INOSITOL TETRAKISPHOSPHATE AS A 2ND MESSENGER - CONFUSIONS, CONTRADICTIONS AND A POTENTIAL RESOLUTION

被引:121
作者
IRVINE, RF
机构
[1] Department of Biochemistry, Institute of Animal Physiology and Genetics Research, Cambridge, CB2 4AT, Babraham
关键词
D O I
10.1002/bies.950130810
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
The second messenger function of inositol 1,4,5-trisphosphate (InsP3) is now well-defined - it mobilizes Ca2+ from intracellular stores so that cytosolic Ca2+ increases. However, the function of inositol 1,3,4,5-tetrakisphosphate (InsP4) has proved much more difficult to fathom, as it has been reported to exert a wide variety of effects in a collection of experimental systems. In this review, a proposed molecular mechanism for InsP4's actions is discussed; it is suggested that InsP4 is the second messenger that controls Ca2+ entry into cells, and that it does so by binding to a receptor which itself interacts, directly or indirectly, with the receptor for InsP3. It is proposed that this is InsP4's true physiological function, but the mechanism by which it exerts this function has led to confusing data concerning its action, and also to some misconceptions about how inositol phosphates control Ca2+ entry.
引用
收藏
页码:419 / 427
页数:9
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[1]   INOSITOL PHOSPHATES AND CELL SIGNALING [J].
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[3]   SPECIFIC BINDING-SITES FOR [H-3] INOSITOL(1,3,4,5)TETRAKISPHOSPHATE ON MEMBRANES OF HL-60 CELLS [J].
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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 149 (02) :680-685
[4]   ATTRACTANT-INDUCED CHANGES AND OSCILLATIONS OF THE EXTRACELLULAR CA++ CONCENTRATION IN SUSPENSIONS OF DIFFERENTIATING DICTYOSTELIUM CELLS [J].
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[5]   HETEROGENEITY OF [H-3] INOSITOL 1,4,5-TRISPHOSPHATE BINDING-SITES IN ADRENAL-CORTICAL MEMBRANES - CHARACTERIZATION AND VALIDATION OF A RADIORECEPTOR ASSAY [J].
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WILLCOCKS, AL ;
NAHORSKI, SR .
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GALLACHER, DV ;
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PETERSEN, OH .
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[7]   ACTIVATION OF SEA-URCHIN EGGS BY INOSITOL PHOSPHATES IS INDEPENDENT OF EXTERNAL CALCIUM [J].
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[8]   SYNERGISTIC CONTROL OF CA2+ MOBILIZATION IN PERMEABILIZED MOUSE L1210 LYMPHOMA-CELLS BY INOSITOL 2,4,5-TRISPHOSPHATE AND INOSITOL 1,3,4,5-TETRAKISPHOSPHATE [J].
CULLEN, PJ ;
IRVINE, RF ;
DAWSON, AP .
BIOCHEMICAL JOURNAL, 1990, 271 (02) :549-553
[9]   INOSITOL 1,3,4,5-TETRAKISPHOSPHATE CAUSES RELEASE OF CA-2+ FROM PERMEABILIZED MOUSE LYMPHOMA L1210 CELLS BY ITS CONVERSION INTO INOSITOL 1,4,5-TRISPHOSPHATE [J].
CULLEN, PJ ;
IRVINE, RF ;
DROBAK, BK ;
DAWSON, AP .
BIOCHEMICAL JOURNAL, 1989, 259 (03) :931-933
[10]   CHARACTERIZATION OF A MEMBRANE-PROTEIN FROM BRAIN MEDIATING THE INHIBITION OF INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR-BINDING BY CALCIUM [J].
DANOFF, SK ;
SUPATTAPONE, S ;
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