CD8型
质量细胞仪
生物
细胞毒性T细胞
流式细胞术
自身免疫性肝炎
T细胞
免疫系统
分子生物学
细胞
免疫学
细胞生物学
基因
肝炎
生物化学
表型
体外
作者
Yuting He,Mingjie Ding,Jiakai Zhang,Changjun Huang,Jihua Shi,Yun Wang,Ruolin Tao,Zeyu Wu,Wenzhi Guo
标识
DOI:10.1002/advs.202403148
摘要
Abstract Astaxanthin (ASX) is an oxygen‐containing non‐vitamin A carotenoid pigment. However, the role of ASX in autoimmune hepatitis (AIH) remains unclear. In this study, a mouse model of AIH is established induced by concanavalin A (ConA). Mass cytometry and single‐cell RNA sequencing (scRNA‐seq) are used to analyze the potential role of ASX in regulating the immune microenvironment of AIH. ASX treatment effectively alleviated liver damage induced by ConA and downregulated pro‐inflammatory cytokines production in mice. Mass cytometry and scRNA‐seq analyses revealed a significant increase in the number of CD8 + T cells following ASX treatment. Functional markers of CD8 + T cells, such as CD69, MHC II, and PD‐1, are significantly downregulated. Additionally, specific CD8 + T cell subclusters (subclusters 4, 13, 24, and 27) are identified, each displaying distinct changes in marker gene expression after ASX treatment. This finding suggests a modulation of CD8 + T cell function by ASX. Finally, the key transcription factors for four subclusters of CD8 + T cells are predicted and constructed a cell‐to‐cell communication network based on receptor‐ligand interactions probability. In conclusion, ASX holds the potential to ameliorate liver damage by regulating the number and function of CD8 + T cells.
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