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TonEBP 在高渗刺激后调节肾近端小管细胞 AAD 表达和多巴胺产生中的作用。

The role of TonEBP in regulation of AAD expression and dopamine production in renal proximal tubule cells upon hypertonic challenge.

机构信息

Department of Life Sciences, National Chung-Hsing University, Taichung 402, Taiwan.

出版信息

Biochem Biophys Res Commun. 2011 Oct 28;414(3):598-603. doi: 10.1016/j.bbrc.2011.09.128. Epub 2011 Oct 1.

Abstract

Renal proximal tubule cells overexpress aromatic l-amino acid decarboxylase (AAD) to produce dopamine, which inhibits salt absorption in the hypertonic environment. We examined the effect of TonEBP on AAD expression in human proximal tubule epithelial cells, HK-2 cell line. Confocal microscopy showed that after 2h of exposure to the hypertonic medium, TonEBP accumulation in nuclei increased as compared to the isotonic control. The activated TonEBP enhanced the mRNA expression of the representative downstream genes (i.e., SMIT and TauT). Meanwhile, AAD protein abundance also increased with TonEBP activation. EMSA and luciferase reporter assay showed that TonEBP was involved in transcriptional regulation of AAD upon hypertonic stress. Inactivation of TonEBP by the p38 inhibitor SB203580, or TonEBP shRNA significantly reduced AAD expression, which was rescued by re-expressing Myc-tagged TonEBP. Up-regulation of AAD increased dopamine synthesis, and dopamine inhibited NKA activity in hypertonic condition. These results suggested that TonEBP played an important role in the epithelial cells of renal proximal tubule upon hypertonic stress by enhancing AAD expression, which could promote dopamine secretion to negative regulate NKA activity. The elucidation of a new mechanism described in this study combined with previous findings provides more insights into this issue.

摘要

肾近端小管细胞过表达芳香族 l-氨基酸脱羧酶 (AAD) 以产生多巴胺,从而抑制高渗环境中的盐吸收。我们研究了 TonEBP 对人近端肾小管上皮细胞 HK-2 系中 AAD 表达的影响。共聚焦显微镜显示,与等渗对照相比,在高渗培养基中暴露 2 小时后,TonEBP 在核内的积累增加。激活的 TonEBP 增强了代表性下游基因(即 SMIT 和 TauT)的 mRNA 表达。同时,AAD 蛋白丰度也随着 TonEBP 的激活而增加。EMSA 和荧光素酶报告基因分析表明,TonEBP 参与了高渗应激下 AAD 的转录调控。用 p38 抑制剂 SB203580 或 TonEBP shRNA 使 TonEBP 失活,显著降低了 AAD 的表达,而过表达 Myc 标记的 TonEBP 则可挽救 AAD 的表达。AAD 的上调增加了多巴胺的合成,而多巴胺在高渗条件下抑制了 NKA 的活性。这些结果表明,TonEBP 通过增强 AAD 的表达在高渗应激下对肾近端小管的上皮细胞发挥重要作用,从而促进多巴胺的分泌,以负调控 NKA 的活性。本研究描述的新机制的阐明结合以前的发现,为这一问题提供了更深入的认识。

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