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酸性孵育导致OKP细胞中NHE3的胞吐插入。

Acid incubation causes exocytic insertion of NHE3 in OKP cells.

作者信息

Yang X, Amemiya M, Peng Y, Moe O W, Preisig P A, Alpern R J

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235, USA.

出版信息

Am J Physiol Cell Physiol. 2000 Aug;279(2):C410-9. doi: 10.1152/ajpcell.2000.279.2.C410.

Abstract

Incubation of opossum kidney clone P (OKP) cells in acid media (pH 6. 8) causes activation of Na(+)/H(+) exchanger 3 (NHE3) at 6, 12, and 24 h. OKP cell NHE3 protein abundance was increased by 45% at 24 h of acid incubation but was unaffected at 3-12 h. By contrast, apical membrane NHE3, measured by surface biotinylation, increased approximately twofold at 6, 12, and 24 h, mirroring the increase in activity. Acid incubation caused a 76% increase in exocytic insertion of NHE3 into the apical membrane but had no effect on endocytic internalization at 6 h. Latrunculin B, an inhibitor of microfilament organization, inhibited the acid-induced increases in apical membrane NHE3, exocytic insertion of NHE3, and NHE3 activity at 6 h. These studies demonstrate two mechanisms for acid-induced increases in NHE3 activity. Beginning at 6 h, there is an increase in apical membrane NHE3 that is due to stimulated exocytic insertion and is required for increased NHE3 activity. At 24 h, there is an additional increase in total cellular NHE3.

摘要

将负鼠肾克隆P(OKP)细胞置于酸性培养基(pH 6.8)中培养6、12和24小时会导致钠氢交换体3(NHE3)激活。酸性培养24小时时,OKP细胞NHE3蛋白丰度增加45%,但在3至12小时时未受影响。相比之下,通过表面生物素化测量的顶端膜NHE3在6、12和24小时时增加约两倍,与活性增加情况相符。酸性培养使NHE3向顶端膜的胞吐插入增加76%,但在6小时时对胞吞内化无影响。微丝组织抑制剂Latrunculin B在6小时时抑制了酸性诱导的顶端膜NHE3增加、NHE3的胞吐插入以及NHE3活性。这些研究证明了酸性诱导NHE3活性增加的两种机制。从6小时开始,顶端膜NHE3增加,这是由于受刺激的胞吐插入所致,且是NHE3活性增加所必需的。在24小时时,细胞内总NHE3进一步增加。

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