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In vivo imaging of virological synapses

机译:病毒突触的体内成像

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Retroviruses such as the human immunodeficiency virus, human T-cell lymphotropic virus and murine leukaemia virus are believed to spread via sites of cell–cell contact designated virological synapses. Support for this model is based on in vitro evidence in which infected cells are observed to specifically establish long-lived cell–cell contact with uninfected cells. Whether virological synapses exist in vivo is unknown. Here we apply intravital microscopy to identify a subpopulation of B cells infected with the Friend murine leukaemia virus that form virological synapses with uninfected leucocytes in the lymph node of living mice. In vivo virological synapses are, like their in vitro counterpart, dependent on the expression of the viral envelope glycoprotein and are characterized by a prolonged polarization of viral capsid to the cell–cell interface. Our results validate the concept of virological synapses and introduce intravital imaging as a tool to visualize retroviral spreading directly in living mice.
机译:诸如人类免疫缺陷病毒,人类T细胞淋巴病毒和鼠白血病病毒等逆转录病毒被认为是通过指定的病毒突触与细胞接触的部位传播的。该模型的支持基于体外证据,其中观察到感染的细胞与未感染的细胞特别建立了长寿命的细胞-细胞接触。体内是否存在病毒突触尚不清楚。在这里,我们应用活体显微镜检查来确定感染了Friend鼠白血病病毒的B细胞的亚群,后者在活小鼠的淋巴结中与未感染的白细胞形成病毒突触。体内病毒学突触像它们在体外的突触一样,取决于病毒包膜糖蛋白的表达,其特征是病毒衣壳向细胞-细胞界面的极化延长。我们的结果验证了病毒突触的概念,并引入了活体成像作为直接可视化逆转录病毒在活小鼠中传播的工具。

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