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HLA - G基因中14碱基对缺失多态性在血浆可溶性HLA - G的表达中起重要作用。

The 14 bp deletion polymorphisms in HLA-G gene play an important role in the expression of soluble HLA-G in plasma.

作者信息

Chen X-Y, Yan W-H, Lin A, Xu H-H, Zhang J-G, Wang X-X

机构信息

Department of Laboratory Medicine, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Tissue Antigens. 2008 Oct;72(4):335-41. doi: 10.1111/j.1399-0039.2008.01107.x. Epub 2008 Aug 12.

Abstract

Soluble human leukocyte antigen-G (sHLA-G) functions as a multiple immunoregulator. A 14 bp insertion (+14 bp)/deletion (-14 bp) polymorphism in exon 8 of the HLA-G gene has been proposed to be associated with HLA-G mRNA stability and the expression of HLA-G. In the current study, a total of 150 normal Chinese Han population had been genotyped for the +14 bp/-14 bp polymorphism, and the expression of plasma sHLA-G was determined with enzyme-linked immunosorbent assay in these case-matched plasma. Data showed that genotype of 14 bp polymorphism was significantly associated with sHLA-G expression. Plasma sHLA-G level with the +14 bp/+14 bp genotype was dramatically lower than that with +14 bp/-14 bp (P = 0.004) and -14 bp/-14 bp genotypes (P = 0.003), while no dramatic difference was observed between the +14 bp/-14 bp and -14 bp/-14 bp genotypes (P > 0.05). In both males and females, plasma sHLA-G with the +14 bp/+14 bp genotype was also significantly lower when compared with other two respective 14 bp genotypes. Data also showed that sHLA-G expression was unrelated to gender. This study suggests that the 14 bp deletion polymorphism in the HLA-G gene plays an important role in sHLA-G expression and that interpretation of the potential biological functions of sHLA-G should be made with caution, taking the polymorphism into consideration.

摘要

可溶性人类白细胞抗原-G(sHLA-G)具有多种免疫调节功能。有人提出,HLA-G基因第8外显子中的14碱基对插入(+14 bp)/缺失(-14 bp)多态性与HLA-G mRNA稳定性及HLA-G表达有关。在本研究中,对150名正常中国汉族人群进行了+14 bp/-14 bp多态性基因分型,并采用酶联免疫吸附测定法测定了这些病例匹配血浆中血浆sHLA-G的表达。数据显示,14碱基对多态性的基因型与sHLA-G表达显著相关。+14 bp/+14 bp基因型的血浆sHLA-G水平显著低于+14 bp/-14 bp基因型(P = 0.004)和-14 bp/-14 bp基因型(P = 0.003),而+14 bp/-14 bp基因型与-14 bp/-14 bp基因型之间未观察到显著差异(P > 0.05)。在男性和女性中,+14 bp/+14 bp基因型的血浆sHLA-G与其他两种14碱基对基因型相比也显著较低。数据还显示,sHLA-G表达与性别无关。本研究表明,HLA-G基因中的14碱基对缺失多态性在sHLA-G表达中起重要作用,在解释sHLA-G的潜在生物学功能时应谨慎考虑该多态性。

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