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低强度脉冲超声刺激骨膜细胞的成骨分化

Low-Intensity Pulsed Ultrasound Stimulates Osteogenic Differentiation of Periosteal Cells .

作者信息

Maung Wai Myo, Nakata Hidemi, Miura Motoi, Miyasaka Munemitsu, Kim You-Kyoung, Kasugai Shohei, Kuroda Shinji

机构信息

Tokyo Medical and Dental University (TMDU), Oral Implantology and Regenerative Dental Medicine Department, Tokyo, Japan.

出版信息

Tissue Eng Part A. 2021 Jan;27(1-2):63-73. doi: 10.1089/ten.TEA.2019.0331. Epub 2020 May 21.

DOI:10.1089/ten.TEA.2019.0331
PMID:32164486
Abstract

Adequate bone volume is required for osseointegrated implants to restore lost teeth and oral function. Several studies have demonstrated potential advantage of stem cells in regenerative medicine using osteoblasts. The periosteum is composed of osteoblasts, fibroblasts, and osteoprogenitor cells. It may be an alternative source for bone tissue engineering because of easy isolation and rapid proliferation and . Low-intensity pulsed ultrasound (LIPUS) has proved successful in recoveries from nonunions, delayed unions, and fracture of the bone in both animal experiments and clinical treatments. The study was to investigate the influence of LIPUS on the osteogenic differentiation in murine periosteum-derived cells (PDCs) and the underlying mechanism of LIPUS. PDCs were treated daily with LIPUS for 20 min up to 21 days with 3 MHz frequency, 30 mW/cm intensity, and pulse repetition frequency of 1 kHz. The effects of LIPUS on cell proliferation and viability were investigated. Osteogenic differentiation was analyzed by alkaline phosphatase (ALP)-positive cell staining, ALP activity assay, mineralized nodule formation, real-time reverse transcription-polymerase chain reaction, as well as western blotting. The results indicated that ultrasound stimulation did not significantly affect the proliferation of PDCs. But LIPUS significantly increased ALP activity on day 7 and markedly promoted formation of mineralized nodules on day 21. mRNA expression of ALP and osteocalcin was significantly upregulated by stimulation with LIPUS. LIPUS enhanced gene expression of both bone morphogenetic protein-2 (BMP-2) and osterix only in the presence of osteogenic medium. LIPUS stimulation did not affect Smad 1 and Smad 5 protein expression, but significantly upregulated protein levels of BMP-2 and phosphor-Smad 1/5/9 in PDCs. Thus, LIPUS stimulation increased early osteogenic differentiation in a normal medium and further enhanced expression of BMP-2 and subsequent osterix expression through the canonical Smad-signaling pathway in an osteogenic medium, leading to mineral apposition. Therefore, LIPUS might have potential to promote osteogenesis in PDCs. Impact statement There are few studies on periosteum-derived cells (PDCs) because conventional methods of their isolation are relatively difficult to procure abundant cells for cell culture and the total cell numbers are limited. In this study, a modified isolation technique of murine calvarial PDCs using gelatin is described. PDCs were initiated to emerge as early as day 3 and showed increased proliferation, which can be used for further studies. Low-intensity pulsed ultrasound stimulation increased early osteogenic differentiation in a normal medium and further enhanced expression of bone morphogenic protein-2 and subsequent osterix expression through the canonical Smad-signaling pathway in an osteogenic medium, leading to mineral apposition.

摘要

骨结合种植体需要足够的骨量来修复缺失牙齿和恢复口腔功能。多项研究已证明干细胞在利用成骨细胞的再生医学中具有潜在优势。骨膜由成骨细胞、成纤维细胞和骨祖细胞组成。由于易于分离、增殖迅速,它可能是骨组织工程的另一种细胞来源。低强度脉冲超声(LIPUS)在动物实验和临床治疗中已被证明能成功促进骨不连、延迟愈合和骨折的恢复。本研究旨在探讨LIPUS对小鼠骨膜来源细胞(PDCs)成骨分化的影响及其潜在机制。使用频率为3MHz、强度为30mW/cm²、脉冲重复频率为1kHz的LIPUS,每天对PDCs进行20分钟的照射,持续21天。研究了LIPUS对细胞增殖和活力的影响。通过碱性磷酸酶(ALP)阳性细胞染色、ALP活性测定、矿化结节形成、实时逆转录-聚合酶链反应以及蛋白质印迹法分析成骨分化情况。结果表明,超声刺激对PDCs的增殖没有显著影响。但LIPUS在第7天显著增加了ALP活性,并在第21天明显促进了矿化结节的形成。LIPUS刺激显著上调了ALP和骨钙素的mRNA表达。仅在存在成骨培养基的情况下,LIPUS增强了骨形态发生蛋白-2(BMP-2)和osterix的基因表达。LIPUS刺激不影响Smad 1和Smad 5蛋白表达,但显著上调了PDCs中BMP-2和磷酸化Smad 1/5/9的蛋白水平。因此,LIPUS刺激在正常培养基中增加了早期成骨分化,并在成骨培养基中通过经典的Smad信号通路进一步增强了BMP-2的表达以及随后osterix的表达,导致矿化沉积。所以,LIPUS可能具有促进PDCs成骨的潜力。影响声明:关于骨膜来源细胞(PDCs)的研究较少,因为传统的分离方法相对难以获取大量细胞用于细胞培养,且细胞总数有限。在本研究中,描述了一种使用明胶改良的小鼠颅骨PDCs分离技术。PDCs最早在第3天开始出现,并显示出增殖增加,可用于进一步研究。低强度脉冲超声刺激在正常培养基中增加了早期成骨分化,并在成骨培养基中通过经典的Smad信号通路进一步增强了骨形态发生蛋白-2的表达以及随后osterix的表达,导致矿化沉积。

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