309th Hospital of Chinese People's Liberation Army, Beijing, 100091, China.
Aging Clin Exp Res. 2013 Apr;25(1):17-23. doi: 10.1007/s40520-013-0006-0. Epub 2013 Apr 3.
Telomere attrition proceeds with the aging process, and is also associated with aging disease conditions, such as Alzheimer's disease (AD). The aging process also affects subtelomeric methylation status. In the present study, the telomere length and the subtelomeric methylation status in female AD patients were analyzed to see how AD affects telomere structure.
Terminal restriction fragment length of 23 AD patients' peripheral leukocytes was analyzed with methylation sensitive- and insensitive-isoschizomer by Southern blot.
AD patients were found to have normal mean telomere lengths (controls; 6.4 ± 0.9 kb, AD; 6.1 ± 0.8 kb, p = 0.131), a proportionally decreased number of the longest telomeres (>9.4 kb) (controls; 30.3 ± 7.9%, AD; 24.4 ± 8.3%, p = 0.013), increased medium-sized telomeres (controls; 51.7 ± 3.3%, AD 55.5 ± 6.4%, p = 0.015) and unchanged numbers of the shortest telomeres (<4.4 kb) (controls; 18.0 ± 7.8, AD; 20.2 ± 8.9%, p = 0.371) in their peripheral leukocytes. The subtelomeres of telomeres in the shortest range (<4.4 kb) were more methylated in AD subjects than in controls (controls; 0.21 ± 0.23, AD; 0.41 ± 0.26, p = 0.016).
These results may indicate that AD contributes to the loss of cells bearing the shortest telomeres, with hypomethylation of subtelomeres occurring in addition to telomere attrition, resulting in an apparent normal mean telomere length in AD patients. The relatively high subtelomeric methylation status of the shortest telomeres in peripheral blood leukocytes may be a characteristic of AD. This report demonstrates that the epigenetic status of the telomeric region is affected by disease conditions.
端粒损耗随着衰老过程而发生,也与衰老疾病状况有关,如阿尔茨海默病(AD)。衰老过程也会影响亚端粒甲基化状态。在本研究中,分析了女性 AD 患者的端粒长度和亚端粒甲基化状态,以观察 AD 如何影响端粒结构。
通过 Southern 印迹分析 23 例 AD 患者外周血白细胞的末端限制片段长度,并用甲基化敏感和非敏感同裂酶进行分析。
AD 患者的平均端粒长度正常(对照组:6.4 ± 0.9 kb,AD 组:6.1 ± 0.8 kb,p = 0.131),最长端粒(>9.4 kb)的比例减少(对照组:30.3 ± 7.9%,AD 组:24.4 ± 8.3%,p = 0.013),中等大小的端粒增加(对照组:51.7 ± 3.3%,AD 组:55.5 ± 6.4%,p = 0.015),最短端粒(<4.4 kb)的数量不变(对照组:18.0 ± 7.8,AD 组:20.2 ± 8.9%,p = 0.371)。在 AD 患者的外周血白细胞中,最短端粒(<4.4 kb)的亚端粒比对照组更甲基化(对照组:0.21 ± 0.23,AD 组:0.41 ± 0.26,p = 0.016)。
这些结果可能表明 AD 导致携带最短端粒的细胞丢失,除了端粒损耗外,亚端粒还发生低甲基化,导致 AD 患者的平均端粒长度正常。外周血白细胞中最短端粒的相对较高的亚端粒甲基化状态可能是 AD 的一个特征。本报告表明,端粒区域的表观遗传状态受疾病状况的影响。