共 39 条
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.
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页数:11
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