Taohong Siwu decoction promotes the process of fracture healing by activating the VEGF-FAK signal pathway and systemically regulating the gut microbiota

骨愈合 细胞生物学 血管内皮生长因子 间充质干细胞 化学 伤口愈合 免疫印迹 血管生成 信号转导 男科 生物 免疫学 癌症研究 医学 血管内皮生长因子受体 解剖 生物化学 基因
作者
Wangyang Li,Tiao Li,Zhi Tang,Xinyu Qi,Youliang Zhou,Tang Xiaolu,Weijie Xu,Hui Xiong
出处
期刊:Journal of Applied Microbiology [Oxford University Press]
卷期号:133 (3): 1363-1377 被引量:9
标识
DOI:10.1111/jam.15598
摘要

Abstract Aims This study aimed to explore the effect of Taohong Siwu Decoction (THSWD) on bone marrow mesenchymal stem cells (BMSCs) at the cellular level and the possible mechanism of systemic regulation of gut microbiota on fracture recovery. Methods and Results Cell Counting Kit-8 (CCK-8) experiments show that THSWD effectively promotes the proliferation of BMSCs. Transwell and wound healing assays show that THSWD effectively promotes the invasion and migration of BMSCs. Alizarin red staining showed that the THSWD model enhanced the osteogenic differentiation of BMSCs. Moreover, the effect of THSWD on BMSCs is time- and concentration-dependent. RT-qPCR and western blot results showed that THSWD treatment up-regulated the expression of vascular endothelial growth factor (VEGF) and focal adhesion kinase (FAK) at mRNA and protein levels, respectively. Haematoxylin–eosin and crocin O-quick green staining showed that after 14 days of THSWD treatment, the area of callus and cartilage regeneration at the fracture site increased significantly in rats with right femoral shaft fractures. Gut microbiota was changed in fractured rats, such as the abundance of Bacteroidetes and Firmicutes was increased. THSWD showed positive regulation of both to a certain extent. Conclusion THSWD up-regulates VEGF and activates the FAK signalling pathway to enhance the development and differentiation of BMSCs, and systematically regulates the gut microbiota to promote fracture healing. Significance and Impact of Study This study provides new insights on the cellular and systemic level to understand the mechanism of THSWD in the treatment of fractures.
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