HIV-1 INFECTION AND MODULATION OF CYTOKINE AND GROWTH-FACTOR EXPRESSION IN KAPOSIS SARCOMA-DERIVED CELLS-INVITRO

被引:19
作者
HUANG, YQ
LI, JJ
KIM, KS
NICOLAIDES, A
ZHANG, WG
LE, JM
POIESZ, BJ
FRIEDMANKIEN, AE
机构
[1] NYU MED CTR, DEPT MICROBIOL, MSB 275, 550 1ST AVE, NEW YORK, NY 10016 USA
[2] NYU MED CTR, DEPT DERMATOL, NEW YORK, NY 10016 USA
[3] SUNY UPSTATE MED CTR, SYRACUSE, NY 13210 USA
关键词
KAPOSIS SARCOMA; HIV-1; GROWTH FACTORS;
D O I
10.1097/00002030-199303000-00002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HIV-1 transcripts have been detected in AIDS-related Kaposi's sarcoma (KS) tissues within the factor XIIIa+ dermal dendrocytes present in the tumor. Various cytokines and growth factors have been shown to influence the growth of KS-derived cells in vitro. HIV-1 preferentially infects CD4+ cells and has also been found to infect some CD4- cells in vitro. The susceptibility of cultured KS cells in vitro to infection with HIV-1 and the expression of interleukin (IL)-1beta, IL-6 and basic fibroblast growth factor (bFGF) after exposure to HIV-1 was examined. Methods: The susceptibility of two different KS-derived cell cultures to HIV-1 infection was examined by the expression of p24 antigen, detection of proviral sequence and electron microscopy. The expression of IL-1beta, IL-6 and bFGF was detected by enzyme-linked immunosorbent assay and reverse transcriptase polymerase chain reaction. Results: KS-derived cells can be infected by HIV-1 in vitro. Both KS-derived cells were found to express CD4 mRNA. The expression of IL-1beta and IL-6 was increased, whereas the expression of bFGF was not stimulated after exposure of KS cells to HIV-1. Conclusion: These experiments describe the in vitro infection of KS-derived cells by HIV-1 and the expression of various cytokines and growth factor following infection. The increased production of cytokines observed following such infection may be involved in the pathogenesis of AIDS-related KS.
引用
收藏
页码:317 / 322
页数:6
相关论文
共 43 条
[1]   ENZYMATIC GENE AMPLIFICATION - QUALITATIVE AND QUANTITATIVE METHODS FOR DETECTING PROVIRAL DNA AMPLIFIED INVITRO [J].
ABBOTT, MA ;
POIESZ, BJ ;
BYRNE, BC ;
KWOK, S ;
SNINSKY, JJ ;
EHRLICH, GD .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (06) :1158-1169
[2]   HUMAN BASIC FIBROBLAST GROWTH-FACTOR - NUCLEOTIDE-SEQUENCE AND GENOMIC ORGANIZATION [J].
ABRAHAM, JA ;
WHANG, JL ;
TUMOLO, A ;
MERGIA, A ;
FRIEDMAN, J ;
GOSPODAROWICZ, D ;
FIDDES, JC .
EMBO JOURNAL, 1986, 5 (10) :2523-2528
[3]   PRODUCTIVE, PERSISTENT INFECTION OF HUMAN COLORECTAL CELL-LINES WITH HUMAN-IMMUNODEFICIENCY-VIRUS [J].
ADACHI, A ;
KOENIG, S ;
GENDELMAN, HE ;
DAUGHERTY, D ;
GATTONICELLI, S ;
FAUCI, AS ;
MARTIN, MA .
JOURNAL OF VIROLOGY, 1987, 61 (01) :209-213
[4]   A GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE PSEUDOGENE ON THE SHORT ARM OF THE HUMAN X-CHROMOSOMES DEFINES A MULTIGENE FAMILY [J].
BENHAM, FJ ;
HODGKINSON, S ;
DAVIES, KE .
EMBO JOURNAL, 1984, 3 (11) :2635-2640
[5]  
BOVI PD, 1986, CANCER RES, V46, P6333
[6]   NUCLEOTIDE-SEQUENCE OF THE ACEB GENE ENCODING MALATE SYNTHASE-A IN ESCHERICHIA-COLI [J].
BYRNE, C ;
STOKES, HW ;
WARD, KA .
NUCLEIC ACIDS RESEARCH, 1988, 16 (19) :9342-9342
[7]   TRANSCRIPTION OF THE DYSTROPHIN GENE IN HUMAN-MUSCLE AND NON-MUSCLE TISSUES [J].
CHELLY, J ;
KAPLAN, JC ;
MAIRE, P ;
GAUTRON, S ;
KAHN, A .
NATURE, 1988, 333 (6176) :858-860
[8]   HUMAN-IMMUNODEFICIENCY-VIRUS CAN PRODUCTIVELY INFECT CULTURED HUMAN GLIAL-CELLS [J].
CHENGMAYER, C ;
RUTKA, JT ;
ROSENBLUM, ML ;
MCHUGH, T ;
STITES, DP ;
LEVY, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) :3526-3530
[9]  
COHEN EA, 1990, J ACQ IMMUN DEF SYND, V3, P11
[10]   REGULATORY PATHWAYS GOVERNING HIV-1 REPLICATION [J].
CULLEN, BR ;
GREENE, WC .
CELL, 1989, 58 (03) :423-426