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骨骼中与年龄相关的体细胞线粒体DNA缺失

Age related somatic mitochondrial DNA deletions in bone.

作者信息

Papiha S S, Rathod H, Briceno I, Pooley J, Datta H K

机构信息

Department of Clinical Biochemistry, The Medical School, University of Newcastle, UK.

出版信息

J Clin Pathol. 1998 Feb;51(2):117-20. doi: 10.1136/jcp.51.2.117.

Abstract

BACKGROUND

It has been suggested that the accumulation of damage to mitochondrial DNA is a major cause of age related, degenerative disease. Aging is known to cause bone loss leading to a fall in bone mineral density and disruption of bone microarchitecture. However, despite the evidence of age related bone loss, no attempt has been made to detect specific deletions of mitochondrial DNA in the bone of aged individuals.

AIMS

To detect bone specific, age related deletions in mitochondrial DNA.

METHOD

Blood leucocytes and bone biopsies from patients who had undergone orthopaedic surgery were used as a source of mitochondrial DNA and screened for deletions using the polymerase chain reaction.

RESULTS

Although no deletions were detected in the blood mitochondrial DNA, specific deletions in bone mitochondrial DNA were found in three of five elderly subjects.

CONCLUSION

The findings of this study suggest that there could be a link between mitochondrial DNA deletions and free radical induced apoptosis of bone cells in the development of age related bone loss.

摘要

背景

有人提出,线粒体DNA损伤的积累是与年龄相关的退行性疾病的主要原因。众所周知,衰老会导致骨质流失,从而导致骨矿物质密度下降和骨微结构破坏。然而,尽管有与年龄相关的骨质流失的证据,但尚未有人尝试检测老年个体骨骼中线粒体DNA的特定缺失。

目的

检测线粒体DNA中与年龄相关的骨骼特异性缺失。

方法

将接受骨科手术患者的血液白细胞和骨活检组织作为线粒体DNA的来源,并使用聚合酶链反应筛选缺失情况。

结果

虽然在血液线粒体DNA中未检测到缺失,但在五名老年受试者中的三名中发现了骨骼线粒体DNA的特异性缺失。

结论

本研究结果表明,在与年龄相关的骨质流失的发展过程中,线粒体DNA缺失与自由基诱导的骨细胞凋亡之间可能存在联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82bd/500505/353b0efa7249/jclinpath00263-0030-a.jpg

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