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拉脱维亚人群不同年龄组端粒长度的动态变化

Dynamics of telomere length in different age groups in a Latvian population.

作者信息

Zole Egija, Pliss Liana, Ranka Renate, Krumina Astrida, Baumanis Viesturs

机构信息

Latvian Biomedical Research and Study Centre, Ratsupites street 1, Riga, LV-1067, Latvia.

出版信息

Curr Aging Sci. 2013 Dec;6(3):244-50. doi: 10.2174/18746098113069990038.

Abstract

The shortening of telomeres with ageing is a well-documented observation; however, the reported number of nucleotides in telomeres varies between different laboratories and studies. Such variability is likely caused by ethnic differences between the populations studied. Until now, there were no studies that investigated the variability of telomere length in a senescent Latvian population of the most common mitochondrial haplogroups, defined as H (45%), U (25%), Y chromosomal N1c (40%) and R1a1 (40%). Telomere length was determined in 121 individuals in different age groups, including a control group containing individuals of 20-40 years old and groups of individuals between 60-70 years old, 71-80 years old, 81-90 years old, and above 90 years old. Telomere length was determined using the Southern blot telomeric restriction fragment assay (TRF). Decreased telomere length with ageing was confirmed, but a comparison of centenarians and individuals between 60-90 years of age did not demonstrate a significant difference in telomere length. However, significant variability in telomere length was observed in the control group, indicating probable rapid telomere shortening in some individuals that could lead up to development of health status decline appearing with ageing. Telomere length measured in mononuclear blood cells (MNC) was compared with the telomere length measured in whole peripheral white blood cells (WBC) using TRF. Telomere length in MNC was longer than in WBC for the control group with individuals 20 to 40 years old; in contrast, for the group of individuals aged 65 to 85 years old, measured telomere length was shorter in MNC when compared to WBC.

摘要

随着年龄增长端粒缩短是一个有充分文献记载的现象;然而,不同实验室和研究报告的端粒核苷酸数量存在差异。这种变异性可能是由于所研究人群的种族差异导致的。到目前为止,还没有研究调查过拉脱维亚衰老人群中最常见线粒体单倍群(定义为H(45%)、U(25%)、Y染色体N1c(40%)和R1a1(40%))的端粒长度变异性。对121名不同年龄组的个体进行了端粒长度测定,包括一个由20至40岁个体组成的对照组以及60至70岁、71至80岁、81至90岁和90岁以上的个体组。使用Southern印迹端粒限制性片段分析(TRF)测定端粒长度。证实了随着年龄增长端粒长度会缩短,但百岁老人与60至90岁个体之间的端粒长度比较未显示出显著差异。然而,在对照组中观察到端粒长度存在显著变异性,表明某些个体可能端粒快速缩短,这可能导致随着年龄增长出现健康状况下降。使用TRF将单核血细胞(MNC)中测得的端粒长度与全外周白细胞(WBC)中测得的端粒长度进行比较。对于20至40岁个体的对照组,MNC中的端粒长度比WBC中的长;相反,对于65至85岁个体组,与WBC相比,MNC中测得的端粒长度较短。

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