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Article: Adipocyte Fatty Acid Binding Protein Promotes the Onset and Progression of Liver Fibrosis via Mediating the Crosstalk between Liver Sinusoidal Endothelial Cells and Hepatic Stellate Cells

TitleAdipocyte Fatty Acid Binding Protein Promotes the Onset and Progression of Liver Fibrosis via Mediating the Crosstalk between Liver Sinusoidal Endothelial Cells and Hepatic Stellate Cells
Authors
Issue Date2021
Citation
Advanced Science, 2021, p. 2003721 How to Cite?
AbstractDevelopment of liver fibrosis results in drastic changes in the liver microenvironment, which in turn accelerates disease progression. Although the pathological function of various hepatic cells in fibrogenesis is identified, the crosstalk between them remains obscure. The present study demonstrates that hepatic expression of adipocyte fatty acid binding protein (A‐FABP) is induced especially in the liver sinusoidal endothelial cells (LSECs) in mice after bile duct ligation (BDL). Genetic ablation and pharmacological inhibition of A‐FABP attenuate BDL‐ or carbon tetrachloride‐induced liver fibrosis in mice associating with reduced collagen accumulation, LSEC capillarization, and hepatic stellate cell (HSC) activation. Mechanistically, elevated A‐FABP promotes LSEC capillarization by activating Hedgehog signaling, thus impairs the gatekeeper function of LSEC on HSC activation. LSEC‐derived A‐FABP also acts on HSCs in paracrine manner to potentiate the transactivation of transforming growth factor β1 (TGFβ1) by activating c‐Jun N‐terminal kinase (JNK)/c‐Jun signaling. Elevated TGFβ1 subsequently exaggerates liver fibrosis. These findings uncover a novel pathological mechanism of liver fibrosis in which LSEC‐derived A‐FABP is a key regulator modulating the onset and progression of the disease. Targeting A‐FABP may represent a potential approach against liver fibrosis.
Persistent Identifierhttp://hdl.handle.net/10722/299152

 

DC FieldValueLanguage
dc.contributor.authorWu, X-
dc.contributor.authorShu, L-
dc.contributor.authorZHANG, Z-
dc.contributor.authorLi, J-
dc.contributor.authorZONG, J-
dc.contributor.authorCheong, LY-
dc.contributor.authorYe, D-
dc.contributor.authorLam, KSL-
dc.contributor.authorSong, E-
dc.contributor.authorWang, C-
dc.contributor.authorXu, A-
dc.contributor.authorHoo, RLC-
dc.date.accessioned2021-04-28T02:26:52Z-
dc.date.available2021-04-28T02:26:52Z-
dc.date.issued2021-
dc.identifier.citationAdvanced Science, 2021, p. 2003721-
dc.identifier.urihttp://hdl.handle.net/10722/299152-
dc.description.abstractDevelopment of liver fibrosis results in drastic changes in the liver microenvironment, which in turn accelerates disease progression. Although the pathological function of various hepatic cells in fibrogenesis is identified, the crosstalk between them remains obscure. The present study demonstrates that hepatic expression of adipocyte fatty acid binding protein (A‐FABP) is induced especially in the liver sinusoidal endothelial cells (LSECs) in mice after bile duct ligation (BDL). Genetic ablation and pharmacological inhibition of A‐FABP attenuate BDL‐ or carbon tetrachloride‐induced liver fibrosis in mice associating with reduced collagen accumulation, LSEC capillarization, and hepatic stellate cell (HSC) activation. Mechanistically, elevated A‐FABP promotes LSEC capillarization by activating Hedgehog signaling, thus impairs the gatekeeper function of LSEC on HSC activation. LSEC‐derived A‐FABP also acts on HSCs in paracrine manner to potentiate the transactivation of transforming growth factor β1 (TGFβ1) by activating c‐Jun N‐terminal kinase (JNK)/c‐Jun signaling. Elevated TGFβ1 subsequently exaggerates liver fibrosis. These findings uncover a novel pathological mechanism of liver fibrosis in which LSEC‐derived A‐FABP is a key regulator modulating the onset and progression of the disease. Targeting A‐FABP may represent a potential approach against liver fibrosis.-
dc.languageeng-
dc.relation.ispartofAdvanced Science-
dc.titleAdipocyte Fatty Acid Binding Protein Promotes the Onset and Progression of Liver Fibrosis via Mediating the Crosstalk between Liver Sinusoidal Endothelial Cells and Hepatic Stellate Cells-
dc.typeArticle-
dc.identifier.emailWu, X: raxpwu@hku.hk-
dc.identifier.emailShu, L: shinyshu@hku.hk-
dc.identifier.emailLi, J: kimli07@hku.hk-
dc.identifier.emailCheong, LY: u3003285@connect.hku.hk-
dc.identifier.emailLam, KSL: ksllam@hku.hk-
dc.identifier.emailXu, A: amxu@hkucc.hku.hk-
dc.identifier.emailHoo, RLC: rubyhoo@hkucc.hku.hk-
dc.identifier.authorityLam, KSL=rp00343-
dc.identifier.authorityXu, A=rp00485-
dc.identifier.authorityHoo, RLC=rp01334-
dc.identifier.doi10.1002/advs.202003721-
dc.identifier.hkuros322236-
dc.identifier.spage2003721-
dc.identifier.epage2003721-

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