3D-bioprinted bone scaffolds incorporating SR1 nanoparticles enhance blood vessel regeneration in rat calvarial defects

IF 6.8 3区 医学 Q1 ENGINEERING, BIOMEDICAL International Journal of Bioprinting Pub Date : 2024-01-19 DOI:10.36922/ijb.1931
KyeongWoong Yang, Donghyun Lee, KyoungHo Lee, W. Jang, Hye ji Lim, Eun Ji Lee, Hojun Jeon, Donggu Kang, Gi Hoon Yang, K. Lee, Yong-Il Shin, Sang-Cheol Han, SangHyun An, Sang-Mo Kwon
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Abstract

The inherent limitations of bone grafting in the treatment of critical-sized bone defects have led to a growing demand for bone repair implants. Three-dimensional (3D) bioprinting has emerged as a promising manufacturing technique for implants, offering flexibility in their structural design and the use of applicable materials. Although numerous 3D-bioprinted bone scaffolds have been developed to enhance osteogenesis, angiogenesis remains a challenge. Angiogenesis is crucial for successful bone healing because the process forms blood vessels to deliver essential nutrients and oxygen. Endothelial progenitor cells (EPCs) play a pivotal role in the early stages of vascularization. These cells, capable of differentiating into endothelial cells (ECs), are recruited from the bone marrow to the injured area during the healing process. CD34+ cells, a subset of EPCs, have gained attention because of their neovascularization potential and ability to contribute to bone regeneration. The incorporation of CD34+ cell-enhancing factors into 3D-printed bone scaffolds may facilitate successful bone healing in critical defects. StemRegenin-1 (SR1), a molecule that promotes CD34+ cell expansion, has shown promising results in increasing CD34+ hematopoietic stem and progenitor cell populations. This study aimed to investigate the sustained release of SR1 from a collagen-based scaffold integrated with mesoporous silica nanoparticles (MSNs) to promote angiogenesis and enhance bone healing. The sustained release of SR1 from the collagen scaffold is hypothesized to promote angiogenesis, thereby facilitating bone repair. In vitro studies have demonstrated the angiogenic potential of SR1; however, further in vivo investigations are required to establish its clinical efficacy. This study contributes to the development of novel therapies targeting CD34+ cells and demonstrates the potential of SR1 as a promising agent for promoting angiogenesis and enhancing bone healing in critical defects.
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含有 SR1 纳米颗粒的三维生物打印骨支架可促进大鼠腓骨缺损处的血管再生
骨移植在治疗临界大小骨缺损方面存在固有的局限性,因此对骨修复植入物的需求日益增长。三维(3D)生物打印技术在结构设计和适用材料的使用方面具有灵活性,已成为一种前景广阔的植入物制造技术。虽然已经开发出许多三维生物打印骨支架来增强骨生成,但血管生成仍然是一个挑战。血管生成对骨的成功愈合至关重要,因为在这一过程中会形成血管,以输送必需的营养物质和氧气。内皮祖细胞(EPCs)在血管生成的早期阶段发挥着关键作用。在愈合过程中,这些能够分化成内皮细胞(EC)的细胞会从骨髓中被招募到受伤部位。CD34+ 细胞是 EPCs 的一个亚群,因其新生血管潜能和促进骨再生的能力而备受关注。在三维打印骨支架中加入 CD34+ 细胞增强因子可促进严重缺损部位的骨愈合。StemRegenin-1(SR1)是一种促进CD34+细胞扩增的分子,在增加CD34+造血干细胞和祖细胞数量方面已显示出良好的效果。本研究旨在探讨从与介孔二氧化硅纳米颗粒(MSNs)集成的胶原基支架中持续释放SR1,以促进血管生成并增强骨愈合。据推测,从胶原支架中持续释放 SR1 可促进血管生成,从而促进骨修复。体外研究已经证明了 SR1 的血管生成潜力,但要确定其临床疗效,还需要进一步的体内研究。这项研究有助于开发以 CD34+ 细胞为靶点的新型疗法,并证明了 SR1 作为一种促进血管生成和增强严重缺损骨愈合的药物所具有的潜力。
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来源期刊
CiteScore
6.90
自引率
4.80%
发文量
81
期刊介绍: The International Journal of Bioprinting is a globally recognized publication that focuses on the advancements, scientific discoveries, and practical implementations of Bioprinting. Bioprinting, in simple terms, involves the utilization of 3D printing technology and materials that contain living cells or biological components to fabricate tissues or other biotechnological products. Our journal encompasses interdisciplinary research that spans across technology, science, and clinical applications within the expansive realm of Bioprinting.
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