Camacho P, Lechleiter J D
Department of Neuroscience, University of Virginia Health Sciences Center, Charlottesville 22908, USA.
Cell. 1995 Sep 8;82(5):765-71. doi: 10.1016/0092-8674(95)90473-5.
Inositol 1,4,5-trisphosphate (IP3)-mediated calcium (Ca2+) signaling is subject to cytosolic and luminal regulatory mechanisms. In Xenopus oocytes, Ca(2+)-sensitive gating of the IP3 receptor (IP3R) produces repetitive waves of Ca2+ release. We examined the role of the luminal Ca(2+)-binding protein calreticulin (CRT) in IP3-mediated Ca2+ signaling by using Ca2+ wave activity as a sensitive Ca2+ release assay. Overexpression of CRT inhibited repetitive IP3-induced Ca2+ waves. Deletion mutagenesis demonstrated that CRT inhibition was mediated by the high affinity-low capacity Ca(2+)-binding domain, which contributes little to Ca2+ storage. This novel function of CRT in intracellular Ca2+ signaling may be regulated by Ca2+ occupancy of the high affinity binding site.
肌醇1,4,5-三磷酸(IP3)介导的钙(Ca2+)信号传导受胞质和内质网腔调节机制的影响。在非洲爪蟾卵母细胞中,IP3受体(IP3R)的Ca2+敏感门控产生重复的Ca2+释放波。我们通过使用Ca2+波活动作为灵敏的Ca2+释放检测方法,研究了内质网腔Ca2+结合蛋白钙网蛋白(CRT)在IP3介导的Ca2+信号传导中的作用。CRT的过表达抑制了IP3诱导的重复Ca2+波。缺失诱变表明,CRT的抑制作用由高亲和力-低容量Ca2+结合结构域介导,该结构域对Ca2+储存的贡献很小。CRT在细胞内Ca2+信号传导中的这一新功能可能受高亲和力结合位点的Ca2+占据情况调节。