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过氧化物酶体增殖物激活受体α(PPARα)调节酰基辅酶A氧化酶1(ACOX1),但不调节过氧化氢酶。

PPARα regulates acyl-CoA oxidase 1 (ACOX1) but not catalase.

作者信息

Chen Xue, Mazur Anna, Xu Wei, Risher W Christopher, Denning Krista L, Lu Yongke

机构信息

Department of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, 1700 3rd Avenue, Huntington, WV, 25755, USA.

Department of Pathology, Joan C. Edwards School of Medicine, Marshall University, 1700 3rd Avenue, Huntington, WV, 25755, USA.

出版信息

Biochem Biophys Res Commun. 2025 Jun 25;777:152247. doi: 10.1016/j.bbrc.2025.152247.

Abstract

Peroxisomes are membranous organelles, and peroxisomal membrane protein 70 (PMP70), a peroxisome transporter, is used as a marker of peroxisomes. Like mitochondria, peroxisomes can also oxidize fatty acids and its rate limiting enzyme is acyl-CoA oxidase 1 (ACOX1). But unlike mitochondria, peroxisomes generate hydrogen peroxide (HO) by ACOX1, and the generated HO is locally detoxified by catalase. PPARα agonist WY-14,643 induces peroxisome proliferation as indicated by the induction of PMP70, ACOX1 and catalase were also induced. However, ACOX1 was induced to a greater extent than catalase. After WY-14,643 withdrawal, the induced ACOX1 started to decrease after 2 days; but catalase remained at higher levels up to10 days. While mRNA levels of ACOX1 were also induced by WY-14,643, mRNA levels of catalase were not induced by WY-14,643. In the livers collected from liver-specific PEX16 knockout (Pex16) mice, peroxisomes are absent but catalase and ACOX1 were somehow upregulated. The mRNA of ACOX1 was also spontaneously elevated, but the catalase mRNA was not changed. When PPARα was abrogated through crossing the Pex16 mice with Pparα mice to create the Pparα/Pex16 mice, the upregulated ACOX1 protein was suppressed in the Pparα/Pex16 mice, but catalase protein remained elevated. These results suggest that ACOX1 but not catalase is regulated by PPARα.

摘要

过氧化物酶体是膜性细胞器,过氧化物酶体膜蛋白70(PMP70)作为一种过氧化物酶体转运蛋白,被用作过氧化物酶体的标志物。与线粒体一样,过氧化物酶体也能氧化脂肪酸,其限速酶是酰基辅酶A氧化酶1(ACOX1)。但与线粒体不同的是,过氧化物酶体通过ACOX1产生过氧化氢(H₂O₂),产生的H₂O₂由过氧化氢酶在局部进行解毒。PPARα激动剂WY-14,643可诱导过氧化物酶体增殖,表现为PMP70的诱导,同时ACOX1和过氧化氢酶也被诱导。然而,ACOX1的诱导程度大于过氧化氢酶。在停用WY-14,643后,诱导的ACOX1在2天后开始下降;但过氧化氢酶在长达10天的时间内仍保持在较高水平。虽然WY-14,643也能诱导ACOX1的mRNA水平,但不能诱导过氧化氢酶的mRNA水平。在从肝脏特异性PEX16基因敲除(Pex16)小鼠收集到的肝脏中,过氧化物酶体缺失,但过氧化氢酶和ACOX1却有所上调。ACOX1的mRNA也自发升高,但过氧化氢酶的mRNA没有变化。当通过将Pex16小鼠与Pparα小鼠杂交以产生Pparα/Pex16小鼠来消除PPARα时,Pparα/Pex16小鼠中上调的ACOX1蛋白受到抑制,但过氧化氢酶蛋白仍保持升高。这些结果表明,ACOX1而非过氧化氢酶受PPARα调控。

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