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Cytosolic Ca2+ alteration mediates both ryanodine receptor and IP3 receptor in TE671/RD cells

フォーマット:
論文
責任表示:
Edahiro, Shigeki ; Yoshikawa, Hiroaki ; Iwasa, Kazuo ; Hashii, Minako ; Yamada, Masahito
言語:
英語
出版情報:
Biomedical Research, 2004-12-01
著者名:
掲載情報:
Biomedical Research
ISSN:
0388-6107  CiNii Research  Webcat Plus  JAIRO
巻:
25
通号:
6
開始ページ:
255
終了ページ:
261
バージョン:
publisher
概要:
金沢大学医薬保健研究域医学系<br />TE671 is a cell line obtained from the rhabdomyosarcoma cells. In the present study, we examined [Ca2+]i alteration induced by acetylcholine (ACh) in TE671/RD cells with the special attention to ryanodine receptor (RyR) and inositol 1,4,5-triphosphate receptor (IP3R). The change of [Ca2+]i was mediated by muscarinic type 3 (m3) AChR. Both phosphatidylinositol-specific phospholipase C blocker (U73122) and IP3R blocker (2-APB) inhibited ACh-induced [Ca2+]i elevation, suggesting that IP3 pathway is involved in [Ca2+]i alteration. Ryanodine and FK506 increased ACh-induced [Ca2+]i elevation, which was decreased by RyR blocker (ruthenium red). These results suggest that RyR and FK506 binding protein 12 kDa (FKBP12) complex was involved in [Ca2+]i change, and that TE671/RD cell line has a hybrid characteristic of smooth and skeletal muscles. Copyright © 2005 Biomedical Research Press. 続きを見る
URL:
http://hdl.handle.net/2297/14432
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