Reference : Expression of the plasma membrane Ca2+-ATPase in myogenic cells.
Scientific journals : Article
Human health sciences : Cardiovascular & respiratory systems
http://hdl.handle.net/10993/18307
Expression of the plasma membrane Ca2+-ATPase in myogenic cells.
English
Hammes, A. [> >]
Oberdorf-Maass, S. [> >]
Jenatschke, S. [> >]
Pelzer, T. [> >]
Maass, A. [> >]
Gollnick, F. [> >]
Meyer, R. [> >]
Afflerbach, J. [> >]
Neyses, Ludwig mailto [University of Luxembourg > Reserach Office]
1996
The Journal of biological chemistry
271
48
30816-22
Yes (verified by ORBilu)
0021-9258
UNITED STATES
[en] Animals ; Calcium/metabolism ; Calcium-Transporting ATPases/metabolism ; Cell Differentiation ; Cell Membrane/enzymology ; Cells, Cultured ; Creatine Kinase/metabolism ; Humans ; Muscles/enzymology ; RNA, Messenger/genetics ; Rats ; Recombinant Proteins
[en] To study the physiological function of the plasma membrane calmodulin-dependent calcium ATPase (PMCA) in intact cells, L6 myogenic cell lines stably overexpressing the human PMCA isoform 4CI (= human PMCA isoform 4b) were generated. Several independent L6 clones and controls stably transfected with the empty expression vector were analyzed in detail. The resting cytosolic calcium level in hPMCA4CI-overexpressing muscle cells (measured by the Fura-2 method) was significantly reduced by 20-30% compared with controls. This was shown in a cytosolic window of 1322 single cells (p < 0.01). Furthermore, the differentiation process of these cells was remarkably accelerated compared with control myoblasts and parental nontransfected L6 cells as assessed by multinucleated myotube formation and creatine phosphokinase activity elevation. After 4 and 6 days of differentiation, PMCA-overexpressing L6 cells from four independent clones displayed a 3- and 4-fold higher creatine phosphokinase activity compared with controls (n = 5, p < 0.02). These results may extend the concept of the function of the PMCA from simple prevention of calcium overload to an active involvement in intracellular calcium regulation with potentially important consequences for cellular functions.
http://hdl.handle.net/10993/18307
10.1074/jbc.271.48.30816
http://www.jbc.org/content/271/48/30816.long

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