Activity of complex III of the mitochondrial electron transport chain is essential for early heart muscle cell differentiation
D Spitkovsky, P Sasse, E Kolossov… - The FASEB …, 2004 - Wiley Online Library
D Spitkovsky, P Sasse, E Kolossov, C Böttinger, BK Fleischmann, J Hescheler, RJ Wiesner
The FASEB Journal, 2004•Wiley Online LibraryDuring development of the heart, mitochondria proliferate within cardiomyocytes. It is
unclear whether this is a response to the increasing energy demand or whether it is part of
the developmental program. To investigate the role of the electron transport chain (ETC) in
this process, we used transgenic murine embryonic stem (ES) cells in which the green
fluorescent protein gene is under control of the a‐myosin heavy chain promoter (a‐MHC),
allowing easy monitoring of cardiomyocyte differentiation. Spontaneous contraction of these …
unclear whether this is a response to the increasing energy demand or whether it is part of
the developmental program. To investigate the role of the electron transport chain (ETC) in
this process, we used transgenic murine embryonic stem (ES) cells in which the green
fluorescent protein gene is under control of the a‐myosin heavy chain promoter (a‐MHC),
allowing easy monitoring of cardiomyocyte differentiation. Spontaneous contraction of these …
Abstract
During development of the heart, mitochondria proliferate within cardiomyocytes. It is unclear whether this is a response to the increasing energy demand or whether it is part of the developmental program. To investigate the role of the electron transport chain (ETC) in this process, we used transgenic murine embryonic stem (ES) cells in which the green fluorescent protein gene is under control of the a‐myosin heavy chain promoter (a‐MHC), allowing easy monitoring of cardiomyocyte differentiation. Spontaneous contraction of these cells within embryoid bodies (EBs) was not affected by inhibition of the ETC, suggesting that early heart cell function is sufficiently supported by anaerobic ATP production. However, heart cell development was completely blocked when adding antimycin A, an inhibitor of ETC complex III, before initiation of differentiation, whereas KCN did not block differentiation, strongly suggesting that specifically complex III function rather than mitochondrial ATP production is necessary for early heart cell development. When the underlying mechanism was examined, we noticed that antimycin A but not KCN lead to inhibition of spontaneous intracellular Ca++ oscillations, whereas both substances decreased mitochondrial membrane potential, as expected. We postulate that mitochondrial complex III activity is necessary for these Ca++ oscillations, which in turn are a prerequisite for cardiomyocyte differentiation.
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