Chaudhary Khuram W, Barrezueta Nestor X, Bauchmann Mary B, Milici Anthony J, Beckius Gretchen, Stedman Donald B, Hambor John E, Blake William L, McNeish John D, Bahinski Anthony, Cezar Gabriela Gebrin
Pfizer Global Research and Development, Chesterfield, Missouri 63017, USA.
Toxicol Sci. 2006 Mar;90(1):149-58. doi: 10.1093/toxsci/kfj078. Epub 2005 Dec 15.
Embryonic stem (ES) cells offer unprecedented opportunities for in vitro drug discovery and safety assessment of compounds. Cardiomyocytes derived from ES cells enable development of predictive cardiotoxicity models to increase the safety of novel drugs. Heterogeneity of differentiated ES cells limits the development of reliable in vitro models for compound screening. We report an innovative and robust approach to isolate ES-derived cardiomyocytes using laser microdissection and pressure catapulting (LMPC). LMPC cells were readily applied onto 96-well format in vitro pharmacology assays. The expression of developmental and functional cardiac markers, Nkx 2.5, MLC2V, GATA-4, Connexin 43, Connexin 45, Serca-2a, cardiac alpha actin, and phospholamban, among others, was confirmed in LMPC ES-derived cardiomyocytes. Functional assays exhibited cardiac-like response to increased extracellular calcium (5.4 mM extracellular Ca2+) and L-type calcium channel antagonist (1 microM nifedipine). In conclusion, laser microdissection and pressure catapulting is a robust technology to isolate homogeneous ES-derived cell types from heterogeneous populations applicable to assay development.
胚胎干细胞(ES细胞)为化合物的体外药物发现和安全性评估提供了前所未有的机会。源自ES细胞的心肌细胞有助于开发预测性心脏毒性模型,以提高新药的安全性。分化的ES细胞的异质性限制了用于化合物筛选的可靠体外模型的开发。我们报告了一种创新且强大的方法,即使用激光显微切割和压力弹射(LMPC)来分离源自ES细胞的心肌细胞。LMPC细胞很容易应用于96孔板形式的体外药理学测定。在LMPC源自ES细胞的心肌细胞中证实了发育和功能性心脏标志物Nkx 2.5、MLC2V、GATA-4、连接蛋白43、连接蛋白45、肌浆网钙ATP酶2a、心肌α-肌动蛋白和受磷蛋白等的表达。功能测定显示,对细胞外钙增加(细胞外Ca2+为5.4 mM)和L型钙通道拮抗剂(1 μM硝苯地平)呈现出类似心脏的反应。总之,激光显微切割和压力弹射是一种强大的技术,可从异质群体中分离出适用于测定开发的同质源自ES细胞的细胞类型。