Influence of nucleotide polymorphisms in the CCR2 gene and the CCR5 promoter on the expression of cell surface CCR5 and CXCR4

被引:74
作者
Shieh, B
Liau, YE
Hsieh, PS
Yan, YP
Wang, ST
Li, C
机构
[1] Natl Cheng Kung Univ, Coll Med, Inst Mol Med, Tainan 701, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Inst Microbiol & Immunol, Tainan 701, Taiwan
[3] Natl Cheng Kung Univ, Coll Med, Dept Publ Hlth, Tainan 701, Taiwan
[4] Chung Shan Med & Dent Coll, Dept Biochem, Sect 1, Taichung 402, Taiwan
关键词
AIDS progression; CCR2; CCR5; HIV-1; nucleotide polymorphism;
D O I
10.1093/intimm/12.9.1311
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Polymorphisms in the CCR2 gene (CCR2-64I) and the CCR5 promoter (pCCR5-59029G) have been correlated with slower HIV-1 disease progression. How these polymorphisms influence the rate of AIDS progression has remained unclear. We have therefore investigated whether these nucleotide polymorphisms will reduce the expression levels of surface CCR5 and CXCR4, and thus lead to slower AIDS progression. For this, a cohort of Chinese volunteers in Taiwan was subjected to the determination of CCR2 and pCCR5 genotypes followed by analysis of the surface CCR5 and CXCR4 expression on five cell types derived from peripheral blood mononuclear cells by flow cytometry. Several significant associations were detected between genotypes and expression levels of the proteins, The most important finding was that an increased number of CD4(+) cells expressing CCR5 correlated with pCCR5-59029A homozygosity without the interference of both the CCR2-64 and the CCR5 Delta 32 (deleted 32 bp) mutations (P = 0.0453), which is consistent with the previous data on the association of the genotype to AIDS progression, Since different genetic polymorphisms co-exist in human beings, the rate of AIDS progression as well as the risk of rheumatoid arthritis may be governed by the interplay of the array of nucleotide changes and their affected proteins.
引用
收藏
页码:1311 / 1318
页数:8
相关论文
共 25 条
[21]   Molecular cloning and functional expression of a new human CC-chemokine receptor gene [J].
Samson, M ;
Labbe, O ;
Mollereau, C ;
Vassart, G ;
Parmentier, M .
BIOCHEMISTRY, 1996, 35 (11) :3362-3367
[22]   Alleles that may influence HIV-1 pathogenesis in Chinese subjects [J].
Shieh, B ;
Liau, YE ;
Yan, YP ;
Sun, HS ;
Chen, MY ;
Liu, YC ;
Ko, NY ;
Li, C .
AIDS, 1999, 13 (03) :421-424
[23]   Contrasting genetic influence of CCR2 and CCR5 variants on HIV-1 infection and disease progression [J].
Smith, MW ;
Dean, M ;
Carrington, M ;
Winkler, C ;
Huttley, GA ;
Lomb, DA ;
Goedert, JJ ;
OBrien, TR ;
Jacobson, LP ;
Kaslow, R ;
Buchbinder, S ;
Vittinghoff, E ;
Vlahov, D ;
Hoots, K ;
Hilgartner, MW ;
OBrien, SJ .
SCIENCE, 1997, 277 (5328) :959-965
[24]   Expression of CCR5 increases during monocyte differentiation and directly mediates macrophage susceptibility to infection by human immunodeficiency virus type 1 [J].
Tuttle, DL ;
Harrison, JK ;
Anders, C ;
Sleasman, JW ;
Goodenow, MM .
JOURNAL OF VIROLOGY, 1998, 72 (06) :4962-4969
[25]   CCR5 levels and expression pattern correlate with infectability by macrophage-tropic HIV-1, in vitro [J].
Wu, LJ ;
Paxton, WA ;
Kassam, N ;
Ruffing, N ;
Rottman, JB ;
Sullivan, N ;
Choe, H ;
Sodroski, J ;
Newman, W ;
Koup, RA ;
Mackay, CR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (09) :1681-1691