A xenogeneic extracellular matrix-based 3D printing scaffold modified by ceria nanoparticles for craniomaxillofacial hard tissue regeneration via osteo-immunomodulation.

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Jiahao Chen, Yibing Huang, Huilin Tang, Xiangchen Qiao, Xiutian Sima, Weihua Guo
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引用次数: 0

Abstract

Hard tissue engineering scaffolds especially 3D printed scaffolds were considered an excellent strategy for craniomaxillofacial hard tissue regeneration, involving crania and facial bones and teeth. Porcine treated dentin matrix (pTDM) as xenogeneic extracellular matrix has the potential to promote the stem cell differentiation and mineralization as it contains plenty of bioactive factors similar with human-derived dentin tissue. However, its application might be impeded by the foreign body response induced by the damage-associated molecular patterns of pTDM, which would cause strong inflammation and hinder the regeneration. Ceria nanoparticles (CNPs) show a great promise at protecting tissue from oxidative stress and influence the macrophages polarization. Using 3D-bioprinting technology, we fabricated a xenogeneic hard tissue scaffold based on pTDM xenogeneic TDM-polycaprolactone (xTDM/PCL) and we modified the scaffolds by CNPs (xTDM/PCL/CNPs). Through series ofin vitroverification, we found xTDM/PCL/CNPs scaffolds held promise at up-regulating the expression of osteogenesis and odontogenesis related genes including collagen type 1, Runt-related transcription factor 2 (RUNX2), bone morphogenetic protein-2, osteoprotegerin, alkaline phosphatase (ALP) and DMP1 and inducing macrophages to polarize to M2 phenotype. Regeneration of bone tissues was further evaluated in rats by conducting the models of mandibular and skull bone defects. Thein vivoevaluation showed that xTDM/PCL/CNPs scaffolds could promote the bone tissue regeneration by up-regulating the expression of osteogenic genes involving ALP, RUNX2 and bone sialoprotein 2 and macrophage polarization into M2. Regeneration of teeth evaluated on beagles demonstrated that xTDM/PCL/CNPs scaffolds expedited the calcification inside the scaffolds and helped form periodontal ligament-like tissues surrounding the scaffolds.
基于异种细胞外基质的三维打印支架经铈纳米颗粒修饰,通过骨免疫调节实现颅颌面硬组织再生。
硬组织工程支架,尤其是三维打印支架,被认为是颅颌面硬组织再生的绝佳策略,涉及颅骨、面部骨骼和牙齿。猪处理过的牙本质基质(pTDM)作为异种细胞外基质,具有促进干细胞分化和矿化的潜力,因为它含有大量与人源牙本质组织相似的生物活性因子。然而,由于 pTDM 的损伤相关分子模式会诱发异物反应,从而引起强烈的炎症并阻碍再生,这可能会阻碍其应用。铈纳米粒子(CNPs)在保护组织免受氧化应激和影响巨噬细胞极化方面显示出巨大的潜力。利用三维生物打印技术,我们制备了基于 pTDM 异种 TDM 聚己内酯(xTDM/PCL)的异种硬组织支架,并用 CNPs(xTDM/PCL/CNPs)对支架进行了修饰。通过一系列体外验证,我们发现 xTDM/PCL/CNPs 支架有望上调成骨和牙体形成相关基因的表达,包括 1 型胶原蛋白、Runt 相关转录因子 2 (RUNX2)、骨形态发生蛋白-2、骨保护素、碱性磷酸酶 (ALP) 和 DMP1,并诱导巨噬细胞极化为 M2 表型。通过建立下颌骨和颅骨缺损模型,进一步评估了大鼠骨组织的再生情况。体内评估结果表明,xTDM/PCL/CNPs 支架可通过上调 ALP、RUNX2 和骨硅蛋白 2 等成骨基因的表达以及巨噬细胞极化为 M2 型促进骨组织再生。在小猎犬身上进行的牙齿再生评估表明,xTDM/PCL/CNPs 支架可加速支架内部的钙化,并有助于在支架周围形成类似牙周韧带的组织。
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来源期刊
Biomedical materials
Biomedical materials 工程技术-材料科学:生物材料
CiteScore
6.70
自引率
7.50%
发文量
294
审稿时长
3 months
期刊介绍: The goal of the journal is to publish original research findings and critical reviews that contribute to our knowledge about the composition, properties, and performance of materials for all applications relevant to human healthcare. Typical areas of interest include (but are not limited to): -Synthesis/characterization of biomedical materials- Nature-inspired synthesis/biomineralization of biomedical materials- In vitro/in vivo performance of biomedical materials- Biofabrication technologies/applications: 3D bioprinting, bioink development, bioassembly & biopatterning- Microfluidic systems (including disease models): fabrication, testing & translational applications- Tissue engineering/regenerative medicine- Interaction of molecules/cells with materials- Effects of biomaterials on stem cell behaviour- Growth factors/genes/cells incorporated into biomedical materials- Biophysical cues/biocompatibility pathways in biomedical materials performance- Clinical applications of biomedical materials for cell therapies in disease (cancer etc)- Nanomedicine, nanotoxicology and nanopathology- Pharmacokinetic considerations in drug delivery systems- Risks of contrast media in imaging systems- Biosafety aspects of gene delivery agents- Preclinical and clinical performance of implantable biomedical materials- Translational and regulatory matters
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