Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/58497

TítuloAdvanced maturation of human cardiac tissue grown from pluripotent stem cells
Autor(es)Ronaldson-Bouchard, Kacey
Ma, Stephen P.
Yeager, Keith
Chen, Timothy
Song, LouJin
Sirabella, Dario
Morikawa, Kumi
Teles, Diogo
Yazawa, Masayuki
Vunjak-Novakovic, Gordana
Palavras-chaveAdult
Calcium
Energy Metabolism
Heart
Humans
Induced Pluripotent Stem Cells
Isoproterenol
Mitochondria
Myocardium
Myocytes, Cardiac
Sarcomeres
Transcriptome
Cell Differentiation
Tissue Culture Techniques
DataAbr-2018
EditoraNature Research
RevistaNature
CitaçãoRonaldson-Bouchard, K., Ma, S. P., Yeager, K., et. al. (2018). Advanced maturation of human cardiac tissue grown from pluripotent stem cells. Nature, 556(7700), 239
Resumo(s)Cardiac tissues generated from human induced pluripotent stem cells (iPSCs) can serve as platforms for patient-specific studies of physiology and disease1-6. However, the predictive power of these models is presently limited by the immature state of the cells1, 2, 5, 6. Here we show that this fundamental limitation can be overcome if cardiac tissues are formed from early-stage iPSC-derived cardiomyocytes soon after the initiation of spontaneous contractions and are subjected to physical conditioning with increasing intensity over time. After only four weeks of culture, for all iPSC lines studied, such tissues displayed adult-like gene expression profiles, remarkably organized ultrastructure, physiological sarcomere length (2.2 µm) and density of mitochondria (30%), the presence of transverse tubules, oxidative metabolism, a positive force-frequency relationship and functional calcium handling. Electromechanical properties developed more slowly and did not achieve the stage of maturity seen in adult human myocardium. Tissue maturity was necessary for achieving physiological responses to isoproterenol and recapitulating pathological hypertrophy, supporting the utility of this tissue model for studies of cardiac development and disease.
TipoArtigo
URIhttps://hdl.handle.net/1822/58497
DOI10.1038/s41586-018-0016-3
ISSN0028-0836
e-ISSN1476-4687
Versão da editorahttps://www.nature.com/articles/s41586-018-0016-3?_ga=2.210913495.338718695.1526860800-1585132472.1526860800
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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