生物
造血
祖细胞
功能(生物学)
个体发育
CD8型
免疫学
细胞生物学
骨髓
干扰素
树突状细胞
抗原
浆细胞样树突状细胞
干细胞
遗传学
作者
David A. Anderson,Charles–Antoine Dutertre,Florent Ginhoux,Kenneth M. Murphy
出处
期刊:Nature Reviews Immunology
[Springer Nature]
日期:2020-09-09
卷期号:21 (2): 101-115
被引量:148
标识
DOI:10.1038/s41577-020-00413-x
摘要
Dendritic cells (DCs) develop in the bone marrow from haematopoietic progenitors that have numerous shared characteristics between mice and humans. Human counterparts of mouse DC progenitors have been identified by their shared transcriptional signatures and developmental potential. New findings continue to revise models of DC ontogeny but it is well accepted that DCs can be divided into two main functional groups. Classical DCs include type 1 and type 2 subsets, which can detect different pathogens, produce specific cytokines and present antigens to polarize mainly naive CD8+ or CD4+ T cells, respectively. By contrast, the function of plasmacytoid DCs is largely innate and restricted to the detection of viral infections and the production of type I interferon. Here, we discuss genetic models of mouse DC development and function that have aided in correlating ontogeny with function, as well as how these findings can be translated to human DCs and their progenitors.
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