Department of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Singapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Nat Rev Immunol. 2021 Feb;21(2):101-115. doi: 10.1038/s41577-020-00413-x. Epub 2020 Sep 9.
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.
树突状细胞(DCs)由造血祖细胞在骨髓中发育而来,这些祖细胞在小鼠和人类之间具有许多共同特征。通过其共享的转录特征和发育潜能,已经鉴定出人类与小鼠 DC 祖细胞相对应的细胞。新的发现不断修正 DC 发生的模型,但人们普遍认为 DC 可以分为两个主要的功能群。经典的 DC 包括 1 型和 2 型亚群,它们可以检测不同的病原体,产生特定的细胞因子,并将抗原呈递给主要的幼稚 CD8 或 CD4 T 细胞,分别。相比之下,浆细胞样 DC 的功能主要是先天的,局限于检测病毒感染和产生 I 型干扰素。在这里,我们讨论了小鼠 DC 发育和功能的遗传模型,这些模型有助于将发生与功能相关联,以及如何将这些发现转化为人类 DC 及其祖细胞。