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- W2567466572 startingPage "352" @default.
- W2567466572 abstract "Biochemical, biophysical, and bioelectrical signaling cues control cardiac myocyte differentiation, maturation, and physiology. These signals may be mediated via cell–cell and cell–extracellular matrix interactions. The development of cellular models of human myocardial physiology and pathophysiology requires the adaptation of these cues for in vitro applications. A cardiogenic biochemical milieu can be enforced in vitro via small-molecule modulation of Wnt signaling. Cardiogenic biophysical cues can be adapted in vitro by controlling growth substrate topography and elasticity, generating 3D myocardial tissue, and applying mechanical stress to cells and tissues. Electrical point stimulation provides physiologic bioelectrical cues and is dependent on cell–cell interactions for signal propagation. Electrical field stimulation is suitable for excitation of cell islands or clusters in vitro and ensures synchronous contraction of myocardial cells. The advent of human pluripotent stem cell (hPSC) biology has opened unprecedented opportunities for the use of tissue engineering to generate human cardiac tissue for in vitro study. Engineering cardiac constructs that recapitulate human development and disease requires faithful recreation of the cardiac niche in vitro. Here we discuss recent progress in translating the in vivo cardiac microenvironment into PSC models of the human heart. We review three key physiologic features required to recreate the cardiac niche and facilitate normal cardiac differentiation and maturation: the biochemical, biophysical, and bioelectrical signaling cues. Finally, we discuss key barriers that must be overcome to fulfill the promise of stem cell biology in preclinical applications and ultimately in clinical practice. The advent of human pluripotent stem cell (hPSC) biology has opened unprecedented opportunities for the use of tissue engineering to generate human cardiac tissue for in vitro study. Engineering cardiac constructs that recapitulate human development and disease requires faithful recreation of the cardiac niche in vitro. Here we discuss recent progress in translating the in vivo cardiac microenvironment into PSC models of the human heart. We review three key physiologic features required to recreate the cardiac niche and facilitate normal cardiac differentiation and maturation: the biochemical, biophysical, and bioelectrical signaling cues. Finally, we discuss key barriers that must be overcome to fulfill the promise of stem cell biology in preclinical applications and ultimately in clinical practice." @default.
- W2567466572 created "2017-01-06" @default.
- W2567466572 creator A5063761119 @default.
- W2567466572 creator A5088957999 @default.
- W2567466572 date "2017-05-01" @default.
- W2567466572 modified "2023-10-16" @default.
- W2567466572 title "Recreating the Cardiac Microenvironment in Pluripotent Stem Cell Models of Human Physiology and Disease" @default.
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