INOSITOL TRISPHOSPHATE RECEPTOR AND CA2+ SIGNALING

被引:13
作者
MIKOSHIBA, K
FURUICHI, T
MIYAWAKI, A
YOSHIKAWA, S
NAKAGAWA, T
YAMADA, N
HAMANAKA, Y
FUJINO, I
MICHIKAWA, T
RYO, Y
OKANO, H
FUJII, S
NAKADE, S
机构
[1] INST PHYS & CHEM RES,DEPT MOLEC NEUROBIOL,IBARAKI,JAPAN
[2] OSAKA UNIV,INST PROT RES,DIV REGULAT MACROMOLEC FUNCT,OSAKA,JAPAN
关键词
D O I
10.1098/rstb.1993.0077
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Inositol 1,4,5-trisphosphate (InsP3) is a second messenger that releases Ca2+ from the intracellular stores. The InsP3 receptor (InsP3-R) was purified and its cDNA was cloned. We have found that InsP3-R is identical to the P400 protein identified as a protein enriched in the cerebellar Purkinje cells. We generated an L fibroblast cell transfectant that produced cDNA derived InsP3-R. The expressed protein displays high affinity and specificity for InsP3. InsP3 induces Ca2+ release from the membrane vesicles of the transfected cells. Incorporation of purified InsP3-R into a lipid bilayer showed InsP3 induced Ca2+ release. These result suggest that InsP3-R is a Ca2+ release channel. Immunogold method using monoclonal antibodies against the receptor showed that it is highly condensed on the smooth surfaced endoplasmic reticulum (ER) and slightly on the outer nuclear membrane and rough ER. Cross linking experiments show that the InsP3-R forms a homotetramer. The approximately 650 N-terminal amino acids are highly conserved between mouse and Drosophila melanogaster, and this region has the critical sequences for InsP3 binding. We found novel subtypes of the InsP3-R resulting from RNA-splicing that are expressed in a tissue-specific and developmentally specific manner and also resulting from different genes. It is believed that there are two Ca2+ release mechanisms, InsP3-induced Ca2+ release (IICR) and Ca2+-induced Ca2+ release (CICR). Eggs are good materials to analyse the machanism of Ca2+ signalling: fertilized hamster eggs exhibit repetitive Ca2+ transients as well as the Ca2+ wave. A monoclonal antibody to the InsP3-R inhibited both IICR and CICR respectively upon injection of InsP3 and Ca2+ into hamster eggs. The antibody completely blocked sperm-induced Ca2+ waves and Ca2+ oscillations. The results indicate that Ca2+ release in fertilized hamster eggs is mediated solely by the InsP3-R, and that Ca2+-sensitized IICR, but not CICR, generates Ca2+ waves and Ca2+ oscillations.
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收藏
页码:345 / 349
页数:5
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共 42 条
[21]   PUTATIVE RECEPTOR FOR INOSITOL 1,4,5-TRISPHOSPHATE SIMILAR TO RYANODINE RECEPTOR [J].
MIGNERY, GA ;
SUDHOF, TC ;
TAKEI, K ;
DECAMILLI, P .
NATURE, 1989, 342 (6246) :192-195
[22]   BIOCHEMICAL AND IMMUNOLOGICAL STUDIES ON THE P-400 PROTEIN, A PROTEIN CHARACTERISTIC OF THE PURKINJE-CELL FROM MOUSE AND RAT CEREBELLUM [J].
MIKOSHIBA, K ;
HUCHET, M ;
CHANGEUX, JP .
DEVELOPMENTAL NEUROSCIENCE, 1979, 2 (06) :254-275
[23]   P400-PROTEIN CHARACTERISTIC TO PURKINJE-CELLS AND RELATED PROTEINS IN CEREBELLA FROM NEUROPATHOLOGICAL MUTANT MICE - AUTORADIOGRAPHIC STUDY BY C-14-LEUCINE AND PHOSPHORYLATION [J].
MIKOSHIBA, K ;
OKANO, H ;
TSUKADA, Y .
DEVELOPMENTAL NEUROSCIENCE, 1985, 7 (03) :179-187
[24]   STRUCTURE-FUNCTION-RELATIONSHIPS OF THE MOUSE INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR [J].
MIYAWAKI, A ;
FURUICHI, T ;
RYOU, Y ;
YOSHIKAWA, S ;
NAKAGAWA, T ;
SAITOH, T ;
MIKOSHIBA, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :4911-4915
[25]   EXPRESSED CEREBELLAR-TYPE INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR, P400, HAS CALCIUM RELEASE ACTIVITY IN A FIBROBLAST L-CELL LINE [J].
MIYAWAKI, A ;
FURUICHI, T ;
MAEDA, N ;
MIKOSHIBA, K .
NEURON, 1990, 5 (01) :11-18
[26]   BLOCK OF CA2+ WAVE AND CA2+ OSCILLATION BY ANTIBODY TO THE INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR IN FERTILIZED HAMSTER EGGS [J].
MIYAZAKI, S ;
YUZAKI, M ;
NAKADA, K ;
SHIRAKAWA, H ;
NAKANISHI, S ;
NAKADE, S ;
MIKOSHIBA, K .
SCIENCE, 1992, 257 (5067) :251-255
[27]   PRIMARY STRUCTURE AND FUNCTIONAL EXPRESSION FROM COMPLEMENTARY-DNA OF A BRAIN CALCIUM-CHANNEL [J].
MORI, Y ;
FRIEDRICH, T ;
KIM, MS ;
MIKAMI, A ;
NAKAI, J ;
RUTH, P ;
BOSSE, E ;
HOFMANN, F ;
FLOCKERZI, V ;
FURUICHI, T ;
MIKOSHIBA, K ;
IMOTO, K ;
TANABE, T ;
NUMA, S .
NATURE, 1991, 350 (6317) :398-402
[28]   INVOLVEMENT OF THE C-TERMINUS OF THE INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR IN CA-2+ RELEASE ANALYZED USING REGION-SPECIFIC MONOCLONAL-ANTIBODIES [J].
NAKADE, S ;
MAEDA, N ;
MIKOSHIBA, K .
BIOCHEMICAL JOURNAL, 1991, 277 :125-131
[29]   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
[30]   IMMUNOGOLD LOCALIZATION OF INOSITOL 1,4,5-TRISPHOSPHATE (INSP3) RECEPTOR IN MOUSE CEREBELLAR PURKINJE-CELLS USING 3 MONOCLONAL-ANTIBODIES [J].
OTSU, H ;
YAMAMOTO, A ;
MAEDA, N ;
MIKOSHIBA, K ;
TASHIRO, Y .
CELL STRUCTURE AND FUNCTION, 1990, 15 (03) :163-173