PPARα调节酰基辅酶a氧化酶1 (ACOX1),但不调节过氧化氢酶

IF 2.5 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xue Chen , Anna Mazur , Wei Xu , W. Christopher Risher , Krista L. Denning , Yongke Lu
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引用次数: 0

摘要

过氧化物酶体是一种膜细胞器,过氧化物酶体膜蛋白70 (PMP70)是一种过氧化物酶体转运体,被用作过氧化物酶体的标记物。像线粒体一样,过氧化物酶体也可以氧化脂肪酸,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被过氧化氢酶局部解毒。PPARα激动剂wy - 14643通过诱导PMP70诱导过氧化物酶体增殖,ACOX1和过氧化氢酶也被诱导。但ACOX1的诱导程度大于过氧化氢酶。wy - 14643停药后,诱导ACOX1在停药2天后开始下降;但过氧化氢酶在10天内仍保持较高水平。wy - 14643对ACOX1 mRNA水平也有诱导作用,但对过氧化氢酶mRNA水平无诱导作用。在肝脏特异性PEX16基因敲除(Pex16Alb-Cre)小鼠的肝脏中,过氧化物酶体缺失,但过氧化氢酶和ACOX1在某种程度上上调。ACOX1 mRNA也自发升高,但过氧化氢酶mRNA没有变化。通过将PPARα与PPARα - / -小鼠杂交来去除PPARα,生成PPARα - / - / ppar16alb - cre小鼠,上调的ACOX1蛋白在PPARα - / - / ppar16alb - cre小鼠中被抑制,但过氧化氢酶蛋白保持升高。这些结果表明ACOX1受PPARα调控,过氧化氢酶不受PPARα调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PPARα regulates acyl-CoA oxidase 1 (ACOX1) but not catalase
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 (H2O2) by ACOX1, and the generated H2O2 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 (Pex16Alb-Cre) 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 Pex16Alb-Cre mice with Pparα−/− mice to create the Pparα−/−/Pex16Alb-Cre mice, the upregulated ACOX1 protein was suppressed in the Pparα−/−/Pex16Alb-Cre mice, but catalase protein remained elevated. These results suggest that ACOX1 but not catalase is regulated by PPARα.
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来源期刊
Biochemical and biophysical research communications
Biochemical and biophysical research communications 生物-生化与分子生物学
CiteScore
6.10
自引率
0.00%
发文量
1400
审稿时长
14 days
期刊介绍: Biochemical and Biophysical Research Communications is the premier international journal devoted to the very rapid dissemination of timely and significant experimental results in diverse fields of biological research. The development of the "Breakthroughs and Views" section brings the minireview format to the journal, and issues often contain collections of special interest manuscripts. BBRC is published weekly (52 issues/year).Research Areas now include: Biochemistry; biophysics; cell biology; developmental biology; immunology ; molecular biology; neurobiology; plant biology and proteomics
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