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Engineered human pluripotent stem cell-derived cardiac cells and tissues for electrophysiological studies.
Lieu, Deborah K; Turnbull, Irene C; Costa, Kevin D; Li, Ronald A.
Afiliação
  • Lieu DK; Cardiovascular Research Center, Mount Sinai School of Medicine, New York, NY, United States.
  • Turnbull IC; Department of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, CA, United States.
  • Costa KD; Cardiovascular Research Center, Mount Sinai School of Medicine, New York, NY, United States.
  • Li RA; Cardiovascular Research Center, Mount Sinai School of Medicine, New York, NY, United States.
Drug Discov Today Dis Models ; 9(4): e209-e217, 2012.
Article em En | MEDLINE | ID: mdl-29422934
Human cardiomyocytes (CMs) do not proliferate in culture and are difficult to obtain for practical reasons. As such, our understanding of the mechanisms that underlie the physiological and pathophysiological development of the human heart is mostly extrapolated from studies of the mouse and other animal models or heterologus expression of defective gene product(s) in non-human cells. Although these studies provided numerous important insights, much of the exact behavior in human cells remains unexplored given that significant species differences exist. With the derivation of human embryonic stem cells (hESC) and induced pluripotent stem cells (iPSCs) from patients with underlying heart disease, a source of human CMs for disease modeling, cardiotoxicity screening and drug discovery is now available. In this review, we focus our discussion on the use of hESC/ iPSC-derived cardiac cells and tissues for studying various heart rhythm disorders and the associated pro-arrhythmogenic properties in relation to advancements in electrophysiology and tissue engineering.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2012 Tipo de documento: Article