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Resolving T cell — T cell transfer of HIV-1 by optical nanoscopy

机译:通过光学纳米技术解决T细胞转移-HIV-1的T细胞转移

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Summary form only given. The Acquired Immune Deficiency Syndrome (AIDS) is caused by the Human Immunodeficiency Virus (HIV). A thorough understanding of the infection on a cellular level is important for the development of new classes of therapeutics or vaccines to combat this virus. HIV can enter CD4+ T cells either as a cell-free virus or by direct cell-cell transmission. An infected T cell can engage in a virus dependent adhesive structure with an uninfected CD4 + T cell, called the Virological Synapse (VS), where virus assembly occurs preferentially within a spatially narrowly confined region and where newly synthesized virus is endocytosed by the target cell. This process occurs on a small spatial scale, while the cells are highly polarized and motile [1, 2]. Resolving the viral transfer involves optical nanoscopy methods that can follow this process with high resolution and high speed. Our method of choice is super-resolved Structured Illumination Microscopy (SRSIM) which provides double the resolution compared to conventional microscopy and has the ability to simultaneously acquire fast, super-resolved three-dimensional images, with multiple colors. [3]. Therefore, the simultaneous observation of several components of the infection process is possible.
机译:仅提供摘要表格。获得性免疫缺陷综合症(AIDS)是由人类免疫缺陷病毒(HIV)引起的。在细胞水平上对感染的透彻了解对于开发新型抗击这种病毒的疗法或疫苗很重要。 HIV可以作为无细胞病毒或通过直接的细胞间传播进入CD4 + T细胞。被感染的T细胞可以与未感染的CD4 + T细胞(称为病毒突触(VS))发生病毒依赖性的粘连结构,其中病毒装配优先在空间狭窄的区域内发生,新合成的病毒被靶细胞内吞。该过程在较小的空间尺度上发生,而细胞高度极化且能活动[1,2]。解决病毒转移涉及光学纳米技术方法,该方法可以高分辨率和高速地遵循该过程。我们选择的方法是超分辨结构照明显微镜(SRSIM),其分辨率是传统显微镜的两倍,并且能够同时获取多种颜色的快速,超分辨三维图像。 [3]。因此,可以同时观察感染过程的几个组成部分。

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