Spatiotemporal dynamics of Ca2+ signaling and its physiological roles

被引:31
作者
Iino, Masamitsu [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Pharmacol, Bunkyo Ku, Tokyo 1130033, Japan
来源
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES | 2010年 / 86卷 / 03期
关键词
Ca2+; IP3; NFAT; imaging; smooth muscle; synapse; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; SMOOTH-MUSCLE-CELLS; INDUCED CALCIUM RELEASE; XENOPUS-LAEVIS OOCYTES; PIG TAENIA CECI; INTRACELLULAR CA2+; SARCOPLASMIC-RETICULUM; ENDOPLASMIC-RETICULUM; RYANODINE RECEPTOR; FUNCTIONAL-CHARACTERIZATION;
D O I
10.2183/pjab.86.244
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Changes in the intracellular Ca2+ concentration regulate numerous cell functions and display diverse spatiotemporal dynamics, which underlie the versatility of Ca2+ in cell signaling. In ninny cell types, an increase in the intracellular Ca2+ concentration starts locally, propagates within the cell (Ca2+ wave) and makes oscillatory changes (Ca2+ oscillation). Studies of the intracellular release mechanism horn the endoplasmic reticulum (ER) snowed that the Ca2+ release mechanism has inherent regenerative properties, which is essential for the generation of Ca2+ waves and oscillations. Ca2+ may shuttle between the ER, and mitochondria, and this appears to be important for pacemaking of Ca2+ oscillations. Importantly, Ca2+ oscillations are an efficient, mechanism in regulating cell functions, having effects supra-proportional to the sum of duration of Ca2+ increase. Furthermore, Ca2+ signaling mechanism studies have led to the development, of a method for specific inhibition of Ca2+ signaling. which has been used to identify hitherto unrecognized functions of Ca2+ signals.
引用
收藏
页码:244 / 256
页数:13
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