CD8 binding to MHC class I molecules is influenced by maturation and T cell glycosylation

被引:158
作者
Daniels, MA
Levine, L
Miller, JD
Moser, JM
Lukacher, AE
Altman, JD
Kavathas, P
Hogquist, KA
Jameson, SC [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Lab Med & Pathol, Ctr Immunol, Minneapolis, MN 55455 USA
[2] Yale Univ, Sch Med, Dept Lab Med, Immunobiol Sect, New Haven, CT 06520 USA
[3] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[5] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
关键词
D O I
10.1016/S1074-7613(01)00252-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8 serves both as an adhesion molecule for class I MHC molecules and as a coreceptor with the TCR for T cell activation. Here we study the developmental regulation of CD8-mediated binding to noncognate peptide/MHC ligands (i.e., those not bound by the TCR). We show that CD8's ability to bind soluble class I MHC tetramers and to mediate T cell adhesion under shear flow conditions diminishes as double-positive thymocytes mature into CD8(+) T cells. Furthermore, we provide evidence that this decreased CD8 binding results from increased T cell sialylation upon T cell maturation. These data suggest that CD8's ability to interact with class I MHC is not fixed and is developmentally regulated through the T cell's glycosylation state.
引用
收藏
页码:1051 / 1061
页数:11
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