3D printed O2-generating scaffolds enhance osteoprogenitor- and type H vessel recruitment during bone healing

被引:3
|
作者
Sarkar, Naboneeta [1 ,2 ]
Zhao, Jingtong [1 ,2 ]
Zhang, Nicholas Y. [1 ,2 ]
Horenberg, Allison L. [1 ,2 ]
Grayson, Warren L. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Univ, Dept Biomed Engn, Sch Med, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Translat Tissue Engn Ctr, Sch Med, Baltimore, MD USA
[3] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD USA
[4] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD USA
[5] Johns Hopkins Univ, Inst NanoBioTechnol, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
Oxygen; Calcium peroxide; Bone regeneration; Angiogenesis; Bone tissue engineering; OXYGEN GENERATING SCAFFOLDS; CALCIUM PEROXIDE; CELL VIABILITY; BETA-CELLS; TISSUE; HYPOXIA; ANGIOGENESIS; VASCULARIZATION; BIOMATERIALS; OSTEOGENESIS;
D O I
10.1016/j.actbio.2024.07.011
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Oxygen (O2 )-delivering tissue substitutes have shown tremendous potential for enhancing tissue regeneration, maturation, and healing. As O2 is both a metabolite and powerful signaling molecule, providing controlled delivery is crucial for optimizing its beneficial effects in the treatment of critical-sized injuries. Here, we report the design and fabrication of 3D-printed, biodegradable, O2-generating bone scaffold comprising calcium peroxide (CPO) that once hydrolytically activated, provides long-term generation of oxygen at a controlled, concentration-dependent manner, and polycaprolactone (PCL), a hydrophobic polymer that regulate the interaction of CPO with water, preventing burst release of O2 at early time points. When anoxic conditions were simulated in vitro , CPO-PCL scaffolds maintained the survival and proliferation of human adipose-derived stem/stromal cells (hASCs) relative to PCL-only controls. We assessed the in vivo osteogenic efficacy of hASC-seeded CPO-PCL scaffolds implanted in a non-healing critical-sized 4mm calvarial defects in nude mice for 8 weeks. Even without exogenous osteoinductive factors, CPO-PCL scaffolds demonstrated increased new bone volume compared to PCL-only scaffolds as verified by both microcomputed tomography analysis and histological assessments. Lastly, we employed a quantitative 3D lightsheet microscopy platform to determine that O2-generating scaffolds had similar vascular volumes with slightly higher presence of CD31hiEmcnhipro-osteogenic, type H vessels and increased number of Osterix+ skeletal progenitor cells relative to PCL-only scaffolds. In summary, 3D-printed O2 generating CPO-PCL scaffolds with tunable O2 release rates provide a facile, customizable strategy for effectively treating, craniofacial bone defects. Statement of significance Oxygen(O2)-delivering bone substitutes show promise in defect repair applications by supplying O2 to the cells within or around the graft, improving cell survivability and enhancing bone matrix mineralization. A novel O2-generating bone scaffold has been 3D printed for the first-time which ensures patient and defect specificity. 3D printed calcium peroxide-polycaprolactone (CPO-PCL) bone scaffold provides uninterrupted O2 supply for 22 days allowing cell survival in deprived O2 and nutrient conditions. For the first time, O2- driven bone regenerative environment in mice calvaria has been captured by light-sheet imaging which illuminates abundance of Osterix+ cells, angiogenesis at a single cell resolution indicating active site of bone remodeling and growth in the presence of O2 . (c) 2024 Acta Materialia Inc. Published by Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:126 / 143
页数:18
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