The Role of Co-receptors in T-cell Actin Barrier Evasion during HIV Entry

描述（由申请人提供）：最近的研究表明，人类免疫缺陷病毒（HIV）能够感染静息T细胞，这些细胞大量存在于宿主体内，通常对病毒具有相当的抵抗力。这种抗性至少部分是由靠近T细胞细胞膜的一层厚的基于肌动蛋白的细胞骨架提供的，这层骨架通常阻止病毒颗粒与宿主细胞完全融合，并将病毒基因组传递到细胞中。然而，病毒偶尔能够通过启动绕过这种防御

DESCRIPTION (provided by applicant): Recent research has shown that the human immunodeficiency virus (HIV) is able to infect resting T cells, which are present in large number in the host and generally quite resistant to the virus. This resistance is at least partially provied by a thick layer of actin-based cytoskeleton near the T cell's plasma membrane that usually prevents the viral particles from fully fusing with the host cell and delivering the viral genome into the cell. However, viruses are able to occasionally circumvent this defense through initiation of a cellular signaling cascade that activates the cell's own actin-regulating enzymes to weaken the cytoskeleton layer. The goal of this project is to (1) find exactly which of these enzymes HIV uses to weaken the T cell's actin layer and (2) determine the order that each enzyme is recruited to the site of HIV entry. This knowledge is the foundation that is needed to enable future work on finding a way to strengthen the T cells' own defense as a new type of HIV/AIDS inhibition. To obtain this information, T-cell derived laboratory cell lines and primary T cells wil be imaged with super-resolution fluorescence microscopy. Various cellular proteins that are known or proposed to be involved with the signaling process that HIV uses to dismantle the actin barrier to entry will be labeled with fluorescent tags. The localization of these tagged proteins will be watched in live cells and determined with high resolution using advanced single- molecule based particle tracking and super-resolution imaging techniques.