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Inhibitory and Regulatory Immune Synapses
被引:19
|作者:
Eissmann, Philipp
[1
]
Davis, Daniel M.
[1
]
机构:
[1] Univ London Imperial Coll Sci Technol & Med, Div Cell & Mol Biol, London SW7 2AZ, England
来源:
基金:
英国惠康基金;
英国生物技术与生命科学研究理事会;
英国医学研究理事会;
关键词:
NATURAL-KILLER-CELLS;
IG-LIKE RECEPTORS;
ACTIVATED NK CELLS;
IMMUNOLOGICAL SYNAPSE;
T-CELLS;
DENDRITIC CELLS;
LIPID RAFTS;
TARGET-CELLS;
CROSS-TALK;
PHOSPHATIDYLINOSITOL;
3-KINASE;
D O I:
10.1007/978-3-642-03858-7_4
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Cell contact-dependent inhibition and regulation of immune responses play an essential role in balancing the need for rapid and efficient responses to a wide variety of pathological challenges, while at the same time maintaining self-tolerance. Much attention has been given to immune synapses that lead to the activation of, for example, cell-mediated cytotoxicity, and here we compare the supramolecular dynamics of synapses that lead to inhibition or regulatory functions. We focus on natural killer cells where such different synapses have been best studied. An emergent principle is that inhibition or regulatory responses are commonly achieved by selective recruitment of signalling proteins to the synapse and exclusion of membrane-proximal intracellular proteins needed for activation. We also discuss evidence that an inhibitory synapse triggers or maintains effector cells in a migratory configuration, which serves to break the synapse before the steps needed for effector cell activation can be completed. This model implies that the concept of kinetic-proofreading, previously used to describe activation of individual T-cell receptors, can also apply in determining the outcome of intercellular conjugation.
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页码:63 / 79
页数:17
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