| Literature DB >> 33488602 |
Dmytro Shytikov1, Deepak Rohila1, Dan Li1, Pengfei Wang1, Mei Jiang1, Mingxu Zhang2,3, Qin Xu3, Linrong Lu1,2,3.
Abstract
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.Entities:
Keywords: CD8 T-cells; Ly49 receptors; NK-cell receptors; anti-viral response; memory phenotype
Year: 2021 PMID: 33488602 PMCID: PMC7817614 DOI: 10.3389/fimmu.2020.602783
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561