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Functional Expression and Regulation of Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels (HCN) in Mouse iPS Cell-derived Cardiomyocytes afterUTF1-Neo Selection
Author(s) -
Judith Semmler,
Martin Lehmann,
Kurt Pfannkuche,
Michael Reppel,
Jürgen Hescheler,
Filomain Nguemo
Publication year - 2014
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000366332
Subject(s) - microbiology and biotechnology , biology , reprogramming , transplantation , hyperpolarization (physics) , transcription factor , electrophysiology , myocyte , hcn channel , membrane potential , ion channel , cell , chemistry , neuroscience , gene , medicine , genetics , receptor , organic chemistry , nuclear magnetic resonance spectroscopy
In vitro reprogramming of somatic cells holds great potential to serve as an autologous source of cells for tissue repair. However, major difficulties in achieving this potential include obtaining homogeneous and stable cells for transplantation. High electrical activity of cells such as cardiomyocytes (CMs) is crucial for both, safety and efficiency of cell replacement therapy. Moreover, the function of the cardiac pacemaker is controlled by the activities of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels. Here we have examined changes in HCN gene expression and function during cardiomyogenesis.

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