PH-DEPENDENCE OF INOSITOL 1,4,5-TRISPHOSPHATE-INDUCED CA2+ RELEASE IN PERMEABILIZED SMOOTH-MUSCLE CELLS OF THE GUINEA-PIG

被引:59
作者
TSUKIOKA, M [1 ]
IINO, M [1 ]
ENDO, M [1 ]
机构
[1] UNIV TOKYO, FAC MED, DEPT PHARMACOL, BUNKYO KU, TOKYO 113, JAPAN
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1994年 / 475卷 / 03期
关键词
D O I
10.1113/jphysiol.1994.sp020078
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. The dependence on pH of inositol 1,4,5-trisphosphate (IP3)-induced Ca2+ release was studied in saponin-skinned smooth muscle cells from guinea-pig portal vein, using the indicator fura-2 to monitor Ca2+ release. 2. Increasing pH between 6.7 and 7.3 enhanced the rate of IP3-induced Ca2+ release at all the Ca2+ concentrations above 30 nM without changing the bell-shaped dependence of the Ca2+ release rate on Ca2+ concentration with a peak near 300 nM. 3. The ascending limb of the biphasic Ca2+ dependence was shifted slightly toward the lower Ca2+ concentration at pH 7.3, suggesting an increase in the Ca2+ sensitivity of IP3-induced Ca2+ release at the higher pH. 4. With the elevation in pH from 6.7 to 7.3 at 100 nM Ca2+, about 7-fold higher IP3 concentration was required to release half of the Ca2+ in the store within 15 s. This pH-dependent change in the IP3 sensitivity was smaller at 1 muM Ca2+ and was indiscernible in the absence of Ca2+. 5. These results suggest that H+ may inhibit binding of IP3 and Ca2+ to the modulator sites of the Ca2+ release mechanism. However, these effects on the binding sites may not fully explain the complex effect of pH, and there may be pH-dependent step(s) involved in the gating mechanism of IP3 channels. The present study demonstrates the importance of pH as a modulator of IP3-induced Ca2+ release.
引用
收藏
页码:369 / 375
页数:7
相关论文
共 33 条
[1]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[2]   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
[3]  
BRASS LF, 1985, J BIOL CHEM, V260, P5172
[4]   ISOLATION AND CHARACTERIZATION OF THE INOSITOL TRISPHOSPHATE RECEPTOR FROM SMOOTH-MUSCLE [J].
CHADWICK, CC ;
SAITO, A ;
FLEISCHER, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (06) :2132-2136
[5]  
CLAPPER DL, 1985, J BIOL CHEM, V260, P3947
[6]  
ENDO M, 1985, CURR TOP MEMBR TRANS, V25, P181
[7]   CALCIUM FLUX MEDIATED BY PURIFIED INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR IN RECONSTITUTED LIPID VESICLES IS ALLOSTERICALLY REGULATED BY ADENINE-NUCLEOTIDES [J].
FERRIS, CD ;
HUGANIR, RL ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (06) :2147-2151
[8]   PURIFIED INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR MEDIATES CALCIUM FLUX IN RECONSTITUTED LIPID VESICLES [J].
FERRIS, CD ;
HUGANIR, RL ;
SUPATTAPONE, S ;
SNYDER, SH .
NATURE, 1989, 342 (6245) :87-89
[9]   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
[10]   PRIMARY STRUCTURE AND FUNCTIONAL EXPRESSION OF THE INOSITOL 1,4,5-TRISPHOSPHATE-BINDING PROTEIN-P400 [J].
FURUICHI, T ;
YOSHIKAWA, S ;
MIYAWAKI, A ;
WADA, K ;
MAEDA, N ;
MIKOSHIBA, K .
NATURE, 1989, 342 (6245) :32-38