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Regulation of hypoxia-inducible factor 2-a is essential for integrity of the glomerular barrier
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital.
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2013 (English)In: American Journal of Physiology - Renal Physiology, ISSN 0363-6127, E-ISSN 1522-1466, Vol. 304, no 1, F120-F126 p.Article in journal (Refereed) Published
Abstract [en]

Deletion of the von Hippel-Lindau tumor suppressor (Vhl) gene from renal podocytes of mice (podVhl KO) leads to rapidly progressive glomerulonephritis (RPGN), a clinical syndrome characterized by rapid loss of renal function and crescents on renal biopsy. Genomic profiling of glomeruli isolated from podVhl knockout (KO) mice and from patients with RPGN identified a fingerprint of genes regulated by hypoxia-inducible factors (HIF), important substrates of the product of the VHL gene. Here, we show that stabilization of Hifs in podocytes is both required and sufficient for the glomerular phenotype observed in podVhl KO mice. Genetic deletion of the obligate dimerization partner Arnt/Hif1b that is essential for Hif transcriptional function rescues the phenotype. Conversely, stabilization of HIF2A alone in podocytes results in crescentic glomerular disease. Together, our results show that the Hif pathway and Hif2a in particular are key players in maintenance of the glomerular barrier.

Place, publisher, year, edition, pages
2013. Vol. 304, no 1, F120-F126 p.
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Medical and Health Sciences
URN: urn:nbn:se:uu:diva-230057DOI: 10.1152/ajprenal.00416.2012PubMedID: 23054256OAI: oai:DiVA.org:uu-230057DiVA: diva2:738799
Available from: 2014-08-19 Created: 2014-08-19 Last updated: 2014-09-16Bibliographically approved

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Jeansson, Marie
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