| Literature DB >> 28801233 |
Myriam Baratin1, Léa Simon2, Audrey Jorquera2, Clément Ghigo2, Doulaye Dembele3, Jonathan Nowak2, Rebecca Gentek2, Stephan Wienert4, Frederick Klauschen4, Bernard Malissen2, Marc Dalod2, Marc Bajénoff5.
Abstract
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.Entities:
Keywords: dendritic cell; efferocytosis; lymph node; macrophage
Mesh:
Substances:
Year: 2017 PMID: 28801233 DOI: 10.1016/j.immuni.2017.07.019
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745