Endoplasmic reticulum calcium. transport ATPase expression during differentiation of colon cancer and leukaemia cells

被引:36
作者
Papp, B
Brouland, JP
Gélébart, P
Kovàcs, T
Chomienne, C
机构
[1] Univ Paris, Hosp St Louis, Inst Hematol, INSERM,EMI0003,Lab Biol Cellulaire Hematopoiet, F-75010 Paris, France
[2] Hop Lariboisiere, Serv Anat Pathol, F-75010 Paris, France
[3] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
[4] Inst Hematol & Immunol, Natl Med Ctr, H-1113 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
D O I
10.1016/j.bbrc.2004.08.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The calcium homeostasis of the endoplasmic reticulum (ER) is connected to a multitude of cell functions involved in intracellular signal transduction, control of proliferation, programmed cell death, or the synthesis of mature proteins. Calcium is accumulated in the ER by various biochemically distinct sarco/endoplasmic reticulum calcium transport ATPase isoenzymes (SERCA isoforms). Experimental data indicate that the SERCA composition of some carcinoma and leukaemia cell types undergoes significant changes during differentiation, and that this is accompanied by modifications of SERCA-dependent calcium accumulation in the ER. Because ER calcium homeostasis can also influence cell differentiation, we propose that the modulation of the expression of various SERCA isoforms, and in particular, the induction of the expression of SERCA3-type proteins, is an integral part of the differentiation program of some cancer and leukaemia cell types. The SERCA content of the ER may constitute a new parameter by which the calcium homeostatic characteristics of the organelle are adjusted. The cross-talk between ER calcium homeostasis and cell differentiation may have some implications for the better understanding of the signalling defects involved in the acquisition and maintenance of the malignant phenotype. (C) 2004 Published by Elsevier Inc.
引用
收藏
页码:1223 / 1236
页数:14
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