Biology Department, Ghent University, K.L. Ledeganckstraat 35, B-9000 Ghent, Belgium.
Laboratory of Cell Biology and Histology, Department of Veterinary Sciences, University of Antwerp, 2610 Antwerp, Belgium.
Dis Model Mech. 2021 Nov 1;14(11). doi: 10.1242/dmm.049169. Epub 2021 Nov 30.
Sarcopenia encompasses a progressive decline in muscle quantity and quality. Given its close association with ageing, it may represent a valuable healthspan marker. The commonalities with human muscle structure and facile visualization possibilities make Caenorhabditis elegans an attractive model for studying the relationship between sarcopenia and healthspan. However, classical visual assessment of muscle architecture is subjective and has low throughput. To resolve this, we have developed an image analysis pipeline for the quantification of muscle integrity in confocal microscopy images from a cohort of ageing myosin::GFP reporter worms. We extracted a variety of morphological descriptors and found a subset to scale linearly with age. This allowed establishing a linear model that predicts biological age from a morphological muscle signature. To validate the model, we evaluated muscle architecture in long-lived worms that are known to experience delayed sarcopenia by targeted knockdown of the daf-2 gene. We conclude that quantitative microscopy allows for staging sarcopenia in C. elegans and may foster the development of image-based screens in this model organism to identify modulators that mitigate age-related muscle frailty and thus improve healthspan.
肌肉减少症包括肌肉数量和质量的逐渐下降。鉴于其与衰老密切相关,它可能代表了一个有价值的健康寿命标志物。与人类肌肉结构的相似性以及易于可视化的可能性,使秀丽隐杆线虫成为研究肌肉减少症与健康寿命之间关系的有吸引力的模型。然而,经典的肌肉结构的视觉评估是主观的,并且通量低。为了解决这个问题,我们开发了一个图像分析管道,用于对肌球蛋白::GFP 报告线虫的共聚焦显微镜图像中的肌肉完整性进行定量。我们提取了各种形态描述符,并发现其中一部分与年龄呈线性关系。这允许建立一个线性模型,该模型可以根据形态学肌肉特征预测生物年龄。为了验证该模型,我们评估了已知通过靶向敲低 daf-2 基因而经历延迟肌肉减少症的长寿线虫的肌肉结构。我们得出结论,定量显微镜允许在秀丽隐杆线虫中分期肌肉减少症,并可能促进基于图像的筛选在这个模式生物中的发展,以识别减轻与年龄相关的肌肉脆弱性并从而改善健康寿命的调节剂。