Department of Gene and Cell Medicine and Immunology Institute, Mount Sinai School of Medicine, New York, NY, USA.
Blood. 2010 Jan 21;115(3):e10-9. doi: 10.1182/blood-2009-07-235028. Epub 2009 Nov 12.
Blood of both humans and mice contains 2 main monocyte subsets. Here, we investigated the extent of their similarity using a microarray approach. Approximately 270 genes in humans and 550 genes in mice were differentially expressed between subsets by 2-fold or more. More than 130 of these gene expression differences were conserved between mouse and human monocyte subsets. We confirmed numerous of these differences at the cell surface protein level. Despite overall conservation, some molecules were conversely expressed between the 2 species' subsets, including CD36, CD9, and TREM-1. Other differences included a prominent peroxisome proliferator-activated receptor gamma (PPARgamma) signature in mouse monocytes, which is absent in humans, and strikingly opposed patterns of receptors involved in uptake of apoptotic cells and other phagocytic cargo between human and mouse monocyte subsets. Thus, whereas human and mouse monocyte subsets are far more broadly conserved than currently recognized, important differences between the species deserve consideration when models of human disease are studied in mice.
人类和小鼠的血液中都含有 2 种主要的单核细胞亚群。在这里,我们使用微阵列方法研究了它们的相似程度。人类单核细胞亚群之间有 2 倍或更多的差异表达约 270 个基因,而小鼠则有 550 个基因。这些基因表达差异中有 130 多个在人和小鼠单核细胞亚群之间是保守的。我们在细胞表面蛋白水平上证实了许多这样的差异。尽管整体上存在保守性,但在这两个物种的亚群之间,一些分子的表达是相反的,包括 CD36、CD9 和 TREM-1。其他差异包括在小鼠单核细胞中存在明显的过氧化物酶体增殖物激活受体 γ (PPARγ) 特征,而在人类中则不存在,并且在人类和小鼠单核细胞亚群之间参与摄取凋亡细胞和其他吞噬性货物的受体模式存在显著差异。因此,尽管人类和小鼠单核细胞亚群比目前认识到的更为广泛保守,但在研究小鼠的人类疾病模型时,应该考虑到物种之间的重要差异。