Podocyte YAP ablation decreases podocyte adhesion and exacerbates FSGS progression through α3β1 integrin

Guangze Shao1, Jitu Xu1, Chencheng Hu1

  • 1Department of Pathology of School of Basic Medical Sciences, Fudan University, Kidney and Dialysis Institute of Shanghai, Shanghai, PR China.

The Journal of Pathology
|December 13, 2024
PubMed

Insights

Yes-associated protein (YAP) promotes podocyte adhesion and regulates focal segmental glomerulosclerosis (FSGS) progression. YAP controls α3β1 integrin expression via TEAD3, offering a potential therapeutic target for FSGS.

Area of Science:

  • Nephrology
  • Molecular Biology
  • Cell Biology

Background:

  • Focal segmental glomerulosclerosis (FSGS) is characterized by podocyte injury and loss, leading to severe proteinuria.
  • Podocyte adhesion is crucial for maintaining glomerular structure, and its disruption is a hallmark of FSGS.
  • The role of Yes-associated protein (YAP) in podocyte adhesion and its specific mechanism in FSGS pathogenesis are not fully understood.

Purpose of the Study:

  • To investigate the role of YAP in podocyte adhesion and its regulatory mechanism in the progression of FSGS.
  • To elucidate the molecular pathway through which YAP influences podocyte integrity and FSGS development.

Main Methods:

  • Established adriamycin (ADR)-induced FSGS models in mice with podocyte-specific Yap knockout (KO) and Itga3 KO.
  • Administered Pyrintegrin (α3β1 integrin agonist) or 1-oleoyl lysophosphatidic acid (LPA, YAP activator) to investigate therapeutic effects.
  • Utilized Western blotting and promoter binding assays to analyze YAP, TEAD3, and integrin interactions.

Main Results:

  • Podocyte-specific Yap KO mice showed reduced α3β1 integrin levels, impaired podocyte adhesion, and exacerbated FSGS with increased proteinuria.
  • YAP activation positively correlated with podocyte adhesion and ameliorated FSGS progression.
  • YAP transcriptionally regulates α3- and β1 integrin expression via TEAD3, which binds to the Itga3 promoter.
  • Itga3 KO or knockdown abrogated the protective effects of YAP activation on podocyte adhesion and FSGS.

Conclusions:

  • YAP plays a critical role in maintaining podocyte adhesion and regulating FSGS progression.
  • The YAP-TEAD3-α3β1 integrin axis is a key molecular pathway governing podocyte integrity in FSGS.
  • Targeting the YAP-TEAD3-α3β1 integrin pathway represents a promising therapeutic strategy for FSGS.