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Enhanced ER Ca2+ store filling by overexpression of SERCA2b promotes IP3-evoked puffs
被引:18
|作者:
Yamasaki-Mann, Michiko
[1
]
Parker, Ian
[1
,2
]
机构:
[1] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92697 USA
基金:
美国国家卫生研究院;
关键词:
SERCA;
ER;
IP3;
INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR;
XENOPUS-LAEVIS OOCYTES;
LUMINAL CA2+;
IP3;
RECEPTORS;
ACTIVATION;
CALCIUM;
RELEASE;
CHANNEL;
TRISPHOSPHATE;
MECHANISM;
D O I:
10.1016/j.ceca.2011.04.008
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Liberation of Ca2+ from the endoplasmic reticulum (ER) through inositol trisphosphate receptors (IP3R) is modulated by the ER Ca2+ content, and overexpression of SERCA2b to accelerate Ca2+ sequestration into the ER has been shown to potentiate the frequency and amplitude of IP3-evoked Ca2+ waves in Xenopus oocytes. Here, we examined the effects of SERCA overexpression on the elementary IP3-evoked puffs to elucidate whether ER [Ca2+] may modulate IP3R function via luminal regulatory sites in addition to simply determining the size of the available store and electrochemical driving force for Ca2+ release. SERCA2b and Ca2+ permeable nicotinic plasmalemmal channels were expressed in oocytes, and hyperpolarizing pulses were delivered to induce Ca2+ influx and thereby load ER stores. Puffs evoked by photoreleased IP3 were significantly potentiated in terms of numbers of responding sites, frequency and amplitude following transient Ca2+ influx in SERCA-overexpressing cells, whereas little change was evident with SERCA overexpression alone or following Ca2+ influx in control cells not overexpressing SERCA. Intriguingly, we observed the appearance of a new population of puffs that arose after long latencies and had prolonged durations supporting the notion of luminal regulation of IP3R gating kinetics. (C) 2011 Elsevier Ltd. All rights reserved.
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页码:36 / 41
页数:6
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