Gene expression profiling during differentiation of human monocytes to macrophages or dendritic cells

被引:126
作者
Lehtonen, Anne
Ahlfors, Helena
Veckman, Ville
Miettinen, Minja
Lahesmaa, Riitta
Julkunen, Ilkka
机构
[1] Natl Publ Hlth Inst, Dept Viral Dis & Immunol, FI-00300 Helsinki, Finland
[2] Univ Turku, Turku Ctr Biotechnol, Turku, Finland
[3] Abo Akad Univ, Turku, Finland
关键词
microarray; GM-CSF; IL-4; WNT5A;
D O I
10.1189/jlb.0307194
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Macrophages and dendritic cells (DC) are APC, which regulate innate and adaptive immune responses. Macrophages function locally mainly, maintaining inflammatory responses in tissues, whereas DC take up microbes, mature, and migrate to local lymph nodes to present microbial antigens to naive T cells to elicit microbe-specific immune responses. Blood monocytes can be differentiated in vitro to macrophages or DC by GM-CSF or GM-CSF + IL-4, respectively. In the present study, we performed global gene expression analyses using Affymetrix HG-U133A Gene Chip oligonucleotide arrays during macrophage and DC differentiation. During the differentiation process, 340 and 350 genes were up-regulated, and 190 and 240 genes were down-regulated in macrophages and DC, respectively. There were also more that 200 genes, which were expressed differentially in fully differentiated macrophages and DC. Macrophage-specific genes include, e. g., CD14, CD163, C5R1, and Fc gamma R1A, and several cell surface adhesion molecules, cytokine receptors, WNT5A and its receptor of the Frizzled family FZD2, fibronectin, and Fc gamma R1A were identified as DC-specific. Our results reveal significant differences in gene expression profiles between macrophages and DC, and these differences can partially explain the functional differences between these two important cell types.
引用
收藏
页码:710 / 720
页数:11
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