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荧光钙指示剂indo-1/AM抑制肾近端小管细胞体积调节。

The fluorescent calcium indicator indo-1/AM inhibits renal proximal tubule cell volume regulation.

作者信息

Kanli H, Brown H M, Terreros D A

机构信息

Veterans Affairs Medical Center, Salt Lake City, UT 84148.

出版信息

Ann Clin Lab Sci. 1992 Jul-Aug;22(4):236-44.

PMID:1503391
Abstract

The intracellular calcium indicator, indo-1, is a fluorescent compound related in structure and function to the calcium chelator ethylene glycol-bis(beta-aminoethyl ether) tetraacetic acid (EGTA) that binds one calcium ion per molecule. In the extracellular range of 1 to 10 microM indo-1/AM, the estimated intracellular concentration of the dye is 0.1 to 3 microM. Therefore, it is likely that intracellular calcium signals could be blunted under these experimental conditions (Cai approximately 0.1 to 0.2 microM). To evaluate the potential effects of indo-1/AM on cellular function, proximal renal tubules of the teleost Carassius auratus (goldfish) were exposed to its acetoxymethyl ester (cell permeable form) in an isotonic Ringer's solution (290 mOsm, 0.1 mM calcium) followed by exposure to a low sodium hypotonic Ringer's (110 mOsm, 0.1 mM calcium). Cellular regulatory volume decreases (RVD) were determined with videometric methods. In proximal renal tubules incubated with indo-1/AM, RVD was inhibited in a dose-dependent fashion (3 to 5 microM). No effects on RVD were observed with the impermeant salt of indo-1. Overt cellular injury was found at 10 microM indo-1/AM as evidenced by mitochondrial and cell swelling, cellular detachment from the tubular basement membrane, and different degrees of cytolysis. It is postulated by us that the inhibitory effects of indo-1/AM (3-5 microM) on RVD are due to intracellular calcium chelation followed by disruption of intracellular signalling.

摘要

细胞内钙指示剂吲哚-1是一种荧光化合物,其结构和功能与每分子结合一个钙离子的钙螯合剂乙二醇双(β-氨基乙基醚)四乙酸(EGTA)相关。在细胞外1至10微摩尔吲哚-1/AM范围内,染料的估计细胞内浓度为0.1至3微摩尔。因此,在这些实验条件下(钙离子浓度约为0.1至0.2微摩尔),细胞内钙信号可能会减弱。为了评估吲哚-1/AM对细胞功能的潜在影响,将硬骨鱼鲫鱼(金鱼)的近端肾小管暴露于等渗林格氏溶液(290毫渗量浓度,0.1毫摩尔钙)中的乙酰氧基甲酯(细胞可渗透形式),然后暴露于低钠低渗林格氏溶液(110毫渗量浓度,0.1毫摩尔钙)。用视频测量方法测定细胞调节性容积减小(RVD)。在用吲哚-1/AM孵育的近端肾小管中,RVD以剂量依赖性方式受到抑制(3至5微摩尔)。用吲哚-1的非渗透性盐未观察到对RVD的影响。在10微摩尔吲哚-1/AM时发现明显的细胞损伤,表现为线粒体肿胀、细胞肿胀、细胞从肾小管基底膜脱离以及不同程度的细胞溶解。我们推测,吲哚-1/AM(3 - 5微摩尔)对RVD的抑制作用是由于细胞内钙螯合,随后细胞内信号传导被破坏。

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