Inositol 1, 4, 5-trisphosphate receptor interacts with the SNARE domain of syntaxin 1B

被引:1
作者
Tanaka, Sayaka [1 ,2 ]
Kabayama, Hiroyuki [1 ,3 ]
Enomoto, Masahiro [1 ]
Saito, Nobuhito [2 ]
Mikoshiba, Katsuhiko [1 ,3 ]
机构
[1] Inst Phys & Chem Res RIKEN, Dev Neurobiol Lab, Brain Sci Inst, Wako, Saitama 3510198, Japan
[2] Univ Tokyo, Dept Neurosurg, Grad Sch Med, Bunkyo Ku, Tokyo 1138655, Japan
[3] Japan Sci & Technol Agcy, ICORP SORST, Kawaguchi, Saitama 3320012, Japan
关键词
Syntaxin; 1B; SNARE domain; Inositol; 1; 4; 5-trisphosphate receptor; Internal coupling domain; LONG-TERM DEPRESSION; 1,4,5-TRISPHOSPHATE RECEPTOR; MEMBRANE-FUSION; CA2+ CHANNELS; IP3; RECEPTOR; MICE LACKING; CALCIUM-CHANNELS; N-TYPE; FUNCTIONAL IMPACT; TYPE-1;
D O I
10.1007/s12576-011-0140-4
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Inositol 1, 4, 5-trisphosphate receptors (IP(3)Rs) are intracellular ligand-gated Ca2+ channels that mediate Ca2+ release from the endoplasmic reticulum (ER) into the cytosol and function in diverse cellular processes including fertilization, muscle contraction, apoptosis, secretion, and synaptic plasticity. The Ca2+ release activity of IP(3)Rs is tightly regulated by many factors including IP3R-binding proteins. We show that IP(3)Rs interact with syntaxin 1 (Syx1), a membrane trafficking protein that regulates various plasma-membrane ion channels including N-, P/Q, and L-type voltage-gated Ca2+ channels, voltage-gated potassium channels, and an epithelial sodium channel. We found that a SNARE-domain of Syx1B, one of the two Syx1 isoforms, directly interacted with the type1 IP3R (IP(3)R1) internal coupling domain, a known modulator for channel opening. These results indicate that Syx1B is an IP3R-interacting protein and that its interaction may play a crucial role in regulating the channel activity of IP3Rs in Syx1B-expressing cells.
引用
收藏
页码:221 / 229
页数:9
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