The Strength of T Cell Receptor Signal Controls the Polarization of Cytotoxic Machinery to the Immunological Synapse

被引:130
作者
Jenkins, Misty R. [1 ]
Tsun, Andy [1 ]
Stinchcombe, Jane C. [1 ]
Griffiths, Gillian M. [1 ]
机构
[1] Addenbrookes Hosp, Cambridge Inst Med Res, Cambridge CB2 0XY, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
MICROTUBULE-ORGANIZING CENTER; ALTERED PEPTIDE LIGANDS; SECRETORY LYSOSOMES; POSITIVE SELECTION; ANTIGEN RECEPTOR; ACTIVATION; TCR; CTL; PHOSPHORYLATION; CYTOSKELETON;
D O I
10.1016/j.immuni.2009.08.024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Killing by cytotoxic T lymphocytes (CTLs) is mediated by the secretion of lytic granules. The centrosome plays a key role in granule delivery, polarizing to the central supramolecular activation complex (cSMAC) within the immunological synapse upon T cell receptor (TCR) activation. Although stronger TCR signals lead to increased target cell death than do weaker signals, it is not known how the strength of TCR signal controls polarization of the centrosome and lytic granules. By using TCR transgenic OT-I CTLs, we showed that both high- and low-avidity interactions led to centrosome polarization to the cSMAC. However, only high-avidity interactions, which induced a higher threshold of intracellular signaling, gave rise to granule recruitment to the polarized centrosome at the synapse. By controlling centrosome and granule polarization independently, the centrosome is able to respond rapidly to weak signals so that CTLs are poised and ready for the trigger for granule delivery.
引用
收藏
页码:621 / 631
页数:11
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