A critical role for the cytoplasmic tail of pTα in T lymphocyte development

被引:70
作者
Aifantis, I
Borowski, C
Gounari, F
Lacorazza, HD
Nikolich-Zugich, J
von Boehmer, H
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, Lab Mol Aspects Hematopoiesis, New York, NY 10021 USA
[3] Vaccine & Gene Therapy Inst, Beaverton, OR 97006 USA
关键词
D O I
10.1038/ni779
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Signals that emanate from the pre-T cell receptor (pre-TCR) regulate multiple processes required for the development of the alphabeta T cell lineage. In contrast to the gammadelta TCR, the pre-TCR localizes cellautonomously to membrane rafts, where it appears to signal in a constitutive and ligand-independent manner.We addressed here the role played by structural features specific to the cytoplasmic domain of the pre-TCRalpha chain (pTalpha). More specifically, we examined a COON-terminal proline-rich sequence that might play a role in signal transduction and a juxtamembrane cysteine residue that could be a target for palmitoylation, thus allowing spontaneous raft localization. Expression of pTalpha mutants in transgenic mice, retrovirally transduced T cell precursors and cell lines showed that the pTalpha cytoplasmic tail, in particular the proline-rich domain, plays a crucial role in pre-TCR signaling and T cell development. In contrast, the pTalpha juxtamembrane cysteine appeared to be dispensable for pre-TCR function.
引用
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页码:483 / 488
页数:6
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