首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Low T cell receptor expression and thermal fluctuations contribute to formation of dynamic multifocal synapses in thymocytes.
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Low T cell receptor expression and thermal fluctuations contribute to formation of dynamic multifocal synapses in thymocytes.

机译:低T细胞受体表达和热波动有助于在胸腺细胞中形成动态多灶突触。

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摘要

Mature T cell activation and selection of immature T cells (thymocytes) are both initiated by binding of T cell receptor (TCR) molecules on the surface of T cells to MHC peptide (MHCp) molecules on the surface of antigen-presenting cells. Recent experiments have shown that the spatial pattern of receptors and ligands in the intercellular junction (synapse) is different during thymocyte selection compared with mature T cell activation. Using a statistical mechanical model, we show that lower TCR expression in thymocytes contributes to effecting these differences. An analogy with the phase behavior of simple fluids helps clarify how, for low TCR expression, thermal fluctuations lead to the dynamic synapse patterns observed for thymocytes. We suggest that a different synapse pattern resulting from lower TCR expression, which could mediate differential signaling, may be the reason why TCR expression level is low in thymocytes.
机译:成熟的T细胞激活和未成熟T细胞(胸腺细胞)的选择均通过T细胞表面的T细胞受体(TCR)分子与抗原呈递细胞表面的MHC肽(MHCp)分子结合而开始。最近的实验表明,与成熟的T细胞活化相比,在胸腺细胞选择过程中,细胞间连接(突触)中受体和配体的空间模式不同。使用统计力学模型,我们显示胸腺细胞中较低的TCR表达有助于实现这些差异。与简单流体的相行为的类比有助于阐明,对于低TCR表达,热波动如何导致观察到的胸腺细胞动态突触模式。我们建议由较低的TCR表达导致的不同突触模式,这可能介导差异信号传导,这可能是胸腺细胞中TCR表达水平较低的原因。

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