Schraml Elisabeth, Grillari Johannes
Department of Biotechnology, BOKU VIBT University of Natural Resources and Life Sciences, Vienna, Austria.
Longev Healthspan. 2012 Dec 3;1(1):10. doi: 10.1186/2046-2395-1-10.
Cellular senescence has evolved from an in-vitro model system to study aging in vitro to a multifaceted phenomenon of in-vivo importance as senescent cells in vivo have been identified and their removal delays the onset of age-associated diseases in a mouse model system. From the large emerging class of non-coding RNAs, miRNAs have only recently been functionally implied in the regulatory networks that are modified during the aging process. Here we summarize examples of similarities between the differential expression of miRNAs during senescence and age-associated diseases and suggest that these similarities might emphasize the importance of senescence for the pathogenesis of age-associated diseases. Understanding such a connection on the level of miRNAs might offer valuable opportunities for designing novel diagnostic and therapeutic strategies.
细胞衰老已从用于体外研究衰老的模型系统演变为一种具有多方面体内重要性的现象,因为体内衰老细胞已被识别,并且在小鼠模型系统中去除这些细胞可延缓与年龄相关疾病的发生。在大量新兴的非编码RNA类别中,微小RNA(miRNA)直到最近才在衰老过程中发生改变的调控网络中被发现具有功能作用。在这里,我们总结了衰老过程中miRNA差异表达与年龄相关疾病之间的相似性实例,并表明这些相似性可能凸显了衰老在年龄相关疾病发病机制中的重要性。在miRNA层面理解这种联系可能为设计新的诊断和治疗策略提供宝贵机会。