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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.
Abstract:
Severe proteinuria in focal segmental glomerulosclerosis (FSGS) is closely associated with decreased adhesion, and subsequent loss, of podocytes. Yes-associated protein (YAP) is a key transcriptional coactivator that plays a significant role in maintaining cellular homeostasis. However, its role in podocyte adhesion and its specific mechanism in FSGS progression remain unclear. In this study, an adriamycin (ADR)-induced FSGS model was established using podocyte-specific Yap knockout (KO) mice and control mice. These mice were further treated with Pyrintegrin, an agonist of α3β1 integrin, or a vehicle. Additionally, an ADR-induced FSGS model was constructed using podocyte-specific Itga3 KO mice, which were subsequently treated with 1-oleoyl lysophosphatidic acid (LPA), a YAP activator, or a vehicle. Our findings demonstrated that YAP was positively correlated with podocyte adhesion. Podocyte-specific Yap KO mice exhibited reduced levels of α3β1 integrin and podocyte adhesion. Yap KO aggravated the ADR-induced reduction in α3β1 integrin and podocyte adhesion, resulting in significantly increased segmental or global glomerulosclerosis and proteinuria. Notably, treatment with a β1 integrin agonist partially ameliorated the decrease of podocyte adhesion and the worsening FSGS progression caused by Yap KO. Mechanistically, YAP was found to transcriptionally regulate α3- and β1 integrin via transcriptional enhanced associate domain 3 (TEAD3), with TEAD3 binding to the promoter region of Itga3. Furthermore, Itga3 KO or knockdown abolished the beneficial effects of YAP activation on podocyte adhesion and FSGS progression. In conclusion, our results demonstrate that YAP regulates podocyte adhesion and FSGS progression through its transcriptional regulation of α3β1 integrin via TEAD3. This suggests that the YAP-TEAD3-α3β1 integrin axis may serve as a promising therapeutic target for FSGS. © 2024 The Pathological Society of Great Britain and Ireland.
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.
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