PARK7 deficiency inhibits fatty acid β-oxidation via PTEN to delay liver regeneration after hepatectomy

PARK7 缺乏通过 PTEN 抑制脂肪酸 β-氧化,从而延缓肝切除术后肝再生

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作者:Xiaoye Qu, Yankai Wen, Junzhe Jiao, Jie Zhao, Xuehua Sun, Fang Wang, Yueqiu Gao, Weifeng Tan, Qiang Xia, Hailong Wu, Xiaoni Kong

Conclusion

Park7/Dj1 is a novel regulator of PTEN-dependent fatty acid β-oxidation, and increasing Park7 expression might be a promising strategy to promote liver regeneration.

Methods

Park7 knockout (Park7-/- ), hepatocyte-specific Park7 knockout (Park7△hep ) and hepatocyte-specific Park7-Pten double knockout mice were subjected to 2/3 partial hepatectomy (PHx)

Results

Increased PARK7 expression was observed in the regenerating liver of mice at 36 and 48 h after PHx. Park7-/- and Park7△hep mice showed delayed liver regeneration and enhanced TRAS after PHx. PPARa, a key regulator of β-oxidation, and carnitine palmitoyltransferase 1a (CPT1a), a rate-limiting enzyme of β-oxidation, had substantially decreased expression in the regenerating liver of Park7△hep mice. Increased phosphatase and tensin homolog (PTEN) expression was observed in the liver of Park7△hep mice, which might contribute to delayed liver regeneration in these mice because genomic depletion or pharmacological inhibition of PTEN restored the delayed liver regeneration by reversing the downregulation of PPARa and CPT1a and in turn accelerating the utilization of TRAS in the regenerating liver of Park7△hep mice

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