Hua Susan, Dias Thilani H
School of Biomedical Sciences and Pharmacy, University of NewcastleCallaghan, NSW, Australia; Hunter Medical Research InstituteNew Lambton Heights, NSW, Australia.
School of Biomedical Sciences and Pharmacy, University of Newcastle Callaghan, NSW, Australia.
Front Pharmacol. 2016 Jun 27;7:184. doi: 10.3389/fphar.2016.00184. eCollection 2016.
Hypoxia is an important micro-environmental characteristic of rheumatoid arthritis (RA). Hypoxia-inducible factors (HIF) are key transcriptional factors that are highly expressed in RA synovium to regulate the adaptive responses to this hypoxic milieu. Accumulating evidence supports hypoxia and HIFs in regulating a number of important pathophysiological characteristics of RA, including synovial inflammation, angiogenesis, and cartilage destruction. Experimental and clinical data have confirmed the upregulation of both HIF-1α and HIF-2α in RA. This review will focus on the differential expression of HIFs within the synovial joint and its functional behavior in different cell types to regulate RA progression. Potential development of new therapeutic strategies targeting HIF-regulated pathways at sites of disease in RA will also be addressed.
缺氧是类风湿关节炎(RA)的一个重要微环境特征。缺氧诱导因子(HIF)是关键的转录因子,在RA滑膜中高表达,以调节对这种缺氧环境的适应性反应。越来越多的证据支持缺氧和HIF在调节RA的一些重要病理生理特征方面的作用,包括滑膜炎症、血管生成和软骨破坏。实验和临床数据已证实RA中HIF-1α和HIF-2α均上调。本综述将聚焦于滑膜关节内HIF的差异表达及其在不同细胞类型中的功能行为,以调节RA的进展。还将探讨针对RA疾病部位HIF调节途径的新治疗策略的潜在发展。