Self-reactive B lymphocytes overexpressing Bcl-xL escape negative selection and are tolerized by clonal anergy and receptor editing

被引:100
作者
Fang, W
Weintraub, BC
Dunlap, B
Garside, P
Pape, KA
Jenkins, MK
Goodnow, CC
Mueller, DL
Behrens, TW [1 ]
机构
[1] Univ Minnesota, Sch Med, Ctr Immunol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[3] Australian Natl Univ, John Curtin Sch Med Res, Med Genome Ctr, Canberra, ACT 2601, Australia
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1074-7613(00)80586-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Self-reactive B cells Tg for both a bcl-x(L) death inhibitory gene and an Ig receptor recognizing hen egg lysozyme (HEL-Ig) efficiently escaped developmental arrest and deletion in mice expressing membrane-bound self-antigen (mHEL). In response to the same antigen, Tg HEL-Ig B cells not expressing bcl-x(L) were deleted, while cells expressing bcl-2 were arrested at the immature B stage. Bcl-x(L) Tg B cells escaping negative selection were anergic in both in vitro and in vivo assays and showed some evidence for receptor editing. These studies suggest that Bcl-x may have a distinct role in controlling survival at the immature stage of B cell development and demonstrate that tolerance is preserved when self-reactive B cells escape central deletion.
引用
收藏
页码:35 / 45
页数:11
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