IL-34 is a tissue-restricted ligand of CSF1R required for the development of Langerhans cells and microglia

被引:706
作者
Wang, Yaming [1 ]
Szretter, Kristy J. [1 ,2 ,3 ]
Vermi, William [1 ,4 ]
Gilfillan, Susan [1 ]
Rossini, Cristina [4 ]
Cella, Marina [1 ]
Barrow, Alexander D. [1 ,5 ]
Diamond, Michael S. [1 ,2 ,3 ]
Colonna, Marco [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[4] Univ Brescia, Dept Pathol, Brescia, Italy
[5] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
基金
美国国家卫生研究院;
关键词
COLONY-STIMULATING-FACTOR; LANGERIN(+) DENDRITIC CELLS; STEADY-STATE; MYELOID CELLS; FACTOR-I; T-CELLS; IDENTIFICATION; MONOCYTES; RECEPTOR; SKIN;
D O I
10.1038/ni.2360
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The differentiation of bone marrow-derived progenitor cells into monocytes, tissue macrophages and some dendritic cell (DC) subtypes requires the growth factor CSF1 and its receptor, CSF1R. Langerhans cells (LCs) and microglia develop from embryonic myeloid precursor cells that populate the epidermis and central nervous system (CNS) before birth. Notably, LCs and microglia are present in CSF1-deficient mice but absent from CSF1R-deficient mice. Here we investigated whether an alternative CSF1R ligand, interleukin 34 (IL-34), is responsible for this discrepancy. Through the use of IL-34-deficient (Il34(LacZ/LacZ)) reporter mice, we found that keratinocytes and neurons were the main sources of IL-34. Il34(LacZ/LacZ) mice selectively lacked LCs and microglia and responded poorly to skin antigens and viral infection of the CNS. Thus, IL-34 specifically directs the differentiation of myeloid cells in the skin epidermis and CNS.
引用
收藏
页码:753 / +
页数:10
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