Fate mapping reveals origins and dynamics of monocytes and tissue macrophages under homeostasis.

Fate mapping reveals origins and dynamics of monocytes and tissue macrophages under homeostasis.
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DOI:
10.1016/j.immuni.2012.12.001
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发表时间:
2013-01-24
期刊:
影响因子:
32.4
通讯作者:
Jung S
Jung S
中科院分区:
医学1区
文献类型:
--
作者:
Yona S;Kim KW;Wolf Y;Mildner A;Varol D;Breker M;Strauss-Ayali D;Viukov S;Guilliams M;Misharin A;Hume DA;Perlman H;Malissen B;Zelzer E;Jung S

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Mononuclear phagocytes, including monocytes, macrophages and dendritic cells, contribute to tissue integrity, as well as innate and adaptive immune defense. Emerging evidence for labour division indicates that manipulation of these cells could bear therapeutic potential. However, specific ontogenies of individual populations and the overall functional organisation of the cellular network are not well-defined. Here we report a fate mapping study of the murine monocyte and macrophage compartment taking advantage of constitutive and conditional CX3CR1 promoter-driven Cre recombinase expression. We have demonstrated that major tissue resident macrophage populations, including liver Kupffer cells, lung alveolar, splenic and peritoneal macrophages, are established prior to birth and maintain themselves subsequently during adulthood independent of replenishment by blood monocytes. Furthermore, we have established that the short-lived Ly6C+ monocytes constitute obligatory steady state precursors of blood-resident Ly6C− cells and that the abundance of Ly6C+ blood monocytes dynamically controls the circulation life span of their progeny.
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