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非相干红光照射对骨髓间充质干细胞增殖及成骨分化的影响。

The effect of noncoherent red light irradiation on proliferation and osteogenic differentiation of bone marrow mesenchymal stem cells.

机构信息

Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, China.

出版信息

Lasers Med Sci. 2012 May;27(3):645-53. doi: 10.1007/s10103-011-1005-z. Epub 2011 Oct 21.

Abstract

Mesenchymal stem cells (MSCs) are promising for use in regenerative medicine. Low-level light irradiation (LLLI) has been shown to modulate various processes in different biological systems. The aim of our study was to investigate the effect of red light emitted from a light-emitting diode (LED) on bone marrow MSCs with or without osteogenic supplements. MSCs both with and without osteogenic supplements were divided into four groups, and each group was irradiated at doses of 0, 1, 2 and 4 J/cm(2). Cellular proliferation was evaluated using WST-8 and 5-ethynyl-2'-deoxyuridine (EdU) fluorescence staining. The alkaline phosphatase activity, mineralization, and expression of osteoblast master genes (Col1α1, Alpl, Bglap and Runx2) were monitored as indicators of MSC differentiation towards osteoblasts. In groups without osteogenic supplements, red light at all doses significantly stimulated cellular proliferation, whereas the osteogenic phenotype of the MSCs was not enhanced. In groups with osteogenic supplements, red light increased alkaline phosphatase activity and mineralized nodule formation, and stimulated the expression of Bglap and Runx2, but decreased cellular proliferation. In conclusion, nonconherent red light can promote proliferation but cannot induce osteogenic differentiation of MSCs in normal media, while it enhances osteogenic differentiation and decreases proliferation of MSCs in media with osteogenic supplements.

摘要

间充质干细胞(MSCs)在再生医学中具有广阔的应用前景。低水平光照射(LLLI)已被证明可以调节不同生物系统中的各种过程。我们的研究旨在研究发光二极管(LED)发出的红光对骨髓间充质干细胞的影响,无论是否有成骨补充剂。有和没有成骨补充剂的间充质干细胞均分为四组,每组分别用 0、1、2 和 4 J/cm(2)的剂量进行照射。使用 WST-8 和 5-乙炔基-2'-脱氧尿苷(EdU)荧光染色评估细胞增殖。碱性磷酸酶活性、矿化以及成骨细胞主基因(Col1α1、Alpl、Bglap 和 Runx2)的表达被监测作为 MSC 向成骨细胞分化的指标。在没有成骨补充剂的组中,所有剂量的红光均显著刺激细胞增殖,而 MSC 的成骨表型并未增强。在有成骨补充剂的组中,红光增加了碱性磷酸酶活性和矿化结节形成,并刺激了 Bglap 和 Runx2 的表达,但降低了细胞增殖。总之,非相干红光可以促进增殖,但不能在正常培养基中诱导 MSC 的成骨分化,而在有成骨补充剂的培养基中,它增强了 MSC 的成骨分化并降低了增殖。

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