He Jia, Han Xuesong, Wang Songmei, Zhang Ying, Dai Xiaoming, Liu Boyan, Liu Liu, Zhao Xian
Department of Plastic Surgery, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, P.R. China.
Department of Obstetrics and Gynecology, Kunming Medical University, Kunming, Yunnan 650031, P.R. China.
Exp Ther Med. 2019 Nov;18(5):3333-3340. doi: 10.3892/etm.2019.7982. Epub 2019 Sep 6.
Bone tissue engineering provides a substitute for bone transplantation to address various bone defects. However, bone regeneration involves a large number of cellular events. In addition, obtaining sufficient source material for autogenous bone or alloplastic bone substitutes remains an unsolved issue. In previous studies, it was confirmed that bone marrow stromal cells (BMSCs) and endothelial progenitor cells (EPCs) had the capacity to promote bone regeneration. Additionally, bone morphogenetic protein-2 (BMP-2) has been demonstrated to be an active inducer of osteoblast differentiation. Therefore, the aim of the present study was to produce an effective integration system, including a scaffold, reparative cells and growth factors, that may enhance bone regeneration. Firstly, bone marrow-derived BMSCs and EPCs were isolated and identified by flow cytometry. Cell proliferation ability, secreted BMP-2 levels and alkaline phosphatase (ALP) activity were highest in the cell sheets containing BMP-2-modified BMSCs and EPCs. In addition, the expression levels of osteogenesis-associated genes, including runt related transcription factor 2 (Runx2), distal-less homeobox 5 (Dlx5), ALP and integrin-binding sialoprotein (Ibsp), and osteogenesis-associated proteins, including Runx2, Dlx, ALP, Ibsp, vascular endothelial growth factor, osteonectin, osteopontin and type I collagen, gradually increased during the co-culture of ad-BMP-2-BMSCs/EPCs. The levels of these genes and proteins were increased compared with those observed in the BMSC, EPC and BMP-2-modified BMSC groups. Finally, scanning electron microscopy observation also demonstrated that the BMP2-modified BMSCs were able to combine well with EPCs to construct a cell sheet for bone formation. Collectively, these results describe an adenovirus (ad)-BMP2-BMSCs/EPCs co-culture system that may significantly accelerate bone regeneration compared with a BMSCs/EPCs co-culture system or ad-BMP2-BMSCs alone.
骨组织工程为骨移植提供了一种替代方法,以解决各种骨缺损问题。然而,骨再生涉及大量细胞事件。此外,获取足够的自体骨或异体骨替代物的源材料仍然是一个未解决的问题。在先前的研究中,已证实骨髓基质细胞(BMSCs)和内皮祖细胞(EPCs)具有促进骨再生的能力。此外,骨形态发生蛋白-2(BMP-2)已被证明是成骨细胞分化的活性诱导剂。因此,本研究的目的是构建一种有效的整合系统,包括支架、修复细胞和生长因子,以增强骨再生。首先,通过流式细胞术分离并鉴定了骨髓来源的BMSCs和EPCs。在含有BMP-2修饰的BMSCs和EPCs的细胞片中,细胞增殖能力、分泌的BMP-2水平和碱性磷酸酶(ALP)活性最高。此外,在腺病毒-BMP-2-BMSCs/EPCs共培养过程中,包括 runt 相关转录因子 2(Runx2)、远端缺失同源盒 5(Dlx5)、ALP 和整合素结合唾液蛋白(Ibsp)等成骨相关基因的表达水平,以及包括 Runx2、Dlx、ALP、Ibsp、血管内皮生长因子、骨连接蛋白、骨桥蛋白和 I 型胶原蛋白等成骨相关蛋白的表达水平逐渐升高。与 BMSC、EPC 和 BMP-2 修饰的 BMSC 组相比,这些基因和蛋白的水平有所增加。最后,扫描电子显微镜观察还表明,BMP2 修饰的 BMSCs 能够与 EPCs 良好结合,构建用于骨形成的细胞片。总体而言,这些结果描述了一种腺病毒(ad)-BMP2-BMSCs/EPCs 共培养系统,与 BMSCs/EPCs 共培养系统或单独的 ad-BMP2-BMSCs 相比,该系统可能显著加速骨再生。