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GRHL2 对于集合管上皮细胞屏障功能和肾脏渗透压调节是必需的。

GRHL2 Is Required for Collecting Duct Epithelial Barrier Function and Renal Osmoregulation.

机构信息

Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.

Berlin Institute of Health, Berlin, Germany.

出版信息

J Am Soc Nephrol. 2018 Mar;29(3):857-868. doi: 10.1681/ASN.2017030353. Epub 2017 Dec 13.

Abstract

Collecting ducts make up the distal-most tubular segments of the kidney, extending from the cortex, where they connect to the nephron proper, into the medulla, where they release urine into the renal pelvis. During water deprivation, body water preservation is ensured by the selective transepithelial reabsorption of water into the hypertonic medullary interstitium mediated by collecting ducts. The collecting duct epithelium forms tight junctions composed of barrier-enforcing claudins and exhibits a higher transepithelial resistance than other segments of the renal tubule exhibit. However, the functional relevance of this strong collecting duct epithelial barrier is unresolved. Here, we report that collecting duct-specific deletion of an epithelial transcription factor, grainyhead-like 2 (GRHL2), in mice led to reduced expression of tight junction-associated barrier components, reduced collecting duct transepithelial resistance, and defective renal medullary accumulation of sodium and other osmolytes. , -deficient collecting duct cells displayed increased paracellular flux of sodium, chloride, and urea. Consistent with these effects, -deficient mice had diabetes insipidus, produced dilute urine, and failed to adequately concentrate their urine after water restriction, resulting in susceptibility to prerenal azotemia. These data indicate a direct functional link between collecting duct epithelial barrier characteristics, which appear to prevent leakage of interstitial osmolytes into urine, and body water homeostasis.

摘要

收集管构成肾脏的最远端管状段,从皮质延伸,在那里它们连接到真正的肾单位,进入髓质,在那里它们将尿液排入肾盂。在缺水期间,通过收集管介导的选择性跨上皮水重吸收到高渗髓质间质,确保了体水的保存。收集管上皮形成由屏障增强的闭合蛋白组成的紧密连接,并表现出比肾小管的其他段更高的跨上皮电阻。然而,这种强大的收集管上皮屏障的功能相关性尚未解决。在这里,我们报告在小鼠中特异性敲除上皮转录因子颗粒头样 2 (GRHL2) 导致紧密连接相关屏障成分的表达减少、收集管跨上皮电阻降低以及钠和其他渗透物在肾髓质的积累受损。GRHL2 缺陷的收集管细胞显示出增加的钠、氯和尿素的细胞旁通量。与这些影响一致,GRHL2 缺陷小鼠患有尿崩症,产生稀释尿液,并且在限制水后无法充分浓缩尿液,导致易发生肾前氮血症。这些数据表明,收集管上皮屏障特性与体水稳态之间存在直接的功能联系,这似乎可以防止间质渗透物漏入尿液。

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