Isoform-specific function of single inositol 1,4,5-trisphosphate receptor channels

被引:150
作者
Ramos-Franco, J
Fill, M
Mignery, GA
机构
[1] Loyola Univ, Stritch Sch Med, Dept Physiol, Maywood, IL 60153 USA
[2] Cardiovasc Inst, Maywood, IL 60153 USA
关键词
D O I
10.1016/S0006-3495(98)77572-1
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The inositol 1,4,5-trisphosphate receptor (InsP(3)R) family of Ca2+ release channels is central to intracellular Ca2+ signaling in mammalian cells. The InsP(3)R channels release Ca2+ from intracellular compartments to generate localized Ca2+ transients that govern a myriad of cellular signaling phenomena (Berridge, 1993, Nature. 361:315-325; Joseph, 1996, Cell Signal. 8:1-7; Kume et al,, 1997, Science. 278:1940-1943; Berridge, 1997, Nature. 368:759-760), Most cells express multiple InsP(3)R isoforms, but only the function of the single type 1 InsP(3)R channel is known. Here the single-channel function of single type 2 InsP(3)R channel is defined for the first time. The type 2 InsP(3)R forms channels with permeation properties similar to that of the type 1 receptor. The InsP(3) regulation and Ca2+ regulation of type 1 and type 2 InsP(3)R channels are strikingly different. Both InsP(3) and Ca2+ are more effective at activating single type 2 InsP(3)R, indicating that single type 2 channels mobilize substantially more Ca2+ than single type 1 channels in cells. Furthermore, high cytoplasmic Ca2+ concentrations inactivate type 1, but not type 2, InsP(3)R channels. This indicates that type 2 InsP(3)R channel is different from the type 1 channel in that its activity will not be inherently self-limiting, because Ca2+ passing through an active type 2 channel cannot feed back and turn the channel off. Thus the InsP(3)R identity will help define the spatial and temporal nature of local Ca2+ signaling events and may contribute to the segregation of parallel InsP(3) signaling cascades in mammalian cells.
引用
收藏
页码:834 / 839
页数:6
相关论文
共 29 条
[1]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[2]   The AM and FM of calcium signalling [J].
Berridge, MJ .
NATURE, 1997, 386 (6627) :759-760
[3]  
BEZPROZVANNY I, 1995, J MEMBRANE BIOL, V145, P205
[4]   BELL-SHAPED CALCIUM-RESPONSE CURVES OF INS(1,4,5)P3-GATED AND CALCIUM-GATED CHANNELS FROM ENDOPLASMIC-RETICULUM OF CEREBELLUM [J].
BEZPROZVANNY, I ;
WATRAS, J ;
EHRLICH, BE .
NATURE, 1991, 351 (6329) :751-754
[5]  
BLONDEL O, 1993, J BIOL CHEM, V268, P11356
[6]   CALCIUM AND INOSITOL 1,4,5-TRISPHOSPHATE-INDUCED CA2+ RELEASE [J].
COMBETTES, L ;
CHAMPEIL, P .
SCIENCE, 1994, 265 (5173) :813-813
[7]  
DeSmedt H, 1997, BIOCHEM J, V322, P575
[8]   CALCIUM AS A COAGONIST OF INOSITOL 1,4,5-TRISPHOSPHATE INDUCED CALCIUM RELEASE [J].
FINCH, EA ;
TURNER, TJ ;
GOLDIN, SM .
SCIENCE, 1991, 252 (5004) :443-446
[9]   LUMINAL CALCIUM REGULATES THE INOSITOL TRISPHOSPHATE RECEPTOR OF RAT BASOPHILIC LEUKEMIA-CELLS AT A CYTOSOLIC SITE [J].
HORNE, JH ;
MEYER, T .
BIOCHEMISTRY, 1995, 34 (39) :12738-12746
[10]   EFFECTS OF ADENINE-NUCLEOTIDES ON INOSITOL 1,4,5-TRISPHOSPHATE-INDUCED CALCIUM RELEASE IN VASCULAR SMOOTH-MUSCLE CELLS [J].
IINO, M .
JOURNAL OF GENERAL PHYSIOLOGY, 1991, 98 (04) :681-698