In vivo distribution of the human immunodeficiency virus simian immunodeficiency virus coreceptors: CXCR4, CCR3, and CCR5

被引:144
作者
Zhang, LQ
He, T
Talal, A
Wang, G
Frankel, SS
Ho, DD
机构
[1] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[2] Walter Reed Army Inst Res, Div Retrovirol, Rockville, MD 20850 USA
[3] Armed Forces Inst Pathol, Dept Infect & Parasit Dis Pathol, Washington, DC 20306 USA
基金
英国惠康基金;
关键词
D O I
10.1128/JVI.72.6.5035-5045.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have evaluated the in vivo distribution of the major human immunodeficiency virus/simian immunodeficiency virus (HIV/SIV) coreceptors, CXCR4, CCR3, and CCR5, in both rhesus macaques and humans, T lymphocytes and macrophages in both lymphoid and nonlymphoid tissues are the major cell populations expressing HIV/SIV coreceptors, reaffirming that these cells are the major targets of HIV/SIV infection in vivo. In lymphoid tissues such as the lymph node and the thymus, approximately 1 to 10% of the T lymphocytes and macrophages are coreceptor positive. However, coreceptor expression was not detected on follicular dendritic cells (FDC) in lymph nodes, suggesting that the ability of FDC to trap extracellular virions is unlikely to be mediated by a coreceptor-specific mechanism. In the thymus, a large number of immature and mature T lymphocytes express CXCR4, which may render these cells susceptible to infection by syncytium-inducing viral variants that use this coreceptor for entry. In addition, various degrees of coreceptor expression are found among different tissues and also among different cells within the same tissues. Coreceptor-positive cells are more frequently identified in the colon than in the rectum and more frequently identified in the cenix than in the vagina, suggesting that the expression levels of coreceptors are differentially regulated at different anatomic sites. Furthermore, extremely high levels of CXCR4 and CCR3 expression are found on the neurons from both the central and peripheral nervous systems. These findings may be helpful in understanding certain aspects of HIV and SIV pathogenesis and transmission.
引用
收藏
页码:5035 / 5045
页数:11
相关论文
共 60 条
[1]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[2]   Infection of human marrow stroma by human immunodeficiency virus-1 (HIV-1) is both required and sufficient for HIV-1-induced hematopoietic suppression in vitro: Demonstration by gene modification of primary human stroma [J].
Bahner, I ;
Kearns, K ;
Coutinho, S ;
Leonard, EH ;
Kohn, DB .
BLOOD, 1997, 90 (05) :1787-1798
[3]   The HIV coreceptors CXCR4 and CCR5 are differentially expressed and regulated on human T lymphocytes [J].
Bleul, CC ;
Wu, LJ ;
Hoxie, JA ;
Springer, TA ;
Mackay, CR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1925-1930
[4]   THE BLOCK TO HIV-1 ENVELOPE GLYCOPROTEIN-MEDIATED MEMBRANE-FUSION IN ANIMAL-CELLS EXPRESSING HUMAN CD4 CAN BE OVERCOME BY A HUMAN CELL COMPONENT(S) [J].
BRODER, CC ;
DIMITROV, DS ;
BLUMENTHAL, R ;
BERGER, EA .
VIROLOGY, 1993, 193 (01) :483-491
[5]  
BURKITT HG, 1994, FUNCTIONAL HISTOLOGY
[6]   SUSCEPTIBILITY OF HUMAN BONE-MARROW STROMAL CELLS TO HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) [J].
CANQUE, B ;
MARANDIN, A ;
ROSENZWAJG, M ;
LOUACHE, F ;
VAINCHENKER, W ;
GLUCKMAN, JC .
VIROLOGY, 1995, 208 (02) :779-783
[7]  
CHENGMAYER C, COMMUNICATION
[8]   The beta-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates [J].
Choe, H ;
Farzan, M ;
Sun, Y ;
Sullivan, N ;
Rollins, B ;
Ponath, PD ;
Wu, LJ ;
Mackay, CR ;
LaRosa, G ;
Newman, W ;
Gerard, N ;
Gerard, C ;
Sodroski, J .
CELL, 1996, 85 (07) :1135-1148
[9]   Differential susceptibility of naive and memory CD4(+) T cells to the cytopathic effects of infection with human immunodeficiency virus type 1 strain LAI [J].
Chun, TW ;
Chadwick, K ;
Margolick, J ;
Siliciano, RF .
JOURNAL OF VIROLOGY, 1997, 71 (06) :4436-4444
[10]   IDENTIFICATION OF RANTES, MIP-1-ALPHA, AND MIP-1-BETA AS THE MAJOR HIV-SUPPRESSIVE FACTORS PRODUCED BY CD8(+) T-CELLS [J].
COCCHI, F ;
DEVICO, AL ;
GARZINODEMO, A ;
ARYA, SK ;
GALLO, RC ;
LUSSO, P .
SCIENCE, 1995, 270 (5243) :1811-1815