The colony-stimulating factor 1 receptor is expressed on dendritic cells during differentiation and regulates their expansion

被引:151
作者
MacDonald, KPA
Rowe, V
Bofinger, HM
Thomas, R
Sasmono, T
Hume, DA
Hill, GR
机构
[1] Queensland Inst Med Res, Bone Marrow Transplantat Lab, Herston, Qld 4006, Australia
[2] Univ Queensland, Princess Alexandra Hosp, Ctr Immunol & Canc Res, Woolloongabba, Qld, Australia
[3] Univ Queensland, Cooperat Res Ctr Chron Inflammatory Dis, Inst Mol Biosci, Woolloongabba, Qld, Australia
[4] Univ Queensland, Australian Res Council, Special Res Ctr Funct Appl Genom, Inst Mol Biosci, Woolloongabba, Qld, Australia
基金
英国惠康基金;
关键词
D O I
10.4049/jimmunol.175.3.1399
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 lineage of dendritic cells (DC), and in particular their relationship to monocytes and macrophages, remains obscure. Furthermore, the requirement for the macrophage growth factor CSF-1 during DC homeostasis is unclear. Using a transgenic mouse in which the promoter for the CSF-1R (c-fms) directs the expression of enhanced GFP in cells of the myeloid lineage, we determined that although the c-fms promoter is inactive in DC precursors, it is up-regulated in all DC subsets during differentiation. Furthermore, plasmacytoid DC and all CD11c(high) DC subsets are reduced by 50-70% in CSF-1-deficient osteopetrotic mice, confirming that CSF-1 signaling is required for the optimal differentiation of DC in vivo. These data provide additional evidence that the majority of tissue DC is of myeloid origin during steady state and supports a close relationship between DC and macrophage biology in vivo.
引用
收藏
页码:1399 / 1405
页数:7
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