发展与衰老是两个相反但又相辅相成的现象。

Interdisciplinary topics in gerontology Pub Date : 2015-01-01 Epub Date: 2014-10-13 DOI:10.1159/000364932
Bruno César Feltes, Joice de Faria Poloni, Diego Bonatto
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引用次数: 15

摘要

衰老是生物体进化的结果,导致生物体发育的特定特征最终促进衰老表型或可能导致与年龄相关的疾病。从这个意义上说,一个广泛探讨发展及其与衰老关系的理论是发育衰老理论(DevAge),它也包括了大多数已知的与年龄相关的理论。因此,我们采用不同的系统生物学工具来展望人类和小鼠模型的发育和衰老相关网络,以进行进化比较。收集到的数据表明了一个模型,其中与炎症、发育、表观遗传机制和氧稳态相关的蛋白质协调发育和衰老之间的相互作用。此外,该机制在两种哺乳动物模型中似乎都是进化保守的,进一步证实了DevAge分子模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and aging: two opposite but complementary phenomena.

Aging is a consequence of an organism's evolution, where specific traits that lead to the organism's development eventually promote aged phenotypes or could lead to age-related diseases. In this sense, one theory that broadly explored development and its association to aging is the developmental aging theory (DevAge), which also encompasses most known age-associated theories. Thus, we employed different systems biology tools to prospect developmental and aging-associated networks for human and murine models for evolutionary comparison. The gathered data suggest a model where proteins related to inflammation, development, epigenetic mechanisms and oxygen homeostasis coordinate the interplay between development and aging. Moreover, the mechanism also appears to be evolutionary conserved in both mammalian models, further corroborating the DevAge molecular model.

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