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本文引用的文献

1
Transcriptional profiling reveals developmental relationship and distinct biological functions of CD16+ and CD16- monocyte subsets.转录谱分析揭示了CD16 +和CD16 -单核细胞亚群的发育关系及不同生物学功能。
BMC Genomics. 2009 Aug 27;10:403. doi: 10.1186/1471-2164-10-403.
2
Fcgamma receptor-dependent expansion of a hyperactive monocyte subset in lupus-prone mice.狼疮易感小鼠中Fcγ受体依赖性高活性单核细胞亚群的扩增
Arthritis Rheum. 2009 Aug;60(8):2408-17. doi: 10.1002/art.24787.
3
Identification of splenic reservoir monocytes and their deployment to inflammatory sites.脾脏储备单核细胞的鉴定及其向炎症部位的募集
Science. 2009 Jul 31;325(5940):612-6. doi: 10.1126/science.1175202.
4
Identification of novel functional differences in monocyte subsets using proteomic and transcriptomic methods.运用蛋白质组学和转录组学方法鉴定单核细胞亚群中的新型功能差异。
J Proteome Res. 2009 Aug;8(8):4028-38. doi: 10.1021/pr900364p.
5
Monocyte subset dynamics in human atherosclerosis can be profiled with magnetic nano-sensors.人类动脉粥样硬化中的单核细胞亚群动态可通过磁性纳米传感器进行分析。
PLoS One. 2009 May 22;4(5):e5663. doi: 10.1371/journal.pone.0005663.
6
Functional role of CD11c+ monocytes in atherogenesis associated with hypercholesterolemia.CD11c⁺单核细胞在高胆固醇血症相关动脉粥样硬化形成中的功能作用。
Circulation. 2009 May 26;119(20):2708-17. doi: 10.1161/CIRCULATIONAHA.108.823740. Epub 2009 May 11.
7
Ly6C(low) monocytes differentiate into dendritic cells and cross-tolerize T cells through PDL-1.Ly6C(低表达)单核细胞分化为树突状细胞,并通过程序性死亡配体-1(PDL-1)诱导T细胞产生交叉耐受。
J Immunol. 2009 Mar 1;182(5):2777-85. doi: 10.4049/jimmunol.0803172.
8
Antibody to Langerin/CD207 localizes large numbers of CD8alpha+ dendritic cells to the marginal zone of mouse spleen.抗朗格汉斯蛋白/CD207抗体将大量CD8α⁺树突状细胞定位到小鼠脾脏的边缘区。
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9
A new triggering receptor expressed on myeloid cells (Trem) family member, Trem-like 4, binds to dead cells and is a DNAX activation protein 12-linked marker for subsets of mouse macrophages and dendritic cells.髓样细胞表达的一种新的触发受体(Trem)家族成员,即类Trem 4,可与死亡细胞结合,并且是小鼠巨噬细胞和树突状细胞亚群的与DNAX激活蛋白12相关的标志物。
J Immunol. 2009 Feb 1;182(3):1278-86. doi: 10.4049/jimmunol.182.3.1278.
10
Lymphotoxin beta receptor signaling promotes tertiary lymphoid organogenesis in the aorta adventitia of aged ApoE-/- mice.淋巴毒素β受体信号传导促进衰老的载脂蛋白E基因敲除(ApoE-/-)小鼠主动脉外膜中的三级淋巴器官生成。
J Exp Med. 2009 Jan 16;206(1):233-48. doi: 10.1084/jem.20080752. Epub 2009 Jan 12.

人源和鼠源单核细胞亚群基因表达谱的比较。

Comparison of gene expression profiles between human and mouse monocyte subsets.

机构信息

Department of Gene and Cell Medicine and Immunology Institute, Mount Sinai School of Medicine, New York, NY, USA.

出版信息

Blood. 2010 Jan 21;115(3):e10-9. doi: 10.1182/blood-2009-07-235028. Epub 2009 Nov 12.

DOI:10.1182/blood-2009-07-235028
PMID:19965649
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2810986/
Abstract

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.

摘要

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。