Institute of Clinical Sciences, School of Dentistry, University of Birmingham, 5 Mill Pool Way, Edgbaston, Birmingham, B5 7EG, UK.
Institute of Microbiology and Infection, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Photochem Photobiol Sci. 2021 May;20(5):699-714. doi: 10.1007/s43630-021-00047-5. Epub 2021 May 4.
Mesenchymal stem cells (MSCs) and photobiomodulation (PBM) both offer significant therapeutic potential in regenerative medicine. MSCs have the ability to self-renew and differentiate; giving rise to multiple cellular and tissue lineages that are utilised in repair and regeneration of damaged tissues. PBM utilises light energy delivered at a range of wavelengths to promote wound healing. The positive effects of light on MSC proliferation are well documented; and recently, several studies have determined the outcomes of PBM on mineralised tissue differentiation in MSC populations. As PBM effects are biphasic, it is important to understand the underlying cellular regulatory mechanisms, as well as, provide accurate details of the irradiation conditions, to optimise and standardise outcomes. This review article focuses on the use of red, near-infra-red (R/NIR) and blue wavelengths to promote the mineralisation potential of MSCs; and also reports on the possible molecular mechanisms which underpin transduction of these effects. A variety of potential photon absorbers have been identified which are reported to mediate the signalling mechanisms, including respiratory chain enzymes, flavins, and cryptochromes. Studies report that R/NIR and blue light stimulate MSC differentiation by enhancing respiratory chain activity and increasing reactive oxygen species levels; however, currently, there are considerable variations between irradiation parameters reported. We conclude that due to its non-invasive properties, PBM may, following optimisation, provide an efficient therapeutic approach to clinically support MSC-mediated hard tissue repair. However, to optimise application, further studies are required to identify appropriate light delivery parameters, as well as elucidate the photo-signalling mechanisms involved.
间充质干细胞(MSCs)和光生物调节(PBM)在再生医学中都具有重要的治疗潜力。MSCs 具有自我更新和分化的能力;产生多种细胞和组织谱系,用于修复和再生受损组织。PBM 利用一系列波长的光能促进伤口愈合。光照对 MSC 增殖的积极影响已有大量文献记载;最近,有几项研究确定了 PBM 对 MSC 群体中矿化组织分化的影响。由于 PBM 效应呈双相性,因此了解潜在的细胞调节机制非常重要,同时还需要提供准确的辐照条件细节,以优化和标准化结果。本文综述了使用红光、近红外光(R/NIR)和蓝光来提高 MSCs 的矿化潜力,并报告了支持这些效应转导的可能分子机制。已经确定了多种潜在的光吸收剂,据报道它们介导信号转导机制,包括呼吸链酶、黄素和隐花色素。研究报告称,R/NIR 和蓝光通过增强呼吸链活性和增加活性氧水平来刺激 MSC 分化;然而,目前报告的辐照参数存在很大差异。我们得出结论,由于 PBM 的非侵入性特性,经过优化后,它可能为临床支持 MSC 介导的硬组织修复提供一种有效的治疗方法。然而,为了优化应用,需要进一步的研究来确定合适的光传递参数,并阐明涉及的光信号转导机制。
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