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Cardiac tissue engineering using human stem cell-derived cardiomyocytes for disease modeling and drug discovery.
Turnbull, Irene C; Lieu, Deborah K; Li, Ronald A; Costa, Kevin D.
Afiliação
  • Turnbull IC; Cardiovascular Research Center, Mount Sinai School of Medicine, New York, NY.
  • Lieu DK; Cardiovascular Research Center, Mount Sinai School of Medicine, New York, NY.
  • Li RA; Department of Internal Medicine, Division of Cardiovascular Medicine, University of California, Davis, CA.
  • Costa KD; Cardiovascular Research Center, Mount Sinai School of Medicine, New York, NY.
Drug Discov Today Dis Models ; 9(4): e219-e227, 2012.
Article em En | MEDLINE | ID: mdl-33968153
ABSTRACT
Cardiovascular disease (CVD) is the most prevalent health problem in the world, and the high mortality rate associated with irreversibly injured heart muscle motivates an urgent need for the development of novel therapies to treat damaged myocardium. Recently, human engineered cardiac tissues (hECT) have been created using cardiomyocytes derived from human embryonic stem cells and human induced pluripotent stem cells. Although a healthy adult phenotype remains elusive, such hECT display structural and functional properties that recapitulate key aspects of natural human myocardium, including dose related responses to compounds with known chronotropic, inotropic and arrhythmogenic effects. Thus, hECT offer the advantage over traditional in vitro culture models of providing a biomimetic 3D environment for the study of myocardial physiopathology, and may be used to generate preclinical models for the development and screening of therapies for CVD.

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

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