C2C12型
心肌细胞
促炎细胞因子
细胞生物学
化学
炎症
细胞分化
一氧化氮
巨噬细胞
生物
分子生物学
肌发生
生物化学
内分泌学
免疫学
体外
基因
作者
Tainá Caroline dos Santos,Kaline de Brito Sousa,Lucas Andreo,Andréia Martinelli,Maria Fernanda Setúbal Destro Rodrigues,Sandra Kalil Bussadori,Kristianne Porta Santos Fernandes,Raquel Agnelli Mesquita‐Ferrari
摘要
Abstract Moderate levels of a proinflammatory macrophages phenotype are indispensable and play an important role in the skeletal muscle repair process since this response depends on their secreted products concentration to influence and modulate muscle inflammation as well as the differentiation of myoblasts. This study investigated the effects of photobiomodulation (PBM) on undifferentiated and differentiation‐induced C2C12 myoblasts cultivated in different concentrations of M1 phenotype macrophage‐conditioned media of J774 cells (MCM1) also submitted to PBM using the same irradiation parameters. Irradiation was performed once with low‐level laser (780 nm, 70 mW, 1 J) and was evaluated cell viability, proliferation and differentiation, nitric oxide (NO) synthesis and IL‐6 and TNF‐α protein levels 24 and 48 h after C2C12 irradiation. PBM treatment in undifferentiated myoblasts exhibited lower IL‐6 levels in the presence of nonirradiated MCM1 at both concentrations. Myoblasts in proliferation condition cultivated with irradiated MCM1 showed lower IL‐6 and TNF‐α levels after 48 h in the presence of both concentrations evaluated. PBM induced a decrease in the synthesis of NO on undifferentiated and differentiation‐induced myoblasts. PBM was able to reduce the level of proinflammatory protein and markers, which are important to allow the differentiation of myoblasts during the muscle repair process.
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