Institute of Inflammation and Ageing, MRC-Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham, UK.
FEBS J. 2021 Oct;288(19):5555-5568. doi: 10.1111/febs.15644. Epub 2020 Dec 17.
Mesenchymal stromal fibroblasts have emerged as key mediators of the inflammatory response and drivers of localised inflammation, in part through their interactions with resident and circulating immune cells at inflammatory sites. As such, they have been implicated in a number of chronic inflammatory conditions as well as in tumour progression through modifying the microenvironment. The connection between metabolic changes and altered phenotype of fibroblasts in inflammatory microenvironments has clear implications for our understanding of how chronic inflammation is regulated and for the development of new anti-inflammatory therapeutics. In this review, we consider the evidence that changes to fibroblast metabolic state underpin chronic inflammation. We examine recent research on fibroblast metabolism in inflammatory microenvironments and consider their involvement in inflammation, providing insight into the role of fibroblasts and metabolism in mediating inflammatory disease progression namely cancer, arthritis and fibrotic disorders including chronic kidney disease, pulmonary fibrosis, heart disease and liver disease.
间充质基质成纤维细胞已成为炎症反应和局部炎症的关键介质,部分原因是它们在炎症部位与常驻和循环免疫细胞相互作用。因此,它们被认为与许多慢性炎症疾病以及肿瘤进展有关,通过改变微环境。代谢变化与炎症微环境中成纤维细胞表型改变之间的联系,对我们理解慢性炎症的调控以及开发新的抗炎治疗方法具有明确的意义。在这篇综述中,我们考虑了纤维化代谢状态改变为慢性炎症提供基础的证据。我们研究了炎症微环境中成纤维细胞代谢的最新研究,并考虑了它们在炎症中的参与,深入了解了成纤维细胞和代谢在介导炎症性疾病进展(即癌症、关节炎和纤维化疾病,包括慢性肾病、肺纤维化、心脏病和肝病)中的作用。