SuperSAGE evidence for CD14++CD16+ monocytes as a third monocyte subset

被引:433
作者
Zawada, Adam M. [1 ]
Rogacev, Kyrill S. [1 ]
Rotter, Bjoern [2 ]
Winter, Peter [2 ]
Marell, Rolf-R. [3 ]
Fliser, Danilo [1 ]
Heine, Gunnar H. [1 ]
机构
[1] Saarland Univ Hosp, Dept Internal Med 4, Hamburg, Germany
[2] GenXPro GmbH, Frankfurt, Germany
[3] Inst Immunol & Genet, Kaiserslautern, Germany
关键词
PREFERENTIALLY HARBORS HIV-1; GENE-EXPRESSION PROFILES; HUMAN PERIPHERAL-BLOOD; CD16(+) MONOCYTES; DIALYSIS PATIENTS; DISEASE; SUBPOPULATIONS; INFECTION; ANGIOPOIETIN-2; IDENTIFICATION;
D O I
10.1182/blood-2011-01-326827
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Monocytes are a heterogeneous cell population with subset-specific functions and phenotypes. The differential expression of CD14 and CD16 distinguishes classical CD14(++)CD16(-), intermediate CD14(++)CD16(+), and nonclassical CD14(+)CD16(++) monocytes. Current knowledge on human monocyte heterogeneity is still incomplete: while it is increasingly acknowledged that CD14(++)CD16(+) monocytes are of outstanding significance in 2 global health issues, namely HIV-1 infection and atherosclerosis, CD14(++)CD16(+) monocytes remain the most poorly characterized subset so far. We therefore developed a method to purify the 3 monocyte subsets from human blood and analyzed their transcriptomes using SuperSAGE in combination with high-throughput sequencing. Analysis of 5 487 603 tags revealed unique identifiers of CD14(++)CD16(+) monocytes, delineating these cells from the 2 other monocyte subsets. Gene Ontology (GO) enrichment analysis suggests diverse immunologic functions, linking CD14(++)CD16(+) monocytes to Ag processing and presentation (eg, CD74, HLA-DR, IFI30, CTSB), to inflammation and monocyte activation (eg, TGFB1, AIF1, PTPN6), and to angiogenesis (eg, TIE2, CD105). In conclusion, we provide genetic evidence for a distinct role of CD14(++)CD16(+) monocytes in human immunity. After CD14(++)CD16(+) monocytes have earlier been discussed as a potential therapeutic target in inflammatory diseases, we are hopeful that our data will spur further research in the field of monocyte heterogeneity. (Blood. 2011;118(12):e50-e61)
引用
收藏
页码:E50 / E61
页数:12
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