Yes-associated protein (YAP) promotes cell survival by inhibiting proapoptotic dendrin signaling

Kirk N. Campbell, Jenny S. Wong, Ritu Gupta, Katsuhiko Asanuma, Marius Sudol, John Cijiang He, Peter Mundel

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Kidney podocytes are highly specialized terminally differentiated cells that form the final barrier to urinary protein loss. Podocytes are a target for injury by metabolic, autoimmune, hereditary, inflammatory, and other stressors. Persistence of podocyte injury leads to podocyte death and loss, which results in progressive kidney damage and ultimately kidney failure. Dendrin is a dual compartment protein with proapoptotic signaling properties. Nuclear relocation of dendrin in response to glomerular injury promotes podocyte apoptosis. Here we show that Yes-associated protein (YAP), a downstream target of Hippo kinases and an inhibitor of apoptosis, is expressed in the nucleus of podocytes. The WW domains of YAP mediate the interaction with the PPXY motifs of dendrin. This interaction is functionally relevant because YAP binding to dendrin reduces dendrin-dependent, staurosporine-induced apoptosis in co-transfected HEK293 cells. Moreover gene silencing of YAP in podocytes increases adriamycin-induced podocyte apoptosis. It also increases staurosporine-induced caspase-3/7 activity, which is rescued by dendrin depletion in YAP knockdown cells. Our findings elucidate YAP binding to dendrin as a prosurvival mechanism. The antiapoptotic signaling properties of YAP in podocytes could hold significance in the quest for targeted therapeutics aimed at preventing podocyte loss.

Original languageEnglish
Pages (from-to)17057-17062
Number of pages6
JournalJournal of Biological Chemistry
Volume288
Issue number24
DOIs
StatePublished - 14 Jun 2013

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