The expression of complement regulatory proteins by adult human oligodendrocytes

被引:58
作者
Scolding, NJ
Morgan, BP
Compston, DAS
机构
[1] Univ Cambridge, Addenbrookes Hosp, Neurol Unit, Cambridge CB2 2QQ, England
[2] MRC, Cambridge Ctr Brain Repair, Cambridge CB2 2SR, England
[3] Univ Wales Coll Med, Dept Med Biochem, Cardiff CF4 4XN, S Glam, Wales
基金
英国医学研究理事会;
关键词
demyelinating disease; CD59; glia;
D O I
10.1016/S0165-5728(97)00241-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In multiple sclerosis, infiltrating T lymphocytes and perivascular microglia may initiate demyelinating lesions, but a role for antibody and complement in the ensuing inflammatory damage to myelin and oligodendrocytes is likely. In most tissues, ubiquitously expressed complement regulatory proteins prevent autologous destruction, protecting host cells from the powerful cytolytic activity of activated complement. We have studied the surface expression of a comprehensive range of complement regulatory proteins by live adult human oligodendrocytes in vitro. Only DAF of the activation pathway regulators was expressed, not CR1 or MCP. Of the membrane attack pathway regulatory proteins, HRF was not expressed, while substantial heterogeneity of CD59 expression by oligodendrocytes was found. Clusterin expression was not found. A relative deficiency of protective complement regulatory proteins on human oligodendrocytes may contribute to their selective damage in multiple sclerosis. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:69 / 75
页数:7
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