自噬
焊剂(冶金)
麦克赫里
细胞生物学
计算生物学
工作流程
骨关节炎
鉴定(生物学)
生物
机制(生物学)
生物信息学
医学
计算机科学
神经科学
化学
病理
绿色荧光蛋白
生物化学
细胞凋亡
物理
替代医学
有机化学
基因
植物
量子力学
数据库
作者
Uxía Nogueira-Recalde,I. Lorenzo-Gómez,Marı́a Isabel Loza,Eduardo Domínguez,B. Caramés
摘要
Autophagy is a central mechanism to regulate homeostasis. Alterations of autophagy contribute to aging-related diseases. Phenotypic methods to identify regulators of autophagy could be used for the identification of novel therapeutics. This article describes a cell-based imaging screening workflow developed to monitor autophagic flux using LC3 as a reporter of autophagic flux (mCherry-EGFP-LC3B) in human chondrocytes. Data acquisition is performed using an automated High Content Imaging Screening System microscope. An algorithm-based automated image analysis protocol was developed and validated to identify molecules activating autophagic flux. Critical steps, explanatory notes, and improvements over current autophagy monitoring protocols are reported. Physiologically relevant phenotypic screening approaches to target hallmarks of aging can facilitate more effective drug discovery strategies for age-related musculoskeletal diseases.
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