T-cell costimulatory molecules B7-1 (CD80) and B7-2 (CD86) are expressed in human microglia but not in astrocytes in culture

被引:110
|
作者
Satoh, J
Lee, YB
Kim, SU
机构
[1] UNIV BRITISH COLUMBIA,VANCOUVER HOSP,DEPT MED,DIV NEUROL,VANCOUVER,BC V6T 2B5,CANADA
[2] UNIV BRITISH COLUMBIA,CTR HLTH SCI,VANCOUVER,BC V6T 2B5,CANADA
基金
英国医学研究理事会;
关键词
antigen-presenting cell; B7-1; B7-2; costimulatory molecule; human astrocyte; human microglia;
D O I
10.1016/0006-8993(95)01177-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The B7-1 and B7-2 expressed on the 'professional' antigen-presenting cells (APC) of the lymphoid system are counterreceptors for the T cell antigens CD28/CTLA-4. The B7/CD28 interaction provides a critical costimulatory signal in the decision between functional activation or clonal anergy of T cells. To investigate the biological role of B7 in the central nervous system, constitutive and cytokine-induced expression of B7 was investigated in fetal human astrocytes and microglia in culture. B7-1 expression was minimally detectable in unstimulated microglia but was increased markedly following exposure to IFN-gamma or GM-CSF. B7-2 was expressed at a high level in untreated microglia and upregulated to a small degree by exposure to IFN-gamma or GM-CSF. In contrast, B7-1 and B7-2 were undetectable in astrocytes under unstimulated or IFN-gamma/GM-CSF-treated conditions. These results indicate that both B7-1 and B7-2 are expressed in cultured human microglia but not in astrocytes.
引用
收藏
页码:92 / 96
页数:5
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