[The role of mitochondrial uniporter in calcium-homeostasis of the exorbital lacrimal gland secretory cells].

A. Kotliarova, V. M. Merlavs'kyĭ, O. Dorosh, V. V. Man'ko
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引用次数: 1

Abstract

The role of mitochondrial calcium-uniporter in calcium-homeostasis maintenance and correlations of calcium-uniporter with other calcium-transport systems of the rat exorbital lacrimal gland secretory cells were studied. The experiments were performed on intact and digitonin-permeabilized cells. The interdependence of calcium-uniporter and other calcium-transporting systems functioning was estimated on the basis of additivity of their inhibitors/agonists effects, which was accompanied with a decrease in the Ca2+ content in the gland cells. It was found that in conditions of simultaneously inhibition of sarco endoplasmic reticulum Ca2+-ATPase (SERCA) and mitochondrial calcium-uniporter Ca2+ passively released from different calcium stores, because the effects of these calcium-transport systems inhibitors (thapsigargin and ruthenium red, respectively) were additive. Similarly, the processes of inositol-1,4,5-trisphosphate receptors (IP3Rs) activation and calcium-uniporter inhibition were additive. In contrast, the effects of ryanodine and ruthenium red on the Ca2+ content in cells were significantly non-additive. In addition, ryanodine at concentrations 1-3 μM reduced respiration rate of studied cells in dose-dependent manner, and this effect was persisted at cells preincubation with ruthenium red or tapsigargin. Thus, besides the activation of ryanodine receptors (RyRs) in endoplasmic reticulum, ryanodine inhibits Ca2+ influx to the mitochondrial matrix, that was insensitive to ruthenium red.
线粒体单转运蛋白在眶外泪腺分泌细胞钙稳态中的作用。
研究了线粒体单输钙在维持大鼠眶外泪腺分泌细胞钙稳态中的作用,以及单输钙与眶外泪腺分泌细胞其他钙转运系统的相关性。实验在完整细胞和地黄皂苷渗透细胞上进行。钙-单转运体和其他钙转运系统功能的相互依赖性是基于它们的抑制剂/激动剂作用的可加性来估计的,这伴随着腺体细胞中Ca2+含量的降低。研究发现,在同时抑制sarco内质网Ca2+- atp酶(SERCA)和线粒体钙转运体Ca2+被动释放的条件下,不同钙储存的钙转运系统抑制剂(分别为thapsigarin和钌红)的作用是加性的。同样,肌醇-1,4,5-三磷酸受体(IP3Rs)的激活和单转运钙的抑制过程是加性的。而ryanodine和钌红对细胞内Ca2+含量的影响呈显著的非相加性。此外,ryanodine浓度在1 ~ 3 μM时,以剂量依赖的方式降低了研究细胞的呼吸速率,并且这种作用在钌红或tapsigarin预孵育细胞时持续存在。因此,除了激活内质网中的ryanodine受体(RyRs)外,ryanodine还抑制Ca2+流入对钌红不敏感的线粒体基质。
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