4.8 Article

Hepatic glucuronyl C5-epimerase combats obesity by stabilising GDF15

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JOURNAL OF HEPATOLOGY
卷 79, 期 3, 页码 -

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ELSEVIER
DOI: 10.1016/j.jhep.2023.05.011

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Glucuronyl C5-epimerase; Growth differentiation factor-15; Obesity; Energy expenditure; Ubiquitination

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This study investigated the role of hepatic glucuronyl C5-epimerase (Glce) in obesity development. It found that hepatic Glce deficiency facilitates obesity progression and reduces secretion of growth differentiation factor 15 (GDF15), disrupting lipid homeostasis.
Background & Aims: Disturbed hepatic metabolism frequently results in excessive lipid accumulation in the adipose tissue. However, the specific role of the liver-adipose axis in maintaining lipid homeostasis, as well as the underlying mechanism, has not yet been fully elucidated. In this study, we investigated the role of hepatic glucuronyl C5-epimerase (Glce) in the progression of obesity. Methods: We determined the association between the expression of hepatic Glce and body mass index (BMI) in obese patients. Obesity models were established in hepatic Glce-knockout and wild-type mice fed a high-fat diet (HFD) to understand the effect of Glce on obesity development. The role of Glce in the progression of disrupted hepatokine secretion was examined via secretome analysis.Results: Hepatic Glce expression was inversely correlated with BMI in obese patients. Moreover, Glce level was found to be decreased in the liver of a HFD murine model. Hepatic Glce deficiency led to impaired thermogenesis in adipose tissue and exacerbated HFD-induced obesity. Interestingly, decreased level of growth differentiation factor 15 (GDF15) was observed in the culture medium of Glce-knockout mouse hepatocytes. Treatment with recombinant GDF15 obstructed obesity progression derived from the absence of hepatic Glce, similar to the effect of Glce or its inactive mutant overexpressed both in vitro and in vivo. Furthermore, liver Glce deficiency led to diminished production and increased degradation of mature GDF15, resulting in reduced hepatic GDF15 secretion.Conclusions: Hepatic Glce deficiency facilitated obesity development, and decreased Glce expression further reduced hepatic secretion of GDF15, thereby perturbing lipid homeostasis in vivo. Therefore, the novel Glce-GDF15 axis plays an important role in maintaining energy balance and may act as a potential target for combating obesity.& COPY; 2023 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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