Macrophage microvesicles induce macrophage differentiation and miR-223 transfer

被引:432
作者
Ismail, Noura [1 ,2 ]
Wang, Yijie [1 ]
Dakhlallah, Duaa [1 ,2 ]
Moldovan, Leni [1 ]
Agarwal, Kitty [3 ,4 ]
Batte, Kara [1 ]
Shah, Prexy [1 ]
Wisler, Jon [5 ]
Eubank, Tim D. [1 ]
Tridandapani, Susheela [1 ]
Paulaitis, Michael E. [6 ]
Piper, Melissa G. [1 ]
Marsh, Clay B. [1 ,2 ]
机构
[1] Ohio State Univ, Davis Heart & Lung Res Inst, Div Pulm Allergy Crit Care & Sleep Med, Columbus, OH 43210 USA
[2] Ohio State Univ, Dev Biol Program, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Chem, Columbus, OH 43210 USA
[4] Ohio State Univ, Nanoscale Sci & Engn Ctr Affordable Nanoengn Poly, Columbus, OH 43210 USA
[5] Ohio State Univ, Coll Med, Dept Surg, Columbus, OH 43210 USA
[6] Ohio State Univ, William G Lowrie Dept Chem & Biomol Engn, Columbus, OH 43210 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
MESSENGER-RNA; CIRCULATING MICRORNAS; ACTIVATED PLATELETS; MEDIATED TRANSFER; CELLS; MICROPARTICLES; EXPRESSION; MECHANISM; EXOSOMES; BIOMARKERS;
D O I
10.1182/blood-2011-08-374793
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Microvesicles are small membrane-bound particles comprised of exosomes and various-sized extracellular vesicles. These are released by several cell types. Microvesicles have a variety of cellular functions from communication to mediating growth and differentiation. Microvesicles contain proteins and nucleic acids. Previously, we showed that plasma microvesicles contain microRNAs (miRNAs). Based on our previous report, the majority of peripheral blood microvesicles are derived from platelets, while mononuclear phagocytes, including macrophages, are the second most abundant population. Here, we characterized macrophage-derived microvesicles and explored their role in the differentiation of naive monocytes. We also identified the miRNA content of the macrophage-derived microvesicles. We found that RNA molecules contained in the macrophage-derived microvesicles were transported to target cells, including monocytes, endothelial cells, epithelial cells, and fibroblasts. Furthermore, we found that miR-223 was transported to target cells and was functionally active. Based on our observations, we hypothesize that microvesicles bind to and activate target cells. Furthermore, we find that microvesicles induce the differentiation of macrophages. Thus, defining key components of this response may identify novel targets to regulate host defense and inflammation. (Blood. 2013;121(6):984-995)
引用
收藏
页码:984 / 995
页数:12
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