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Marked upregulation of cholesterol 25-hydroxylase expression by lipopolysaccharide

机译:脂多糖显着上调胆固醇25-羟化酶的表达

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摘要

During screening of genes upregulated by lipopolysaccharide (LPS; endotoxin) treatment of bone marrow-derived mouse macrophages, it was unexpectedly found that cholesterol 25-hydroxylase (Ch25h) was strongly upregulated. Treatment of macrophages with 10 ng/ml of LPS for 2 h resulted in a 35-fold increase in the expression of Ch25h. In contrast, LPS treatment did not increase the expression of Cyp27a1 or Cyp7b1. The increased Ch25h expression was found to be independent of Myeloid differentiation protein 88 signaling but dependent on Toll-like receptor 4 signaling. LPS treatment of macrophages caused a 6- to 7-fold increase in cellular 25-hydroxycholesterol concentration. When macrophages were treated with increasing concentrations of 25-hydroxycholesterol, a dose-dependent release of CCL5 into the culture medium was observed. Intravenous injection of LPS in eight healthy volunteers resulted in an increase in plasma 25-hydroxycholesterol concentration. The possibility is discussed that 25-hydroxycholesterol may have a role in the inflammatory response, in addition to its more established role in the regulation of cholesterol homeostasis.
机译:在筛选通过脂多糖(LPS;内毒素)处理的骨髓源性小鼠巨噬细胞上调的基因时,出乎意料地发现胆固醇25-羟化酶(Ch25h)被上调。用10 ng / ml LPS处理巨噬细胞2小时,导致Ch25h表达增加35倍。相反,LPS处理并未增加Cyp27a1或Cyp7b1的表达。发现增加的Ch25h表达不依赖于骨髓分化蛋白88信号传导,但依赖于Toll样受体4信号传导。 LPS处理巨噬细胞导致细胞25-羟基胆固醇浓度增加6到7倍。当用增加浓度的25-羟基胆固醇处理巨噬细胞时,观察到剂量依赖性地将CCL5释放到培养基中。在八名健康志愿者中静脉注射LPS导致血浆25-羟胆固醇浓度增加。讨论了25-羟基胆固醇除了在胆固醇稳态调节中更确定的作用外,还可能在炎症反应中起作用的可能性。

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