Weill Cornell/Rockefeller/Sloan-Kettering Tri-Institutional MD-PhD Program, New York, NY 10065, USA; Autoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA.
Autoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA.
Curr Opin Immunol. 2020 Jun;64:63-70. doi: 10.1016/j.coi.2020.03.002. Epub 2020 May 5.
The recent advent of single-cell technologies has fast-tracked the discovery of multiple fibroblast subsets in tissues affected by autoimmune disease. In recent years, interest in lymph node fibroblasts that support and regulate immune cells has also grown, leading to an expanding framework of stromal cell subsets with distinct spatial, transcriptional, and functional characteristics. Inflammation can drive tissue fibroblasts to adopt a lymphoid tissue stromal cell phenotype, suggesting that fibroblasts in diseased tissues can have counterparts in lymphoid tissues. Here, we examine fibroblast subsets in tissues affected by autoimmunity in the context of knowledge gained from studies on lymph node fibroblasts, with the ultimate aim to better understand stromal cell heterogeneity in these immunologically reactive tissues.
近年来,人们对支持和调节免疫细胞的淋巴结成纤维细胞也产生了兴趣,这导致了具有不同空间、转录和功能特征的基质细胞亚群的扩展框架。炎症可以促使组织成纤维细胞采用淋巴组织基质细胞表型,这表明病变组织中的成纤维细胞可以与淋巴组织中的成纤维细胞相对应。在这里,我们在淋巴结成纤维细胞研究中获得的知识的背景下,研究自身免疫性疾病相关组织中的成纤维细胞亚群,最终目的是更好地了解这些免疫反应性组织中的基质细胞异质性。