Friborg J, Kong W P, Flowers C C, Flowers S L, Sun Y, Foreman K E, Nickoloff B J, Nabel G J
Departments of Internal Medicine and Biological Chemistry, Howard Hughes Medical Institute, University of Michigan Medical Center, Ann Arbor, Michigan 48109-0650, USA.
J Virol. 1998 Dec;72(12):10073-82. doi: 10.1128/JVI.72.12.10073-10082.1998.
The DNA sequence for Kaposi's sarcoma-associated herpesvirus was originally detected in Kaposi's sarcoma biopsy specimens. Since its discovery, it has been possible to detect virus in cell lines established from AIDS-associated body cavity-based B-cell lymphoma and to propagate virus from primary Kaposi's sarcoma lesions in a human renal embryonic cell line, 293. In this study, we analyzed the infectivity of Kaposi's sarcoma-associated herpesvirus produced from these two sources. Viral isolates from cultured cutaneous primary KS cells was transmitted to an Epstein-Barr virus-negative Burkitt's B-lymphoma cell line, Louckes, and compared to virus induced from a body cavity-based B-cell lymphoma cell line. While propagation of body cavity-based B-cell lymphoma-derived virus was not observed in 293 cell cultures, infection with viral isolates obtained from primary Kaposi's sarcoma lesions induced injury in 293 cells typical of herpesvirus infection and was associated with apoptotic cell death. Interestingly, transient overexpression of the Kaposi's sarcoma-associated herpesvirus v-Bcl-2 homolog delayed the process of apoptosis and prolonged the survival of infected 293 cells. In contrast, the broad-spectrum caspase inhibitors Z-VAD-fmk and Z-DEVD-fmk failed to protect infected cell cultures, suggesting that Kaposi's sarcoma-associated herpesvirus-induced apoptosis occurs through a Bcl-2-dependent pathway. Kaposi's sarcoma-associated herpesvirus isolates from primary Kaposi's sarcoma lesions and body cavity-based lymphomas therefore may differ and are likely to have distinct contributions to the pathophysiology of Kaposi's sarcoma.
卡波西肉瘤相关疱疹病毒的DNA序列最初是在卡波西肉瘤活检标本中检测到的。自发现以来,已能够在从艾滋病相关体腔B细胞淋巴瘤建立的细胞系中检测到该病毒,并能在人肾胚胎细胞系293中从原发性卡波西肉瘤病变中繁殖病毒。在本研究中,我们分析了从这两种来源产生的卡波西肉瘤相关疱疹病毒的感染性。将来自培养的皮肤原发性卡波西肉瘤细胞的病毒分离株接种到爱泼斯坦-巴尔病毒阴性的伯基特B淋巴瘤细胞系Louckes中,并与从体腔B细胞淋巴瘤细胞系诱导的病毒进行比较。虽然在293细胞培养物中未观察到体腔B细胞淋巴瘤衍生病毒的繁殖,但用从原发性卡波西肉瘤病变中获得的病毒分离株感染可诱导293细胞出现典型的疱疹病毒感染损伤,并伴有凋亡性细胞死亡。有趣的是,卡波西肉瘤相关疱疹病毒v-Bcl-2同源物的瞬时过表达延迟了凋亡过程,延长了受感染293细胞的存活时间。相比之下,广谱半胱天冬酶抑制剂Z-VAD-fmk和Z-DEVD-fmk未能保护受感染的细胞培养物,这表明卡波西肉瘤相关疱疹病毒诱导的凋亡是通过Bcl-2依赖性途径发生的。因此,来自原发性卡波西肉瘤病变和体腔淋巴瘤的卡波西肉瘤相关疱疹病毒分离株可能不同,并且可能对卡波西肉瘤的病理生理学有不同的贡献。