单克隆抗体
中性粒细胞胞外陷阱
免疫荧光
细胞质
化学
细胞外
分子生物学
单克隆
生物
抗体
生物化学
遗传学
免疫学
炎症
作者
Lívia P. Mendes,Kobra Rostamizadeh,Kandace Gollomp,Jacob W. Myerson,Oscar A. Marcos‐Contreras,Marco E. Zamora,Ed Luther,Jacob S. Brenner,Nina Filipczak,Xiang Li,Vladimir P. Torchilin
出处
期刊:mAbs
[Landes Bioscience]
日期:2020-01-01
卷期号:12 (1)
被引量:8
标识
DOI:10.1080/19420862.2020.1850394
摘要
Neutrophils can release DNA and granular cytoplasmic proteins that form smooth filaments of stacked nucleosomes (NS). These structures, called neutrophil extracellular traps (NETs), are involved in multiple pathological processes, and NET formation and removal are clinically significant. The monoclonal antibody 2C5 has strong specificity toward intact NS but not to individual NS components, indicating that 2C5 could potentially target NS in NETs. In this study, NETs were generated in vitro using neutrophils and HL-60 cells differentiated into granulocyte-like cells. The specificity of 2C5 toward NETs was evaluated by ELISA, which showed that it binds to NETs with the specificity similar to that for purified nucleohistone substrate. Immunofluorescence showed that 2C5 stains NETs in both static and perfused microfluidic cell cultures, even after NET compaction. Modification of liposomes with 2C5 dramatically enhanced liposome association with NETs. Our results suggest that 2C5 could be used to identify and visualize NETs and serve as a ligand for NET-targeted diagnostics and therapies.
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