Activation and function of murine primary microglia in the absence of the prion protein

被引:9
作者
Pinheiro, Livia P. [1 ]
Linden, Rafael [1 ]
Mariante, Rafael M. [1 ,2 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Biophys, Rio De Janeiro, Brazil
[2] Fiocruz MS, Inst Oswaldo Cruz, Lab Biol Estrutural, BR-43652104 Rio De Janeiro, RJ, Brazil
关键词
Prion protein; Microglia; Inflammation; Cytokine; Phagocytosis; Cell migration; ALPHA SIRP-ALPHA; NITRIC-OXIDE; CELL-LINES; KAPPA-B; EXPRESSION; PHAGOCYTOSIS; PRP; INFLAMMATION; MACROPHAGES; CLEARANCE;
D O I
10.1016/j.jneuroim.2015.07.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The prion protein (PrPc) is predominantly expressed in the nervous and immune systems and is involved in relevant cell signaling. Microglia participate in neuroimmune interactions, and their regulatory mechanisms are critical for both health and disease. Despite recent reports with a microglial cell line, little is known about the relevance of PrPc in brain microglia. We investigated the role of PrPc in mouse primary microglia, and found no differences between wild type and Prop-null cells in cell morphology or the expression of a microglial marker. Translocation of NF-kappa B to the nucleus also did not differ, nor did cytokine production. The levels of iNOS were also similar and, finally, microglia of either genotype showed no differences in either rates of phagocytosis or migration, even following activation. Thus, functional roles of PrPc in primary microglial cells are if present much more subtle than in transformed microglial cell lines. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 32
页数:8
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