The Aging Stress Response

被引:397
作者
Haigis, Marcia C. [1 ]
Yankner, Bruce A. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
LIFE-SPAN EXTENSION; ACTIVATED PROTEIN-KINASE; GENE-EXPRESSION PROFILE; FATTY-ACID OXIDATION; DNA-DAMAGE RESPONSE; CAENORHABDITIS-ELEGANS; CALORIE RESTRICTION; SKELETAL-MUSCLE; MITOCHONDRIAL BIOGENESIS; NEURODEGENERATIVE DISEASE;
D O I
10.1016/j.molcel.2010.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aging is the outcome of a balance between damage and repair. The rate of aging and the appearance of age-related pathology are modulated by stress response and repair pathways that gradually decline, including the proteostasis and DNA damage repair networks and mitochondrial respiratory metabolism. Highly conserved insulin/IGF-1, TOR, and sirtuin signaling pathways in turn control these critical cellular responses. The coordinated action of these signaling pathways maintains cellular and organismal homeostasis in the face of external perturbations, such as changes in nutrient availability, temperature, and oxygen level, as well as internal perturbations, such as protein misfolding and DNA damage. Studies in model organisms suggest that changes in signaling can augment these critical stress response systems, increasing life span and reducing age-related pathology. The systems biology of stress response signaling thus provides a new approach to the understanding and potential treatment of age-related diseases.
引用
收藏
页码:333 / 344
页数:12
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