Ackert-Bicknell Cheryl L, Anderson Laura C, Sheehan Susan, Hill Warren G, Chang Bo, Churchill Gary A, Chesler Elissa J, Korstanje Ron, Peters Luanne L
The Jackson Laboratory, Bar Harbor, Maine.
Present address: University of Rochester, Department of Orthopaedics and Rehabilitation, Rochester, New York.
Curr Protoc Mouse Biol. 2015 Jun 1;5(2):95-133. doi: 10.1002/9780470942390.mo140195.
Despite the dramatic increase in human lifespan over the past century, there remains pronounced variability in "health-span," or the period of time in which one is generally healthy and free of disease. Much of the variability in health-span and lifespan is thought to be genetic in origin. Understanding the genetic mechanisms of aging and identifying ways to boost longevity is a primary goal in aging research. Here, we describe a pipeline of phenotypic assays for assessing mouse models of aging. This pipeline includes behavior/cognition testing, body composition analysis, and tests of kidney function, hematopoiesis, and immune function, as well as physical parameters. We also describe study design methods for assessing lifespan and health-span, and other important considerations when conducting aging research in the laboratory mouse. The tools and assays provided can assist researchers with understanding the correlative relationships between age-associated phenotypes and, ultimately, the role of specific genes in the aging process.
尽管在过去一个世纪人类寿命显著延长,但“健康寿命”(即一个人总体健康且无疾病的时间段)仍存在明显差异。健康寿命和寿命的大部分差异被认为源于基因。了解衰老的遗传机制并确定延长寿命的方法是衰老研究的主要目标。在此,我们描述了一套用于评估衰老小鼠模型的表型分析流程。该流程包括行为/认知测试、身体成分分析、肾功能测试、造血功能测试、免疫功能测试以及身体参数测试。我们还描述了评估寿命和健康寿命的研究设计方法,以及在实验室小鼠中进行衰老研究时的其他重要注意事项。所提供的工具和分析方法可帮助研究人员了解与年龄相关的表型之间的相关关系,并最终了解特定基因在衰老过程中的作用。