Ishii Masaru, Fujita Akikazu, Iwai Kaori, Kusaka Shunji, Higashi Kayoko, Inanobe Atsushi, Hibino Hiroshi, Kurachi Yoshihisa
Department of Pharmacology II, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0871, Japan.
Am J Physiol Cell Physiol. 2003 Aug;285(2):C260-7. doi: 10.1152/ajpcell.00560.2002. Epub 2003 Apr 9.
Kir5.1 is an inwardly rectifying K+ channel subunit whose functional role has not been fully elucidated. Expression and distribution of Kir5.1 in retina were examined with a specific polyclonal antibody. Kir5.1 immunoreactivity was detected in glial Müller cells and in some retinal neurons. In the Kir5.1-positive neurons the expression of glutamic acid decarboxylase (GAD65) was detected, suggesting that they may be GABAergic-amacrine cells. In Müller cells, spots of Kir5.1 immunoreactivity distributed diffusely at the cell body and in the distal portions, where Kir4.1 immunoreactivity largely overlapped. In addition, Kir4.1 immunoreactivity without Kir5.1 was strongly concentrated at the endfoot of Müller cells facing the vitreous surface or in the processes surrounding vessels. The immunoprecipitant obtained from retina with anti-Kir4.1 antibody contained Kir5.1. These results suggest that heterotetrameric Kir4.1/Kir5.1 channels may exist in the cell body and distal portion of Müller cells, whereas homomeric Kir4.1 channels are clustered in the endfeet and surrounding vessels. It is possible that homomeric Kir4.1 and heteromeric Kir4.1/Kir5.1 channels play different functional roles in the K+-buffering action of Müller cells.
Kir5.1是一种内向整流钾离子通道亚基,其功能作用尚未完全阐明。使用特异性多克隆抗体检测Kir5.1在视网膜中的表达和分布。在神经胶质Müller细胞和一些视网膜神经元中检测到Kir5.1免疫反应性。在Kir5.1阳性神经元中检测到谷氨酸脱羧酶(GAD65)的表达,表明它们可能是γ-氨基丁酸能无长突细胞。在Müller细胞中,Kir5.1免疫反应性斑点在细胞体和远端部分呈弥漫性分布,Kir4.1免疫反应性在很大程度上与之重叠。此外,没有Kir5.1的Kir4.1免疫反应性强烈集中在Müller细胞面向玻璃体表面的终足或血管周围的突起中。用抗Kir4.1抗体从视网膜获得的免疫沉淀物中含有Kir5.1。这些结果表明,异源四聚体Kir4.1/Kir5.1通道可能存在于Müller细胞的细胞体和远端部分,而同源Kir4.1通道则聚集在终足和血管周围。同源Kir4.1和异源Kir4.1/Kir5.1通道可能在Müller细胞的钾离子缓冲作用中发挥不同的功能作用。