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

Tissue Engineering Part A Pub Date : 2021-01-01 Epub Date: 2020-05-21 DOI:10.1089/ten.TEA.2019.0331
Wai Myo Maung, Hidemi Nakata, Motoi Miura, Munemitsu Miyasaka, You-Kyoung Kim, Shohei Kasugai, Shinji Kuroda
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引用次数: 22

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 in vivo and in vitro. 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/cm2 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.

低强度脉冲超声刺激骨膜细胞体外成骨分化。
骨整合种植体需要足够的骨容量来修复失去的牙齿和口腔功能。一些研究已经证明了干细胞在成骨细胞再生医学中的潜在优势。骨膜由成骨细胞、成纤维细胞和骨祖细胞组成。由于其在体内和体外易于分离和快速增殖,可能成为骨组织工程的替代来源。在动物实验和临床治疗中,低强度脉冲超声(LIPUS)已被证明在骨不连、延迟愈合和骨折的恢复中是成功的。本研究旨在探讨LIPUS对小鼠骨膜源性细胞成骨分化的影响及其作用机制。每天用LIPUS治疗PDCs 20分钟,持续21天,频率为3 MHz,强度为30 mW/cm2,脉冲重复频率为1 kHz。研究了LIPUS对细胞增殖和活力的影响。采用碱性磷酸酶(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及western blotting分析成骨分化情况。结果表明,超声刺激对PDCs的增殖无明显影响。但LIPUS在第7天显著提高ALP活性,并在第21天显著促进矿化结节的形成。在LIPUS的刺激下,ALP和骨钙素的mRNA表达显著上调。LIPUS仅在成骨培养基存在的情况下增强骨形态发生蛋白2 (BMP-2)和成骨细胞的基因表达。LIPUS刺激不影响Smad 1和Smad 5蛋白表达,但显著上调PDCs中BMP-2和磷酸化Smad 1/5/9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,并通过成骨培养基中规范的smad信号通路进一步增强BMP-2的表达和随后的成骨表达,导致矿物质沉积。因此,LIPUS可能具有促进PDCs成骨的潜力。对骨膜源性细胞(PDCs)的研究很少,因为传统的分离方法相对难以获得丰富的细胞进行细胞培养,而且细胞总数有限。本研究描述了一种改良的用明胶分离小鼠颅骨PDCs的方法。PDCs早在第3天就开始出现,并表现出增殖增强,这可以用于进一步的研究。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,并通过成骨培养基中规范的smad信号通路进一步增强骨形态发生蛋白-2的表达和随后的成骨表达,导致矿物质相结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tissue Engineering Part A
Tissue Engineering Part A CELL & TISSUE ENGINEERING-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
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