Carrisoza-Gaytán Rolando, Salvador Carolina, Diaz-Bello Beatriz, Escobar Laura I
Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, 04510, México, DF, Mexico.
J Mol Histol. 2014 Oct;45(5):583-97. doi: 10.1007/s10735-014-9581-4. Epub 2014 Jun 20.
Several potassium (K(+)) channels contribute to maintaining the resting membrane potential of renal epithelial cells. Apart from buffering the cell membrane potential and cell volume, K(+) channels allow sodium reabsorption in the proximal tubule (PT), K(+) recycling and K(+) reabsorption in the thick ascending limb (TAL) and K(+) secretion and K(+) reabsorption in the distal convoluted tubule (DCT), connecting tubule (CNT) and collecting duct. Previously, we identified Kv.1.1, Kv1.3 and Kv1.6 channels in collecting ducts of the rat inner medulla. We also detected intracellular Kv1.3 channel in the acid secretory intercalated cells, which is trafficked to the apical membrane in response to dietary K(+) to function as a secretory K(+) channel. In this work we sought to characterize the expression of all members of the Kv1 family in the rat nephron. mRNA and protein expression were detected for all Kv1 channels. Immunoblots identified differential expression of each Kv1 in the cortex, outer and inner medulla. Immunofluorescence labeling detected Kv1.5 in Bowman´s capsule and endothelial cells and Kv1.7 in podocytes, endothelial cells and macula densa in glomeruli; Kv1.4, Kv1.5 and Kv1.7 in PT; Kv1.2, Kv1.4 and Kv1.6 in TAL; Kv1.1, Kv1.4 and Kv1.6 in DCT and CNT and Kv1.3 in DCT, and all the Kv1 family in the cortical and medullary collecting ducts. Recently, some hereditary renal syndromes have been attributed to mutations in K(+) channels. Our results expand the repertoire of K(+) channels that contribute to K(+) homeostasis to include the Kv1 family.
几种钾(K⁺)通道有助于维持肾上皮细胞的静息膜电位。除了缓冲细胞膜电位和细胞体积外,K⁺通道还允许近端小管(PT)中的钠重吸收、厚壁升支(TAL)中的K⁺循环和K⁺重吸收以及远曲小管(DCT)、连接小管(CNT)和集合管中的K⁺分泌和K⁺重吸收。此前,我们在大鼠内髓集合管中鉴定出Kv.1.1、Kv1.3和Kv1.6通道。我们还在酸性分泌性闰细胞中检测到细胞内Kv1.3通道,该通道在饮食中K⁺的作用下被转运至顶端膜,作为分泌性K⁺通道发挥作用。在这项工作中,我们试图表征Kv1家族所有成员在大鼠肾单位中的表达。检测了所有Kv1通道的mRNA和蛋白质表达。免疫印迹法鉴定了每个Kv1在皮质、外髓和内髓中的差异表达。免疫荧光标记在肾小球的鲍曼囊和内皮细胞中检测到Kv1.5,在足细胞、内皮细胞和致密斑中检测到Kv1.7;在近端小管中检测到Kv1.4、Kv1.5和Kv1.7;在厚壁升支中检测到Kv1.2、Kv1.4和Kv1.6;在远曲小管和连接小管中检测到Kv1.1、Kv1.4和Kv1.6,在远曲小管中检测到Kv1.3,在皮质和髓质集合管中检测到所有Kv1家族成员。最近,一些遗传性肾脏综合征被归因于K⁺通道的突变。我们的结果扩展了有助于K⁺稳态的K⁺通道库,将Kv1家族包括在内。