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TAT AND REV DIFFERENTIALLY AFFECT RESTRICTED REPLICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-I IN VARIOUS CELLS
被引:30
作者:
DUAN, LX
[1
]
OAKES, JW
[1
]
FERRARO, A
[1
]
BAGASRA, O
[1
]
POMERANTZ, RJ
[1
]
机构:
[1] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT MED,DIV INFECT DIS,MOLEC RETROVIROL SECT,PHILADELPHIA,PA 19107
来源:
关键词:
D O I:
10.1006/viro.1994.1148
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Human immunodeficiency virus type 1 (HIV-1) can infect various cell lines in culture and be maintained in a chronic state of restricted replication. These states of proviral latency are characterized by a predominance of spliced compared to unspliced viral RNA species. The proximate molecular mechanisms leading to restricted HIV-1 replication may differ in various cell lines. Importantly, recent studies have demonstrated that the site of integration is the critical parameter leading to proviral latency in ACH-2 cells. Utilizing murine retroviral shuttle vectors, the HIV-1 Tat protein was demonstrated to dramatically increase HIV-1 expression in the restrictively infected U1 monocytic cell line but not in the ACH-2 T-lymphocytic line. The HIV-1 Rev protein only modestly increased viral expression in both of these cell types. Thus, these data support the hypothesis that the mechanisms which initiate and/or maintain restricted HIV-1 expression may differ in various cell types in cell culture, and possibly in vivo. (C) 1994 Academic Press, Inc.
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页码:474 / 478
页数:5
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