Xue Chen , Anna Mazur , Wei Xu , W. Christopher Risher , Krista L. Denning , Yongke Lu
{"title":"PPARα调节酰基辅酶a氧化酶1 (ACOX1),但不调节过氧化氢酶","authors":"Xue Chen , Anna Mazur , Wei Xu , W. Christopher Risher , Krista L. Denning , Yongke Lu","doi":"10.1016/j.bbrc.2025.152247","DOIUrl":null,"url":null,"abstract":"<div><div>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 (H<sub>2</sub>O<sub>2</sub>) by ACOX1, and the generated H<sub>2</sub>O<sub>2</sub> 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 (<em>Pex16</em><sup><em>Alb-Cre</em></sup>) 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 <em>Pex16</em><sup><em>Alb-Cre</em></sup> mice with <em>Pparα</em><sup><em>−/−</em></sup> mice to create the <em>Pparα</em><sup><em>−/−</em></sup>/<em>Pex16</em><sup><em>Alb-Cre</em></sup> mice, the upregulated ACOX1 protein was suppressed in the <em>Pparα</em><sup><em>−/−</em></sup>/<em>Pex16</em><sup><em>Alb-Cre</em></sup> mice, but catalase protein remained elevated. These results suggest that ACOX1 but not catalase is regulated by PPARα.</div></div>","PeriodicalId":8779,"journal":{"name":"Biochemical and biophysical research communications","volume":"777 ","pages":"Article 152247"},"PeriodicalIF":2.5000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PPARα regulates acyl-CoA oxidase 1 (ACOX1) but not catalase\",\"authors\":\"Xue Chen , Anna Mazur , Wei Xu , W. Christopher Risher , Krista L. Denning , Yongke Lu\",\"doi\":\"10.1016/j.bbrc.2025.152247\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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 (H<sub>2</sub>O<sub>2</sub>) by ACOX1, and the generated H<sub>2</sub>O<sub>2</sub> 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 (<em>Pex16</em><sup><em>Alb-Cre</em></sup>) 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 <em>Pex16</em><sup><em>Alb-Cre</em></sup> mice with <em>Pparα</em><sup><em>−/−</em></sup> mice to create the <em>Pparα</em><sup><em>−/−</em></sup>/<em>Pex16</em><sup><em>Alb-Cre</em></sup> mice, the upregulated ACOX1 protein was suppressed in the <em>Pparα</em><sup><em>−/−</em></sup>/<em>Pex16</em><sup><em>Alb-Cre</em></sup> mice, but catalase protein remained elevated. These results suggest that ACOX1 but not catalase is regulated by PPARα.</div></div>\",\"PeriodicalId\":8779,\"journal\":{\"name\":\"Biochemical and biophysical research communications\",\"volume\":\"777 \",\"pages\":\"Article 152247\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-06-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical and biophysical research communications\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0006291X25009623\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical and biophysical research communications","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0006291X25009623","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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.
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