HLA-G expression in placenta in relation to HLA-G genotype and polymorphisms

被引:21
作者
Hviid, TVF
Larsen, LG
Hoegh, AM
Bzorek, M
机构
[1] Univ Copenhagen Hosp, Rigshosp, Dept Clin Biochem, DK-2100 Copenhagen O, Denmark
[2] Storstrommens Hosp Naestved, Dept Pathol, Naestved, Denmark
[3] Univ Copenhagen Hosp, Hvidovre Hosp, Dept Clin Biochem, Hvidovre, Denmark
关键词
human leukocyte antigen-G; placenta; polymorphism; preeclampsia;
D O I
10.1111/j.1600-0897.2004.00208.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
PROBLEM: The expression of the non-classical human leukocyte antigen (HLA) class Ib gene, HLA-G, seems to be important at the feto-maternal interface. The HLA-G molecule is almost monomorphic and expressed in both membrane-bound and soluble isoforms. It has been shown to inhibit natural killer cell -mediated lysis and influence cytokine expression. HLA-G gene polymorphism has been linked to differences in gene expression profile of alternatively spliced HLA-G transcripts and levels of specific HLA-G messenger RNA (mRNA) isoforms. Furthermore, aberrant HLA-G expression has been reported in preeclamptic placentas. On this background it is of general interest to further elucidate any associations between HLA-G polymorphism and protein expression. METHODS: We have investigated HLA-G protein expression by immunohistochemistry in HLA-G genotyped placentas from term. HLA-G mRNA expression in preeclamptic placentas and in control placentas was also studied by microarray technology. RESULTS AND CONCLUSIONS: The studies of HLA-G protein expression in term placentas by immunohistochemical analysis showed no clear associations with HLA-G genotypes although this could be because of the very semi-quantitative nature of this technique. However, we found a tendency towards reduction of HLA-G mRNA expression in placentas from preeclamptic cases compared to matched controls with the use of microarray technology.
引用
收藏
页码:212 / 217
页数:6
相关论文
共 30 条
[1]   Mother-to-child discordance in HLA-G exon 2 is associated with a reduced risk of perinatal HIV-1 transmission [J].
Aikhionbare, FO ;
Hodge, T ;
Kuhn, L ;
Bulterys, M ;
Abrams, EJ ;
Bond, VC .
AIDS, 2001, 15 (16) :2196-2198
[2]   Human cytomegalovirus-encoded US2 differentially affects surface expression of MHC class I locus products and targets membrane-bound, but not soluble HLA-G1 for degradation [J].
Barel, MT ;
Ressing, M ;
Pizzato, N ;
van Leeuwen, D ;
Le Bouteiller, P ;
Lenfant, F ;
Wiertz, EJHJ .
JOURNAL OF IMMUNOLOGY, 2003, 171 (12) :6757-6765
[3]   Altered phenotype of HLA-G expressing trophoblast and decidual natural killer cells in pathological pregnancies [J].
Emmer, PM ;
Steegers, EAP ;
Kerstens, HMJ ;
Bulten, J ;
Nelen, WLDM ;
Boer, K ;
Joosten, I .
HUMAN REPRODUCTION, 2002, 17 (04) :1072-1080
[4]  
FUJII T, 1994, J IMMUNOL, V153, P5516
[5]  
Fuzzi B, 2002, EUR J IMMUNOL, V32, P311, DOI 10.1002/1521-4141(200202)32:2<311::AID-IMMU311>3.3.CO
[6]  
2-#
[7]   Lack of human leukocyte antigen-G expression in extravillous trophoblasts is associated with pre-eclampsia [J].
Goldman-Wohl, DS ;
Ariel, I ;
Greenfield, C ;
Hochner-Celnikier, D ;
Cross, J ;
Fisher, S ;
Yagel, S .
MOLECULAR HUMAN REPRODUCTION, 2000, 6 (01) :88-95
[8]  
Hara N, 1996, AM J REPROD IMMUNOL, V36, P349
[9]   14 BP DELETION POLYMORPHISM IN THE HLA-G GENE [J].
HARRISON, GA ;
HUMPHREY, KE ;
JAKOBSEN, IB ;
COOPER, DW .
HUMAN MOLECULAR GENETICS, 1993, 2 (12) :2200-2200
[10]   HLA-G polymorphisms in couples with recurrent spontaneous abortions [J].
Hviid, TV ;
Hylenius, S ;
Hoegh, AM ;
Kruse, C ;
Christiansen, OB .
TISSUE ANTIGENS, 2002, 60 (02) :122-132