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PTPN22 1858C>T(R620W)功能多态性与人类长寿。

PTPN22 1858C>T (R620W) functional polymorphism and human longevity.

机构信息

Laboratory of Human Genetics, School of Biosciences and Biotechnologies, University of Camerino, Via Gentile III da Varano, 62032, Camerino, Italy.

出版信息

Mol Biol Rep. 2011 Aug;38(6):4231-5. doi: 10.1007/s11033-010-0546-8. Epub 2010 Nov 27.

Abstract

The PTPN22 gene, located on chromosome 1p13, encoding lymphoid protein tyrosine phosphatase (LYP), plays a crucial role in the negative control of T lymphocyte activation. Since the age-related change in T-cell signal transduction may be one of the most important causes of cell-mediated immune response decline with ageing, we performed a population-based association study to test whether the PTPN22 1858C>T (R620W) functional polymorphism affects the ability to survive to old age and to reach even exceptional life expectancy. 892 unrelated healthy individuals (age range 8-106 years, 403 males and 489 females) from central Italy were studied. For both gender, the frequency of PTPN22T1858 carriers does not differ significantly in nona/centenarians and in octogenarians respect to young group. Allele and genotype frequencies of age groups were compared to those reported in previously published studied carried out on control individuals with Italic ancestry (N = 1393), further confirming results obtained from our sample population. Overall, our study suggests that PTPN22T1858 allele is not negatively selected at oldest ages and we speculate that its increased ability to protect individuals against development of infectious diseases may counteract its deleterious effect on immune system leading to autoimmunity.

摘要

PTPN22 基因位于染色体 1p13,编码淋巴样蛋白酪氨酸磷酸酶(LYP),在 T 淋巴细胞活化的负性调控中发挥重要作用。由于 T 细胞信号转导的年龄相关性变化可能是细胞介导的免疫反应随年龄衰退的最重要原因之一,我们进行了一项基于人群的关联研究,以测试 PTPN22 1858C>T(R620W)功能多态性是否影响达到长寿甚至超长寿命的能力。 来自意大利中部的 892 名无血缘关系的健康个体(年龄 8-106 岁,男性 403 名,女性 489 名)参与了此项研究。对于两性而言,非百岁/百岁以上老人和 80 岁以上老人与年轻组相比,PTPN22T1858 携带者的频率没有显著差异。将年龄组的等位基因和基因型频率与具有意大利血统的对照组个体(N=1393)之前发表的研究中报告的频率进行比较,进一步证实了我们样本人群的研究结果。总的来说,我们的研究表明,PTPN22T1858 等位基因在最年长的年龄阶段不会被负性选择,我们推测其增加的保护个体免受感染性疾病发展的能力可能会抵消其对免疫系统导致自身免疫的有害影响。

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