4.5 Article

FGF15 promotes hepatic NPC1L1 degradation in lithogenic diet-fed mice

期刊

LIPIDS IN HEALTH AND DISEASE
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12944-022-01709-8

关键词

Cholesterol gallstone disease; NPC1L1; Ezetimibe; Ubiquitination; FGF15

资金

  1. National Natural Science Foundation of China [81870433, 82170649]
  2. Basic Public Welfare Research Program of Zhejiang Province [LGJ18H030001]

向作者/读者索取更多资源

This study found that ezetimibe can effectively prevent cholesterol gallstone disease. LD induces the degradation of hepatic NPC1L1 via the FGF15-FGFR4 pathway. These findings contribute to a better understanding of the pathogenesis of CGD and the identification of effective strategies for prevention and treatment of the disease.
Background: Cholesterol gallstone disease (CGD) is accompanied by biliary cholesterol supersaturation. Hepatic Niemann-Pick C1-like 1 (NPC1L1), which is present in humans but not in wild-type (WT) mice, promotes hepatocyte cholesterol uptake and decreases biliary cholesterol supersaturation. In contrast, intestinal NPC1L1 promotes intestinal cholesterol absorption, increasing biliary cholesterol supersaturation. Ezetimibe (EZE) can inhibit both hepatic and intestinal NPC1L1. However, whether hepatic NPC1L1 can affect CGD progress remains unknown. Methods: Mice expressing hepatic NPC1 L1 (NPC1L1(hepatic-OE) mice) were generated using Adeno-associated viruses (AAV) gene delivery. The protein level and function of hepatic NPC1L1 were examined under chow diet, high fat-cholesterol diet (HFCD), and lithogenic diet (LD) feeding. Gallstone formation rates were examined with or without EZE treatment. Fibroblast growth factor 15 (FGF15) treatment and inhibition of fibroblast growth factor receptor 4 (FGFR4) were applied to verify the mechanism of hepatic NPC1L1 degradation. Results: The HFCD-fed NPC1L1(hepatic-OE) mice retained the biliary cholesterol desaturation function of hepatic NPC1L1, whereas EZE treatment decreased biliary cholesterol saturation and did not cause CGD. The ubiquitination and degradation of hepatic NPC1 L1 were discovered in LD-fed NPC1 L1(hepatic-OE) mice. Treatment of FGF15 during HFCD feeding and inhibition of FGFR4 during LD feeding could affect the protein level and function of hepatic NPC1L1. Conclusions: LD induces the ubiquitination and degradation of hepatic NPC1L1 via the FGF15-FGFR4 pathway. EZE may act as an effective preventative agent for CGD.

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