Division of Medical Research Support, Advanced Research Support Center, Ehime University, Ehime, Japan.
Division of Integrative Pathophysiology, Proteo-Science Center, Ehime University, Ehime, Japan.
Histol Histopathol. 2023 Nov;38(11):1231-1238. doi: 10.14670/HH-18-628. Epub 2023 May 12.
Rheumatoid arthritis (RA) is an autoimmune disease associated with chronic inflammation of joints. Abnormally activated cells such as synovial macrophages and synovial fibroblasts induce RA pathogenesis and ultimately joint destruction. Since macrophages can change their own characteristics depending on the microenvironmental condition, it has been suggested that activation and remission of RA are regulated by crosstalk between synovial macrophages and other cells. Moreover, recent findings of heterogeneity of synovial macrophages and fibroblasts support the idea that complex interactions regulate RA from its onset to remission. Importantly, an understanding of the intercellular crosstalk in RA is far from complete. Here, we summarize the molecular mechanisms underlying the pathological development of RA with particular reference to the crosstalk between synovial macrophages and fibroblasts.
类风湿关节炎(RA)是一种与关节慢性炎症相关的自身免疫性疾病。异常激活的细胞,如滑膜巨噬细胞和滑膜成纤维细胞,诱导 RA 的发病机制,并最终导致关节破坏。由于巨噬细胞可以根据微环境条件改变自身的特征,因此有人提出 RA 的激活和缓解是由滑膜巨噬细胞和其他细胞之间的串扰调节的。此外,最近发现滑膜巨噬细胞和成纤维细胞的异质性支持这样一种观点,即复杂的相互作用从 RA 的发病到缓解都在调节着它。重要的是,对 RA 中细胞间串扰的理解还远远不够。在这里,我们总结了 RA 病理发展的分子机制,特别提到了滑膜巨噬细胞和成纤维细胞之间的串扰。