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
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