Cutting edge:: Distinct motifs within CD28 regulate T cell proliferation and induction of Bcl-XL

被引:126
作者
Burr, JS
Savage, NDL
Messah, GE
Kimzey, SL
Shaw, AS
Arch, RH
Green, JM
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
D O I
10.4049/jimmunol.166.9.5331
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD28 provides an important costimulatory signal in T cell activation that regulates multiple cellular processes including proliferation and survival. Several signal transduction pathways are activated by CD28; however, the precise biochemical mechanism by which CD28 regulates T cell function remains controversial. Retroviral gene transfer into primary T cells from TCR-transgenic, CD28-deficient mice was used to determine the specific sequences within CD28 that determine function. Discrete regions of the cytoplasmic domain of CD28 were identified that differentially regulate T cell proliferation and induction of the anti-apoptotic protein Bcl-X-L, Mutation of C-terminal proline residues abrogated the proliferative and cytokine regulatory features of CD28 costimulation while preserving Bcl-X-L induction. Conversely, mutation of residues important in phosphatidylinositol 3-kinase activation partially inhibited proliferation but prevented induction of Bcl-X-L. Thus the ability of CD28 to regulate proliferation and induction of Bcl-X-L map to distinct motifs, suggesting independent signaling cascades modulate these biologic effects.
引用
收藏
页码:5331 / 5335
页数:5
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