在人子宫内膜细胞中可视化表达荧光蛋白的X4和R5嗜性HIV-1病毒:在嗜性研究中的应用。

Visualization of X4- and R5-Tropic HIV-1 Viruses Expressing Fluorescent Proteins in Human Endometrial Cells: Application to Tropism Study.

作者信息

Terrasse Rachel, Memmi Meriam, Palle Sabine, Heyndrickx Leo, Vanham Guido, Pozzetto Bruno, Bourlet Thomas

机构信息

Groupe Immunité des Muqueuses et Agents Pathogènes EA3064, University of Lyon, Faculté de Médecine Jacques Lisfranc de Saint-Etienne, Saint-Etienne cedex 02, France.

Centre de Microscopie Confocale Multiphotonique, Université Jean Monnet, Pôle Optique et Vision, Saint-Etienne cedex 2, France.

出版信息

PLoS One. 2017 Jan 6;12(1):e0169453. doi: 10.1371/journal.pone.0169453. eCollection 2017.

Abstract

Worldwide most HIV infections occur through heterosexual transmission, involving complex interactions of cell-free and cell-associated particles with cells of the female genital tract mucosa. The ability of HIV-1 to "infect" epithelial cells remains poorly understood. To address this question, replicative-competent chimeric constructs expressing fluorescent proteins and harboring the envelope of X4- or R5-tropic HIV-1 strains were used to "infect" endometrial HEC1-A cells. The virus-cell interactions were visualized using confocal microscopy (CM) at various times post infection. Combined with quantification of viral RNA and total HIV DNA in infected cells, the CM pictures suggest that epithelial cells do not support a complete viral replication cycle: X4-tropic viruses are imported into the nucleus in a non-productive way, whereas R5-tropic viruses transit through the cytoplasm without replication and are preferentially transmitted to susceptible activated peripheral blood mononuclear cells. Within the limit of experiments conducted in vitro on a continued cell line, these results indicate that the epithelial mucosa may participate to the selection of HIV-1 strains at the mucosal level.

摘要

在全球范围内,大多数HIV感染是通过异性传播发生的,这涉及游离病毒颗粒和细胞相关颗粒与女性生殖道黏膜细胞的复杂相互作用。HIV-1 “感染” 上皮细胞的能力仍知之甚少。为了解决这个问题,研究人员使用了表达荧光蛋白并携带X4或R5嗜性HIV-1毒株包膜的具有复制能力的嵌合构建体来 “感染” 子宫内膜HEC1-A细胞。在感染后的不同时间,使用共聚焦显微镜(CM)观察病毒与细胞的相互作用。结合对感染细胞中病毒RNA和总HIV DNA的定量分析,CM图像表明上皮细胞不支持完整的病毒复制周期:X4嗜性病毒以非生产性方式导入细胞核,而R5嗜性病毒在不复制的情况下穿过细胞质,并优先传播给易感的活化外周血单核细胞。在对连续细胞系进行的体外实验范围内,这些结果表明上皮黏膜可能在黏膜水平参与HIV-1毒株的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aba/5218496/a196fc73b399/pone.0169453.g001.jpg

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