2. Academic Validation
  3. Valtrate alleviates inflammation by targeting USP9X to enhance NLRP3 degradation

Valtrate alleviates inflammation by targeting USP9X to enhance NLRP3 degradation

  • Phytomedicine. 2025 Jul 25:143:156835. doi: 10.1016/j.phymed.2025.156835.
Kaiyue Su 1,  Neng Ye 2,  Lei Lin 1,  Jie Wu 3,  Min Zhao 4,  Xueqin Jiang 1,  Ruijia Zhang 1,  Xiaoying Cai 1,  Xinlu Zhang 1,  Jing Peng 1,  Minghai Tang 1,  Na Li 1,  Lijuan Chen 5,  Haoyu Ye 6,  Wenshuang Wu 7
Affiliations

Affiliations

  • 1 Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
  • 2 Scaled Manufacturing Center of Biological Products, Management Office of National Facility for Translational Medicine, West China Hospital, Sichuan University Chengdu, 610041, China.
  • 3 Key Laboratory of Hydrodynamics (Ministry of Education), School of Ocean and Civil Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
  • 4 Laboratory of Metabolomics and Drug-induced Liver Injury, Department of Gastroenterology & Hepatology, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, 610041, China.
  • 5 Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China; Chengdu Zenitar Biomedical Technology Co., Ltd, Chengdu, 610041, China.
  • 6 Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China. Electronic address: haoyu_ye@scu.edu.cn.
  • 7 Division of Thyroid Surgery, Department of General Surgery and Laboratory of Thyroid and Parathyroid Disease, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, 610041, China. Electronic address: wenshuang_wu@163.com.
PMID: 40378590 DOI: 10.1016/j.phymed.2025.156835
Abstract

Background: The NLRP3 inflammasome is a key regulator of innate immunity and plays a critical role in the pathogenesis of various inflammatory diseases. Regulating NLRP3 has emerged as a promising strategy for the development of anti-inflammatory therapies. Valtrate (Val), a natural compound derived from Valeriana officinalis Jones, has demonstrated significant anti-inflammatory activity. However, its precise mechanism of action remains unclear.

Purpose: This study elucidates the molecular mechanisms of Val suppressing NLRP3 inflammasome activation.

Methods: We screened 100 natural compounds for anti-pyroptotic in lipopolysaccharide (LPS)/nigericin-stimulated THP-1 cells and bone marrow-derived macrophages (BMDMs) using Lactate Dehydrogenase (LDH) release assays. Val's effect on NLRP3 were assessed via immunoblotting and ELISA. Target identification employed DARTS, proteomics, thermal shift assay (TSA), microscale thermophoresis (MST), and molecular dynamics (MD) simulations. In vivo efficacy was evaluated in acetaminophen (APAP)- and LPS-induced liver injury models.

Results: Val potently inhibited Pyroptosis (99.20 % LDH reduction) and selectively degraded NLRP3 via post-translation mechanisms (PTMs) without altering its mRNA. DARTS and CETSA confirmed that Val directly interacts with the C2 fragment of USP9X without inhibiting its enzymatic activity, while RMSD, RMSF, and Gibbs energy landscape analyses supported its stable binding to USP9X, which was further confirmed by MST. Mechanistically, Val downregulated USP9X protein expression and promoted K48- and K63-linked ubiquitination and proteasomal degradation of NLRP3. In vivo, Val exhibited therapeutic potential in murine models of acute liver injury induced by APAP and LPS. Val reduced serum ALT and AST levels, inflammatory cytokines, and liver injury (histopathological analysis (H&E) and TUNEL).

Conclusion: This study uncovers an unrecognized mechanism by which Val attenuates NLRP3 inflammasome activation by disrupting the USP9X-NLRP3 axis, thereby promoting NLRP3 ubiquitination and proteasomal degradation. Notably, Val down-regulates USP9X protein levels without impairing its catalytic activity, representing a distinct mechanism from existing USP9X inhibitors. These findings not only deepen our understanding of Val's anti-inflammatory action but also underscore its promise as a lead compound for the development of novel therapeutics targeting NLRP3-driven inflammatory diseases.

Keywords

NLRP3 inflammasome; USP9X; Ubiquitin-proteasome pathway; Valtrate.

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