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.
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收藏
页码:447 / 455
页数:9
相关论文
共 53 条
[41]   Calmodulin regulation of Drosophila light-activated channels and receptor function mediates termination of the light response in vivo [J].
Scott, K ;
Sun, YM ;
Beckingham, K ;
Zuker, CS .
CELL, 1997, 91 (03) :375-383
[42]   Camstatins are peptide antagonists of calmodulin based upon a conserved structural motif in PEP-19, neurogranin, and neuromodulin [J].
Slemmon, JR ;
Morgan, JI ;
Fullerton, SM ;
Danho, W ;
Hilbush, BS ;
Wengenack, TM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (27) :15911-15917
[43]   PHOTORECEPTOR DEACTIVATION AND RETINAL DEGENERATION MEDIATED BY A PHOTORECEPTOR-SPECIFIC PROTEIN-KINASE-C [J].
SMITH, DP ;
RANGANATHAN, R ;
HARDY, RW ;
MARX, J ;
TSUCHIDA, T ;
ZUKER, CS .
SCIENCE, 1991, 254 (5037) :1478-1484
[44]   Genetic evidence for involvement of type 1, type 2 and type 3 inositol 1,4,5-trisphosphate receptors in signal transduction through the B-cell antigen receptor [J].
Sugawara, H ;
Kurosaki, M ;
Takata, M ;
Kurosaki, T .
EMBO JOURNAL, 1997, 16 (11) :3078-3088
[45]  
SUPATTAPONE S, 1988, J BIOL CHEM, V263, P1530
[46]   CALMODULIN ACTIVATION AND INHIBITION OF SKELETAL-MUSCLE CA2+ RELEASE CHANNEL (RYANODINE RECEPTOR) [J].
TRIPATHY, A ;
XU, L ;
MANN, G ;
MEISSNER, G .
BIOPHYSICAL JOURNAL, 1995, 69 (01) :106-119
[47]   R-24-571 - A POTENT INHIBITOR OF CALMODULIN-ACTIVATED ENZYMES [J].
VANBELLE, H .
CELL CALCIUM, 1981, 2 (05) :483-494
[48]   Identification and characterization of two distinct calmodulin-binding sites in the Trpl ion-channel protein of Drosophila melanogaster [J].
Warr, CG ;
Kelly, LE .
BIOCHEMICAL JOURNAL, 1996, 314 :497-503
[49]   TYPE-I, TYPE-II, AND TYPE-III INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS ARE UNEQUALLY SUSCEPTIBLE TO DOWN-REGULATION AND ARE EXPRESSED IN MARKEDLY DIFFERENT PROPORTIONS IN DIFFERENT CELL-TYPES [J].
WOJCIKIEWICZ, RJH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (19) :11678-11683
[50]   REGULATION OF CALMODULIN-BINDING MYOSINS [J].
WOLENSKI, JS .
TRENDS IN CELL BIOLOGY, 1995, 5 (08) :310-316