Shaping the heart: Structural and functional maturation of iPSC-cardiomyocytes in 3D-micro-scaffolds.

Biomaterials

Institute of Physiology and Pathophysiology, Department of Cardiovascular Research, Heidelberg University, Im Neuenheimer Feld 307, 69120, Heidelberg, Germany; German Center for Cardiovascular Research (DZHK) Partner Site Heidelberg-Mannheim, Germany; Heidelberg-Karlsruhe Research Partnership (HEiKA

Published: January 2020


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Article Abstract

Cardiomyocytes derived from induced pluripotent stem cells (iPSC-CMs) represent the best cell source for cardiac regenerative purposes but retain an immature phenotype after differentiation with significant limitations compared to adult cardiomyocytes. Apart from an incomplete cardiomyocyte-specific structure and microarchitecture, cells show at the level of Ca signaling only slow Ca release and reuptake properties. Here, we investigated the effect of restructuring single iPSC-CMs in specially designed 3D-micro-scaffolds on cell morphology and Ca handling. Using direct laser writing, rectangular-shaped scaffolds were produced and single iPSC-CMs were seeded into these forms. Structural analyses revealed strong sarcolemmal remodeling processes and myofilament reorientation in 3D-shaped cells leading to enhanced clustered expression of L-type Ca channels and ryanodine receptors and consequently, to faster Ca transient kinetics. Spontaneous beating activity was enhanced and Ca handling was more robust compared to non-patterned cells. Overall, our data demonstrate for the first time significant improvement of Ca signaling properties in reshaped iPSC-CMs indicative of functional maturation by structural remodeling.

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http://dx.doi.org/10.1016/j.biomaterials.2019.119551DOI Listing

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