Effects of 660 and 940nm Low-Level Laser Irradiation on Viability and Proliferation of Stem Cells from Human Exfoliated Deciduous Teeth.

Q3 Dentistry
Frontiers in Dentistry Pub Date : 2026-02-10 eCollection Date: 2026-01-01 DOI:10.18502/fid.v23i7.21236
Samar Rahimpour, Arash Azizi, Mahshid Hodjat, Mohammad Vahedi
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Abstract

Objectives: This study evaluated the effects of 660 and 940nm lasers on viability and proliferation of stem cells from human exfoliated deciduous teeth (SHED). Materials and Methods: SHED were cultured and divided into six groups for laser irradiation: 660nm laser at 25mW with energy densities of 1 and 2J/cm2 for 8 and 16 seconds, and 940nm laser at 100mW with the same energy densities and durations. Two additional groups served as controls with no laser exposure. Cell viability was evaluated by the methyl thiazolyl tetrazolium (MTT) assay, and cell proliferation was measured by cell counting with a Neubauer chamber and qualitatively evaluated by 4',6-diamidino-2-phenylindole (DAPI) staining at 24 and 72 hours post- irradiation. Data were analyzed using one-way ANOVA, followed by Tamhane's and Tukey's tests. Results: Irradiation with 940nm laser enhanced cell proliferation compared to both 660nm laser and control groups at 24 and 72 hours (P<0.05), as confirmed by DAPI staining. At 24 hours, all laser-treated groups showed increased cell viability relative to the control, although the increase in the 660nm/2J/cm² group was not statistically significant (P>0.05). At 72 hours, only 940nm laser group showed significantly higher cell viability and proliferation than the control group (P<0.05). Conclusion: These findings suggest low-level laser therapy, particularly at the wavelength of 940nm enhances the viability and proliferation of stem cell, supporting its potential as a promising tool in regenerative medicine and tissue engineering.

660和940nm低强度激光照射对人脱落乳牙干细胞活力和增殖的影响。
目的:研究660 nm和940nm激光对人脱落乳牙(SHED)干细胞活力和增殖的影响。材料与方法:培养SHED,将其分为6组进行激光照射:660nm 25mW激光照射,能量密度分别为1和2J/cm2,照射时间分别为8和16秒;940nm 100mW激光照射,能量密度和持续时间相同。另外两组作为没有激光照射的对照组。采用甲基噻唑四氮唑(MTT)法测定细胞活力,采用Neubauer室细胞计数法测定细胞增殖,并在辐照后24和72小时采用4′,6-二氨基-2-苯基吲哚(DAPI)染色法定性评价细胞增殖。数据分析采用单因素方差分析,然后进行Tamhane和Tukey检验。结果:与660nm激光照射组和对照组相比,940nm激光照射组在24和72 h时细胞增殖能力增强(P0.05)。结论:低强度激光治疗,特别是940nm波长的激光治疗可提高干细胞的活力和增殖能力,支持其在再生医学和组织工程中的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Dentistry
Frontiers in Dentistry Dentistry-General Dentistry
CiteScore
1.00
自引率
0.00%
发文量
34
审稿时长
12 weeks
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