A self-forming bone membrane generated by periosteum-derived stem cell spheroids enhances the repair of bone defects

IF 9.4 1区 医学 Q1 ENGINEERING, BIOMEDICAL Acta Biomaterialia Pub Date : 2025-02-01 DOI:10.1016/j.actbio.2024.12.058
Jintao Zhong , Wenhua Li , Hetong Li , Jin Zhang , Zuoxu Hou , Xiao Wang , Enhui Zhou , Ke Lu , Weida Zhuang , Hongxun Sang
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Abstract

The periosteum, a highly specialized thin tissue, is instrumental in contributing to as much as 70 % of early bone formation. Recognizing the periosteum's vital physiological roles, the fabrication of a biomimetic periosteum has risen as an auspicious strategy for addressing extensive bone defects. In the study, we obtained such biomimetic periosteum by utilizing periosteum-derived stem cells (PDSCs) spheroids. These spheroids are induced to spontaneously generate a bioactive membrane on a delicate 3D-printed polycaprolactone (PCL) substrate. This process yields a biomimetic periosteum rich in the resources needed for bone repair. The in vitro evaluations demonstrated that this membrane can act as a repository for growth factors and stem cells. The release kinetics confirmed a sustained delivery of BMP-2 and VEGF, which promoted enhanced osteogenesis and angiogenesis in vitro, respectively. The in vivo results further highlighted robust bone regeneration from critical cranial defects upon the application of this biomimetic periosteum. The biomimetic periosteum, easily harvested and potent in bioactivity, presents substantial clinical potential, particularly for the treatment of critical-sized bone defects.

Statement of Significance

PDSC theoretically demonstrates substantial potential in membrane construction, a value we've harnessed in this pioneering application. By employing cell spheroids, we've successfully integrated a substantial number of cells into the membrane framework. PDSC spheroids exhibit the remarkable ability to self-assemble into functional membranes, endowing them with robust biological capabilities that enhance their performance in biological systems. The in vitro evaluations demonstrated that this membrane can act as a repository for growth factors and stem cells. The in vivo bone repair facilitated by this membrane is notably effective, characterized by superior bone quality and accelerated formation rates. This process mirrors the natural intramembrane ossification, offering a promising approach to bone integration and regeneration.

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由骨膜来源的干细胞球体生成的自形成骨膜增强骨缺损的修复。
骨膜是一种高度特化的薄组织,在早期骨形成中起着70%的作用。认识到骨膜的重要生理作用,仿生骨膜的制造已经上升为解决广泛的骨缺陷的一个吉祥的策略。在这项研究中,我们利用骨膜来源的干细胞(PDSCs)球体获得了这种仿生骨膜。这些球体被诱导在精细的3d打印聚己内酯(PCL)底物上自发地产生生物活性膜。这一过程产生了一种富含骨修复所需资源的仿生骨膜。体外评价表明,该膜可作为生长因子和干细胞的储存库。释放动力学证实BMP-2和VEGF的持续递送,分别促进体外骨生成和血管生成。在体内的结果进一步强调了在应用这种仿生骨膜后,严重颅骨缺陷的骨再生能力很强。该仿生骨膜易于获取且具有强大的生物活性,具有巨大的临床潜力,特别是用于治疗临界大小的骨缺损。意义声明:理论上,PDSC在膜结构中展示了巨大的潜力,这是我们在这一开创性应用中所利用的价值。通过使用细胞球体,我们成功地将大量细胞整合到膜框架中。PDSC球体表现出非凡的自组装成功能性膜的能力,赋予它们强大的生物能力,提高了它们在生物系统中的性能。体外评价表明,该膜可作为生长因子和干细胞的储存库。该膜促进体内骨修复效果显著,其特点是骨质量好,形成速度快。这一过程反映了自然的膜内骨化,为骨整合和再生提供了一种有前途的方法。
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来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
期刊最新文献
Editorial Board Corrigendum to “A composite hydrogel with co-delivery of antimicrobial peptides and platelet-rich plasma to enhance healing of infected wounds in diabetes” [Acta Biomaterialia 2021, 124, 205-218] Corrigendum to “Vascular Endothelial Growth Factor-Capturing Aligned Electrospun Polycaprolactone/Gelatin Nanofibers Promote Patellar Ligament Regeneration” [Acta Biomaterialia 140, 2022, 122-246] Physical exercise impacts bone remodeling around bio-resorbable magnesium implants A metal-organic framework functionalized CaO2-based cascade nanoreactor induces synergistic cuproptosis/ferroptosis and Ca2+ overload-mediated mitochondrial damage for enhanced sono-chemodynamic immunotherapy
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