Histatin 1 enhanced the speed and quality of wound healing through regulating the behaviour of fibroblast

成纤维细胞 伤口愈合 肌成纤维细胞 细胞生物学 体外 化学 医学 免疫学 生物 病理 生物化学 纤维化
作者
Liuhanghang Cheng,Xiaoxuan Lei,Zengjun Yang,Yanan Kong,Pengcheng Xu,Shiya Peng,Jue Wang,Cheng Chen,Yunqing Dong,Xiaohong Hu,Xiaorong Zhang,Tymour Forouzanfar,Gang Wu,Xiaobing Fu
出处
期刊:Cell Proliferation [Wiley]
卷期号:54 (8) 被引量:13
标识
DOI:10.1111/cpr.13087
摘要

Abstract Objectives Histatin 1(Hst 1) has been proved to promote wound healing. However, there was no specific study on the regulation made by Hst 1 of fibroblasts in the process of wound healing. This research comprehensively studied the regulation of Hst 1 on the function of fibroblasts in the process of wound healing and preliminary mechanism about it. Materials and methods The full‐thickness skin wound model was made on the back of C57/BL6 mice. The wound healing, collagen deposition and fibroblast distribution were detected on days 3, 5 and 7 after injury. Fibroblast was cultured in vitro and stimulated with Hst 1, and then, their biological characteristics and functions were detected. Results Histatin 1 can effectively promote wound healing, improve collagen deposition during and after healing and increase the number and function of fibroblasts. After healing, the mechanical properties of the skin also improved. In vitro, the migration ability of fibroblasts stimulated by Hst 1 was significantly improved, and the fibroblasts transformed more into myofibroblasts, which improved the function of contraction and collagen secretion. In fibroblasts, mTOR signalling pathway can be activated by Hst 1. Conclusions Histatin 1 can accelerate wound healing and improve the mechanical properties of healed skin by promoting the function of fibroblasts. The intermolecular mechanisms need to be further studied, and this study provides a direction about mTOR signalling pathway.
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