Chen Z and Guo Z
Volume6-Issue12
Dates: Received: 2025-12-05 | Accepted: 2025-12-15 | Published: 2025-12-16
Pages: 1911-1928
Abstract
Background: Focal Segmental Glomerulosclerosis (FSGS), a major cause of end-stage renal disease, is characterized by podocyte loss via apoptosis and cytoskeletal disruption. Although dysregulation of the Hippo-YAP pathway is implicated in podocyte injury, upstream regulators of this pathway in FSGS pathogenesis remain elusive.
Methods: To determine whether FAM40A deficiency precipitates FSGS, we generated heterozygous FAM40A+/− mice by CRISPR/Cas9-mediated deletion of exons 3-8 (Δex3-8 allele). At specified time points, kidneys were collected for histological examination (PAS, TEM), immunofluorescence, and Western blotting to quantify podocyte apoptosis and Hippo pathway activation. Finally, FAM40A+/− mice were randomly assigned to receive treatment with the MST1/2 inhibitor XMU-MP-1 (1 mg/kg/day) via intraperitoneal injection or vehicle treatment for 10 days. Endpoints included urinary Albumin-to-Creatinine Ratio (ACR), renal histology, podocyte density, and podocyte apoptosis markers.
Results: We identified FAM40A as a novel negative regulator of the Hippo pathway in podocytes. FAM40A directly suppressed the kinase activity of Mst1/2, thereby preventing phosphorylation and inactivation of the downstream effector YAP. FAM40A deficiency triggered Mst1/2 activation, leading to YAP phosphorylation, nuclear exclusion, and transcriptional repression. This cascade resulted in podocyte apoptosis and exacerbated FSGS phenotypes In vivo.
Conclusion: Our study defines the FAM40A-Mst1/2-YAP axis as a critical signalling pathway governing podocyte survival. Loss of FAM40A activates Hippo signalling to promote podocyte apoptosis and FSGS progression. While short-term MST1/2 inhibition ameliorates disease features in mice, further evaluation of safety and feasibility is required. These findings highlight FAM40A as a potential therapeutic target for FSGS.
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DOI: 10.37871/jbres2240
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© 2025 Chen Z, et al. Distributed under Creative Commons CC-BY 4.0
How to cite this article
Chen Z, Guo Z. FAM40A Defi ciency Activates the Hippo Pathway to Promote Podocyte Apoptosis and Contribute to FSGS. J Biomed Res Environ Sci. 2025 Dec 16; 6(12): 1911-1928. doi: 10.37871/jbres2240, Article ID: JBRES2240, Available at: https://www.jelsciences.com/articles/jbres2240.pdf
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