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Verfasst von:Kermani, Fatemeh [VerfasserIn]   i
 Mosqueira, Matias [VerfasserIn]   i
 Peters, Kyra [VerfasserIn]   i
 Lemma, Enrico D. [VerfasserIn]   i
 Rapti, Kleopatra [VerfasserIn]   i
 Grimm, Dirk [VerfasserIn]   i
 Bastmeyer, Martin [VerfasserIn]   i
 Laugsch, Magdalena [VerfasserIn]   i
 Hecker, Markus [VerfasserIn]   i
 Ullrich, Nina D. [VerfasserIn]   i
Titel:Membrane remodelling triggers maturation of excitation-contraction coupling in 3D-shaped human-induced pluripotent stem cell-derived cardiomyocytes
Verf.angabe:Fatemeh Kermani, Matias Mosqueira, Kyra Peters, Enrico D. Lemma, Kleopatra Rapti, Dirk Grimm, Martin Bastmeyer, Magdalena Laugsch, Markus Hecker, Nina D. Ullrich
E-Jahr:2023
Jahr:29 March 2023
Umfang:16 S.
Fussnoten:Gesehen am 12.06.2023
Titel Quelle:Enthalten in: Basic research in cardiology
Ort Quelle:[Darmstadt u.a.] : Steinkopff, 1937
Jahr Quelle:2023
Band/Heft Quelle:118(2023) vom: März, Artikel-ID 13, Seite 1-16
ISSN Quelle:1435-1803
Abstract:The prospective use of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) for cardiac regenerative medicine strongly depends on the electro-mechanical properties of these cells, especially regarding the Ca2+-dependent excitation-contraction (EC) coupling mechanism. Currently, the immature structural and functional features of hiPSC-CM limit the progression towards clinical applications. Here, we show that a specific microarchitecture is essential for functional maturation of hiPSC-CM. Structural remodelling towards a cuboid cell shape and induction of BIN1, a facilitator of membrane invaginations, lead to transverse (t)-tubule-like structures. This transformation brings two Ca2+ channels critical for EC coupling in close proximity, the L-type Ca2+ channel at the sarcolemma and the ryanodine receptor at the sarcoplasmic reticulum. Consequently, the Ca2+-dependent functional interaction of these channels becomes more efficient, leading to improved spatio-temporal synchronisation of Ca2+ transients and higher EC coupling gain. Thus, functional maturation of hiPSC-cardiomyocytes by optimised cell microarchitecture needs to be considered for future cardiac regenerative approaches.
DOI:doi:10.1007/s00395-023-00984-5
URL:kostenfrei: Volltext: https://doi.org/10.1007/s00395-023-00984-5
 kostenfrei: Volltext: https://link.springer.com/article/10.1007/s00395-023-00984-5
 DOI: https://doi.org/10.1007/s00395-023-00984-5
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:3D reshaping
 BIN1
 Excitation-contraction coupling
 hiPSC cardiomyocytes
 Maturation
 t-tubules
K10plus-PPN:1848795246
Verknüpfungen:→ Zeitschrift
 
 
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