免疫学
生物
单核细胞
骨髓
免疫系统
MHC II级
获得性免疫系统
抗原呈递
脾脏
细胞生物学
先天免疫系统
单核吞噬细胞系统
抗原提呈细胞
抗原
巨噬细胞
主要组织相容性复合体
T细胞
体外
遗传学
作者
Naoka Kamio,Asumi Yokota,Yuichi Tokuda,Chie Ogasawara,Masakazu Nakano,Miki Nagao,Kei Tashiro,Taira Maekawa,Nobuyuki Onai,Hideyo Hirai
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2022-08-01
卷期号:209 (3): 498-509
标识
DOI:10.4049/jimmunol.2100024
摘要
Abstract The mononuclear phagocyte system (MPS), composed of monocytes/macrophages and dendritic cells (DCs), plays a critical role at the interface of the innate and adaptive immune systems. However, the simplicity of MPS has been challenged recently by discoveries of novel cellular components. In the current study, we identified the CD135+ subset of monocytes as a novel class of APCs in mice. CD135+ monocytes were readily found in the bone marrow, spleen, and peripheral blood at steady state, and they expressed markers specific to DCs, including MHC class II and CD209a, along with markers for monocytes/macrophages. In addition, this subset phagocytosed bacteria and activated naive T lymphocytes, fulfilling the criteria for APCs. CD135+ monocytes were derived directly from macrophage DC progenitors, not from common monocyte progenitors or other monocytes, suggesting that these are distinct from conventional monocytes. These findings facilitate our understanding of the MPS network that regulates immune responses for host defense.
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