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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.
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页码:97 / 104
页数:8
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