Wu Tinghui, Zhang Yan Man, Krishnan Sasirekha, Jaisankar Abinaya, Wan Yu, Gong Shu Juan, Zhou Hang Zhen, Wang Hai Tao, Ramalingam Murugan, Li Shu-Wei
Xinjiang Production & Construction Corps Key Laboratory of Protection and Utilization of Biological Resources in Tarim Basin, College of Life Science and Technology, Tarim University, Alar 843300, Xinjiang, China.
Department of Immunology, Nanjing Medical University, Nanjing 211166, Jiangsu, China.
J Biomed Nanotechnol. 2022 Feb 1;18(2):463-473. doi: 10.1166/jbn.2022.3251.
: A bioactive small molecule of precision medicine involves targeted therapies. Shikonin, a herbal extract, is an active small molecule that is traditionally used in wound healing for its anti-tumor and anti-inflammatory properties. Therefore, the present study aims to evaluate the anti-inflammatory role of shikonin in skin burn wound healing and hair follicle regeneration and to identify molecular signaling pathways that promote the regeneration. : A secondary skin burn model of mice was established by conventional method. The burn wound was externally treated with shikonin ointment and excipient treated mice were used as controls. Skin samples were taken on the day 3 and 7 after drug treatment and the dosage was unified in the experiments. The wound healing process was observed by histopathological and immunofluorescence (IF) staining. The proliferation of hair follicle cells in wound skin was tracked by 5-Ethynyl-2'-deoxyuridne (EdU) staining. The inflammatory factors at the wound healing site were quantified by polymerase chain reaction (qPCR). The PI3K/Akt, P65, Ki67 signaling proteins and Bax/BCL2 apoptosis proteins were studied by western blot analysis. The functionality of PI3K/Akt signaling pathway was tested using LY294002, an inhibitor of PI3K. : Shikonin treated mice group exhibited better and faster skin burn wound healing in comparison with the controls. The proliferation of new skin cells and hair follicle regeneration in the wound site of the shikonin treated group was more active. The recruitment of macrophages in shikonin treated group was inhibited inturn decreased the expression of inflammatory factors. However, LY294002 inhibited the shikonin-mediated PI3K/Akt signaling pathway and affected the wound healing process. : In conclusion, this study strengthens the hypothesis that bioactive small molecule, shikonin, inhibits inflammation, promotes wound healing and has a significant protective effect on the deep hair follicles against burn skin injury by activating the PI3K/Akt signaling pathway.
一种用于精准医学的生物活性小分子涉及靶向治疗。紫草素是一种草药提取物,是一种活性小分子,传统上因其抗肿瘤和抗炎特性而用于伤口愈合。因此,本研究旨在评估紫草素在皮肤烧伤创面愈合和毛囊再生中的抗炎作用,并确定促进再生的分子信号通路。通过常规方法建立小鼠继发性皮肤烧伤模型。用紫草素软膏对烧伤创面进行外部处理,以赋形剂处理的小鼠作为对照。在药物治疗后第3天和第7天采集皮肤样本,实验中剂量统一。通过组织病理学和免疫荧光(IF)染色观察伤口愈合过程。用5-乙炔基-2'-脱氧尿苷(EdU)染色追踪伤口皮肤中毛囊细胞的增殖。通过聚合酶链反应(qPCR)对伤口愈合部位的炎症因子进行定量。通过蛋白质免疫印迹分析研究PI3K/Akt、P65、Ki67信号蛋白和Bax/BCL2凋亡蛋白。使用PI3K抑制剂LY294002测试PI3K/Akt信号通路的功能。与对照组相比,紫草素处理的小鼠组表现出更好、更快的皮肤烧伤创面愈合。紫草素处理组伤口部位新皮肤细胞的增殖和毛囊再生更活跃。紫草素处理组中巨噬细胞的募集受到抑制,进而降低了炎症因子的表达。然而,LY294002抑制了紫草素介导的PI3K/Akt信号通路,并影响了伤口愈合过程。总之,本研究强化了这样一种假设,即生物活性小分子紫草素通过激活PI3K/Akt信号通路抑制炎症、促进伤口愈合,并对深部毛囊免受烧伤皮肤损伤具有显著的保护作用。