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Photobiomodulation Therapy in the Proliferation and Differentiation of Human Umbilical Cord Mesenchymal Stem Cells: An Study.光生物调节疗法对人脐带间充质干细胞增殖与分化的影响:一项研究
J Lasers Med Sci. 2020 Fall;11(4):469-474. doi: 10.34172/jlms.2020.73. Epub 2020 Oct 3.
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Effect of Low- Level Laser Therapy on Bone Regeneration of Critical-Size Bone Defects: A Systematic Review of In Vivo Studies and Meta-Analysis.低水平激光疗法对临界尺寸骨缺损骨再生的影响:体内研究的系统评价和荟萃分析。
Arch Oral Biol. 2020 Sep;117:104782. doi: 10.1016/j.archoralbio.2020.104782. Epub 2020 May 28.
3
Irradiation with blue light-emitting diode enhances osteogenic differentiation of stem cells from the apical papilla.蓝光发光二极管照射增强根尖乳头干细胞的成骨分化。
Lasers Med Sci. 2020 Dec;35(9):1981-1988. doi: 10.1007/s10103-020-02995-3. Epub 2020 Mar 16.
4
The Effect of Photobiomodulation Therapy on the Differentiation, Proliferation, and Migration of the Mesenchymal Stem Cell: A Review.光生物调节疗法对间充质干细胞分化、增殖和迁移的影响:综述
J Lasers Med Sci. 2019 Fall;10(Suppl 1):S96-S103. doi: 10.15171/jlms.2019.S17. Epub 2019 Dec 1.
5
Evaluation of the Apical Complex and the Coronal Pulp as a Stem Cell Source for Dentin-pulp Regeneration.根尖复合体和冠髓作为牙本质-牙髓再生的干细胞源的评价。
J Endod. 2020 Feb;46(2):224-231.e3. doi: 10.1016/j.joen.2019.10.025. Epub 2019 Dec 10.
6
Biomaterials and Scaffold Design Strategies for Regenerative Endodontic Therapy.再生牙髓治疗的生物材料与支架设计策略
Front Bioeng Biotechnol. 2019 Nov 15;7:317. doi: 10.3389/fbioe.2019.00317. eCollection 2019.
7
Effect of Photobiomodulation Therapy on the Increase of Viability and Proliferation of Human Mesenchymal Stem Cells.光生物调节疗法对人骨髓间充质干细胞活力增加和增殖的影响。
Lasers Surg Med. 2019 Nov;51(9):824-833. doi: 10.1002/lsm.23107. Epub 2019 Jun 4.
8
Stem Cells from the Apical Papilla: A Promising Source for Stem Cell-Based Therapy.根尖乳头干细胞:基于干细胞治疗的有前途的来源。
Biomed Res Int. 2019 Jan 29;2019:6104738. doi: 10.1155/2019/6104738. eCollection 2019.
9
Stem Cells From the Apical Papilla (SCAP) as a Tool for Endogenous Tissue Regeneration.根尖乳头干细胞(SCAP)作为内源性组织再生的工具
Front Bioeng Biotechnol. 2018 Jul 24;6:103. doi: 10.3389/fbioe.2018.00103. eCollection 2018.
10
The Angiogenic Potential of DPSCs and SCAPs in an Model of Dental Pulp Regeneration.牙髓再生模型中牙髓干细胞和成体牙髓干细胞的血管生成潜力
Stem Cells Int. 2017;2017:2582080. doi: 10.1155/2017/2582080. Epub 2017 Sep 5.

低强度激光照射促进根尖乳头干细胞的增殖与分化。

Low-Level Laser Irradiation Promotes Proliferation and Differentiation on Apical Papilla Stem Cells.

作者信息

Gutiérrez David, Rouabhia Mahmoud, Ortiz Javiera, Gaviria Diego, Alfonso Camilo, Muñoz Ana, Inostroza Carolina

机构信息

Faculty of dentistry, Buccal Innovation research group, Antonio Nariño University, Bogotá, Colombia.

Faculty of Dentistry, Laval University, Quebec, Canada.

出版信息

J Lasers Med Sci. 2021 Dec 1;12:e75. doi: 10.34172/jlms.2021.75. eCollection 2021.

DOI:10.34172/jlms.2021.75
PMID:35155160
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8837851/
Abstract

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.

摘要

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。