Subtype-specific and ER lumenal environment-dependent regulation of inositol 1,4,5-trisphosphate receptor type 1 by ERp44

被引:311
作者
Higo, T
Hattori, M
Nakamura, T
Natsume, T
Michikawa, T
Mikoshiba, K
机构
[1] Univ Tokyo, Dept Mol Neurobiol, Inst Med Sci, Minato Ku, Tokyo 1088639, Japan
[2] RIKEN, Dev Neurobiol Lab, Brain Sci Inst, Wako, Saitama 3510198, Japan
[3] JST, ICORP, Calcium Oscillat Project, Kawaguchi, Saitama 3320012, Japan
[4] Japan Biol Informat Res Ctr, Prot Network Team, Funct Genome Grp, Koto Ku, Tokyo 1358073, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1016/j.cell.2004.11.048
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
Inositol 1,4,5-trisphosphate receptors (IP(3)Rs) are intracellular channel proteins that mediate Ca2+ release from the endoplasmic reticulum (ER) and are involved in many biological processes and diseases. IP(3)Rs are differentially regulated by a variety of cytosolic proteins, but their regulation by ER lumenal protein(s) remains largely unexplored. In this study, we found that ERp44, an ER lumenal protein of the thioredoxin family, directly interacts with the third lumenal loop of IP3R type 1 (IP(3)R1) and that the interaction is dependent on pH, Call concentration, and redox state: the presence of free cysteine residues in the loop is required. Ca2+-imaging experiments and single-channel recording Of IP3R1 activity with a planar lipid bilayer system demonstrated that IP3R1 is directly inhibited by ERp44. Thus, ERp44 senses the environment in the ER lumen and modulates IP3R1 activity accordingly, which should in turn contribute to regulating both intralumenal conditions and the complex patterns of cytosolic Ca2+ concentrations.
引用
收藏
页码:85 / 98
页数:14
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