Genetic and pharmacological inhibition of microRNA-92a maintains podocyte cell cycle quiescence and limits crescentic glomerulonephritis

Abstract: Crescentic rapidly progressive glomerulonephritis (RPGN) represents the most aggressive form of acquired glomerular disease. While most therapeutic approaches involve potentially toxic immunosuppressive strategies, the pathophysiology remains incompletely understood. Podocytes are glomerular epithelial cells that are normally growth-arrested because of the expression of cyclin-dependent kinase (CDK) inhibitors. An exception is in RPGN where podocytes undergo a deregulation of their differentiated phenotype and proliferate. Here we demonstrate that microRNA-92a (miR-92a) is enriched in podocytes of patients and mice with RPGN. The CDK inhibitor p57Kip2 is a major target of miR-92a that constitutively safeguards podocyte cell cycle quiescence. Podocyte-specific deletion of miR-92a in mice de-repressed the expression of p57Kip2 and prevented glomerular injury in RPGN. Administration of an anti-miR-92a after disease initiation prevented albuminuria and kidney failure, indicating miR-92a inhibition as a potential therapeutic strategy for RPGN. We demonstrate that miRNA induction in epithelial cells can break glomerular tolerance to immune injury

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
Nature communications. - 8, 1 (2017) , 1829, ISSN: 2041-1723

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2019
Creator
Henique, Carole
Bollée, Guillaume
Loyer, Xavier
Grahammer, Florian
Dhaun, Neeraj
Camus, Marine
Vernerey, Julien
Guyonnet, Léa
Gaillard, François
Lazareth, Hélène
Meyer, Charlotte
Bensaada, Imane
Legrès, Luc
Satoh, Takashi
Akira, Shizuo
Bruneval, Patrick
Dimmeler, Stefanie
Tedgui, Alain
Karras, Alexandre
Thervet, Eric
Nochy, Dominique
Huber, Tobias
Mesnard, Laurent
Lenoir, Olivia
Tharaux, Pierre-Louis
Contributor

DOI
10.1038/s41467-017-01885-7
URN
urn:nbn:de:bsz:25-freidok-1429893
Rights
Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 11:01 AM CEST

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Associated

Time of origin

  • 2019

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