脂肪组织
CCL5
干细胞
白色脂肪组织
炎症
细胞生物学
肿瘤坏死因子α
趋化因子
脂肪组织巨噬细胞
内科学
内分泌学
生物
医学
T细胞
癌症研究
免疫学
免疫系统
白细胞介素2受体
作者
Xiyan Liao,Qin Zeng,Limin Xie,Haowei Zhang,Wanyu Hu,Liuling Xiao,Hui Zhou,Fanqi Wang,Wanqin Xie,Jianfeng Song,Xiaoxiao Sun,Dandan Wang,Yujin Ding,Yuanyuan Jiao,Wuqian Mai,Wufuer Aini,Xiaoyan Hui,Wei Liu,Willa A. Hsueh,Tuo Deng
出处
期刊:Cell Reports
[Elsevier]
日期:2024-03-01
卷期号:43 (3): 113963-113963
被引量:1
标识
DOI:10.1016/j.celrep.2024.113963
摘要
Summary
T cell infiltration into white adipose tissue (WAT) drives obesity-induced adipose inflammation, but the mechanisms of obesity-induced T cell infiltration into WAT remain unclear. Our single-cell RNA sequencing reveals a significant impact of adipose stem cells (ASCs) on T cells. Transplanting ASCs from obese mice into WAT enhances T cell accumulation. C-C motif chemokine ligand 5 (CCL5) is upregulated in ASCs as early as 4 weeks of high-fat diet feeding, coinciding with the onset of T cell infiltration into WAT during obesity. ASCs and bone marrow transplantation experiments demonstrate that CCL5 from ASCs plays a crucial role in T cell accumulation during obesity. The production of CCL5 in ASCs is induced by tumor necrosis factor alpha via the nuclear factor κB pathway. Overall, our findings underscore the pivotal role of ASCs in regulating T cell accumulation in WAT during the early phases of obesity, emphasizing their importance in modulating adaptive immunity in obesity-induced adipose inflammation.
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