Garcia-Merino Jose Angel, Carrabs Vittoria, Ferrini Fabio, Salucci Sara, Battistelli Michela, Burattini Sabrina, Luchetti Francesca, Nasoni Maria Gemma, Annibalini Giosuè, Micucci Matteo, Gianfanti Federico, Sestili Piero, Larrosa Mar, Barbieri Elena
Faculty of Health Sciences, Universidad Europea de Canarias, La Orotava, Spain.
MAS Microbiota Group, Faculty of Biomedical and Health Sciences, Universidad Europea de Madrid, Villaviciosa de Odón, Spain.
Microsc Res Tech. 2025 Mar;88(3):905-912. doi: 10.1002/jemt.24755. Epub 2024 Nov 30.
In this study, we describe the effect of cocoa polyphenol extract (CPE, from flavanols-rich cocoa) on myogenic differentiation in murine myoblasts (C2C12 cells) exposed to HO. The myogenic program was monitored using morphological, ultrastructural, and molecular approaches. Treatment with 100 μM of HO for 1 h decreased cell viability. C2C12 (D1) exposed to HO shows more apoptotic and necrotic cells, and mitochondria appear emptied, with cristae heavily damaged. To evaluate the effect of CPE on myoblast viability and myotube formation, 10 μg/mL of CPE were added 24 h prior to HO treatment and cells were supplemented with fresh CPE every 24 h during differentiation. Supplementation with CPE protected C2C12 myoblasts from HO-induced oxidative damage both at early (D1) and late (D6) phases of differentiation, preventing cell death and mitochondrial damage. The number of mitochondria (per area of cell surface) increased 2-fold in both control and in CPE-supplemented and mitochondria in myotubes D6 showed a greater extension of mitochondrial cristae than mitochondria in D1. At D1 and D6 the monolayers showed surface and inner cell features relatively comparable to the untreated control suggesting that CPE supplementation significantly mitigated the effect of HO. Preliminary data obtained by the myogenic index (Giemsa staining) suggested that CPE-supplemented cells were partially protected from HO-induced myogenesis inhibition. The CPE supplementation seems to preserve the mitochondrial integrity and the myogenic differentiation ability of oxidatively injured C2C12 ensuing further nutraceutical perspectives.
在本研究中,我们描述了可可多酚提取物(CPE,来自富含黄烷醇的可可)对暴露于过氧化氢(HO)的小鼠成肌细胞(C2C12细胞)成肌分化的影响。使用形态学、超微结构和分子方法监测成肌程序。用100μM的HO处理1小时会降低细胞活力。暴露于HO的C2C12(D1)显示出更多的凋亡和坏死细胞,线粒体似乎排空,嵴严重受损。为了评估CPE对成肌细胞活力和肌管形成的影响,在HO处理前24小时添加10μg/mL的CPE,并且在分化过程中每24小时向细胞补充新鲜的CPE。补充CPE在分化的早期(D1)和晚期(D6)均保护C2C12成肌细胞免受HO诱导的氧化损伤,防止细胞死亡和线粒体损伤。在对照和补充CPE的细胞中,线粒体数量(每细胞表面积)增加了2倍,并且在D6肌管中的线粒体嵴比D1中的线粒体嵴具有更大的延伸。在D1和D6时,单层细胞显示出与未处理对照相对可比的表面和内部细胞特征,这表明补充CPE显著减轻了HO的影响。通过成肌指数(吉姆萨染色)获得的初步数据表明,补充CPE的细胞部分免受HO诱导的成肌抑制。补充CPE似乎能保持氧化损伤的C2C12的线粒体完整性和成肌分化能力,从而带来进一步的营养保健前景。