Progeria syndromes and ageing: what is the connection?

被引:281
作者
Burtner, Christopher R. [1 ]
Kennedy, Brian K. [1 ,2 ,3 ]
机构
[1] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[2] Buck Inst Age Res, Novato, CA 94945 USA
[3] Guangdong Med Coll, Aging Res Inst, Dongguan 523808, Guangdong, Peoples R China
基金
美国国家卫生研究院;
关键词
HUTCHINSON-GILFORD-PROGERIA; A-TYPE LAMINS; ACTIVATED PROTEIN-KINASE; RETINOBLASTOMA GENE-PRODUCT; LIFE-SPAN EXTENSION; DIETARY RESTRICTION; CALORIC RESTRICTION; TELOMERE LENGTH; DNA-DAMAGE; STEM-CELLS;
D O I
10.1038/nrm2944
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
One of the many debated topics in ageing research is whether progeroid syndromes are really accelerated forms of human ageing. The answer requires a better understanding of the normal ageing process and the molecular pathology underlying these rare diseases. Exciting recent findings regarding a severe human progeria, Hutchinson-Gilford progeria syndrome, have implicated molecular changes that are also linked to normal ageing, such as genome instability, telomere attrition, premature senescence and defective stem cell homeostasis in disease development. These observations, coupled with genetic studies of longevity, lead to a hypothesis whereby progeria syndromes accelerate a subset of the pathological changes that together drive the normal ageing process.
引用
收藏
页码:567 / 578
页数:12
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