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Effects of low-intensity pulsed ultrasound on the differentiation of C2C12 cells

机译:低强度脉冲超声对C2C12细胞分化的影响

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摘要

Low-intensity pulsed ultrasound (LIPUS) is known to accelerate bone regeneration, but the precise cellular mechanism is still unclear. The purpose of this study was to determine the effect of LIPUS on the differentiation of pluripotent mesenchymal cell line C2C12. The cells were cultured in differentiation medium with or without the addition of LIPUS stimulation. The ultrasound signal consisted of 1.5 MHz at an intensity of 70 mW/cm(2) for 20 min for all cultures. To verify the cell lineage after LIPUS stimulation, mRNA expression of cellular phenotype-specific markers characterizing osteoblasts (Runx2, Msx2, Dlx5, AJ18), chondroblasts (Sox9), myoblasts (MyoD), and adipocytes (C/EBP, PPAR gamma) was studied using real-time polymerase chain reaction analysis. The protein expression of Runx2 and activated phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2) and p38 mitogen-activated protein kinase (p38 MAPK) were performed using Western blotting. The mRNA expression of Runx2, Msx2, Dlx5, AJ18, and Sox9 was increased markedly by the LIPUS stimulation, whereas the expression of MyoD, C/EBP, and PPAR gamma was drastically decreased. In the Western blot analysis, LIPUS stimulation increased Runx2 protein expression and phosphorylation of ERK1/2 and p38 MAPK. Our study demonstrated that LIPUS stimulation converts the differentiation pathway of C2C12 cells into the osteoblast and/or chondroblast lineage via activated phosphorylation of ERK1/2 and p38 MAPK. (c) 2006 Elsevier Inc. All rights reserved.
机译:低强度脉冲超声(LIPUS)可以促进骨骼再生,但是确切的细胞机制仍不清楚。这项研究的目的是确定LIPUS对多能间充质细胞系C2C12分化的影响。将细胞在分化培养基中培养,添加或不添加LIPUS刺激。对于所有培养物,超声信号由1.5 MHz的信号组成,强度为70 mW / cm(2),持续20分钟。为了验证LIPUS刺激后的细胞谱系,使用了表征成骨细胞(Runx2,Msx2,Dlx5,AJ18),软骨母细胞(Sox9),成肌细胞(MyoD)和脂肪细胞(C / EBP,PPARγ)的细胞表型特异性标志物的mRNA表达。使用实时聚合酶链反应分析进行了研究。使用蛋白质印迹法进行Runx2的蛋白表达以及细胞外信号调节激酶1/2(ERK1 / 2)和p38丝裂原活化蛋白激酶(p38 MAPK)的活化磷酸化。 LIPUS刺激显着增加Runx2,Msx2,Dlx5,AJ18和Sox9的mRNA表达,而MyoD,C / EBP和PPARγ的表达则大大降低。在蛋白质印迹分析中,LIPUS刺激增加了Runx2蛋白的表达以及ERK1 / 2和p38 MAPK的磷酸化。我们的研究表明,LIPUS刺激通过ERK1 / 2和p38 MAPK的活化磷酸化将C2C12细胞的分化途径转化为成骨细胞和/或成软骨细胞谱系。 (c)2006 Elsevier Inc.保留所有权利。

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