成纤维细胞
ETS1型
兰克尔
生物
细胞生物学
癌症研究
转录因子
炎症
表型
激活剂(遗传学)
免疫学
病理
医学
遗传学
受体
细胞培养
基因
作者
Minglu Yan,Noriko Komatsu,Ryunosuke Muro,Nam Cong‐Nhat Huynh,Yoshihiko Tomofuji,Yukinori Okada,Hiroshi Suzuki,Hiroyuki Takaba,Riko Kitazawa,Sohei Kitazawa,Warunee Pluemsakunthai,Yuichi Mitsui,Takashi Satoh,Tadashi Okamura,Takeshi Nitta,Sin‐Hyeog Im,Chan Johng Kim,George Kollias,Sakae Tanaka,Kazuo Okamoto
出处
期刊:Nature Immunology
[Nature Portfolio]
日期:2022-08-23
卷期号:23 (9): 1330-1341
被引量:37
标识
DOI:10.1038/s41590-022-01285-0
摘要
Fibroblasts, the most abundant structural cells, exert homeostatic functions but also drive disease pathogenesis. Single-cell technologies have illuminated the shared characteristics of pathogenic fibroblasts in multiple diseases including autoimmune arthritis, cancer and inflammatory colitis. However, the molecular mechanisms underlying the disease-associated fibroblast phenotypes remain largely unclear. Here, we identify ETS1 as the key transcription factor governing the pathological tissue-remodeling programs in fibroblasts. In arthritis, ETS1 drives polarization toward tissue-destructive fibroblasts by orchestrating hitherto undescribed regulatory elements of the osteoclast differentiation factor receptor activator of nuclear factor-κB ligand (RANKL) as well as matrix metalloproteinases. Fibroblast-specific ETS1 deletion resulted in ameliorated bone and cartilage damage under arthritic conditions without affecting the inflammation level. Cross-tissue fibroblast single-cell data analyses and genetic loss-of-function experiments lent support to the notion that ETS1 defines the perturbation-specific fibroblasts shared among various disease settings. These findings provide a mechanistic basis for pathogenic fibroblast polarization and have important therapeutic implications.
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