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鱿鱼轴突中细胞内钙调节的质膜机制。

Plasma membrane mechanisms for intracellular calcium regulation in squid axons.

作者信息

DiPolo R, Beaugé L

机构信息

Centro de Biofísica y Bioquímica, Instituto Venezolano de Investigaciones Científicas, Caracas.

出版信息

Acta Physiol Pharmacol Latinoam. 1987;37(4):437-44.

PMID:2856239
Abstract

The long term regulation of the cytosolic ionized Ca is the consequence of two separate Ca transport mechanisms present in most eucaryotic cells: a high-affinity and low-capacity system which is in charge of extruding Ca during resting conditions (the Ca pump) and a low affinity and high-capacity system (Na/Ca exchange) designed not only to extrude Ca2+ ions when the Cai raises above certain levels, but also to led Ca into the cell under conditions that favor the reverse reaction of the exchange, such as increase in Nai, decrease in external Na and membrane depolarization. Experiments in dialyzed and voltage clamped squid axons show that the Na/Ca exchange system is a complex mechanism in which several ligands normally present in the cytosol interact with the carrier. This should be taken into account when measuring kinetic properties of the Na/Ca exchange. Of great interest is the fact that Na/Ca exchange is subject of enzymatic regulation (phosphorylation/dephosphorylation), which in turn is regulated by the levels of Cai2+. More evidence is needed from both isolated membrane preparations and in vivo systems to answer several questions including the characterization of the partial reactions of the exchange system, the factors that modulate the affinity of the transport sites for Na and Ca, the stoichiometry (constant or variable?), the current generated by the exchanger and finally, the biochemical structure of the antiporter.

摘要

胞质游离钙的长期调节是大多数真核细胞中两种独立的钙转运机制作用的结果

一种是高亲和力、低容量系统,负责在静息状态下排出钙(钙泵);另一种是低亲和力、高容量系统(钠/钙交换),其设计目的不仅是在胞内钙升高到一定水平时排出钙离子,而且在有利于交换逆向反应的条件下,如胞内钠增加、胞外钠减少和膜去极化时,将钙导入细胞。对经透析和电压钳制的枪乌贼轴突进行的实验表明,钠/钙交换系统是一种复杂的机制,胞质中通常存在的几种配体与载体相互作用。在测量钠/钙交换的动力学特性时应考虑到这一点。一个非常有趣的事实是,钠/钙交换受酶促调节(磷酸化/去磷酸化),而这又受胞内钙水平的调节。需要从分离的膜制剂和体内系统中获得更多证据,以回答几个问题,包括交换系统部分反应的特征、调节转运位点对钠和钙亲和力的因素、化学计量(恒定还是可变?)、交换体产生的电流,以及最后,反向转运体的生化结构。

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