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[CTLA-4基因启动子区域单核苷酸多态性与特发性扩张型心肌病的相关性研究]

[The research on associating the single nucleotide polymorphism of CTLA-4 gene promoter region with idiopathic dilated cardiomyopathy].

作者信息

Liu Wei, Li Wei-min, Gao Cheng, Li Yue, Kong Yi-hui

机构信息

Department of Cardiology, First Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, 150001 P.R.China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):198-201.

Abstract

OBJECTIVE

To investigate the expression of cytotoxic T lymphocyte associated antigen-4 (CTLA-4) in patients with idiopathic dilated cardiomyopathy (IDC) and to explore genetic susceptibility to IDC caused possibly by single nucleotide polymorphism (SNP) of CTLA-4 gene promoter.

METHODS

PCR-restriction fragment length polymorphism techniques were used to analyze the SNPs of CTLA-4 gene at position -1772, -1661 and -318 in the promoter region. Serum sCTLA-4, IFN-gamma and IL-4 were tested by ELISA.

RESULTS

sCTLA-4 levels of IDC patients were associated with the haplotype and genotype. Patients with -1772 TC genotype or -1772 TC -1661 AA, -1772 TC -1661 AG haplotypes had higher sCTLA-4 levels than patients with other haplotypes did. The frequency of -1772 TC genotype was significantly high in patients with low ejection factor(EF) values. Whereas the frequencies of -1661 G allele and -1661 GG genotype were lower in IDC patients. Levels of IL-4 were increased in IDC group.

CONCLUSION

Patients with IDC have an aberrant expression of the CTLA-4 products, and the -1772 C/T and -1661 A/G polymorphisms. The two SNPs may function as genetic markers for disease susceptibility.

摘要

目的

研究细胞毒性T淋巴细胞相关抗原4(CTLA-4)在特发性扩张型心肌病(IDC)患者中的表达情况,并探讨CTLA-4基因启动子单核苷酸多态性(SNP)可能导致的IDC遗传易感性。

方法

采用聚合酶链反应-限制性片段长度多态性技术分析启动子区域CTLA-4基因-1772、-1661和-318位点的SNP。采用酶联免疫吸附测定法检测血清可溶性CTLA-4(sCTLA-4)、γ干扰素(IFN-γ)和白细胞介素4(IL-4)。

结果

IDC患者的sCTLA-4水平与单倍型和基因型有关。-1772 TC基因型或-1772 TC -1661 AA、-1772 TC -1661 AG单倍型的患者sCTLA-4水平高于其他单倍型的患者。射血分数(EF)值低的患者中-1772 TC基因型频率显著较高。而IDC患者中-1661 G等位基因和-1661 GG基因型频率较低。IDC组IL-4水平升高。

结论

IDC患者存在CTLA-4产物异常表达以及-1772 C/T和-1661 A/G多态性。这两个SNP可能作为疾病易感性的遗传标记。

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