Spatial Growth Factor Delivery for 3D Bioprinting of Vascularized Bone with Adipose-Derived Stem/Stromal Cells as a Single Cell Source

被引:1
|
作者
Goker, Meric [1 ,2 ]
Derici, Utku Serhat [1 ]
Gokyer, Seyda [1 ]
Parmaksiz, Mehmet Goktug [1 ]
Kaya, Burak [3 ,4 ]
Can, Alp [5 ]
Yilgor, Pinar [1 ,4 ]
机构
[1] Ankara Univ, Fac Engn, Dept Biomed Engn, TR-06830 Ankara, Turkiye
[2] Royal Coll Surgeons Ireland, Dept Anat & Regenerat Med, Dublin D02 YN77, Ireland
[3] Ankara Univ, Med Fac, Dept Plast Reconstruct & Aesthet Surg, TR-06620 Ankara, Turkiye
[4] MEDITAM, Ankara Univ Med Design Res & Applicat Ctr, TR-06520 Ankara, Turkiye
[5] Ankara Univ, Dept Histol & Embryol, Fac Med, TR-06230 Ankara, Turkiye
关键词
vascularized bone; bioprinting; controlledrelease; microencapsulation; perfusion culture; bioreactor; SEQUENTIAL BMP-2/BMP-7 DELIVERY; MESENCHYMAL STEM-CELLS; AVASCULAR NECROSIS; TISSUE; DIFFERENTIATION; RECONSTRUCTION; EXPRESSION; SCAFFOLDS; RELEASE; GRAFTS;
D O I
10.1021/acsbiomaterials.3c01222
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
Encapsulating multiple growth factors within a scaffold enhances the regenerative capacity of engineered bone grafts through their localization and controls the spatiotemporal release profile. In this study, we bioprinted hybrid bone grafts with an inherent built-in controlled growth factor delivery system, which would contribute to vascularized bone formation using a single stem cell source, human adipose-derived stem/stromal cells (ASCs) in vitro. The strategy was to provide precise control over the ASC-derived osteogenesis and angiogenesis at certain regions of the graft through the activity of spatially positioned microencapsulated BMP-2 and VEGF within the osteogenic and angiogenic bioink during bioprinting. The 3D-bioprinted vascularized bone grafts were cultured in a perfusion bioreactor. Results proved localized expression of osteopontin and CD31 by the ASCs, which was made possible through the localized delivery activity of the built-in delivery system. In conclusion, this approach provided a methodology for generating off-the-shelf constructs for vascularized bone regeneration and has the potential to enable single-step, in situ bioprinting procedures for creating vascularized bone implants when applied to bone defects.
引用
收藏
页码:1607 / 1619
页数:13
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