Expression of a truncated form of inositol 1,4,5-trisphosphate receptor type III in the cytosol of DT40 triple inositol 1,4,5-trisphosphate receptor-knockout cells

被引:9
作者
Guillemette, J
Caron, AZ
Regimbald-Dumas, Y
Arguin, G
Mignery, GA
Boulay, G
Guillemette, G [1 ]
机构
[1] Univ Sherbrooke, Fac Med, Dept Pharmacol, Sherbrooke, PQ J1H 5N4, Canada
[2] Loyola Univ Chicago, Stritch Sch Med, Dept Physiol, Maywood, IL 60153 USA
基金
加拿大健康研究院;
关键词
inositol 1,4,5-trisphosphate; cytosol; knockout cells;
D O I
10.1016/j.ceca.2004.03.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In non-excitable cells, the inositol 1,4,5-trisphosphate receptor (IP3R) is an intracellular Ca2+ channel playing a major role in Ca2+ signaling. Three isoforms Of IP3R have been identified and most cell types express different proportions of each isoform. The DT40 B lymphocyte cell line lacking all three IP3R isoforms (DT40IP(3)R-KO cells) represents an excellent model to re-express any recombinant IP3R and analyze its specific properties. In the study presented here, we confirmed that DT40IP(3)R-KO cells do not express any IP3-sensitive Ca2+ release channel. However, with an immunoblot approach and a [H-3]IP3 binding approach we demonstrated the presence of a C-terminally truncated form Of IP3R type III in the cytosolic fraction of DT40IP(3)R-KO cells. We further showed that this truncated IP3R retained the ability to couple to the Ca2+ entry channel TRPC6. Therefore, a word of caution is offered about the interpretation of results obtained in using DT40IP3R-KO cells to study the cellular mechanisms of Ca2+ entry. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:97 / 104
页数:8
相关论文
共 35 条
[31]   Modulation of inositol 1,4,5-trisphosphate binding to the various inositol 1,4,5-trisphosphate receptor isoforms by thimerosal and cyclic ADP-ribose [J].
Vanlingen, S ;
Sipma, H ;
De Smet, P ;
Callewaert, G ;
Missiaen, L ;
De Smedt, H ;
Parys, JB .
BIOCHEMICAL PHARMACOLOGY, 2001, 61 (07) :803-809
[32]   TYPE-I, TYPE-II, AND TYPE-III INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS ARE UNEQUALLY SUSCEPTIBLE TO DOWN-REGULATION AND ARE EXPRESSED IN MARKEDLY DIFFERENT PROPORTIONS IN DIFFERENT CELL-TYPES [J].
WOJCIKIEWICZ, RJH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (19) :11678-11683
[33]   Phosphorylation of inositol 1,4,5-trisphosphate receptors by cAMP-dependent protein kinase - Type I, II and III receptors are differentially susceptible to phosphorylation and are phosphorylated in intact cells [J].
Wojcikiewicz, RJH ;
Luo, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5670-5677
[34]   TYPE-I, TYPE-II AND TYPE-III INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR CO-IMMUNOPRECIPITATION AS EVIDENCE FOR THE EXISTENCE OF HETEROTETRAMERIC RECEPTOR COMPLEXES [J].
WOJCIKIEWICZ, RJH ;
HE, YQ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 213 (01) :334-341
[35]   Ca2+ differentially regulates the ligand-affinity states of type 1 and type 3 inositol 1,4,5-trisphosphate receptors [J].
Yoneshima, H ;
Miyawaki, A ;
Michikawa, T ;
Furuichi, T ;
Mikoshiba, K .
BIOCHEMICAL JOURNAL, 1997, 322 :591-596