Kelly Caleb J, Colgan Sean P
Mucosal Inflammation Program, Department of Medicine, University of Colorado Health Sciences Center, Aurora, CO USA.
J Epithel Biol Pharmacol. 2012;5(Suppl 1-M10):67-76. doi: 10.2174/1875044301205010067. Epub 2012 Jan 16.
Sites of inflammation are associated with profound changes in tissue metabolism. Studies and have shown that the activation of the hypoxia-inducible factor (HIF) serves as an adaptive pathway for the resolution of inflammation associated with various murine disease models. The resolution of disease occurs, at least in part, through transcriptional regulation of non-classical epithelial barrier genes. There is significant recent interest in harnessing hypoxia-inducible pathways, including targeting the HIF and the proyl-hydroxylase (PHD) enzymes that stabilize HIF, to promote mucosal healing. Here, we review the signaling pathways involved and define how hypoxia-associated signaling provides mechanistic insight into augmenting barrier function in mucosal inflammatory disease.
炎症部位与组织代谢的深刻变化相关。研究表明,缺氧诱导因子(HIF)的激活是与各种小鼠疾病模型相关的炎症消退的适应性途径。疾病的消退至少部分是通过非经典上皮屏障基因的转录调控实现的。最近人们对利用缺氧诱导途径产生了浓厚兴趣,包括靶向HIF和稳定HIF的脯氨酰羟化酶(PHD),以促进黏膜愈合。在此,我们综述相关信号通路,并阐述缺氧相关信号如何为增强黏膜炎症性疾病中的屏障功能提供机制性见解。