| Literature DB >> 29237740 |
Christian Hinze1,2,3, Janett Ruffert1,4, Katharina Walentin1, Nina Himmerkus5, Elham Nikpey6,7, Olav Tenstad6, Helge Wiig6, Kerim Mutig8, Zeliha Yesim Yurtdas1,4, Janet D Klein9, Jeff M Sands9, Federica Branchi10, Michael Schumann10, Sebastian Bachmann8, Markus Bleich5, Kai M Schmidt-Ott11,3.
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. In vitro, Grhl2-deficient collecting duct cells displayed increased paracellular flux of sodium, chloride, and urea. Consistent with these effects, Grhl2-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.Entities:
Keywords: diabetes insipidus; epithelial barrier function; grainyhead-like 2 transcription factor; prerenal azotemia; renal collecting duct epithelium; urinary concentration
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Year: 2017 PMID: 29237740 PMCID: PMC5827589 DOI: 10.1681/ASN.2017030353
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121