High-content image screening to identify chemical modulators for peroxisome and ferroptosis

• Published in: Cellular & molecular biology letters 2024-02, Vol.29 (1), p.26-26, Article 26
• Main Authors: Zheng, Daheng, Li, Fei, Wang, Shanshan, Liu, Pu-Ste, Xie, Xin
• Format: Article
• Language: English
• Subjects: Automation; Biosynthesis; Brief Report; Cancer; Cell cycle; Cell death; Chemicals; Fatty acids; Ferroptosis; Flow cytometry; High-content screening; Homeostasis; Lipids; Metabolism; Metabolites; Oxidation; Oxidative stress; Peroxisome; Proteins; Reactive oxygen species; S phase; Software; Spheroids; U-2OS
• ISSN: 1689-1392; 1425-8153; 1689-1392
• DOI: 10.1186/s11658-024-00544-2

The peroxisome is a dynamic organelle with variety in number, size, shape, and activity in different cell types and physiological states. Recent studies have implicated peroxisomal homeostasis in ferroptosis susceptibility. Here, we developed a U-2OS cell line with a fluorescent peroxisomal tag and screened a target-selective chemical library through high-content imaging analysis. U-2OS cells stably expressing the mOrange2-Peroxisomes2 tag were generated to screen a target-selective inhibitor library. The nuclear DNA was counterstained with Hoechst 33342 for cell cycle analysis. Cellular images were recorded and quantitatively analyzed through a high-content imaging platform. The effect of selected compounds on ferroptosis induction was analyzed in combination with ferroptosis inducers (RSL3 and erastin). Flow cytometry analysis was conducted to assess the level of reactive oxygen species (ROS) and cell death events. Through the quantification of DNA content and peroxisomal signals in single cells, we demonstrated that peroxisomal abundance was closely linked with cell cycle progression and that peroxisomal biogenesis mainly occurred in the G1/S phase. We further identified compounds that positively and negatively regulated peroxisomal abundance without significantly affecting the cell cycle distribution. Some compounds promoted peroxisomal signals by inducing oxidative stress, while others regulated peroxisomal abundance independent of redox status. Importantly, compounds with peroxisome-enhancing activity potentiated ferroptosis induction. Our findings pinpoint novel cellular targets that might be involved in peroxisome homeostasis and indicate that compounds promoting peroxisomal abundance could be jointly applied with ferroptosis inducers to potentiate anticancer effect.