肾中IP(3)受体基因家族的细胞特异性表达

M Hayashi, T Monkawa, T Saruta
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引用次数: 7

摘要

背景/目的:本文讨论了肌醇三磷酸(IP(3))受体1-3型在肾脏中的定位及其在调节细胞内钙浓度[Ca(2+)](i) -中的作用。方法:采用同种异构体特异性抗体进行免疫组织学研究,揭示IP(3)受体同种异构体的定位。为了研究IP(3)受体1型在肾小球中的作用,我们在IP(3)受体1型敲除小鼠中检测了[Ca(2+)](i)对激素刺激的反应。结果:在免疫组织学研究中,1型受体存在于动脉、传入小动脉和系膜细胞中。水通道蛋白2和IP(3) 2型受体抗体双染色显示2型受体主要定位于插层细胞。3型受体在皮层至外髓质的集管细胞中表现出特征性的细胞内定位。3型受体的免疫染色在基底外侧膜侧细胞质中最为强烈,而在根尖侧未见。在IP(3)受体1型敲除小鼠中,[Ca(2+)](i)对肾小球血管紧张素II和内皮素的反应明显减弱。结论:IP(3)受体的三种亚型在肾脏中表现出不同的定位,其中1型受体在肾小球[Ca(2+)](i)的调控中起主要作用。然而,细胞特异性定位的生理意义仍有待确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell-specific expression of the IP(3) receptor gene family in the kidney.

Background/aim: The localization of inositol trisphosphate (IP(3)) receptor isoforms, types 1-3, in the kidney and their role in the regulation of the intracellular calcium concentration - [Ca(2+)](i) - are discussed.

Methods: Immunohistological studies with isoform-specific antibodies were performed to reveal the localization of IP(3) receptor isoforms. To examine the role of IP(3) receptor type 1 in the glomeruli, the responses of [Ca(2+)](i) to hormonal stimuli were examined in IP(3) receptor type 1 knockout mice.

Results: In the immunohistological study, type 1 receptor was present in arteries, afferent arterioles, and mesangial cells. Double staining with antibodies against aquaporin 2 and IP(3) type 2 receptor revealed that type 2 receptor was localized mainly in the intercalated cells. The type 3 receptor showed characteristic intracellular localization in the collecting duct cells of the cortex to the outer medulla. Immunostaining of type 3 receptor was most intense in the cytoplasm on the basolateral membrane side and was not seen on the apical side. The responses of [Ca(2+)](i) to angiotensin II and endothelin in the glomeruli were markedly attenuated in IP(3) receptor type 1 knockout mice.

Conclusions: The three isoforms of the IP(3) receptor showed distinctive localization in the kidney, and the type 1 receptor plays a major role in the regulation of [Ca(2+)](i) in the glomeruli. The physiological significance of the cell-specific localization, however, remains to be determined.

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