| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10801788 | Biochimica et Biophysica Acta (BBA) - Molecular Cell Research | 2016 | 46 Pages | 
Abstract
												Plasma membrane Ca2 + ATPases (PMCAs) are intimately involved in the control of intracellular Ca2 + concentration. They reduce Ca2 + in the cytosol not only by direct ejection, but also by controlling the formation of inositol-1,4,5-trisphosphate and decreasing Ca2 + release from the endoplasmic reticulum Ca2 + pool. In mammals four genes (PMCA1-4) are expressed, and alternative RNA splicing generates more than twenty variants. The variants differ in their regulatory characteristics. They localize into highly specialized membrane compartments and respond to the incoming Ca2 + with distinct temporal resolution. The expression pattern of variants depends on cell type; a change in this pattern can result in perturbed Ca2 + homeostasis and thus altered cell function. Indeed, PMCAs undergo remarkable changes in their expression pattern during tumorigenesis that might significantly contribute to the unbalanced Ca2 + homeostasis of cancer cells. This article is part of a Special Issue entitled: Calcium and Cell Fate . Guest Editors: Jacques Haiech, Claus Heizmann, Joachim Krebs, Thierry Capiod and Olivier Mignen.
											Keywords
												VSMCSTIM1PKCSOCECBSNHERF2nNOSIP3SPCAPMCAHUVECMLECHDACERKRANKLCa2 + signalingNCXplasma membrane Ca2 + ATPaseNFATsarco/endoplasmic reticulum Ca2 + ATPaseinositol-1,4,5-trisphosphatePI(4,5)P2DifferentiationRas association domain familyRASSFCAMVascular smooth muscle cellHuman umbilical vein endothelial cellsneuronal nitric oxide synthaseendoplasmic reticulumnuclear factor of activated T-cellsVascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)phosphatidylinositol-4,5-bisphosphateSERCAStromal interaction molecule 1histone deacetylaseProtein kinase CTumor progressionCalmodulinextracellular signal-regulated kinase
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											Authors
												Rita Padányi, Katalin Pászty, Luca Hegedűs, Karolina Varga, Béla Papp, John T. Penniston, Ágnes Enyedi, 
											