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光生物调节在体外促进间充质干细胞的成骨分化并提高磷酸化蛋白激酶B(P-Akt)水平。

Photobiomodulation promotes osteogenic differentiation of mesenchymal stem cells and increases P-Akt levels in vitro.

作者信息

Ma Chunyan, Ye Yutong, Shi Xinyu, Li Na, Chen Yufei, Shi Xiafei, Chen Hongli

机构信息

State Key Laboratory of Separation Membranes and Membrane Processes & Key Laboratory of Hollow Fiber Membrane Materials and Membrane Processes, Tianjin Key Laboratory of Optoelectronic Detection Technology and Systems, Tiangong University, Tianjin, 300387, China.

State Key Laboratory of Advanced Medical Materials and Devices, Tianjin Key Laboratory of Neuromodulation and Neurorepair, Integrative regeneration laboratory, Institute of Biomedical Engineering, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, 300192, China.

出版信息

Sci Rep. 2025 May 22;15(1):17844. doi: 10.1038/s41598-025-02428-7.

Abstract

Bone defects are common orthopedic conditions, and due to the limited regenerative capacity of bone tissue, their repair remains a challenge in orthopedic surgery. Mesenchymal stem cells (MSCs) have demonstrated strong potential for osteogenic differentiation; however, their efficiency in vivo remains restricted, particularly in terms of differentiation and migration. Photobiomodulation (PBM), a non-invasive therapeutic technique, has shown great promise in promoting stem cell differentiation. In this study, we cultured human umbilical cord mesenchymal stem cells (hUCMSCs) in vitro and treated them with 635/808 nm laser light. We measured alkaline phosphatase (ALP) activity, mineralized nodule formation, and the expression of osteogenesis-related genes and factors after 7, 14, and 21 days. The results showed that PBM treatment significantly enhanced hUCMSC proliferation and osteogenic differentiation. The mechanism behind this effect involves PBM activating the upstream Akt signaling pathway, increasing P-Akt expression, and elevating reactive oxygen species (ROS) levels to induce mild oxidative stress. This process enhances ALP activity, mineralized nodule formation, and the expression of osteogenesis-related genes and factors, thus promoting the osteogenic differentiation of hUCMSCs.

摘要

骨缺损是常见的骨科病症,由于骨组织的再生能力有限,其修复仍是骨科手术中的一项挑战。间充质干细胞(MSCs)已显示出强大的成骨分化潜力;然而,它们在体内的效率仍然受限,特别是在分化和迁移方面。光生物调节(PBM)是一种非侵入性治疗技术,在促进干细胞分化方面已显示出巨大潜力。在本研究中,我们在体外培养人脐带间充质干细胞(hUCMSCs),并用635/808 nm激光对其进行处理。我们在7天、14天和21天后测量了碱性磷酸酶(ALP)活性、矿化结节形成以及成骨相关基因和因子的表达。结果表明,PBM处理显著增强了hUCMSC的增殖和成骨分化。这种效应背后的机制涉及PBM激活上游Akt信号通路,增加P-Akt表达,并提高活性氧(ROS)水平以诱导轻度氧化应激。这一过程增强了ALP活性、矿化结节形成以及成骨相关基因和因子的表达,从而促进了hUCMSCs的成骨分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8918/12098891/ade7088e0d04/41598_2025_2428_Fig1_HTML.jpg

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