T细胞受体
等位基因排除
CD3型
生物
细胞生物学
受体
T细胞
信号转导
免疫球蛋白结构域
分子生物学
CD8型
抗原
遗传学
免疫系统
作者
Harald von Boehmer,Iannis Aifantis,Orly Azogui,Claude Saint‐Ruf,Fabio Grassi
出处
期刊:Cold Spring Harbor Symposia on Quantitative Biology
[Cold Spring Harbor Laboratory]
日期:1999-01-01
卷期号:64: 283-290
被引量:33
标识
DOI:10.1101/sqb.1999.64.283
摘要
The pre-T-cell receptor (pre-TCR), which is composedof the pre-TCR-α (pTα) and TCR-β chains, is the first receptor in the development of αβ T cells that associateswith signal-transducing CD3 molecules and mediates themost effective entry into the αβ lineage. The pre-TCR,which signals via a signaling cascade similar to that of theαβ TCR, is also absolutely essential for TCRβ allelic exclusion, even though signals that determine entry into theCD4+8+ compartment of thymocytes and that mediate allelic exclusion bifurcate below the adapter protein SLP76. The pre-TCR takes away from the γδ-lineage cellswith productive TCRβ rearrangements and may thus instruct entry into the αβ lineage. It is mostly, if not exclusively, expressed on the surface of developing thymocytes as a heterodimer, utilizing the long pTα form withone extracellular immunoglobulin (Ig)-like domain.Some experiments suggest that the pre-TCR spontaneously localizes together with glycolipid-enrichedmembrane domains and may signal in a cell-autonomousfashion without binding to a ligand. Thus, the pre-TCRαprotein may not represent a mere TCRα surrogate chain,but a protein that in association with the TCRβ chain actsas a cell-autonomous developmental switch...
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