Characteristics of ?dTCR on myeloid cells from C57BL/6 mice with Plasmodium yoelii nigeriensis infection

MOLECULAR AND BIOCHEMICAL PARASITOLOGY(2023)

引用 0|浏览6
暂无评分
摘要
Recently, there is a paucity of studies focus on the characteristics of myeloid cells which expressed ?dTCR. The aim of this study was to observe the properties of ?dTCR-expressing myeloid cells in the spleen of C57BL/6 mice infected by P. yoelii nigeriensis NSM. Haematoxylin-eosin (HE) staining was used to observe pathological changes in the spleens from infected mice. The differentially expressed genes (DEGs) between the infection and control groups were analyzed by RNA sequencing (RNA -seq). Flow cytometry (FCM) was used to evaluate the frequency of ?dTCR+ cells and the characteristics of ?8TCR(+) cells in P. yoelii nigeriensis NSM-infected mice. Obvious infiltration of inflammatory were observed in the spleens from infected C57BL/6 mouse. The proportions of ?dTCR(+) cells and CD11b(+) ?dTCR+ cells from infected group were higher than that from normal group. CD11b(+) ?dTCR(+) cells expressed high levels of activated-mediated genes and inflammatory-mediated genes. The heterogeneous pathway activities among CD11b(+) ?dTCR(+) cells from normal and infected group were characterized. The oxidative phosphorylation, respiratory electron transport chain and leukocyte activation involved in immune response pathways were up-regulated, while the alpha-beta T cell activation and myeloid leukocyte migration pathways were down-regulated in infected mice. Importantly, Ly6c2 was higher expressed in CD11b(+) ?dTCR(+) cells than Ly6g. Consistent with it, flow cytometry results revealed that a subset of Ly6C(+) cells was higher than Ly6G(+) cells in the spleen. Taken together, our data suggest the existence of a population of ?dTCR-expressing myeloid cells and they might be multifunctional cells, which play a role in couse of Plasmodium infection.
更多
查看译文
关键词
Plasmodium yoelii nigeriensis, CD11b (+)?8TCR (+) cells, Pathways
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要