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11型人乳头瘤病毒通过脱落的角质化细胞传播。

Transmission of human papillomavirus type 11 infection by desquamated cornified cells.

作者信息

Bryan J T, Brown D R

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.

出版信息

Virology. 2001 Mar 1;281(1):35-42. doi: 10.1006/viro.2000.0777.

Abstract

While much is known about the human papillomavirus (HPV) productive cycle, the mechanisms of virion transmission from person to person are poorly understood. The keratinocyte is the target cell of HPV infection. As keratinocytes differentiate, nuclei are lost and the cornified cell envelope develops. Layers of these desquamated cornified cells (DCCs) are continuously shed from the stratum corneum. Release of HPV requires the cornified cell envelope, a normally very durable structure, to break apart, liberating the contents of the cell. In differentiated keratinocytes infected with HPV 11, the cornified cell envelope is abnormally thin and fragile. In this study, DCCs from HPV 11-infected genital epithelium were used to investigate the mechanisms of viral transmission. First, HPV 11-infected tissue was examined for the presence of virions by transmission electron microscopy. Virions were observed in the nuclei of differentiated keratinocytes. In addition, virions were detected in the cytoplasm of DCCs that had undergone nuclear dissolution. Rarely, virions were observed outside of cells. Next, infectivity of intact and ruptured DCCs was tested in an assay performed in the athymic mouse xenograft system. High-titer cesium chloride gradient-purified HPV 11 virions infected 100% of recovered xenografts. Using intact DCCs derived from HPV 11-infected tissue, 62.5% of recovered xenografts were infected. To test the effects of mechanical stress on infectivity, DCCs were ruptured by sonication and used in the infectivity assay. The infectivity rate increased to 90%. We conclude that DCCs serve as vehicles for efficient, concentrated delivery of virions in HPV 11 infection.

摘要

虽然人们对人乳头瘤病毒(HPV)的增殖周期了解颇多,但对病毒粒子在人与人之间传播的机制却知之甚少。角质形成细胞是HPV感染的靶细胞。随着角质形成细胞分化,细胞核消失,角质化细胞包膜形成。这些脱屑的角质化细胞(DCCs)层不断从角质层脱落。HPV的释放需要角质化细胞包膜(一种通常非常耐用的结构)破裂,从而释放细胞内容物。在感染HPV 11的分化角质形成细胞中,角质化细胞包膜异常薄且脆弱。在本研究中,来自HPV 11感染的生殖器上皮的DCCs被用于研究病毒传播的机制。首先,通过透射电子显微镜检查HPV 11感染的组织中是否存在病毒粒子。在分化角质形成细胞的细胞核中观察到了病毒粒子。此外,在经历核溶解的DCCs的细胞质中也检测到了病毒粒子。很少在细胞外观察到病毒粒子。接下来,在无胸腺小鼠异种移植系统中进行的一项试验中测试了完整和破裂的DCCs的感染性。高滴度氯化铯梯度纯化的HPV 11病毒粒子感染了100%回收的异种移植物。使用来自HPV 11感染组织的完整DCCs,62.5%回收的异种移植物被感染。为了测试机械应力对感染性的影响,通过超声处理使DCCs破裂并用于感染性试验。感染率提高到了90%。我们得出结论,在HPV 11感染中,DCCs作为病毒粒子高效、集中递送的载体。

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