Department of Biochemistry, Institute of Experimental Medicine, Russian Academy of Medical Sciences, 197376 St. Petersburg, Russia.
Biochem Biophys Res Commun. 2010 Jul 23;398(2):224-30. doi: 10.1016/j.bbrc.2010.06.064. Epub 2010 Jun 18.
Human apolipoprotein A-I (ApoA-I) is a major structural and functional protein component of high-density lipoproteins. The expression of the apolipoprotein A-I gene (apoA-I) in hepatocytes is repressed by pro-inflammatory cytokines such as IL-1beta and TNFalpha. Recently, two novel additional (alternative) promoters for human apoA-I gene have been identified. Nothing is known about the role of alternative promoters in TNFalpha-mediated downregulation of apoA-I gene. In this article we report for the first time about the different effects of TNFalpha on two alternative promoters of human apoA-I gene. Stimulation of HepG2 cells by TNFalpha leads to activation of the distal alternative apoA-I promoter and downregulation of the proximal alternative and the canonical apoA-I promoters. This effect is mediated by weakening of the promoter competition within human apoA-I 5'-regulatory region (apoA-I promoter switching) in the cells treated by TNFalpha. The MEK1/2-ERK1/2 cascade and nuclear receptors PPARalpha and LXRs are important for TNFalpha-mediated apoA-I promoter switching.
人载脂蛋白 A-I(ApoA-I)是高密度脂蛋白的主要结构和功能蛋白成分。肝细胞中载脂蛋白 A-I 基因(apoA-I)的表达受炎性细胞因子如 IL-1beta 和 TNFalpha 的抑制。最近,已经鉴定出人类 apoA-I 基因的两个新的额外(替代)启动子。关于替代启动子在 TNFalpha 介导的 apoA-I 基因下调中的作用尚不清楚。在本文中,我们首次报道了 TNFalpha 对人类 apoA-I 基因两个替代启动子的不同影响。TNFalpha 刺激 HepG2 细胞导致远端替代 apoA-I 启动子的激活和近端替代和典型 apoA-I 启动子的下调。这种效应是通过在 TNFalpha 处理的细胞中削弱人 apoA-I 5'-调控区(apoA-I 启动子转换)内的启动子竞争介导的。MEK1/2-ERK1/2 级联和核受体 PPARalpha 和 LXRs 对于 TNFalpha 介导的 apoA-I 启动子转换很重要。