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FXYD2c 在高渗刺激 HK-2 细胞时可能起到调节 Na(+)/K (+)-ATP 酶活性的作用。

FXYD2c plays a potential role in modulating Na(+)/K (+)-ATPase activity in HK-2 cells upon hypertonic challenge.

机构信息

Graduate Institute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan.

出版信息

J Membr Biol. 2014 Jan;247(1):93-105. doi: 10.1007/s00232-013-9615-y. Epub 2013 Nov 21.

Abstract

Na(+)/K(+)-ATPase (NKA) is a widely found and important transporter in mammals. The kidney is a major osmoregulatory organ of which the proximal tubules play a crucial role in the maintenance of ionic homeostasis functioning via salt and water reabsorption. FXYD (FXYD domain-containing protein) 2, the γ-subunit of NKA, is the first identified and the most abundant member of FXYD family, affecting the sodium/potassium affinity of NKA in the kidney. Based on DNA microarray analysis, the expression levels of fxyd2 gene are markedly increased upon hypertonic challenge. Combined with bioinformatic analysis using the NCBI database, we identified an unnamed protein with 145 amino acids, of which the N-terminus involved the FXYD sequence similar to FXYD2a and FXYD2b, and thus, named as FXYD2c. However, the role of FXYD2c protein in the regulation of NKA expression in the kidney has not been elucidated. In this study, we found that the mRNA and protein levels of FXYD2c were significantly increased upon hypertonic challenge. Immunoprecipitation data revealed that FXYD2c interacts with the NKA α1 subunit. Subsequently, the functional inhibition of fxyd2c using short hairpin RNA abrogated NKA activity. Taken together, our study offers novel insight into the potential function of FXYD2c in promoting NKA activity upon hypertonic challenge in HK-2 cells.

摘要

钠钾泵(NKA)是哺乳动物中广泛存在且重要的转运蛋白。肾脏是主要的渗透压调节器官,其中近端小管通过盐和水的重吸收在维持离子稳态方面发挥着关键作用。FXYD(含 FXYD 结构域蛋白)家族的第一个被发现的也是最丰富的成员 FXYD2 是 NKA 的γ亚基,它影响肾脏中 NKA 的钠/钾亲和力。基于 DNA 微阵列分析,在高渗刺激下,fxyd2 基因的表达水平显著增加。结合使用 NCBI 数据库的生物信息学分析,我们鉴定出一个具有 145 个氨基酸的未命名蛋白,其 N 端涉及与 FXYD2a 和 FXYD2b 相似的 FXYD 序列,因此将其命名为 FXYD2c。然而,FXYD2c 蛋白在调节肾脏中 NKA 表达中的作用尚未阐明。在这项研究中,我们发现 FXYD2c 的 mRNA 和蛋白水平在高渗刺激下显著增加。免疫沉淀数据显示 FXYD2c 与 NKA α1 亚基相互作用。随后,使用短发夹 RNA 功能性抑制 fxyd2c 可消除 NKA 活性。总之,我们的研究为 FXYD2c 在促进 HK-2 细胞高渗刺激下 NKA 活性方面的潜在功能提供了新的见解。

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