Granulocyte-macrophage colony-stimulating factor induces an expression program in neonatal microglia that primes them for antigen presentation

被引:83
作者
Re, FB
Belyanskaya, SL
Riese, RJ
Cipriani, B
Fischer, FR
Granucci, F
Ricciardi-Castagnoli, P
Brosman, C
Stern, LJ
Strominger, JL
Santambrogio, L
机构
[1] Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] MIT, Dept Chem, Cambridge, MA 02139 USA
[5] Univ Milano Bicocca, Dept Biosci & Biotechnol, I-20126 Milan, Italy
[6] Univ Giessen, Dept Neurol, Giessen, Germany
[7] Yeshiva Univ Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
关键词
D O I
10.4049/jimmunol.169.5.2264
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neonatal microglial cells respond to GM-CSF and M-CSF by acquiring different morphologies and phenotypes. To investigate the extent and consequences of this process, a global gene expression analysis was performed, with significant changes in transcript levels confirmed by biochemical analyses. Primary murine microglial cells underwent substantial expression reprogramming after treatment with GM-CSF or M-CSF with many differentially expressed transcripts important in innate and adaptive immunity. In particular, many gene products involved in Ag presentation were induced by GM-CSF, but not M-CSF, thus potentially priming relatively quiescent microglia cells for Ag presentation. This function of GM-CSF is distinct from its primary function in cell proliferation and survival.
引用
收藏
页码:2264 / 2273
页数:10
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