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

被引:1
作者
Daghrery, Arwa [1 ,2 ]
Dal-Fabbro, Renan [2 ]
Xu, Jinping [2 ]
Kaigler, Darnell [3 ,8 ]
de Ruijter, Mylene [4 ,5 ,7 ]
Gawlitta, Debby [4 ,6 ]
Malda, Jos [4 ,5 ,7 ]
Bottino, Marco C. [2 ,8 ]
机构
[1] Jazan Univ, Sch Dent, Dept Restorat Dent Sci, Jazan, Saudi Arabia
[2] Univ Michigan, Sch Dent, Dept Cariol Restorat Sci & Endodont, 1011 N Univ Ave,Room 2303, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI USA
[4] Regenerat Med Ctr Utrecht, Utrecht, Netherlands
[5] Univ Med Ctr Utrecht, Dept Orthoped, Utrecht, Netherlands
[6] Univ Utrecht, Dept Oral & Maxillofacial Surg & Special Dent Care, Div Surg Specialties, Utrecht, Netherlands
[7] Univ Utrecht, Fac Vet Med, Dept Clin Sci, Utrecht, Netherlands
[8] Univ Michigan, Coll Engn, Dept Biomed Engn, Ann Arbor, MI USA
来源
BIOMATERIALS ADVANCES | 2025年 / 170卷
基金
美国国家卫生研究院;
关键词
Bone; Collagen; Melt electrowriting; Regeneration; Stem cells; Transplantation; Engineering; PULP STEM-CELLS; IN-VITRO; HYDROGEL;
D O I
10.1016/j.bioadv.2025.214222
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
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 mu m) polymeric fibers forming a porous (500 mu m 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/CaPcoated 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.
引用
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页数:11
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