Embryonic stem cells in predictive cardiotoxicity: Laser capture microscopy enables assay development

被引:28
作者
Chaudhary, KW
Barrezueta, NX
Bauchmann, MB
Milici, AJ
Beckius, G
Stedman, DB
Hambor, JE
Blake, WL
McNeish, JD
Bahinski, A
Cezar, GG
机构
[1] Pfizer Global Res & Dev, Chesterfield, MO 63017 USA
[2] Pfizer Global Res & Dev, Groton, CT 06340 USA
关键词
embryonic stem cells; cardiomyocytes; cardiotoxicity; laser microdissection and pressure catapulting;
D O I
10.1093/toxsci/kfj078
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
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 mu M 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.
引用
收藏
页码:149 / 158
页数:10
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