Gutiérrez David, Rouabhia Mahmoud, Ortiz Javiera, Gaviria Diego, Alfonso Camilo, Muñoz Ana, Inostroza Carolina
Faculty of dentistry, Buccal Innovation research group, Antonio Nariño University, Bogotá, Colombia.
Faculty of Dentistry, Laval University, Quebec, Canada.
J Lasers Med Sci. 2021 Dec 1;12:e75. doi: 10.34172/jlms.2021.75. eCollection 2021.
Low-level laser therapy (LLLT) has been reported to improve cell proliferation and differentiation. The stem cells derived from dental apical papilla (SCAPs) are a promising therapy because they are easily obtained from immature human teeth. The effect of LLLT over SCAPs is still unknown. This study aimed to evaluate the proliferation and osteogenic potential of the SCAPs stimulated with LLLT. SCAPs were isolated from the third molars of a healthy donor and characterized according to the minimum established criteria. SCAPs were cultured for 24 hours before being exposed to LLLT. Cells were exposed to different doses, energy, and wavelengths for selecting the irradiation parameters. SCAPs proliferation was evaluated with the MTT assay at 24 hours and 7-day post-laser exposure. VEGF and TGFβ2 expression were assessed with a specific enzyme-linked immunosorbent assay (ELISA). The osteogenic differentiation potential was analyzed with alizarin red staining, and the nodule quantification was performed by the relative optical density (ROD) analysis using ImageJ software. The cells isolated from the apical papilla showed phenotype and stem cell properties. SCAPs irradiated with one dose at 6 J/m and 650 nm exhibited significantly higher proliferation (>0.05) than the controls nonirradiated. LLLT stimulated SCAPs' expression of factors VEGF and TGFβ2. Also, SCAPs irradiated showed higher osteogenic activity (<0.05). LLLT promotes proliferation, osteogenic differentiation, and VEGF and TGFβ2 expression on SCAPs. LLLT is a practical approach for the preconditioning of SCAPs for future regenerative therapies. More studies are needed to determine the underlying molecular processes that determine the mechanism of the LLLT.
据报道,低强度激光疗法(LLLT)可促进细胞增殖和分化。源自根尖乳头的干细胞(SCAPs)是一种很有前景的治疗方法,因为它们很容易从未成熟的人类牙齿中获取。LLLT对SCAPs的影响尚不清楚。本研究旨在评估经LLLT刺激的SCAPs的增殖和成骨潜力。从一名健康供体的第三磨牙中分离出SCAPs,并根据既定的最低标准进行鉴定。SCAPs在暴露于LLLT之前培养24小时。细胞暴露于不同剂量、能量和波长下以选择照射参数。在激光照射后24小时和7天,用MTT法评估SCAPs的增殖。用特异性酶联免疫吸附测定(ELISA)评估血管内皮生长因子(VEGF)和转化生长因子β2(TGFβ2)的表达。用茜素红染色分析成骨分化潜力,并使用ImageJ软件通过相对光密度(ROD)分析进行结节定量。从根尖乳头分离出的细胞表现出表型和干细胞特性。在6 J/m和650 nm波长下以单一剂量照射的SCAPs的增殖明显高于未照射的对照组(>0.05)。LLLT刺激了SCAPs中VEGF和TGFβ2因子的表达。此外,照射后的SCAPs表现出更高的成骨活性(<0.05)。LLLT促进SCAPs的增殖、成骨分化以及VEGF和TGFβ2的表达。LLLT是一种用于SCAPs预处理以用于未来再生治疗的实用方法。需要更多的研究来确定决定LLLT机制的潜在分子过程。