细胞毒性T细胞
生物
CD8型
细胞生物学
白细胞介素21
白细胞介素2受体
受体
免疫系统
细胞因子
ZAP70型
T细胞
免疫学
体外
生物化学
作者
Dmytro Shytikov,Deepak Rohila,Dan Li,Pengfei Wang,Mei Jiang,Mingxu Zhang,Qin Xu,Linrong Lu
标识
DOI:10.3389/fimmu.2020.602783
摘要
The role of Ly49 + CD8 T-cells in the immune system is not clear. Previously, several papers suggested Ly49 + CD8 T-cells as immunosuppressors, while multiple studies also suggested their role as potent participants of the immune response. The mechanism of Ly49 expression on CD8 T-cells is also not clear. We investigated phenotype, functions, and regulation of Ly49 expression on murine CD8 T-cells in both normal state and during LCMV infection. CD8 T-cells express different Ly49 receptors compared with NK-cells. In intact mice, Ly49 + CD8 T-cells have a phenotype similar to resting central memory CD8 T-cells and do not show impaired proliferation and cytokine production. Conventional CD8 T-cells upregulate Ly49 receptors during TCR-induced stimulation, and IL-2, as well as IL-15, affect it. At the same time, Ly49 + CD8 T-cells change the Ly49 expression profile dramatically upon re-stimulation downregulating inhibitory and upregulating activating Ly49 receptors. We observed the expression of Ly49 receptors on the virus-specific CD8 T-cells during LCMV infection, especially marked in the early stages, and participation of Ly49 + CD8 T-cells in the anti-viral response. Thus, CD8 T-cells acquire Ly49 receptors during the T-cell activation and show dynamic regulation of Ly49 receptors during stimulation.
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