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Multifaceted plasma membrane Ca(2+) pumps: From structure to intracellular Ca(2+) handling and cancer.
Padányi, Rita; Pászty, Katalin; Hegedus, Luca; Varga, Karolina; Papp, Béla; Penniston, John T; Enyedi, Ágnes.
Afiliação
  • Padányi R; 2(nd) Department of Pathology, Semmelweis University, Budapest, Hungary.
  • Pászty K; Molecular Biophysics Research Group of the Hungarian Academy of Sciences and Department of Biophysics, Semmelweis University, Budapest, Hungary.
  • Hegedus L; Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria.
  • Varga K; 2(nd) Department of Pathology, Semmelweis University, Budapest, Hungary.
  • Papp B; Institut National de la Santé et de la Recherche Médicale, UMR U978 and Université Paris-13, PRES Sorbonne Paris-Cité, Bobigny, France.
  • Penniston JT; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Enyedi Á; 2(nd) Department of Pathology, Semmelweis University, Budapest, Hungary; Molecular Oncology Research Group of the Hungarian Academy of Sciences and Semmelweis University, Budapest, Hungary. Electronic address: enyedi.agnes@med.semmelweis-univ.hu.
Biochim Biophys Acta ; 1863(6 Pt B): 1351-63, 2016 Jun.
Article em En | MEDLINE | ID: mdl-26707182
Plasma membrane Ca(2+) ATPases (PMCAs) are intimately involved in the control of intracellular Ca(2+) concentration. They reduce Ca(2+) in the cytosol not only by direct ejection, but also by controlling the formation of inositol-1,4,5-trisphosphate and decreasing Ca(2+) release from the endoplasmic reticulum Ca(2+) 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 Ca(2+) with distinct temporal resolution. The expression pattern of variants depends on cell type; a change in this pattern can result in perturbed Ca(2+) homeostasis and thus altered cell function. Indeed, PMCAs undergo remarkable changes in their expression pattern during tumorigenesis that might significantly contribute to the unbalanced Ca(2+) 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Membrana Celular / Cálcio / Sinalização do Cálcio / ATPases Transportadoras de Cálcio da Membrana Plasmática Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Membrana Celular / Cálcio / Sinalização do Cálcio / ATPases Transportadoras de Cálcio da Membrana Plasmática Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article