Minimal differentiation of classical monocytes as they survey steady-state tissues and transport antigen to lymph nodes.

Minimal differentiation of classical monocytes as they survey steady-state tissues and transport antigen to lymph nodes.
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DOI:
10.1016/j.immuni.2013.08.007
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发表时间:
2013-09-19
期刊:
影响因子:
32.4
通讯作者:
Randolph GJ
Randolph GJ
中科院分区:
医学1区
文献类型:
--
作者:
Jakubzick C;Gautier EL;Gibbings SL;Sojka DK;Schlitzer A;Johnson TE;Ivanov S;Duan Q;Bala S;Condon T;van Rooijen N;Grainger JR;Belkaid Y;Ma'ayan A;Riches DW;Yokoyama WM;Ginhoux F;Henson PM;Randolph GJ

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It is thought that monocytes rapidly differentiate to macrophages or dendritic cells (DCs) upon leaving blood. Here we have shown that Ly-6C+ monocytes constitutively trafficked into skin, lung, and lymph nodes (LNs). Entry was unaffected in gnotobiotic mice. Monocytes in resting lung and LN had similar gene expression profiles to blood monocytes, but elevated transcripts of a limited number of genes including cyclo-oxygenase-2 (COX-2) and major histocompatibility complex class II (MHC II), induced by monocyte interaction with endothelium. Parabiosis, bromodoxyuridine (BrdU) pulse-chase analysis, and intranasal instillation of tracers indicated that instead of contributing to resident macrophages in the lung, recruited endogenous monocytes acquired antigen for carriage to draining LNs, a function redundant with DCs though differentiation to DCs did not occur. Thus, monocytes can enter steady state non-lymphoid organs and recirculate to LNs without differentiation to macrophages or DCs, revising a long-held view that monocytes become tissue-resident macrophages by default.
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