Niche-inspired collagen infused melt electrowritten scaffolds for craniofacial bone regeneration

IF 6 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS Materials Science & Engineering C-Materials for Biological Applications Pub Date : 2025-02-06 DOI:10.1016/j.bioadv.2025.214222
Arwa Daghrery , Renan Dal-Fabbro , Jinping Xu , Darnell Kaigler , Mylène de Ruijter , Debby Gawlitta , Jos Malda , Marco C. Bottino
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Abstract

Advances in tissue engineering are focused on devising improved therapeutics to reconstruct craniofacial bones. In cell-based strategies, biomaterials with specific physicochemical properties can mimic natural environments, supporting stem cell renewal, survivability, and cell fate. This study highlights the engineering of a 3D-printed (Melt Electrowritten, MEW) fluorinated‑calcium phosphate (F/CaP)-coated polymeric scaffold infused with collagen (COL) that boosts the performance of transplanted alveolar bone-derived mesenchymal stem cells (aBMSCs). Electron microscopy revealed micron-sized (2.7 μm) polymeric fibers forming a porous (500 μm fiber strand spacing) composite scaffold with a uniform F/CaP coating homogeneously infiltrated with collagen. In vitro, our findings underscored the cytocompatibility of the collagen-infused F/CaP-coated composite scaffold, fostering a suitable environment for aBMSCs proliferation and differentiation. Cells within the F/CaP-coated constructs exhibited upregulated osteogenic gene activity, and the addition of collagen augmented the expression of critical bone-forming genes (i.e., Runx2 and OCN). After in vivo implantation, the scaffolds integrated well with the surrounding host tissue, supporting extensive blood vessel infiltration. Notably, the collagen-infused F/CaP-coated composite scaffolds showed an increased CD31-positive vessel growth compared to the non-coated counterparts. At 8 weeks, aBMSCs-laden F/CaP-Coated+COL composite scaffolds exhibited robust bone formation, creating connecting bony bridges in calvarial defects. Importantly, F/CaP-Coated+COL composite scaffolds displayed pronounced OCN expression, indicating enhanced osteogenic potential. Thus, the engineered F/CaP-coated polymeric scaffold laden with aBMSCs and infused with collagen has proven effective in supporting cell growth, vascularization, and rapid bone regeneration, suggesting potential for future clinical use.
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小生境启发胶原注入熔融电写支架颅面骨再生
组织工程的进展集中在设计改进的治疗方法来重建颅面骨。在基于细胞的策略中,具有特定物理化学特性的生物材料可以模拟自然环境,支持干细胞的更新、生存能力和细胞命运。这项研究强调了一种注入胶原蛋白(COL)的3d打印(熔融电写,MEW)氟化磷酸钙(F/CaP)涂层聚合物支架的工程设计,该支架可以提高移植的牙槽骨源性间充质干细胞(aBMSCs)的性能。电镜显示,微米级(2.7 μm)的聚合物纤维形成了多孔(纤维链间距500 μm)的复合支架,其F/CaP涂层均匀浸润胶原蛋白。在体外,我们的研究结果强调了胶原注入的F/ cap涂层复合支架的细胞相容性,为aBMSCs的增殖和分化提供了合适的环境。F/ cap包被构建物内的细胞表现出上调的成骨基因活性,胶原的加入增强了关键成骨基因(即Runx2和OCN)的表达。在体内植入后,支架与周围宿主组织结合良好,支持广泛的血管浸润。值得注意的是,与未包被复合支架相比,胶原注入的F/ cap包被复合支架显示出cd31阳性血管生长的增加。8周时,载abmscs的F/ cap涂层+COL复合支架表现出强劲的骨形成,在颅骨缺损中形成连接骨桥。重要的是,F/ cap涂层+COL复合支架显示明显的OCN表达,表明成骨潜力增强。因此,经改造的F/ cap包覆的聚合物支架装载aBMSCs并注入胶原蛋白,已被证明在支持细胞生长、血管形成和快速骨再生方面有效,这表明了未来临床应用的潜力。
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来源期刊
CiteScore
17.80
自引率
0.00%
发文量
501
审稿时长
27 days
期刊介绍: Biomaterials Advances, previously known as Materials Science and Engineering: C-Materials for Biological Applications (P-ISSN: 0928-4931, E-ISSN: 1873-0191). Includes topics at the interface of the biomedical sciences and materials engineering. These topics include: • Bioinspired and biomimetic materials for medical applications • Materials of biological origin for medical applications • Materials for "active" medical applications • Self-assembling and self-healing materials for medical applications • "Smart" (i.e., stimulus-response) materials for medical applications • Ceramic, metallic, polymeric, and composite materials for medical applications • Materials for in vivo sensing • Materials for in vivo imaging • Materials for delivery of pharmacologic agents and vaccines • Novel approaches for characterizing and modeling materials for medical applications Manuscripts on biological topics without a materials science component, or manuscripts on materials science without biological applications, will not be considered for publication in Materials Science and Engineering C. New submissions are first assessed for language, scope and originality (plagiarism check) and can be desk rejected before review if they need English language improvements, are out of scope or present excessive duplication with published sources. Biomaterials Advances sits within Elsevier''s biomaterials science portfolio alongside Biomaterials, Materials Today Bio and Biomaterials and Biosystems. As part of the broader Materials Today family, Biomaterials Advances offers authors rigorous peer review, rapid decisions, and high visibility. We look forward to receiving your submissions!
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