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转录因子 TonEBP 刺激小鼠下丘脑中渗透压依赖的精氨酸血管加压素基因表达。

Transcription Factor TonEBP Stimulates Hyperosmolality-Dependent Arginine Vasopressin Gene Expression in the Mouse Hypothalamus.

机构信息

Department of Biological Sciences, College of Natural Sciences, University of Ulsan, Ulsan, South Korea.

Department of Pharmacology and Physiology, School of Medicine & Health Sciences, The George Washington University, Washington, DC, United States.

出版信息

Front Endocrinol (Lausanne). 2021 Mar 16;12:627343. doi: 10.3389/fendo.2021.627343. eCollection 2021.

DOI:10.3389/fendo.2021.627343
PMID:33796071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8008816/
Abstract

The hypothalamic neuroendocrine system is strongly implicated in body energy homeostasis. In particular, the degree of production and release of arginine vasopressin (AVP) in the hypothalamus is affected by plasma osmolality, and that hypothalamic AVP is responsible for thirst and osmolality-dependent water and metabolic balance. However, the osmolality-responsive intracellular mechanism within AVP cells that regulates AVP synthesis is not clearly understood. Here, we report a role for tonicity-responsive enhancer binding protein (TonEBP), a transcription factor sensitive to cellular tonicity, in regulating osmosensitive hypothalamic AVP gene transcription. Our immunohistochemical work shows that hypothalamic AVP cellular activity, as recognized by c-fos, was enhanced in parallel with an elevation in TonEBP expression within AVP cells following water deprivation. Interestingly, our investigations found a synchronized pattern of TonEBP and AVP gene expression in response to osmotic stress. Those results indicate a positive correlation between hypothalamic TonEBP and AVP production during dehydration. Promoter and chromatin immunoprecipitation assays confirmed that TonEBP can bind directly to conserved binding motifs in the 5'-flanking promoter regions of the AVP gene. Furthermore, dehydration- and TonEBP-mediated hypothalamic AVP gene activation was reduced in TonEBP haploinsufficiency mice, compared with wild TonEBP homozygote animals. Therefore, our result support the idea that TonEBP is directly necessary, at least in part, for the elevation of AVP transcription in dehydration conditions. Additionally, dehydration-induced reductions in body weight were rescued in TonEBP haploinsufficiency mice. Altogether, our results demonstrate an intracellular machinery within hypothalamic AVP cells that is responsible for dehydration-induced AVP synthesis.

摘要

下丘脑神经内分泌系统强烈参与身体能量稳态。特别是,下丘脑精氨酸加压素 (AVP) 的产生和释放程度受血浆渗透压的影响,而下丘脑 AVP 负责口渴和渗透压依赖性水和代谢平衡。然而,调节 AVP 合成的 AVP 细胞内渗透压反应性细胞内机制尚不清楚。在这里,我们报告了渗透压反应增强子结合蛋白 (TonEBP) 的作用,TonEBP 是一种对细胞渗透压敏感的转录因子,它在调节渗透压敏感的下丘脑 AVP 基因转录中起作用。我们的免疫组织化学工作表明,在断水后,下丘脑 AVP 细胞活性(通过 c-fos 识别)与 AVP 细胞中 TonEBP 表达的升高平行增强。有趣的是,我们的研究发现 TonEBP 和 AVP 基因表达对渗透压应激呈同步模式。这些结果表明,在脱水期间,下丘脑 TonEBP 和 AVP 产生之间存在正相关。启动子和染色质免疫沉淀测定证实,TonEBP 可以直接结合 AVP 基因 5'-侧翼启动子区域中的保守结合基序。此外,与野生型 TonEBP 纯合动物相比,TonEBP 半不足小鼠的脱水和 TonEBP 介导的下丘脑 AVP 基因激活减少。因此,我们的结果支持这样一种观点,即 TonEBP 至少部分直接参与脱水条件下 AVP 转录的升高。此外,TonEBP 半不足小鼠的体重减轻在脱水时得到挽救。总之,我们的研究结果证明了下丘脑 AVP 细胞内的一种细胞内机制,负责脱水诱导的 AVP 合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/096291104457/fendo-12-627343-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/82e8679d9751/fendo-12-627343-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/2aa77ee8a6dc/fendo-12-627343-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/588b94c3c2f7/fendo-12-627343-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/c3bac75ae242/fendo-12-627343-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/9f59ee521ab7/fendo-12-627343-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/096291104457/fendo-12-627343-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/82e8679d9751/fendo-12-627343-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/2aa77ee8a6dc/fendo-12-627343-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/588b94c3c2f7/fendo-12-627343-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/c3bac75ae242/fendo-12-627343-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/9f59ee521ab7/fendo-12-627343-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b923/8008816/096291104457/fendo-12-627343-g006.jpg

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