Details

Autor(en) / Beteiligte

• Rinschen, Markus M
• Grahammer, Florian
• Hoppe, Ann-Kathrin
• Kohli, Priyanka
• Hagmann, Henning
• Kretz, Oliver
• Bertsch, Sabine
• Höhne, Martin
• Göbel, Heike
• Bartram, Malte P
• Gandhirajan, Rajesh Kumar
• Krüger, Marcus
• Brinkkoetter, Paul-Thomas
• Huber, Tobias B
• Kann, Martin
• Wickström, Sara A
• Benzing, Thomas
• Schermer, Bernhard

Titel

YAP-mediated mechanotransduction determines the podocyte's response to damage

Ist Teil von

• Science signaling, 2017-04, Vol.10 (474)

Ort / Verlag

United States

Erscheinungsjahr

2017

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Podocytes are terminally differentiated cells of the kidney filtration barrier. They are subjected to physiological filtration pressure and considerable mechanical strain, which can be further increased in various kidney diseases. When injury causes cytoskeletal reorganization and morphological alterations of these cells, the filtration barrier may become compromised and allow proteins to leak into the urine (a condition called proteinuria). Using time-resolved proteomics, we showed that podocyte injury stimulated the activity of the transcriptional coactivator YAP and the expression of YAP target genes in a rat model of glomerular disease before the development of proteinuria. Although the activities of YAP and its ortholog TAZ are activated by mechanical stress in most cell types, injury reduced YAP and TAZ activity in cultured human and mouse podocyte cell lines grown on stiff substrates. Culturing these cells on soft matrix or inhibiting stress fiber formation recapitulated the damage-induced YAP up-regulation observed in vivo, indicating a mechanotransduction-dependent mechanism of YAP activation in podocytes. YAP overexpression in cultured podocytes increased the abundance of extracellular matrix-related proteins that can contribute to fibrosis. YAP activity was increased in mouse models of diabetic nephropathy, and the YAP target was highly expressed in renal biopsies from glomerular disease patients. Although overexpression of human YAP in mice induced mild proteinuria, pharmacological inhibition of the interaction between YAP and its partner TEAD in rats ameliorated glomerular disease and reduced damage-induced mechanosignaling in the glomeruli. Thus, perturbation of YAP-dependent mechanosignaling is a potential therapeutic target for treating some glomerular diseases.