A Three-Dimensional Microporous Decalcified Bone Matrix Combined with Bone Marrow Mesenchymal Stem Cells Enhances Bone Regeneration in Critical-Sized Calvarial Defect of Nude Mouse.

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS
Ying He, Tianze Sun, Jiazhou Wu, Zexian Liu, Yingzhuan Ye, Jie Li, Tao Qian, Xiantong Hu, Jiayi Wang, Xiaomei Bie, Gang Xu, Yantao Zhao
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Abstract

The clinical repair of bone defects is hindered by limitations in donor material and complications arising from autologous bone grafting. Consequently, the development of efficient bone regeneration materials is of great clinical importance. The present study investigated a three-dimensional microporous demineralized bone matrix (DBM) combined with bone marrow mesenchymal stem cells (BMSCs) to enhance the outcomes of bone defect repair. The DBM has been developed to enhance the collagen preparation process, with the aim of retaining the collagen fiber network of the natural bone matrix and forming a three-dimensional microporous structure with good mechanical property. In vitro experiments demonstrated that the biocompatibility of DBM was superior to that of traditional cancellous and cortical bone materials, and they promoted cell adhesion, proliferation, and osteogenic differentiation as well as osteogenesis-related genes. In vivo experimentation was conducted to verify the efficacy of the treatment on a critical-sized cranial bone defect in nude mice. Micro-CT and histological analysis showed more formation of bone at 4 weeks and 8 weeks postsurgery. The DBM with optimized pore structure, degradation rate, and bioactivity enhanced the efficiency of bone defect repair by synergizing the osteogenic activity of BMSCs. The DBM with a porous and cross-linked structure could provide BMSCs with more internal surface area for attachment space to promote cell adhesion and growth and create advantages for the bone formation. Moreover, the DBM contains multifarious osteoinductive growth factors such as transforming growth factor-β (TGF-β), fibroblast growth factors (FGFs), bone morphogenetic proteins (BMPs) and insulin growth factors (IGFs), which can enhance osteogenic differentiation of BMSCs. This study may provide an innovative strategy for bone regeneration and bone defect repair.

三维微孔脱钙骨基质联合骨髓间充质干细胞促进裸鼠临界尺寸颅骨缺损骨再生。
由于供体材料的限制和自体骨移植引起的并发症,骨缺损的临床修复受到阻碍。因此,开发高效的骨再生材料具有重要的临床意义。本研究研究了三维微孔脱矿骨基质(DBM)与骨髓间充质干细胞(BMSCs)联合用于骨缺损修复的效果。DBM的开发是为了增强胶原蛋白的制备过程,目的是保留天然骨基质的胶原纤维网络,形成具有良好力学性能的三维微孔结构。体外实验表明DBM的生物相容性优于传统的松质骨和皮质骨材料,促进细胞粘附、增殖、成骨分化以及成骨相关基因的表达。通过体内实验验证了该方法对裸鼠临界颅骨缺损的治疗效果。显微ct和组织学分析显示术后4周和8周骨形成增多。经优化的孔结构、降解速率和生物活性的DBM通过协同BMSCs的成骨活性来提高骨缺损修复效率。DBM具有多孔交联结构,可为骨髓间充质干细胞提供更大的内表面积作为附着空间,促进细胞粘附生长,为成骨创造有利条件。此外,DBM中含有多种骨诱导生长因子,如转化生长因子-β (TGF-β)、成纤维细胞生长因子(FGFs)、骨形态发生蛋白(BMPs)和胰岛素生长因子(IGFs),可促进BMSCs的成骨分化。本研究可能为骨再生和骨缺损修复提供一种创新策略。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
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