Fabrice Magnino , Marie St-Pierre , Michael Lüthi , Mauricette Hilly , Jean-Pierre Mauger , Jean-François Dufour
{"title":"Expression of Intracellular Calcium Channels and Pumps after Partial Hepatectomy in Rat","authors":"Fabrice Magnino , Marie St-Pierre , Michael Lüthi , Mauricette Hilly , Jean-Pierre Mauger , Jean-François Dufour","doi":"10.1006/mcbr.2000.0242","DOIUrl":null,"url":null,"abstract":"<div><p>Ca<sup>2+</sup> signals regulate many cellular functions, including proliferation. They are governed by the inositol 1,4,5-trisphosphate receptor (IP<sub>3</sub>R), the only intracellular hepatic Ca<sup>2+</sup> channel and by the endoplasmic reticulum Ca<sup>2+</sup> pumps, SERCA. To characterise their role in regeneration, expression of their isoforms was studied after 2/3 hepatectomy by real-time quantitative PCR, Western blot and binding studies. We found an early increase in the expression of the IP<sub>3</sub>R isoform 1 which contrasted with the decrease of the expression of the IP<sub>3</sub>R isoforms 2 and 3 and of SERCA3. This results in a transient switch between IP<sub>3</sub>R isoforms 1 and 2, IP<sub>3</sub>R isoform 1 becoming predominant before the first round of mitosis. Binding studies detected a 30% diminution of the IP<sub>3</sub>R population at 24 h. In conclusion, the Ca<sup>2+</sup> signalling machinery is regulated, after hepatectomy, by changes in expression of the IP<sub>3</sub>R and SERCA isoforms to adapt Ca<sup>2+</sup> signals to the regenerative state.</p></div>","PeriodicalId":80086,"journal":{"name":"Molecular cell biology research communications : MCBRC","volume":"3 6","pages":"Pages 374-379"},"PeriodicalIF":0.0000,"publicationDate":"2000-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/mcbr.2000.0242","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular cell biology research communications : MCBRC","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1522472400902423","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 19
Abstract
Ca2+ signals regulate many cellular functions, including proliferation. They are governed by the inositol 1,4,5-trisphosphate receptor (IP3R), the only intracellular hepatic Ca2+ channel and by the endoplasmic reticulum Ca2+ pumps, SERCA. To characterise their role in regeneration, expression of their isoforms was studied after 2/3 hepatectomy by real-time quantitative PCR, Western blot and binding studies. We found an early increase in the expression of the IP3R isoform 1 which contrasted with the decrease of the expression of the IP3R isoforms 2 and 3 and of SERCA3. This results in a transient switch between IP3R isoforms 1 and 2, IP3R isoform 1 becoming predominant before the first round of mitosis. Binding studies detected a 30% diminution of the IP3R population at 24 h. In conclusion, the Ca2+ signalling machinery is regulated, after hepatectomy, by changes in expression of the IP3R and SERCA isoforms to adapt Ca2+ signals to the regenerative state.