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Enhanced ER Ca2+ store filling by overexpression of SERCA2b promotes IP3-evoked puffs.

机译:SERCA2b的过表达增强了ER Ca2 +存储量,促进了IP3引起的粉扑。

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摘要

Liberation of Ca(2+) from the endoplasmic reticulum (ER) through inositol trisphosphate receptors (IP(3)R) is modulated by the ER Ca(2+) content, and overexpression of SERCA2b to accelerate Ca(2+) sequestration into the ER has been shown to potentiate the frequency and amplitude of IP(3)-evoked Ca(2+) waves in Xenopus oocytes. Here, we examined the effects of SERCA overexpression on the elementary IP(3)-evoked puffs to elucidate whether ER [Ca(2+)] may modulate IP(3)R function via luminal regulatory sites in addition to simply determining the size of the available store and electrochemical driving force for Ca(2+) release. SERCA2b and Ca(2+) permeable nicotinic plasmalemmal channels were expressed in oocytes, and hyperpolarizing pulses were delivered to induce Ca(2+) influx and thereby load ER stores. Puffs evoked by photoreleased IP(3) were significantly potentiated in terms of numbers of responding sites, frequency and amplitude following transient Ca(2+) influx in SERCA-overexpressing cells, whereas little change was evident with SERCA overexpression alone or following Ca(2+) 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 IP(3)R gating kinetics.
机译:Ca(2+)通过肌醇三磷酸受体(IP(3)R)从内质网(ER)的释放由ER Ca(2+)含量和SERCA2b的过表达来加速Ca(2+)螯合ER已显示增强爪蟾卵母细胞中IP(3)诱发的Ca(2+)波的频率和振幅。在这里,我们检查了SERCA过表达对基本IP(3)引起的抽吸的影响,以阐明ER [Ca(2+)]是否可以通过腔调节位点调节IP(3)R功能,而不仅仅是确定其大小。 Ca(2+)释放的可用存储和电化学驱动力。 SERCA2b和Ca(2+)渗透性烟碱质膜通道在卵母细胞中表达,并传递超极化脉冲以诱导Ca(2+)流入,从而加载ER储存。由光释放的IP(3)引起的粉扑在SERCA过表达的细胞中瞬时Ca(2+)大量涌入后的响应部位数量,频率和幅度方面显着增强,而单独或跟随SERCA过表达的Ca(2)几乎没有明显变化+)流入未过表达SERCA的对照细胞。有趣的是,我们观察到出现了新的抽吸现象,这些抽吸现象是在长时间延迟后出现的,并持续了很长时间,从而支持了IP(3)R门控动力学的管腔调节概念。

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    Yamasaki-Mann, M; Parker, I;

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  • 年度 2011
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  • 原文格式 PDF
  • 正文语种 eng
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