Ninth Department of Plastic Surgery, Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 33, Badachu Road, Shijingshan District, Beijing, 100144, China.
Lasers Med Sci. 2022 Apr;37(3):1699-1707. doi: 10.1007/s10103-021-03419-6. Epub 2021 Sep 21.
The aim of the study was to explore the effect and mechanism of a low-level laser on hair follicle stem cells in full-thickness skin wound healing in mice. Full-thickness skin defects were generated by a 5-mm punch biopsy tool on the backs of depilated C57/BL6N mice, which were randomly divided thereafter into a low-dose laser treatment group (LLLT-Low), a high-dose laser treatment group (LLLT-High), and a control group (control). From the day of modeling to the day before the skin samples were taken, the wound area and wound edge of the mice in the LLLT-Low and LLLT-High groups were irradiated with a laser comb every 24 h, and the energy density was 1 J/cm and 10 J/cm, respectively. The control group was irradiated with an ordinary fluorescent lamp. At 0, 3, 5, 10, and 14 days after modeling, pictures of each wound were taken, and the percent wound closure was analyzed. At 3, 5, 10, and 14 days after modeling, the samples were observed by hematoxylin and eosin (HE) and immunofluorescence (IF) staining. Whole transcriptome sequencing (RNA-Seq) was performed on the samples on day 10. Gene Ontology (GO) analysis was performed, and the results were validated by Western blot analysis and enzyme-linked immunosorbent assay (ELISA). The analysis of the percent of wound closure showed that healing was accelerated (significantly from 5 to 10 days) in the LLLT-Low group, but there was no clear change in the LLLT-High group. HE staining showed that the LLLT-Low group had an increasing number of hair follicles and a tendency to migrate to the center of the wound. There was no significant increase in the number of hair follicles and no obvious migration in the LLLT-High group. Immunofluorescence staining showed that the total number of CK15 + hair follicle stem cells in the LLLT-Low group was higher than that in the control group and LLLT-High group at all time points. The number and farthest migration distance of CK15 + hair follicle stem cells increased significantly with time, and after 5 days, they were significantly higher than those in the control group and LLLT-High group. RNA-Seq and Western blot analysis showed that the expression of related genes in hair follicle stem cells, including CK15, in the LLLT-Low group was upregulated. GO analysis and ELISA showed that the expression of many cytokines, represented by IL34, in the LLLT-Low group was upregulated. Low-level laser treatment can promote the proliferation, differentiation, and migration of CK15 + hair follicle stem cells by upregulating the cytokine IL34, thereby promoting skin wound healing in mice.
本研究旨在探讨低水平激光对小鼠全层皮肤创面愈合中毛囊干细胞的作用及机制。通过使用 5mm 打孔活检工具在去毛 C57/BL6N 小鼠背部制造全层皮肤缺损,此后将其随机分为低剂量激光治疗组(LLLT-Low)、高剂量激光治疗组(LLLT-High)和对照组(control)。从建模当天到采集皮肤样本前一天,用激光梳每天照射 LLLT-Low 和 LLLT-High 组的小鼠创面和创缘,能量密度分别为 1 J/cm 和 10 J/cm。对照组用普通荧光灯照射。在建模后 0、3、5、10 和 14 天,拍摄每个伤口的图片,并分析伤口闭合百分比。在建模后 3、5、10 和 14 天,通过苏木精和伊红(HE)和免疫荧光(IF)染色观察样本。在第 10 天对样本进行全转录组测序(RNA-Seq)。进行基因本体论(GO)分析,并通过 Western blot 分析和酶联免疫吸附测定(ELISA)验证结果。伤口闭合百分比的分析表明,LLLT-Low 组的愈合速度加快(从第 5 天到第 10 天明显加快),而 LLLT-High 组则没有明显变化。HE 染色显示,LLLT-Low 组的毛囊数量增加,并呈向伤口中心迁移的趋势。LLLT-High 组的毛囊数量没有明显增加,也没有明显的迁移。免疫荧光染色显示,在所有时间点,LLLT-Low 组的 CK15+毛囊干细胞总数均高于对照组和 LLLT-High 组。CK15+毛囊干细胞的数量和最远迁移距离随时间显著增加,第 5 天后,明显高于对照组和 LLLT-High 组。RNA-Seq 和 Western blot 分析显示,LLLT-Low 组毛囊干细胞相关基因(包括 CK15)的表达上调。GO 分析和 ELISA 显示,以 IL34 为代表的许多细胞因子的表达在 LLLT-Low 组上调。低水平激光治疗可通过上调细胞因子 IL34 促进 CK15+毛囊干细胞的增殖、分化和迁移,从而促进小鼠皮肤伤口愈合。