Ikhlef Souade, Berrougui Hicham, Kamtchueng Simo Olivier, Khalil Abdelouahed
Research Centre on Aging, CSSS-IUGS, Sherbrooke, Canada.
Department of Biology, University Sultan My Slimane, Beni Mellal, Morocco.
FEBS Lett. 2016 Jun;590(11):1614-29. doi: 10.1002/1873-3468.12198. Epub 2016 May 23.
Here, we investigate the mechanism through which paraoxonase 1 (PON1) may regulate cholesterol efflux. Pretreatment of oxLDL with PON1 (oxLDL-PON1) contributed to the formation of LysoPC. In J774 macrophages, oxLDL-PON1 increased cholesterol efflux by more than 47% compared to oxLDL alone. oxLDL-PON1 significantly increased mRNA and protein expression of ABCA1 and ABCG1, as well as of PPARγ and LXRα compared to oxLDL alone. Intraperitoneal injection of oxLDL-PON1- or LysoPC-treated J774 macrophages significantly increased the fecal elimination of macrophage-derived cholesterol in these mice. Our results suggest that PON1 stimulates cholesterol efflux via a mechanism that involves oxidized phospholipid hydrolysis.
在此,我们研究对氧磷酶1(PON1)可能调节胆固醇流出的机制。用PON1预处理氧化型低密度脂蛋白(oxLDL-PON1)有助于溶血磷脂酰胆碱(LysoPC)的形成。在J774巨噬细胞中,与单独的oxLDL相比,oxLDL-PON1使胆固醇流出增加了47%以上。与单独的oxLDL相比,oxLDL-PON1显著增加了ABCA1和ABCG1以及PPARγ和LXRα的mRNA和蛋白表达。腹腔注射经oxLDL-PON1或LysoPC处理的J774巨噬细胞显著增加了这些小鼠粪便中巨噬细胞源性胆固醇的清除。我们的结果表明,PON1通过涉及氧化磷脂水解的机制刺激胆固醇流出。