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Accelerated in vivo epidermal telomere loss in Werner syndrome

机译:Werner综合征的体内表皮端粒加速丢失

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摘要

Many data pertaining to the accelerated telomere loss in cultured cells derived from Werner syndrome (WS), a representative premature aging syndrome, have been accumulated. However, there have been no definitive data on in vivo telomere shortening in WS patients. In the present study, we measured terminal restriction fragment (TRF) lengths of 10 skin samples collected from extremities of 8 WS patients aged between 30 and 61 years that had been surgically amputated because of skin ulceration, and estimated the annual telomere loss. Whereas the values of TRF length in younger WS patients (in their thirties) were within the normal range, those in older WS patients were markedly shorter relative to non-WS controls. Regression analyses indicated that the TRF length in WS was significantly shorter than that in controls (p < 0.001). Furthermore, we found that TRF lengths in muscle adjacent to the examined epidermis were also significantly shorter than those of controls (p = 0.047). These data demonstrate for the first time that in vivo telomere loss is accelerated in systemic organs of WS patients, suggesting that abnormal telomere erosion is one of the major causes of early onset of age-related symptoms and a predisposition to sarcoma and carcinoma in WS.
机译:已经积累了许多与Werner综合征(WS)(一种典型的过早衰老综合征)有关的培养细胞中端粒加速丢失的数据。但是,尚无关于WS患者体内端粒缩短的确切数据。在本研究中,我们测量了10例皮肤样本的末端限制性片段(TRF)长度,这些样本是从8例30至61岁的WS患者的肢体收集的,这些患者由于皮肤溃疡而被手术截肢,并估算了每年的端粒损失。相对于非WS对照,年轻的WS患者(三十多岁)的TRF长度值在正常范围内,而老年WS患者的TRF长度明显短。回归分析表明,WS中的TRF长度显着短于对照组(p <0.001)。此外,我们发现与检查的表皮相邻的肌肉的TRF长度也明显短于对照组(p = 0.047)。这些数据首次证明,WS患者全身器官中的端粒丢失在体内加速,这表明端粒异常侵蚀是与年龄相关的症状及对肉瘤和癌的易感性的主要起因之一。

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