Perotti M E, Tan X, Phillips D M
Department of General Physiology and Biochemistry, University of Milan, Italy.
J Virol. 1996 Sep;70(9):5916-21. doi: 10.1128/JVI.70.9.5916-5921.1996.
Time-lapse cinematography revealed that activated human immunodeficiency virus (HIV)-infected monocytes crawl along surfaces, putting forward a leading pseudopod. Scanning electron micrographs showed monocyte pseudopods associated with spherical structures the size of HIV virions, and transmission electron micrographs revealed HIV virions budding from pseudopods. Filamentous actin (F-actin) was localized by electron microscopy in the pseudopod by heavy meromyosin decoration. Colocalization of F-actin and p24 viral antigen by light microscopy immunofluorescence indicated that F-actin and virus were present on the same pseudopod. These observations indicate that monocytes produce virus from a leading pseudopod. We suggest that HIV secretion at the leading edges of donor monocytes/macrophages may be an efficient way for HIV to infect target cells.
延时摄影显示,被激活的人类免疫缺陷病毒(HIV)感染的单核细胞沿着表面爬行,伸出一个前端伪足。扫描电子显微镜图像显示单核细胞伪足与HIV病毒粒子大小的球形结构相关,而透射电子显微镜图像显示HIV病毒粒子从伪足中芽生。通过电子显微镜用重酶解肌球蛋白标记法将丝状肌动蛋白(F-肌动蛋白)定位在伪足中。通过光学显微镜免疫荧光法检测F-肌动蛋白和p24病毒抗原的共定位,表明F-肌动蛋白和病毒存在于同一个伪足上。这些观察结果表明单核细胞从前端伪足产生病毒。我们认为,供体单核细胞/巨噬细胞前沿的HIV分泌可能是HIV感染靶细胞的一种有效方式。