Spivey Eric C, Finkelstein Ilya J
Department of Molecular Biosciences, The University of Texas at Austin, Austin, Texas 78712, USA.
Mol Biosyst. 2014 Jul;10(7):1658-67. doi: 10.1039/c3mb70604d. Epub 2014 Feb 18.
Aging-the progressive decline of biological functions-is a universal fact of life. Decades of intense research in unicellular and metazoan model organisms have highlighted that aging manifests at all levels of biological organization - from the decline of individual cells, to tissue and organism degeneration. To better understand the aging process, we must first aim to integrate quantitative biological understanding on the systems and cellular levels. A second key challenge is to then understand the many heterogeneous outcomes that may result in aging cells, and to connect cellular aging to organism-wide degeneration. Addressing these challenges requires the development of high-throughput aging and longevity assays. In this review, we highlight the emergence of high-throughput aging approaches in the most commonly used model organisms. We conclude with a discussion of the critical questions that can be addressed with these new methods.
衰老——生物功能的渐进性衰退——是生活中普遍存在的事实。几十年来,在单细胞和后生动物模式生物中的深入研究突出表明,衰老表现在生物组织的各个层面——从单个细胞的衰退到组织和生物体的退化。为了更好地理解衰老过程,我们首先必须致力于整合系统和细胞层面的定量生物学理解。第二个关键挑战是理解可能导致细胞衰老的众多异质性结果,并将细胞衰老与整个生物体的退化联系起来。应对这些挑战需要开发高通量衰老和寿命测定方法。在本综述中,我们重点介绍了在最常用的模式生物中高通量衰老方法的出现。最后,我们讨论了可以用这些新方法解决的关键问题。