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血管升压素对布拉特洛伯大鼠集合管水通道蛋白表达的调节

Regulation of collecting duct water channel expression by vasopressin in Brattleboro rat.

作者信息

DiGiovanni S R, Nielsen S, Christensen E I, Knepper M A

机构信息

Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):8984-8. doi: 10.1073/pnas.91.19.8984.

Abstract

AQP-CD is a vasopressin-regulated water channel expressed exclusively in the renal collecting duct. We have previously shown that AQP-CD is present in the apical plasma membrane and subapical vesicles of collecting duct cells, consistent with membrane-shuttling mechanisms that have been proposed to explain the short-term action of [Arg8] vasopressin (AVP) to regulate apical water permeability. We propose here that AVP may also have long-term actions on the collecting duct to regulate the expression of the AQP-CD water channel. We used immunoblotting, immunohistochemistry, and in vitro perfusion of renal tubules to investigate water channel regulation in collecting ducts of diabetes insipidus (Brattleboro) rats treated with a 5-day infusion of AVP or vehicle. Immunoblotting and immunohistochemistry demonstrated that collecting ducts of vehicle-infused Brattleboro rats had markedly reduced expression of AQP-CD relative to normal rats. In response to AVP infusion there was a nearly 3-fold increase in AQP-CD expression as detected by immunoblotting. Immunocytochemistry demonstrated that the increased expression was predominantly in the apical plasma membrane and subapical vesicles of collecting duct cells. Inner medullary collecting ducts of AVP-infused Brattleboro rats displayed a 3-fold increase in osmotic water permeability relative to vehicle-infused controls, in parallel with the change in AQP-CD expression. Based on these findings, we conclude that (i) long-term infusion of AVP, acting either directly or indirectly, regulates expression of the AQP-CD water channel and (ii) AQP-CD is the predominant AVP-regulated water channel.

摘要

水通道蛋白-CD是一种仅在肾集合管中表达的血管升压素调节性水通道。我们之前已经表明,水通道蛋白-CD存在于集合管细胞的顶端质膜和顶端下小泡中,这与为解释[精氨酸8]血管升压素(AVP)调节顶端水通透性的短期作用而提出的膜穿梭机制一致。我们在此提出,AVP对集合管可能也有长期作用,以调节水通道蛋白-CD水通道的表达。我们使用免疫印迹、免疫组织化学和肾小管体外灌注来研究用AVP或载体进行5天输注治疗的尿崩症(布拉特洛维)大鼠集合管中的水通道调节。免疫印迹和免疫组织化学表明,相对于正常大鼠,输注载体的布拉特洛维大鼠的集合管中,水通道蛋白-CD的表达明显降低。通过免疫印迹检测,对AVP输注的反应是水通道蛋白-CD表达增加了近3倍。免疫细胞化学表明,增加的表达主要在集合管细胞的顶端质膜和顶端下小泡中。与载体输注对照组相比,输注AVP的布拉特洛维大鼠的内髓集合管的渗透水通透性增加了3倍,与水通道蛋白-CD表达的变化平行。基于这些发现,我们得出结论:(i)长期输注AVP,无论是直接还是间接作用,都能调节水通道蛋白-CD水通道的表达;(ii)水通道蛋白-CD是主要的AVP调节性水通道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180d/44731/d516db0a911b/pnas01141-0267-a.jpg

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