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808纳米和915纳米二极管激光对颊脂垫干细胞增殖和成骨分化的光生物调节作用

Photobiomodulation effects of 808 nm and 915 nm diode lasers on proliferation and osteogenic differentiation of Buccal fat pad stem cells.

作者信息

Etemadi Ardavan, Norouzinia Raika, Hodjat Mahshid, Hakimiha Neda

机构信息

Department of Periodontics, Faculty of Dentistry, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

出版信息

Photodiagnosis Photodyn Ther. 2025 Aug;54:104703. doi: 10.1016/j.pdpdt.2025.104703. Epub 2025 Jul 5.

Abstract

AIM

Photobiomodulation therapy (PBM) is a promising adjunct in tissue engineering due to its ability to stimulate cell proliferation and differentiation. This study evaluated the effects of PBM on buccal fat pad-derived stem cells (BFPSCs) using two diode laser wavelengths.

METHODS

BFPSCs were divided into seven groups: six received laser irradiation and one served as control. Three groups were treated with a 915 nm laser and three with an 808 nm diode laser, each at energy densities of 2, 4, and 6 J/cm². Cell proliferation was assessed using the MTT assay, while osteogenic differentiation was evaluated by Alizarin red staining after 14 days. Alkaline phosphatase activity was measured after 7 days. Expression levels of osteocalcin (OCN), Osteopontin (OPN), and Runt-related transcription factor 2 (RUNX2) were measured by RT-PCR on days 7 and 14.

RESULTS

PBM significantly enhanced cell proliferation, particularly at 4 J/cm² (808 nm) and at 4 and 6 J/cm² (915 nm). Upregulation of OCN and OPN were detected in most irradiated groups. RUNX2 expression was higher in all PBM groups. Alizarin Red staining and alkaline phosphatase activity results confirmed PBM's stimulatory effects.

CONCLUSION

PBM, especially at 915 nm, enhances the proliferation and osteogenic differentiation of BFPSCs, suggesting potential benefits for bone reconstruction.

摘要

目的

光生物调节疗法(PBM)因其能够刺激细胞增殖和分化,在组织工程领域是一种很有前景的辅助手段。本研究使用两种二极管激光波长评估了PBM对颊脂垫来源干细胞(BFPSCs)的影响。

方法

将BFPSCs分为七组:六组接受激光照射,一组作为对照。三组用915 nm激光治疗,三组用808 nm二极管激光治疗,能量密度均为2、4和6 J/cm²。使用MTT法评估细胞增殖,14天后通过茜素红染色评估成骨分化。7天后测量碱性磷酸酶活性。在第7天和第14天通过RT-PCR测量骨钙素(OCN)、骨桥蛋白(OPN)和 runt相关转录因子2(RUNX2)的表达水平。

结果

PBM显著增强了细胞增殖,特别是在4 J/cm²(808 nm)以及4和6 J/cm²(915 nm)时。在大多数照射组中检测到OCN和OPN上调。所有PBM组中RUNX2表达均较高。茜素红染色和碱性磷酸酶活性结果证实了PBM的刺激作用。

结论

PBM,尤其是915 nm的PBM,可增强BFPSCs的增殖和成骨分化,提示其在骨重建方面具有潜在益处。

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