Distribution and characterization of tumor-associated macrophages/microglia in rat C6 glioma

被引:10
|
作者
Zhang, Zhi-Ming [1 ]
Yang, Zicheng [2 ]
Zhang, Zhiren [2 ]
机构
[1] Shunde Polytech, Dept Med, Foshan 528300, Guangdong, Peoples R China
[2] Third Mil Med Univ Peoples Liberat Army, Inst Immunol, Chongqing 400038, Peoples R China
关键词
glioblastoma; microglia; macrophages; endothelial monocyte-activating polypeptide II; CD68; CD8; MONOCYTE CHEMOATTRACTANT PROTEIN-1; TRAUMATIC BRAIN-INJURY; CENTRAL-NERVOUS-SYSTEM; EMAP-II; MICROGLIA; CELLS; EXPRESSION; CD8; IMMUNOTHERAPY; INFILTRATION;
D O I
10.3892/ol.2015.3533
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunity responses and immunotherapy are novel areas of research for the pathological development and treatment of glioma, the most common brain cancer. Characterization of the subpopulations of infiltrated immune cells may aid in our understanding of the tumor immune response and contribute to the identification of cellular targets for selective immunotherapy. Using a rat C6 glioma model, the present study observed a significant heterogeneity of active macrophages and microglia, including cluster of differentiation 8 (CD8)(+), endothelial monocyte-activating polypeptide II (EMAPII)(+) and EDP cells, mostly in the areas of compact tumor growth and inside or around the pannecrosis. Moreover, the CD8(+) cells were similar to reactive ED1(+) and EMAPII(+) microglia/macrophages in morphology and distribution, but different from the W3/13(+) T cells. These observations suggest that different subtypes of macrophages and microglia are involved in glioma development and thus, may be potential targets for immunotherapeutic antitumor strategies.
引用
收藏
页码:2442 / 2446
页数:5
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