Does CD40 ligation induce B cell negative selection?

被引:6
作者
Martínez-Barnetche, J
Madrid-Marina, V
Flavell, RA
Moreno, J
机构
[1] Inst Mexicano Seguro Social, Ctr Med Nacl XXI, Autoimmune Dis Res Unit, Mexico City 03020, DF, Mexico
[2] Inst Nacl Salud Publ, Ctr Res Infect Dis, Dept Mol Virol, Cuernavaca, Morelos, Mexico
[3] Yale Univ, Sch Med, Immunobiol Sect, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
D O I
10.4049/jimmunol.168.3.1042
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Binding of CD154 to its receptor, CD40, provides costimulation for mature B cell activation and differentiation in response to Ag receptor signals. In mice, early B cell precursors express CD40, but its function at this stage is unknown. We examined the effects of CD40 ligation during B cell ontogeny in transgenic mice constitutively expressing CD154 on B cells (kappaEP-CD154). Precursors beyond pro-B cells were absent in adult bone marrow but were increased in the fetal liver. Newborn kappaEP-CD154 mice had largely increased numbers of peripheral B cells,which were CD154(+), and that 36 h after birth expressed high surface levels of CD23 and MHC class II, resembling activated mature B cells. Nevertheless, kappaEP-CD154 mice were hypogammaglobulinemic, indicating that the expanded population of apparently activated B cells was nonfunctional. Further analysis revealed that soon after birth, kappaEP-CD154 mice-derived B cells became CD5(+)/Fas(+), after which progressively decreased in the periphery in a CD154-CD40-dependent manner. These results indicate that CD40 ligation during B cell ontogeny induces negative selection characterized by either hyporesponsiveness or an arrest in maturation depending on the time of analysis and the anatomic site studied.
引用
收藏
页码:1042 / 1049
页数:8
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