Vitamin C regulates skeletal muscle post-injury regeneration by promoting myoblast proliferation through its direct interaction with the Pax7 protein.

Previous studies have shown that vitamin C (VC), an essential vitamin for the human body, can promote the differentiation of muscle satellite cells (MuSCs) in vitro and play an important role in skeletal muscle post-injury regeneration. However, the molecular mechanism of VC regulating MuSC proliferation has not been elucidated. In this study, the role of VC in promoting MuSC proliferation and its molecular mechanism were explored using cell molecular biology and animal experiments. The results showed that VC accelerates the progress of skeletal muscle post-injury regeneration by promoting MuSC proliferation in vivo. VC can also promote skeletal muscle regeneration in the case of atrophy. Using the C2C12 myoblast murine cell line, we observed that VC also stimulated cell proliferation. In addition, after an in vitro study establishing the occurrence of a physical interaction between VC and Pax7, we observed that VC also upregulated the total and nuclear Pax7 protein levels. This mechanism increased the expression of Myf5 (Myogenic Factor 5), a Pax7 target gene. This study establishes a theoretical foundation for understanding the regulatory mechanisms underlying VC-mediated MuSC proliferation and skeletal muscle regeneration. Moreover, it develops the application of VC in animal muscle nutritional supplements and treatment of skeletal muscle-related diseases.

Interaction of lignin and xylan in the hydrothermal synthesis of lignocellulose-based carbon quantum dots and their application in in-vivo bioimaging.

The complex interaction of lignin, cellulose, and hemicellulose in the hydrothermal degradation progress of lignocellulose, has led to uncertainty in the hydrothermal synthesis of lignocellulose-based CQDs (LC-CQDs). This makes it difficult to identify the specific formation mechanism of LC-CQDs. To simplify the reaction system and comprehensively describe the formation of LC-CQDs, both lignin and hemicellulose, the main hydrothermal degradation products of lignocellulose, were used as precursor to simulate and explore the synthesis of LC-CQDs at different time intervals (2-12 h). First, different lignin models were employed for preparing CQDs to determine the key lignin structure that govern CQDs formation. G-type lignin-model based CQDs were shown to have higher fluorescence intensity than H- and S-type. Then, G-type lignin model and hemicellulose model (xylan) were used simultaneously hydrothermal to prepare LC-CQDs. The analysis shows that the carbon nucleus preferentially formed by the lignin provides growth sites for small molecules degraded from hemicellulose, which gradually grow around the carbon core over time, thus forming a "sunflower" structure of CQDs. The presence of a lignin model could effectively guide the small molecules toward CQDs formation instead of carbonization. Additionally, the CQDs exhibit good in-vivo imaging performance.