Lehtonen Anne, Ahlfors Helena, Veckman Ville, Miettinen Minja, Lahesmaa Riitta, Julkunen Ilkka
Department of Viral Diseases and Immunology, National Public Health Institute, Mannerheimintie 166, FI-00300 Helsinki, Finland.
J Leukoc Biol. 2007 Sep;82(3):710-20. doi: 10.1189/jlb.0307194. Epub 2007 Jun 26.
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 naïve 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 FcgammaR1A, and several cell surface adhesion molecules, cytokine receptors, WNT5A and its receptor of the Frizzled family FZD2, fibronectin, and FcepsilonR1A 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.
巨噬细胞和树突状细胞(DC)是抗原呈递细胞(APC),它们调节先天性和适应性免疫反应。巨噬细胞主要在局部发挥作用,维持组织中的炎症反应,而DC摄取微生物,成熟并迁移至局部淋巴结,将微生物抗原呈递给幼稚T细胞以引发针对微生物的特异性免疫反应。血液单核细胞可分别通过粒细胞巨噬细胞集落刺激因子(GM-CSF)或GM-CSF +白细胞介素-4(IL-4)在体外分化为巨噬细胞或DC。在本研究中,我们在巨噬细胞和DC分化过程中使用Affymetrix HG-U133A基因芯片寡核苷酸阵列进行了全基因组表达分析。在分化过程中,巨噬细胞和DC中分别有340和350个基因上调,190和240个基因下调。在完全分化的巨噬细胞和DC中也有200多个基因差异表达。巨噬细胞特异性基因包括例如CD14、CD163、C5R1和FcγR1A,并且几种细胞表面粘附分子、细胞因子受体、WNT5A及其卷曲蛋白家族FZD2的受体、纤连蛋白和FcεR1A被鉴定为DC特异性。我们的结果揭示了巨噬细胞和DC之间基因表达谱的显著差异,这些差异可以部分解释这两种重要细胞类型之间的功能差异。