental and disease processes.

Murin Vana Endotel Hücreleri İzolasyon

Normal valve structures consist of stratified layers of specialized extracellular matrix (ECM) interspersed with valve interstitial cells (VICs) and ...

Isolation, Culture and Transduction of Adult Mouse Cardiomyocytes

Cultured cardiomyocytes can be used to study cardiomyocyte biology using techniques that are complementary to in vivo systems. For example, the purity and accessibility of in vitro culture enables fine control over biochemical analyses, live imaging, and electrophysiology. Long-term culture of cardiomyocytes offers access to additional experimental approaches that cannot be completed in short term cultures. For example, the in vitro investigation of dedifferentiation, cell cycle re-entry, and cell division has thus far largely been restricted to rat cardiomyocytes, which appear to be more robust in long-term culture. However, the availability of a rich toolset of transgenic mouse lines and well-developed disease models make mouse systems attractive for cardiac research. Although several reports exist of adult mouse cardiomyocyte isolation, few studies demonstrate their long-term culture. Presented here, is a step-by-step method for the isolation and long-term culture of adult mouse cardiomyocytes. First, retrograde Langendorff perfusion is used to efficiently digest the heart with proteases, followed by gravity sedimentation purification. After a period of dedifferentiation following isolation, the cells gradually attach to the culture and can be cultured for weeks. Adenovirus cell lysate is used to efficiently transduce the isolated cardiomyocytes. These methods provide a simple, yet powerful model system to study cardiac biology.

This protocol describes a step-by-step method for the reproducible isolation and long-term culture of adult mouse cardiomyocytes with high yield, purity, and viability.

İzolasyon, Kültür ve Yetişkin Fare kardiyomiyositlerde İletimi

Cultured cardiomyocytes can be used to study cardiomyocyte biology using techniques that are complementary to in vivo systems. For example, the purity and ...

Isolation, Characterization, and Differentiation of Cardiac Stem Cells from the Adult Mouse Heart

Myocardial infarction (MI) is a leading cause of morbidity and mortality around the world. A major goal of regenerative medicine is to replenish the dead myocardium after MI. Although several strategies have been used to regenerate myocardium, stem cell therapy remains a major approach to replenish the dead myocardium of an MI heart. Accumulating evidence suggests the presence of resident cardiac stem cells (CSCs) in the adult heart and their endocrine and/or paracrine effects on cardiac regeneration. However, CSC isolation and their characterization and differentiation toward myocardial cells, especially cardiomyocytes, remains a technical challenge. In the present study, we provided a simple method for the isolation, characterization, and differentiation of CSCs from the adult mouse heart. Here, we describe a density gradient method for the isolation of CSCs, where the heart is digested by a 0.2% collagenase II solution. To characterize the isolated CSCs, we evaluated the expression of CSCs/cardiac markers Sca-1, NKX2-5, and GATA4, and pluripotency/stemness markers OCT4, SOX2, and Nanog. We also determined the proliferation potential of isolated CSCs by culturing them in a Petri dish and assessing the expression of the proliferation marker Ki-67. For evaluating the differentiation potential of CSCs, we selected seven- to ten-days cultured CSCs. We transferred them to a new plate with a cardiomyocyte differentiation medium. They are incubated in a cell culture incubator for 12 days, while the differentiation medium is changed every three days. The differentiated CSCs express cardiomyocyte-specific markers: actinin and troponin I. Thus, CSCs isolated with this protocol have stemness and cardiac markers, and they have a potential for proliferation and differentiation toward cardiomyocyte lineage.

The overall goal of this article is to standardize the protocol for the isolation, characterization, and differentiation of cardiac stem cells (CSCs) from the adult mouse heart. Here, we describe a density gradient centrifugation method to isolate murine CSCs and elaborated methods for CSC culture, proliferation, and differentiation into cardiomyocytes.

Yalıtım, karakterizasyonu ve yetişkin fare kalp kalp kök hücre farklılaşma

Myocardial infarction (MI) is a leading cause of morbidity and mortality around the world. A major goal of regenerative medicine is to replenish the dead ...

Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts

Cardiac fibrosis in response to injury is a physiological response to wound healing. Efforts have been made to study and target fibroblast subtypes that mitigate fibrosis. However, fibroblast research has been hindered due to the lack of universally acceptable fibroblast markers to identify quiescent as well as activated fibroblasts. Fibroblasts are a heterogenous cell population, making them difficult to isolate and characterize. The presented protocol describes three different methods to enrich fibroblasts and myofibroblasts from uninjured and injured mouse hearts. Using a standard and reliable protocol to isolate fibroblasts will enable the study of their roles in homeostasis as well as fibrosis modulation.

Obtaining a pure population of fibroblasts is crucial to studying their role in wound repair and fibrosis. Described here is a detailed method to isolate fibroblasts and myofibroblasts from uninjured and injured mouse hearts followed by characterization of their purity and functionality by immunofluorescence, RTPCR, fluorescence-assisted cell sorting, and collagen gel contraction.

Erişkin Kardiyak Fibroblastlar ve Miyofibroblastların İzolasyon ve Karakterizasyonu

Cardiac fibrosis in response to injury is a physiological response to wound healing. Efforts have been made to study and target fibroblast subtypes that ...

Isolation of Cardiomyocytes from Fixed Hearts for Immunocytochemistry and Ploidy Analysis

The adult mammalian heart is composed of various cell types including cardiomyocytes, endothelial cells and fibroblasts. Since it is difficult to reliably identify nuclei of cardiomyocytes on histological sections, many groups rely on isolating viable cardiomyocytes prior to fixation to perform immunostaining. However, these live cardiomyocyte isolation techniques require optimization to maximize the yield, viability and quality of the samples, with inherent fluctuations from sample to sample despite maximum optimization. Here, we report a reproducible protocol, involving fixation prior to enzymatic digestion of the heart, which leads to maximum yield while preserving the in vivo morphology of individual cardiomyocytes. We further developed an automated analysis platform to determine the number of nuclei and DNA content per nucleus for individual cardiomyocytes. After exposing the chest cavity, the heart was arrested in diastole by perfusion with 60 mM KCl in PBS. Next, the heart was fixed in 4% paraformaldehyde (PFA) solution, and then digested with 60 mg/mL collagenase solution. After digestions, cells were singularized by trituration, and the cardiomyocyte fraction was enriched via differential centrifugation. Isolated cardiomyocytes were stained for Troponin T and &#945;-actinin to assess purity of the obtained population. Furthermore, we developed an image analysis platform to determine cardiomyocyte nucleation and ploidy status following DAPI staining. Image based ploidy assessments led to consistent and reproducible results. Thus, with this protocol, it is possible to preserve native morphology of individual cardiomyocytes to allow immunocytochemistry and DNA content analysis while achieving maximum yield.

The goal of this work is to develop a method to reproducibly isolate cardiomyocytes from the adult heart and measure DNA content and nucleation.

İmmünsitokimya ve Ploidi Analizi için Sabit Kalplerden Kardiyomiyositlerin İzolasyon

The adult mammalian heart is composed of various cell types including cardiomyocytes, endothelial cells and fibroblasts. Since it is difficult to reliably ...