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Article: A natural small molecule alleviates liver fibrosis by targeting apolipoprotein L2

TitleA natural small molecule alleviates liver fibrosis by targeting apolipoprotein L2
Authors
Issue Date5-Aug-2024
PublisherNature Research
Citation
Nature Chemical Biology, 2024 How to Cite?
Abstract

Liver fibrosis is an urgent clinical problem without effective therapies. Here we conducted a high-content screening on a natural Euphorbiaceae diterpenoid library to identify a potent anti-liver fibrosis lead, 12-deoxyphorbol 13-palmitate (DP). Leveraging a photo-affinity labeling approach, apolipoprotein L2 (APOL2), an endoplasmic reticulum (ER)-rich protein, was identified as the direct target of DP. Mechanistically, APOL2 is induced in activated hepatic stellate cells upon transforming growth factor-β1 (TGF-β1) stimulation, which then binds to sarcoplasmic/ER calcium ATPase 2 (SERCA2) to trigger ER stress and elevate its downstream protein kinase R-like ER kinase (PERK)–hairy and enhancer of split 1 (HES1) axis, ultimately promoting liver fibrosis. As a result, targeting APOL2 by DP or ablation of APOL2 significantly impairs APOL2–SERCA2–PERK–HES1 signaling and mitigates fibrosis progression. Our findings not only define APOL2 as a novel therapeutic target for liver fibrosis but also highlight DP as a promising lead for treatment of this symptom.


Persistent Identifierhttp://hdl.handle.net/10722/348837
ISSN
2023 Impact Factor: 12.9
2023 SCImago Journal Rankings: 5.558

 

DC FieldValueLanguage
dc.contributor.authorGan, Lu-
dc.contributor.authorJiang, Qiwei-
dc.contributor.authorHuang, Dong-
dc.contributor.authorWu, Xueji-
dc.contributor.authorZhu, Xinying-
dc.contributor.authorWang, Lei-
dc.contributor.authorXie, Wei-
dc.contributor.authorHuang, Jialuo-
dc.contributor.authorFan, Runzhu-
dc.contributor.authorJing, Yihang-
dc.contributor.authorTang, Guihua-
dc.contributor.authorLi, Xiang David-
dc.contributor.authorGuo, Jianping-
dc.contributor.authorYin, Sheng-
dc.date.accessioned2024-10-17T00:30:21Z-
dc.date.available2024-10-17T00:30:21Z-
dc.date.issued2024-08-05-
dc.identifier.citationNature Chemical Biology, 2024-
dc.identifier.issn1552-4450-
dc.identifier.urihttp://hdl.handle.net/10722/348837-
dc.description.abstract<p>Liver fibrosis is an urgent clinical problem without effective therapies. Here we conducted a high-content screening on a natural Euphorbiaceae diterpenoid library to identify a potent anti-liver fibrosis lead, 12-deoxyphorbol 13-palmitate (DP). Leveraging a photo-affinity labeling approach, apolipoprotein L2 (APOL2), an endoplasmic reticulum (ER)-rich protein, was identified as the direct target of DP. Mechanistically, APOL2 is induced in activated hepatic stellate cells upon transforming growth factor-β1 (TGF-β1) stimulation, which then binds to sarcoplasmic/ER calcium ATPase 2 (SERCA2) to trigger ER stress and elevate its downstream protein kinase R-like ER kinase (PERK)–hairy and enhancer of split 1 (HES1) axis, ultimately promoting liver fibrosis. As a result, targeting APOL2 by DP or ablation of APOL2 significantly impairs APOL2–SERCA2–PERK–HES1 signaling and mitigates fibrosis progression. Our findings not only define APOL2 as a novel therapeutic target for liver fibrosis but also highlight DP as a promising lead for treatment of this symptom.</p>-
dc.languageeng-
dc.publisherNature Research-
dc.relation.ispartofNature Chemical Biology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleA natural small molecule alleviates liver fibrosis by targeting apolipoprotein L2-
dc.typeArticle-
dc.identifier.doi10.1038/s41589-024-01704-3-
dc.identifier.scopuseid_2-s2.0-85200421048-
dc.identifier.eissn1552-4469-
dc.identifier.issnl1552-4450-

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