Miyazawa N, Leopold P L, Hackett N R, Ferris B, Worgall S, Falck-Pedersen E, Crystal R G
Departments of Medicine, Weill Medical College of Cornell University-New York Presbyterian Hospital, New York, New York, USA.
J Virol. 1999 Jul;73(7):6056-65. doi: 10.1128/JVI.73.7.6056-6065.1999.
Following receptor binding and internalization, intracellular trafficking of adenovirus (Ad) among subgroups B and C is different, with significant amounts of Ad serotype 7 (Ad7) (subgroup B) virions found in cytoplasm during the initial hours of infection while Ad5 (subgroup C) virions rapidly translocate to the nucleus. To evaluate the role of the fiber in these differences, we examined intracellular trafficking of Ad5, Ad7, and Ad5f7 (a chimeric vector composed of the Ad5 capsid with the fiber replaced by the Ad7 fiber) by conjugating Ad capsids directly with Cy3 fluorescent dye, permitting the trafficking of the capsids to be examined by fluorescence microscopy. The human lung carcinoma cell line A549 was infected with Cy3-conjugated viruses for 10 min followed by a 1-h incubation. Ad5 virions rapidly translocated to the nucleus (within 1 h of infection), while Ad7 virions were widely distributed in the cytoplasm at the same time point. Interestingly, chimeric Ad5f7 virions behaved similarly to Ad7 but not Ad5. In this regard, the percentages of nuclear localization of Ad5, Ad7, and Ad5f7 at 1 h following infection were 72% +/- 4%, 32% +/- 6%, and 38% +/- 2%, respectively. Consistent with these observations, fluorescence in situ hybridization demonstrated that most of the Ad5 DNA was detected at the nucleus after 1 h, but at the same time point, DNA of Ad7 and Ad5f7 was distributed in both the nucleus and cytoplasm. Quantification of the kinetics of Ad genomic DNA delivery to the nucleus using a fluorogenic probe-based PCR assay (TaqMan PCR) demonstrated that the percentages of nuclear association of Ad5 DNA and Ad5f7 DNA at 1 h postinfection were 80% +/- 13% and 43% +/- 1%, respectively. Although it has been generally accepted that Ad fiber protein mediates attachment of virions to cells and that fibers dissociate during endocytic uptake, these data suggest that in addition to mediating binding to the cell surface, fiber likely modulates intracellular trafficking as well.
在受体结合和内化之后,B 亚组和 C 亚组腺病毒(Ad)的细胞内运输情况不同,在感染最初数小时内,在细胞质中可发现大量血清型 7(Ad7)(B 亚组)病毒粒子,而 Ad5(C 亚组)病毒粒子则迅速转运至细胞核。为评估纤维在这些差异中的作用,我们通过将 Ad 衣壳直接与 Cy3 荧光染料偶联,利用荧光显微镜观察衣壳的运输情况,从而检测了 Ad5、Ad7 和 Ad5f7(一种由 Ad5 衣壳与被 Ad7 纤维取代的纤维组成的嵌合载体)的细胞内运输。用 Cy3 偶联病毒感染人肺癌细胞系 A549 10 分钟,随后孵育 1 小时。Ad5 病毒粒子迅速转运至细胞核(感染后 1 小时内),而在同一时间点,Ad7 病毒粒子广泛分布于细胞质中。有趣的是,嵌合 Ad5f7 病毒粒子的行为与 Ad7 相似,而与 Ad5 不同。在这方面,感染后 1 小时 Ad5、Ad7 和 Ad5f7 的核定位百分比分别为 72%±4%、32%±6%和 38%±2%。与这些观察结果一致,荧光原位杂交显示,1 小时后大部分 Ad5 DNA 在细胞核中被检测到,但在同一时间点,Ad7 和 Ad5f7 的 DNA 分布于细胞核和细胞质中。使用基于荧光探针的 PCR 测定法(TaqMan PCR)对 Ad 基因组 DNA 向细胞核递送的动力学进行定量分析表明,感染后 1 小时 Ad5 DNA 和 Ad5f7 DNA 的核关联百分比分别为 80%±13%和 43%±1%。尽管人们普遍认为 Ad 纤维蛋白介导病毒粒子与细胞的附着,并且纤维在胞吞摄取过程中会解离,但这些数据表明,纤维除介导与细胞表面的结合外,可能还会调节细胞内运输。