Transgenic expression of Fas in T cells blocks lymphoproliferation but not autoimmune disease in MRL-lpr mice

被引:0
|
作者
Fukuyama, H
Adachi, M
Suematsu, S
Miwa, K
Suda, T
Yoshida, N
Nagata, S
机构
[1] Osaka Univ, Sch Med, Dept Genet, Suita, Osaka 565, Japan
[2] Osaka Med Ctr Maternal & Child Hlth, Osaka, Japan
[3] Osaka Biosci Inst, Suita, Osaka 565, Japan
来源
JOURNAL OF IMMUNOLOGY | 1998年 / 160卷 / 08期
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fas is a member of the TNF receptor family, Binding of Fas ligand to Fas induces apoptosis in Fas-bearing cells. Fas is expressed in various cells, including thymocytes, peripheral T cells, and activated B cells, The mouse lr mutation is a loss of function mutation of Fas, MRL-lpr/lpr mice develop lymphadenopathy and spIenomegaly, and produce multiple autoantibodies, which results in autoimmune disease. In this report, we describe the establishment of a line of Fas transgenic MRL-lpr mice in which mouse Fas cDNA was expressed using the T cell-specific murine lck promoter, The transgenic mice expressed functional Fas in thymocytes and peripheral T cells, but not in B cells, The transgenic mice did not accumulate abnormal T cells (Thy-1(+) B220(+)), but still accumulated B cells (Thy-1(-) B220(+)); they produced a large quantity of Igs (IgG1 and IgG2a), including anti-DNA Abs, and developed glomerulonephritis. These results suggest that autoreactice or activated B cells must be killed through Fas expressed in the B cells by the Fas ligand expressed in activated T cells.
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页码:3805 / 3811
页数:7
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