Overexpression of T-type calcium channels in HEK-293 cells increases intracellular calcium without affecting cellular proliferation

被引:91
作者
Chemin, J
Monteil, A
Briquaire, C
Richard, S
Perez-Reyes, E
Nargeot, J
Lory, P
机构
[1] IGH, CNRS UPR 1142, F-34396 Montpellier 05, France
[2] Univ Virginia, Dept Pharmacol, Charlottesville, VA 22908 USA
关键词
calcium channel; T-type; calcium imaging; proliferation; flow cytometry; HEK-293; cell;
D O I
10.1016/S0014-5793(00)01832-9
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
Increased expression of low voltage-activated T-type Ca2+ channels has been correlated with a variety of cellular events including cell proliferation and cell cycle kinetics. The recent cloning of three genes encoding T-type alpha(1) subunits, alpha(1G), alpha(1H) and alpha(11), non allows direct assessment of their involvement in mediating cellular proliferation, By overexpressing the human alpha(1G) and alpha(1H) subunits in human embryonic kidney (HEK-293) cells, we describe here that. although T-type channels mediate increases in intracellular Ca2+ concentrations, there is no significant change in bromodeoxyuridine incorporation and flow cytometric analysis. These results demonstrate that expressions of T-type Ca2+ channels are not sufficient to modulate cellular proliferation of HEK-293 cells. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:166 / 172
页数:7
相关论文
共 31 条
[1]   EFFECT OF POSTNATAL-DEVELOPMENT ON CALCIUM CURRENTS AND SLOW CHARGE MOVEMENT IN MAMMALIAN SKELETAL-MUSCLE [J].
BEAM, KG ;
KNUDSON, CM .
JOURNAL OF GENERAL PHYSIOLOGY, 1988, 91 (06) :799-815
[2]   Ectopic expression of MmKin17 protein inhibits cell proliferation of human tumor-derived cells [J].
Biard, DSF ;
Kannouche, P ;
Lannuzel-Drogou, C ;
Mauffrey, P ;
Apiou, F ;
Angulo, JF .
EXPERIMENTAL CELL RESEARCH, 1999, 250 (02) :499-509
[3]   The Us9 gene product of pseudorabies virus, an alphaherpesvirus, is a phosphorylated, tail-anchored type II membrane protein [J].
Brideau, AD ;
Banfield, BW ;
Enquist, LW .
JOURNAL OF VIROLOGY, 1998, 72 (06) :4560-4570
[4]   VOLTAGE-SENSITIVE CALCIUM CHANNELS IN NORMAL AND TRANSFORMED 3T3 FIBROBLASTS [J].
CHEN, CF ;
CORBLEY, MJ ;
ROBERTS, TM ;
HESS, P .
SCIENCE, 1988, 239 (4843) :1024-1026
[5]   Cloning and characterization of α1H from human heart, a member of the T-type Ca2+ channel gene family [J].
Cribbs, LL ;
Lee, JH ;
Yang, J ;
Satin, J ;
Zhang, Y ;
Daud, A ;
Barclay, J ;
Williamson, MP ;
Fox, M ;
Rees, M ;
Perez-Reyes, E .
CIRCULATION RESEARCH, 1998, 83 (01) :103-109
[6]   Cell cycle regulation of a T-type calcium current in early mouse embryos [J].
Day, ML ;
Johnson, MH ;
Cook, DI .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1998, 436 (06) :834-842
[7]   Cell cycle-related changes in the voltage-gated Ca2+ currents in cultured newborn rat ventricular myocytes [J].
Guo, W ;
Kamiya, K ;
Kodama, I ;
Toyama, T .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1998, 30 (06) :1095-1103
[8]   An integral membrane green fluorescent protein marker, Us9-GFP, is quantitatively retained in cells during propidium iodide-based cell cycle analysis by flow cytometry [J].
Kalejta, RF ;
Brideau, AD ;
Banfield, BW ;
Beavis, AJ .
EXPERIMENTAL CELL RESEARCH, 1999, 248 (01) :322-328
[9]   Cell cycle-dependent expression of L- and T-Type Ca2+ currents in rat aortic smooth muscle cells in primary culture [J].
Kuga, T ;
Kobayashi, S ;
Hirakawa, Y ;
Kanaide, H ;
Takeshita, A .
CIRCULATION RESEARCH, 1996, 79 (01) :14-19
[10]   Nickel block of three cloned T-type calcium channels:: Low concentrations selectively block α1H [J].
Lee, JH ;
Gomora, JC ;
Cribbs, LL ;
Perez-Reyes, E .
BIOPHYSICAL JOURNAL, 1999, 77 (06) :3034-3042