首页> 外文会议>International conference on Artificial immune systems(ICARIS 2007); 20070826-29; Santos(BR) >Modeling Migration, Compartmentalization and Exit of Naive T Cells in Lymph Nodes Without Chemotaxis
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Modeling Migration, Compartmentalization and Exit of Naive T Cells in Lymph Nodes Without Chemotaxis

机译:在没有趋化性的淋巴结中模拟幼稚T细胞的迁移,分隔和退出

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The migration of lymphocytes through secondary lymphoid organs was believed to be mainly controlled by chemokine gradients. This theory has recently been called into question since na?ve lymphocytes observed in vivo by two-photon microscopy show no evidence of directed migration. We have constructed a simple mathematical model of na?ve T cell migration in lymph nodes that is solely based on local mechanisms. The model was validated against findings from histological analysis and experimentally determined lymphocyte recirculation kinetics. Our results suggest that T cell compartmentalization in lymph nodes can be explained without long-range chemokine gradients. However, the T cell residence time predicted by our model is significantly lower than observed in vivo, indicating the existence of a mechanism which alters the T cell random walk over time.
机译:据信淋巴细胞通过次要淋巴器官的迁移主要受趋化因子梯度控制。该理论最近受到质疑,因为通过双光子显微镜在体内观察到的幼稚淋巴细胞没有显示出定向迁移的证据。我们已经建立了一个简单的单纯T细胞在淋巴结中迁移的数学模型,该模型仅基于局部机制。根据组织学分析结果和实验确定的淋巴细胞再循环动力学对模型进行验证。我们的结果表明,无需长期趋化因子梯度就可以解释淋巴结中的T细胞区室化。但是,我们的模型预测的T细胞停留时间显着低于体内观察到的时间,这表明存在着随时间改变T细胞随机游走的机制。

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