Viard Mathias, Parolini Isabella, Rawat Satinder S, Fecchi Katia, Sargiacomo Massimo, Puri Anu, Blumenthal Robert
Laboratory of Experimental and Computational Biology, Center for Cancer Research, National Cancer Institute-Frederick, National Institutes of Health, Frederick, MD, USA.
Glycoconj J. 2004;20(3):213-22. doi: 10.1023/B:GLYC.0000024253.48791.d9.
Although HIV uses CD4 and coreceptors (CCR5 and CXCR4) for productive infection of T cells, glycosphingolipids (GSL) may play ancillary roles in lymphoid and non-lymphoid cells. Interactions of the HIV Envelope Glycoprotein (Env) with GSL may help HIV in various steps of its pathogenesis. Physical-chemical aspects of the interactions between HIV Env and GSL leading to CD4-dependent entry into lymphocytes, the role of GSL in HIV transcytosis, and CD4-independent entry into non-lymphoid cells are reviewed. An overview of signaling properties of HIV receptors is provided with some speculation on how GSL may play a role in these events by virtue of being in membrane rafts. Finally, we summarize how interactions between HIV and coreceptors leading to signaling and/or fusion can be analyzed by the use of various tyrosine kinase and cytoskeletal inhibitors.
尽管HIV利用CD4和共受体(CCR5和CXCR4)对T细胞进行有效感染,但糖鞘脂(GSL)可能在淋巴细胞和非淋巴细胞中发挥辅助作用。HIV包膜糖蛋白(Env)与GSL的相互作用可能在HIV发病机制的各个步骤中发挥作用。本文综述了HIV Env与GSL相互作用的物理化学方面,这些相互作用导致HIV依赖CD4进入淋巴细胞、GSL在HIV转胞吞作用中的作用以及HIV不依赖CD4进入非淋巴细胞的过程。本文还概述了HIV受体的信号特性,并推测了GSL如何通过存在于膜筏中在这些事件中发挥作用。最后,我们总结了如何通过使用各种酪氨酸激酶和细胞骨架抑制剂来分析HIV与共受体之间导致信号传导和/或融合的相互作用。