Polystyrene microplastics-induced ROS overproduction disrupts the skeletal muscle regeneration by converting myoblasts into adipocytes

• Published in: Journal of hazardous materials 2021-09, Vol.417, p.125962-125962, Article 125962
• Main Authors: Shengchen, Wang, Jing, Liu, Yujie, Yao, Yue, Wang, Shiwen, Xu
• Format: Article
• Language: English
• Subjects: Adipocytes; Microplastic; Myogenic differentiation; Oxidative stress; Skeletal muscle
• ISSN: 0304-3894; 1873-3336
• DOI: 10.1016/j.jhazmat.2021.125962

The environmental problem of Microplastics (MPs) pollution poses a great threat to human and animal health, which has attracted global attention. The physiological integrity of skeletal muscle is extremely important for the survival of animals. Here, we investigated the effect of two size polystyrene microplastics (PS-MPs, 1–10 µm and 50–100 µm) on the growth of anterior tibial (TA) muscle and repair after injury in mice. Results showed that the regeneration of skeletal muscle was delayed by PS-MPs exposure and was negatively correlated with particle size. H&E staining and Oil red O staining showed that PS-MPs exposure reduced the average cross-sectional area (CSA) and diameter of the muscle fibers, increased lipid deposition. Further mechanistic research displayed that though PS-MPs treatment did not affect cell viability of myoblast, it aggravated intracellular ROS generation and oxidative stress, inhibited myogenic differentiation by decreasing the phosphorylation of p38 MAPK, and promote adipogenic differentiation by increasing the expression of NF-κB, which could be alleviated by NAC. In brief, our data demonstrated that the ROS overproduction caused by PS-MPs disturbed the regeneration of skeletal muscle and directed the fate of satellite cells in mice. [Display omitted] •PS-MPs exposure caused failed muscle fiber regeneration.•PS-MPs disrupted the balance between myogenic and adipogenic differentiation.•PS-MPs exposure induced the ROS overproduction in satellite cells.•PS-MPs changed the activation of p38 MAPK and NF-κB during muscle regeneration.