Muallem S, Zhao H, Mayer E, Sachs G
Department of Physiology, U.T. Southwestern Medical Center, Dallas 75235.
Semin Cell Biol. 1990 Aug;1(4):305-10.
The role of [Ca2+]i as a second messenger in non-excitable cells has been appreciated for almost 3 decades. The advent of fluorescent Ca2+ indicators has allowed the monitoring of Ca2+ signalling in suspensions of these cells. Agonist mediated changes in [Ca2+]i usually show an initial Ca2+ transient followed by a maintained increase. The former has been shown to be due to Ca2+ release from one or more intracellular stores, the latter due to activation of receptor operated Ca2+ entry (ROCE). More recently it has been recognized that many cells show distinct maintained oscillatory behavior when examined by single cell optical methods. It is proposed here that these oscillations are the consequence of IP3 and Ca2+ stimulation of Ca2+ release and ligand activation of ROCE followed by Ca2+ inhibition of Ca2+ and ROCE as Ca2+ pumps are activated. These oscillations allow more exact regulation of a pump/leak controlled second messenger such as [Ca2+]i.
细胞内钙离子([Ca2+]i)作为非兴奋性细胞中第二信使的作用已被认识近30年。荧光钙指示剂的出现使得对这些细胞悬浮液中的钙信号进行监测成为可能。激动剂介导的[Ca2+]i变化通常表现为最初的钙瞬变,随后是持续增加。前者已被证明是由于从一个或多个细胞内储存库释放钙,后者是由于受体操纵的钙内流(ROCE)激活。最近人们认识到,当通过单细胞光学方法检测时,许多细胞表现出明显的持续振荡行为。本文提出,这些振荡是IP3和钙对钙释放的刺激以及ROCE的配体激活的结果,随后随着钙泵被激活,钙对钙和ROCE产生抑制作用。这些振荡允许对诸如[Ca2+]i这样的由泵/渗漏控制的第二信使进行更精确的调节。