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Updated: May 24, 2025

Author Spotlight: Exploring the Antibacterial Effects of Zinc Oxide Nanoparticles in Overcoming Antibiotic Resistance
Published on: September 27, 2024
Zinc oxide nanoparticles promote migrasomes formation
Ang Li1, Chengxiong Yang2, Leiliang Zhang3
1Department of Clinical Laboratory Medicine, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, Shandong, China; School of Pharmaceutical Sciences & Institute of Materia Medica, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong, China; Department of Pathogen Biology, School of Clinical and Basic Medical Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong, China; Medical Science and Technology Innovation Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Zinc oxide nanoparticles (ZnO-NPs) boost migrasome formation and protect cells from mitochondrial damage. These findings highlight ZnO-NPs
Area of Science:
- Nanotechnology
- Cell Biology
- Environmental Science
Background:
- Zinc oxide nanoparticles (ZnO-NPs) are increasingly prevalent environmental pollutants.
- Their impact on cellular processes, particularly migrasome formation, remains largely unexplored.
- Understanding these interactions is crucial for assessing health and environmental risks.
Purpose of the Study:
- To investigate the effects of ZnO-NPs on migrasome formation.
- To determine the molecular mechanisms underlying ZnO-NP-induced migrasome biogenesis.
- To assess the protective role of ZnO-NPs against mitochondrial dysfunction.
Main Methods:
- Exposure of cells to 28 nm ZnO-NPs.
- Analysis of migrasome formation and cellular component content.
- Measurement of phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2] and GTP-RhoA levels.
- Evaluation of mitochondrial integrity and mitocytosis induction.
Main Results:
- 28 nm ZnO-NPs significantly enhanced migrasome formation.
- Increased levels of PI(4,5)P2 and GTP-RhoA were observed in ZnO-NP-treated cells.
- ZnO-NPs mitigated mitochondrial damage induced by CCCP via mitocytosis.
- Migrasomes induced by ZnO-NPs contained mitochondria, lysosomes, lipid droplets, and ZnO-NPs.
Conclusions:
- ZnO-NPs promote migrasome formation through specific molecular pathways.
- ZnO-NPs offer protection against mitochondrial damage by enhancing mitocytosis.
- These findings have implications for cellular communication, potential therapeutics, and environmental safety assessments.
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