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爱泼斯坦-巴尔病毒在口腔毛状白斑角质形成细胞中的亚细胞分布及生命周期

Subcellular distribution and life cycle of Epstein-Barr virus in keratinocytes of oral hairy leukoplakia.

作者信息

Rabanus J P, Greenspan D, Petersen V, Leser U, Wolf H, Greenspan J S

机构信息

Department of Stomatology, School of Dentistry, University of California, San Francisco 94143-0512.

出版信息

Am J Pathol. 1991 Jul;139(1):185-97.

Abstract

The authors investigated the life cycle of Epstein-Barr virus (EBV) in keratinocytes of oral hairy leukoplakia by combining immunohistochemistry. DNA in situ hybridization, and lectin histochemistry with electron microscopy. Diffuse-staining components of the EBV early antigen complex (EA-D), EBV 150-kd capsid antigen (VCA), EBV membrane antigen (gp350/220), and double-stranded DNA were labeled with monoclonal antibodies. An EBV-DNA probe was used to locate EBV DNA. Wheat-germ agglutinin (WGA) was employed to distinguish Golgi-associated compartments. The authors found EBV proteins and EBV DNA only in keratinocytes with apparent viral assembly. In situ hybridization showed EBV DNA in free corelike material and in electron-dense cores of mature nucleocapsids. Monoclonal antibodies to nonspecific double-stranded DNA attached to the same structures and to marginated chromatin. Components of EA-D were dispersed throughout the nuclei but accumulated near condensed chromatin and in 'punched-out' regions of the chromatin. Epstein-Barr virus 150-kd capsid antigen was found only in the nuclei, where it appeared preferentially on mature nucleocapsids. As yet unexplained arrays of intranuclear particles that remained unlabeled with all EBV-specific probes reacted intensely with an antiserum against common papillomavirus antigen. Gp350/220 was detectable in various cellular membrane compartments and was highly concentrated on EBV envelopes in peripheral Golgi-associated secretory vesicles. It was less abundant on the extracellular EBV, indicating that viral membrane antigen partly dissociates from the mature virus. Combined lectin-binding histochemistry and electron microscopy demonstrated for the first time that EBV is processed in the Golgi apparatus, which eventually releases the virus by fusion with the plasma membrane. These results provide insight into the biologic events that occur during complete EBV replication in vivo.

摘要

作者通过将免疫组织化学、DNA原位杂交、凝集素组织化学与电子显微镜相结合,研究了口腔毛状白斑角质形成细胞中EB病毒(EBV)的生命周期。EBV早期抗原复合物(EA-D)、EBV 150-kd衣壳抗原(VCA)、EBV膜抗原(gp350/220)和双链DNA的弥漫性染色成分用单克隆抗体标记。使用EBV-DNA探针定位EBV DNA。采用麦胚凝集素(WGA)区分与高尔基体相关的区室。作者仅在具有明显病毒装配的角质形成细胞中发现了EBV蛋白和EBV DNA。原位杂交显示EBV DNA存在于游离的类核心物质和成熟核衣壳的电子致密核心中。针对非特异性双链DNA的单克隆抗体附着于相同结构和边缘化染色质。EA-D成分分散在整个细胞核中,但在浓缩染色质附近和染色质的“穿孔”区域积累。仅在细胞核中发现EBV 150-kd衣壳抗原,它优先出现在成熟核衣壳上。尚未解释的核内颗粒阵列,用所有EBV特异性探针均未标记,但与抗人乳头瘤病毒共同抗原的抗血清发生强烈反应。在各种细胞膜区室中可检测到gp350/220,并且在与高尔基体相关的外周分泌小泡中的EBV包膜上高度浓缩。在细胞外EBV上含量较少,表明病毒膜抗原部分与成熟病毒解离。凝集素结合组织化学与电子显微镜相结合首次证明EBV在高尔基体中进行加工,最终通过与质膜融合释放病毒。这些结果为体内完整EBV复制过程中发生的生物学事件提供了深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04a2/1886136/4b7e225d93b9/amjpathol00091-0180-a.jpg

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