生物
造血
细胞生物学
祖细胞
树突状细胞
干细胞
获得性免疫系统
单核吞噬细胞系统
受体酪氨酸激酶
人口
免疫学
信号转导
免疫系统
社会学
人口学
作者
Pierre Guermonprez,Yohan Gerber-Ferder,Kristīne Vaivode,Pierre Bourdely,Julie Helft
标识
DOI:10.1016/bs.ircmb.2019.08.002
摘要
Classical dendritic cells (cDCs) are mononuclear phagocytes of hematopoietic origin specialized in the induction and regulation of adaptive immunity. Initially defined by their unique T cell activation potential, it became quickly apparent that cDCs would be difficult to distinguish from other phagocyte lineages, by solely relying on marker-based approaches. Today, cDCs definition increasingly embed their unique ontogenetic features. A growing consensus defines cDCs on multiple criteria including: (1) dependency on the fms-like tyrosine kinase 3 ligand hematopoietic growth factor, (2) development from the common DC bone marrow progenitor, (3) constitutive expression of the transcription factor ZBTB46 and (4) the ability to induce, after adequate stimulation, the activation of naïve T lymphocytes. cDCs are a heterogeneous cell population that contains two main subsets, named type 1 and type 2 cDCs, arising from divergent ontogenetic pathways and populating multiple lymphoid and non-lymphoid tissues. Here, we present recent knowledge on the cellular and molecular pathways controlling the specification and commitment of cDC subsets from murine and human hematopoietic stem cells.
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