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低水平激光照射通过刺激 BMP/Smad 信号通路增强 BMP 诱导的成骨细胞分化。

Low-level laser irradiation enhances BMP-induced osteoblast differentiation by stimulating the BMP/Smad signaling pathway.

机构信息

Division of Molecular Signaling and Biochemistry, Department of Biosciences, Kyushu Dental College, 2-6-1 Manazuru, Kokurakita-ku, Kitakyushu, Fukuoka 803-8580, Japan.

出版信息

J Cell Biochem. 2010 Dec 15;111(6):1445-52. doi: 10.1002/jcb.22872.

Abstract

Low-level laser irradiation (LLLI) has been shown to induce bone formation and osteoblast differentiation both in vivo and in vitro. However, the molecular mechanism by which LLLI stimulates osteoblast differentiation is still unclear. The aim of the present study was to examine whether Ga-Al-As laser irradiation could enhance BMP2-induced alkaline phosphatase (ALP) activity in C2C12 cells. Laser irradiation at 0.5 W for 20 min enhanced BMP2-induced ALP activity. Laser treatment alone did not affect ALP activity. To exclude the effect of pH or temperature changes during irradiation, we shortened the exposure time to 2 min, with various levels of laser power. At 2.5 W, irradiation stimulated BMP2-induced ALP activity but not cell proliferation, whereas 1 or 5 W laser power did not induce any significant effects. Irradiation stimulated BMP2-induced phosphorylation of Smad1/5/8 and BMP2 expression, but had no effect on the expression of inhibitory Smads 6 and 7, BMP4, or insulin-like growth factor 1. Laser irradiation enhanced Smad-induced Id1 reporter activity as well as expression of bone morphogenetic protein (BMP)-induced transcription factors such as Id1, Osterix, and Runx2. Laser irradiation also stimulated BMP-induced expressions of type I collagen, osteonectin, and osteocalcin mRNA, markers of osteoblasts. This enhancement of BMP2-induced ALP activity and Smad phosphorylation by laser irradiation was also observed in primary osteoblasts. These results suggest that LLLI accelerates the differentiation of BMP-induced osteoblasts by stimulating the BMP/Smad signaling pathway.

摘要

低水平激光照射(LLLI)已被证明在体内和体外均可诱导骨形成和成骨细胞分化。然而,LLLI 刺激成骨细胞分化的分子机制尚不清楚。本研究旨在探讨 Ga-Al-As 激光照射是否能增强 BMP2 诱导的 C2C12 细胞碱性磷酸酶(ALP)活性。0.5W 激光照射 20 分钟可增强 BMP2 诱导的 ALP 活性。单独激光处理不会影响 ALP 活性。为了排除照射过程中 pH 值或温度变化的影响,我们将暴露时间缩短至 2 分钟,并采用不同的激光功率。2.5W 激光照射可刺激 BMP2 诱导的 ALP 活性,但不刺激细胞增殖,而 1W 或 5W 激光功率则没有引起任何显著的效果。照射刺激 BMP2 诱导的 Smad1/5/8 磷酸化和 BMP2 表达,但对抑制性 Smads 6 和 7、BMP4 或胰岛素样生长因子 1 的表达没有影响。激光照射还增强了 Smad 诱导的 Id1 报告基因活性以及骨形态发生蛋白(BMP)诱导的转录因子如 Id1、Osterix 和 Runx2 的表达。激光照射还刺激 BMP 诱导的 I 型胶原、骨粘连蛋白和骨钙素 mRNA 的表达,这些都是成骨细胞的标志物。激光照射还观察到这种增强的 BMP2 诱导的 ALP 活性和 Smad 磷酸化作用在原代成骨细胞中也存在。这些结果表明,LLLI 通过刺激 BMP/Smad 信号通路加速了 BMP 诱导的成骨细胞的分化。

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