Wu Hao, Liu Qiannan, Meng Caiyun, Xia Qing, Pan Yue, Zhang Hanxu, Zhang Fengmin, Song Wuqi, Liu Hailiang
The Heilongjiang Key Laboratory of Immunity and Infection Harbin Medical University, Department of Microbiology, Wu Lien-Teh Institute, Harbin, P.R. China.
Photobiomodul Photomed Laser Surg. 2022 Apr;40(4):252-260. doi: 10.1089/photob.2021.0142.
Photobiomodulation (PBM) is praised as a promising physical therapy, which has many advantages, such as being noninvasive and painless. However, the mechanisms are not fully elucidated. Using web crawling, mRNA sequence, and bioinformatics analysis, we selected genes, functional annotation, and mechanisms. The expressions of inflammatory cytokines were measured using quantitative real-time PCR (RT-qPCR). A total of 146 human genes and 57 pathways were identified about PBM. The 630 nm light-emitting diode (LED)-stimulated-MH7A cells were sequenced to further analyze the mechanism of PBM. Two thousand nine hundred fifty differentially expressed genes were identified, and the gene ontology term enrichment analysis and Kyoto encyclopedia of genes and genomes pathway analysis were performed to better understand functions and pathways. The 12 pathways were matched with the KEGG results of PBM and MH7A cells. A protein-protein interaction network was performed among genes in 12 pathways, and 10 outstanding proteins were identified. Importantly, the 9 genes were predicted with potential research value. And we also demonstrated that expression of inflammatory factors [interleukin (IL)-6, IL-1β, IL-8, and matrix metalloproteinase-3 (MMP-3)] was reduced; meanwhile, the expression of anti-inflammatory factor IL-10 was promoted after 630 nm LED. Using web crawling, bioinformatics analysis, and mRNA sequence, we obtained 9 key genes and 12 important pathways about PBM. Importantly, we demonstrated the anti-inflammatory effect of 630 nm LED red light by RT-qPCR.
光生物调节作用(PBM)被誉为一种很有前景的物理治疗方法,它具有许多优点,比如无创且无痛。然而,其作用机制尚未完全阐明。通过网络爬虫、mRNA序列和生物信息学分析,我们筛选出了相关基因、功能注释及作用机制。使用定量实时聚合酶链反应(RT-qPCR)检测炎症细胞因子的表达。共鉴定出146个人类基因和57条关于PBM的信号通路。对630纳米发光二极管(LED)刺激的MH7A细胞进行测序,以进一步分析PBM的作用机制。鉴定出2950个差异表达基因,并进行基因本体术语富集分析和京都基因与基因组百科全书通路分析,以更好地了解其功能和信号通路。将这12条信号通路与PBM和MH7A细胞的KEGG结果进行匹配。在12条信号通路中的基因之间构建了蛋白质-蛋白质相互作用网络,鉴定出10个关键蛋白。重要的是,预测出9个具有潜在研究价值的基因。并且我们还证明,630纳米LED照射后炎症因子[白细胞介素(IL)-6、IL-1β、IL-8和基质金属蛋白酶-3(MMP-3)]的表达降低;同时,抗炎因子IL-10的表达升高。通过网络爬虫、生物信息学分析和mRNA序列,我们获得了9个关于PBM的关键基因和12条重要信号通路。重要的是,我们通过RT-qPCR证明了630纳米LED红光的抗炎作用。