生物
处置模式
淋巴结
吞噬作用
细胞生物学
免疫学
淋巴
癌症研究
细胞
细胞凋亡
病理
遗传学
医学
计算机科学
程序设计语言
作者
Myriam Baratin,Léa Simon,Audrey Jorquera,Clément Ghigo,Doulaye Dembélé,Jonathan A. Nowak,Rebecca Gentek,Stephan Wienert,Frederick Klauschen,Bernard Malissen,Marc Dalod,Marc Bajénoff
出处
期刊:Immunity
[Cell Press]
日期:2017-08-01
卷期号:47 (2): 349-362.e5
被引量:116
标识
DOI:10.1016/j.immuni.2017.07.019
摘要
Summary In lymph nodes (LNs), dendritic cells (DCs) are thought to dispose of apoptotic cells, a function pertaining to macrophages in other tissues. We found that a population of CX3CR1 + MERTK + cells located in the T cell zone of LNs, previously identified as DCs, are efferocytic macrophages. Lineage-tracing experiments and shield chimeras indicated that these T zone macrophages (TZM) are long-lived macrophages seeded in utero and slowly replaced by blood monocytes after birth. Imaging the LNs of mice in which TZM and DCs express different fluorescent proteins revealed that TZM—and not DCs—act as the only professional scavengers, clearing apoptotic cells in the LN T cell zone in a CX3CR1-dependent manner. Furthermore, similar to other macrophages, TZM appear inefficient in priming CD4 T cells. Thus, efferocytosis and T cell activation in the LN are uncoupled processes designated to macrophages and DCs, respectively, with implications to the maintenance of immune homeostasis.
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