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EXTRACHROMOSOMAL HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 DNA CAN INITIATE A SPREADING INFECTION OF HL-60 CELLS
被引:8
作者:
BUTERA, ST
PEREZ, VL
BESANSKY, NJ
CHAN, WC
WU, BY
NABEL, GJ
FOLKS, TM
机构:
[1] CTR DIS CONTROL,CTR INFECT DIS,DIV VIRAL & RICKETTSIAL DIS,RETROVIRUS DIS BRANCH,MAIL STOP G19,ATLANTA,GA 30333
[2] EMORY UNIV HOSP,DEPT PATHOL & LAB MED,ATLANTA,GA 30322
[3] UNIV MICHIGAN,MED CTR,HOWARD HUGHES MED INST,DEPT INTERNAL MED,ANN ARBOR,MI 48109
[4] UNIV MICHIGAN,MED CTR,HOWARD HUGHES MED INST,DEPT BIOL CHEM,ANN ARBOR,MI 48109
关键词:
HIV-1 INFECTION OF PROMYELOCYTES;
UNINTEGRATED HIV-1 DNA;
AZIDOTHYMIDINE;
CD4;
CLONAL ANALYSIS;
D O I:
10.1002/jcb.240450410
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In this report, we describe a human immunodeficiency virus type-1 (HIV-1)-infected promyelocytic cell line, OM, derived from HL-60 cells. Although the OM cell line was biologically cloned twice, the pattern of HIV-1 expression during culture appeared analogous to a classical acute spreading infection and was inhibited by both azidothymidine and recombinant soluble CD4 treatment. The number of OM cells actually expressing HIV-1 at the beginning of culture was 0%, reached a peak of nearly 100% at 6 weeks, and then fell to < 10% HIV-1+ cells by 10 weeks. Clonal analysis of the surviving cells verified that stable HIV-1+ OM cells resulted from the spreading infection. Southern analysis confirmed the transmission of HIV-1 through these OM cultures and the occurrence of stable clones which resulted. The initial percentage of OM cells actually harboring the HIV-1 genome was < 0.1%, indicating nonfaithful transmission of an unintegrated HIV-1 genome during clonal expansion. These results demonstrate that extrachromosomal HIV-1 DNA can contribute to the spread of HIV-1 infection and give rise to cells which have stably integrated HIV-1 provirus.
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页码:366 / 373
页数:8
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