Photobiomodulation Facilitates Rat Cutaneous Wound Healing by Promoting Epidermal Stem Cells and Hair Follicle Stem Cells Proliferation.

IF 4.4 4区 医学 Q2 CELL & TISSUE ENGINEERING Tissue engineering and regenerative medicine Pub Date : 2024-01-01 Epub Date: 2023-10-26 DOI:10.1007/s13770-023-00601-5
Tong Wang, Yajuan Song, Liu Yang, Wei Liu, Zhen'an He, Yi Shi, Baoqiang Song, Zhou Yu
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Abstract

Background: Cutaneous wound healing represents a common fundamental phenomenon requiring the participation of cells of distinct types and a major concern for the public. Evidence has confirmed that photobiomodulation (PBM) using near-infrared (NIR) can promote wound healing, but the  cells involved and the precise molecular mechanisms remain elusive.

Methods: Full-thickness skin defects with a diameter of 1.0 cm were made on the back of rats and randomly divided into the control group, 10 J, 15 J, and 30 J groups. The wound healing rate at days 4, 8, and 12 postoperatively was measured. HE and Masson staining was conducted to reveal the histological characteristics. Immunofluorescence staining was performed to label the epidermal stem cells (ESCs) and hair follicle stem cells (HFSCs). Western blot was performed to detect the expressions of proteins associated with ESCs and HFSCs. Cutaneous wound tissues were collected for RNA sequencing. Gene ontology and the Kyoto Encyclopedia of Genes and Genomes analysis was performed, and the hub genes were identified using CytoHubba and validated by qRT-PCR.

Results: PBM can promote reepithelialization, extracellular matrix deposition, and wound healing, increase the number of KRT14+/PCNA+ ESCs and KRT15+/PCNA+ HFSCs, and upregulate the protein expression of P63, Krt14, and PCNA. Three hundred and sixty-six differentially expressed genes (DEGs) and 7 hub genes including Sox9, Krt5, Epcam, Cdh1, Cdh3, Dsp, and Pkp3 were identified. These DEGs are enriched in skin development, cell junction, and cadherin binding involved in cell-cell adhesion etc., while these hub genes are related to skin derived stem cells and cell adhesion.

Conclusion: PBM accelerates wound healing by enhancing reepithelialization through promoting ESCs and HFSCs proliferation and elevating the expression of genes associated with stem cells and cell adhesion. This may provide a valuable alternative strategy to promote wound healing and reepithelialization by modulating the proliferation of skin derived stem cells and regulating genes related to cell adhesion.

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光生物调节通过促进表皮干细胞和毛囊干细胞增殖促进大鼠皮肤伤口愈合。
背景:皮肤伤口愈合是一种常见的基本现象,需要不同类型的细胞参与,也是公众关注的主要问题。有证据证实,使用近红外(NIR)的光生物调制(PBM)可以促进伤口愈合,但所涉及的细胞和确切的分子机制仍然难以捉摸。方法:在大鼠背部制作直径1.0cm的全厚皮肤缺损,随机分为对照组、10J组、15J组和30J组。测量术后第4、8和12天的伤口愈合率。HE和Masson染色显示组织学特征。免疫荧光染色标记表皮干细胞(ESCs)和毛囊干细胞(HFSC)。进行蛋白质印迹以检测与ESCs和HFSC相关的蛋白质的表达。收集皮肤伤口组织进行RNA测序。结果:PBM能促进再上皮化、细胞外基质沉积和伤口愈合,增加KRT14+/PCNA的数量+ ESCs和KRT15+/PCNA+ HFSC,并上调P63、Krt14和PCNA的蛋白表达。鉴定了366个差异表达基因(DEG)和7个枢纽基因,包括Sox9、Krt5、Epcam、Cdh1、Cdh3、Dsp和Pkp3。这些DEG富含皮肤发育、细胞连接和参与细胞-细胞粘附的钙粘蛋白结合等,而这些中枢基因与皮肤来源的干细胞和细胞粘附有关。结论:PBM通过促进ESCs和HFSCs的增殖和提高干细胞和细胞粘附相关基因的表达,促进再上皮化,从而加速伤口愈合。这可能提供一种有价值的替代策略,通过调节皮肤来源的干细胞的增殖和调节与细胞粘附相关的基因来促进伤口愈合和再上皮化。
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来源期刊
Tissue engineering and regenerative medicine
Tissue engineering and regenerative medicine CELL & TISSUE ENGINEERING-ENGINEERING, BIOMEDICAL
CiteScore
6.80
自引率
5.60%
发文量
83
审稿时长
6-12 weeks
期刊介绍: Tissue Engineering and Regenerative Medicine (Tissue Eng Regen Med, TERM), the official journal of the Korean Tissue Engineering and Regenerative Medicine Society, is a publication dedicated to providing research- based solutions to issues related to human diseases. This journal publishes articles that report substantial information and original findings on tissue engineering, medical biomaterials, cells therapy, stem cell biology and regenerative medicine.
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