非人灵长类动物老年病理学分级平台的建立。

Katie J Olstad, Denise M Imai, Rebekah I Keesler, Rachel Reader, John H Morrison, Jeffery A Roberts, John P Capitanio, Elizabeth S Didier, Marcelo J Kuroda, Heather Simmons, Shabnam Salimi, Julie A Mattison, Yuji Ikeno, Warren Ladiges
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引用次数: 3

摘要

一种用于评估年龄相关病变的老年病理学分级平台(GGP)已经建立并在近交系小鼠中得到验证。由于非人灵长类动物(NHPs)在衰老和自发性慢性疾病方面与人类有着显著的相似性,因此它们在将组织病理学与与年龄增长相关的生物和病理事件联系起来方面提供了极好的翻译价值。恒河猴和狨猴的描述性年龄相关病理已被描述,但类似于小鼠GGP的分级平台尚不存在。来自临床、生物行为和社会领域的大量历史数据与这些动物的健康跨度相一致,增强了这些NHP模型的价值。小鼠GGP对NHPs的成功适应将包括:1)扩大检查器官的范围;2)标准化尸检收集、组织修剪和描述病变术语;3)将研究对象从恒河猴和狨猴扩展到其他常用的NHPs;4)创建与年龄相关的病理学的国家资源,以补充广泛的生活数据集。适应GGP以包括小鼠以外的转译模型对于推进旨在加强衰老研究的老年病理学至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Development of a Geropathology Grading Platform for nonhuman primates.

A geropathology grading platform (GGP) for assessing age-related lesions has been established and validated for in inbred strain of mice. Because nonhuman primates (NHPs) share significant similarities in aging and spontaneous chronic diseases with humans, they provide excellent translational value for correlating histopathology with biological and pathological events associated with increasing age. Descriptive age-associated pathology has been described for rhesus macaques and marmosets, but a grading platform similar to the mouse GGP does not exist. The value of these NHP models is enhanced by considerable historical data from clinical, bio-behavioral, and social domains that align with health span in these animals. Successful adaptation of the mouse GGP for NHPs will include 1) expanding the range of organs examined; 2) standardizing necropsy collection, tissue trimming, and descriptive lesion terminology; 3) expanding beyond rhesus macaques and marmosets to include other commonly used NHPs in research; and 4) creating a national resource for age-related pathology to complement the extensive in-life datasets. Adaptation of the GGP to include translational models other than mice will be crucial to advance geropathology designed to enhance aging research.

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