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质膜钠氢交换体NHE1 - 3的半衰期:质膜NHE2具有快速降解速率。

Half-lives of plasma membrane Na(+)/H(+) exchangers NHE1-3: plasma membrane NHE2 has a rapid rate of degradation.

作者信息

Cavet M E, Akhter S, Murtazina R, Sanchez de Medina F, Tse C M, Donowitz M

机构信息

Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

Am J Physiol Cell Physiol. 2001 Dec;281(6):C2039-48. doi: 10.1152/ajpcell.2001.281.6.C2039.

Abstract

The Na(+)/H(+) exchangers NHE2 and NHE3 are involved in epithelial Na(+) and HCO absorption. To increase insights into the functions of NHE2 vs. NHE3, we compared their cellular processing with each other and with the housekeeping isoform NHE1. Using biotinylated exchanger, we determined that the half-life of plasma membrane NHE2 was short (3 h) compared with that of NHE1 (24 h) and NHE3 (14 h) in both PS120 fibroblasts and Caco-2 cells. NHE2 transport and plasma membrane levels were reduced by 3 h of Brefeldin A treatment, whereas NHE1 was unaffected. NHE2 was degraded by the lysosomes but not proteosomes, as demonstrated by increasing levels of endocytosed NHE2 protein after inhibition of the lysosomes, but not with proteosome inhibition. Unlike that of NHE3, basal NHE2 transport activity was not affected by phosphatidylinositol 3-kinase inhibition and did not appear to be localized in the juxtanuclear recycling endosome. Therefore, for NHE2, protein degradation and/or protein synthesis probably play important roles in its basal and regulated states. These results suggest fundamental differences in the cellular processing and trafficking of NHE2 and NHE3. These differences may underlie the specialized roles that these exchangers play in epithelial cells.

摘要

钠氢交换体NHE2和NHE3参与上皮细胞钠和碳酸氢根的吸收。为了更深入了解NHE2与NHE3的功能,我们将它们彼此之间以及与管家异构体NHE1的细胞加工过程进行了比较。使用生物素化的交换体,我们发现在PS120成纤维细胞和Caco-2细胞中,质膜NHE2的半衰期较短(3小时),而NHE1的半衰期为24小时,NHE3的半衰期为14小时。布雷菲德菌素A处理3小时会降低NHE2的转运和质膜水平,而NHE1不受影响。如通过抑制溶酶体后内吞的NHE2蛋白水平升高所证明的那样,NHE2被溶酶体而非蛋白酶体降解,而蛋白酶体抑制则不会出现这种情况。与NHE3不同,基础NHE2转运活性不受磷脂酰肌醇3激酶抑制的影响,并且似乎并不定位于近核循环内体。因此,对于NHE2而言,蛋白质降解和/或蛋白质合成可能在其基础状态和调节状态中发挥重要作用。这些结果表明NHE2和NHE3在细胞加工和运输方面存在根本差异。这些差异可能是这些交换体在上皮细胞中发挥特殊作用的基础。

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