作者
Daniel P Gold, Jennifer M Puck, Carolyn L Pettey, Mildred Cho, John Coligan, James N Woody, Cox Terhorst
发表日期
1986/5/22
期刊
Nature
卷号
321
期号
6068
页码范围
431-434
出版商
Nature Publishing Group UK
简介
The antigen receptor on human T lymphocytes consists of two variable immunoglobulin-like glycoproteins, α and β, which occur in association with three invariable T3 membrane proteins1–3. In humans two of these proteins, T3-γ and T3-δ, are glycoproteins of relative molecular mass (Mr) 25,000 (25K) and 20,000 (20K), respectively, while the third, T3-ε, is a 20K non-glycosylated protein4–6. On the surface of murine T cells, a non-glycosylated protein dimer composed of 17K subunits (T3-ζ) is found associated with the T-cell receptor α and β chains and the three T3-like polypeptide chains7,8. It is generally accepted that major histocompatibility complex-restricted antigen recognition is a function of the αβ heterodimer. This has led to the postulation that the proteins of the T3 complex are involved in the signal transduction that immediately follows antigen recognition via the antigen receptor9. Events believed to be …
引用总数
19851986198719881989199019911992199319941995199619971998199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020211727271617154156447252123311411412321