A novel role for calmodulin:: Ca2+-independent inhibition of type-1 inositol trisphosphate receptors

被引:68
作者
Cardy, TJA [1 ]
Taylor, CW [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
基金
英国惠康基金;
关键词
D O I
10.1042/bj3340447
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
Calmodulin inhibits both inositol 1,4,5-trisphosphate (IP3) binding to, and IP3-evoked Ca2+ release by, cerebellar IP3 receptors [Patel, Morris, Adkins, O' Beirne and Taylor (1997) Proc. Natl. Acad. Sci. U.S.A, 94, 11627-11632]. In the present study, full-length rat type-1 and -3 IP3 receptors were expressed at high levels in insect Spodoptera frugiperda 9 cells and the effects of calmodulin were examined. In the absence of Ca2+, calmodulin caused a concentration-dependent and reversible inhibition of [H-3]IP3 binding to type-1 IP3 receptors by decreasing their apparent affinity for IP3. The effect was not reproduced by high concentrations of troponin C, parvalbumin or S-100. Increasing the medium free [Ca2+] ([Ca2+](m)) inhibited [H-3]IP3 binding to type-1 receptors, but the further inhibition caused by a submaximal concentration of calmodulin was similar at each [Ca2+](m). In the absence of Ca2+, I-125-calmodulin bound to a single site on each type-1 receptor subunit and to an additional site in the presence of Ca2+. There was no detectable binding of I-125-calmodulin to type-3 receptors and binding of [H-3]IP3 was insensitive to calmodulin at all [Ca2+](m). Both peptide and conventional Ca2+-calmodulin antagonists affected neither [H-3]IP3 binding directly nor the inhibitory effect of calmodulin in the absence of Ca2+, but each caused a [Ca2+](m)-dependent reversal of the inhibition of [H-3]IP3, binding caused by calmodulin. Camstatin, a peptide that binds to calmodulin equally well in the presence or absence of Ca2+, reversed the inhibitory effects of calmodulin on [H-3]IP3 binding at all [Ca2+](m). We conclude that calmodulin specifically inhibits [H-3]IP3 binding to type-1 IP3 receptors: the first example of a protein regulated by calmodulin in an entirely Ca2+-independent manner. Inhibition of type-1 IP3 receptors by calmodulin may dynamically regulate their sensitivity to IP3 in response to the changes in cytosolic free calmodulin concentration thought to accompany stimulation of neurones.
引用
收藏
页码:447 / 455
页数:9
相关论文
共 53 条
[31]  
MAEDA N, 1991, J BIOL CHEM, V266, P1109
[32]  
MIGNERY GA, 1990, J BIOL CHEM, V265, P12679
[33]   The InsP(3) receptor and intracellular Ca2+ signaling [J].
Mikoshiba, K .
CURRENT OPINION IN NEUROBIOLOGY, 1997, 7 (03) :339-345
[34]   THE SUBTYPES OF THE MOUSE INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR ARE EXPRESSED IN A TISSUE-SPECIFIC AND DEVELOPMENTALLY SPECIFIC MANNER [J].
NAKAGAWA, T ;
OKANO, H ;
FURUICHI, T ;
ARUGA, J ;
MIKOSHIBA, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) :6244-6248
[35]  
NEWTON CL, 1994, J BIOL CHEM, V269, P28613
[36]   HOW CALMODULIN BINDS ITS TARGETS - SEQUENCE INDEPENDENT RECOGNITION OF AMPHIPHILIC ALPHA-HELICES [J].
ONEIL, KT ;
DEGRADO, WF .
TRENDS IN BIOCHEMICAL SCIENCES, 1990, 15 (02) :59-64
[37]   Ca2+-independent inhibition of inositol trisphosphate receptors by calmodulin: Redistribution of calmodulin as a possible means of regulating Ca2+ mobilization [J].
Patel, S ;
Morris, SA ;
Adkins, CE ;
OBeirne, G ;
Taylor, CW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11627-11632
[38]   IDENTIFICATION OF A DROSOPHILA GENE ENCODING A CALMODULIN-BINDING PROTEIN WITH HOMOLOGY TO THE TRP PHOTOTRANSDUCTION GENE [J].
PHILLIPS, AM ;
BULL, A ;
KELLY, LE .
NEURON, 1992, 8 (04) :631-642
[39]   CALMODULIN-BINDING TO DROSOPHILA NINAC REQUIRED FOR TERMINATION OF PHOTOTRANSDUCTION [J].
PORTER, JA ;
MINKE, B ;
MONTELL, C .
EMBO JOURNAL, 1995, 14 (18) :4450-4459
[40]  
RICHARDSON CD, 1995, BACULOVIRUS EXPRESSI