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Activation of the Liver X Receptor Prevents Lipopolysaccharide-induced Lung Injury

  作者 Gong, HBA; He, JH; Lee, JH; Mallick, E; Gao, X; Li, S; Homanics, GE; Xie, W  
  选自 期刊  Journal of Biological Chemistry;  卷期  2009年284-44;  页码  30113-30121  
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[摘要]The liver X receptors (LXRs) have been known as sterol sensors that impact cholesterol and lipid homeostasis, as well as inflammation. Although the hepatic functions of LXRs are well documented, whether and how LXRs play a pathophysiological role in the lung remain largely unknown. Here we show that LXR alpha and LXR beta are expressed in both type I and type II mouse lung epithelial cells, as well as in human lung cancer cells. To study the role of LXR alpha in vivo including the pulmonary function of this LXR isoform, we created LXR alpha knock-in (LXR-KI) mice in which a constitutively activated LXR alpha (VP-LXR alpha) was inserted into the mouse LXR alpha locus. We show that activation of LXR in LXR-KI mice or LXR agonist-treated wild type mice induced pulmonary expression of genes encoding multiple antioxidant enzymes. Consistent with the induction of antioxidant enzymes, LXR-KI mice and LXR ligand-treated wild type mice showed a substantial resistance to lipopolysaccharide-induced lung injury and decreased production of reactive oxygen species. In summary, we have uncovered a novel role of LXR in regulating antioxidant enzymes in the lung and the implication of this regulation in pulmonary tissue protection.

 
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