Optimal Scaffold Design and Effective Progenitor Cell Identification for the Regeneration of Vascularized Bone

被引:0
作者
Nukavarapu, Syam P. [1 ,2 ]
Amini, Ami R. [1 ]
机构
[1] Univ Connecticut, Orthopaed Surg, Farmington, CT 06030 USA
[2] Univ Connecticut, Chem Mat & Biomol Dept, Farmington, CT 06030 USA
来源
2011 ANNUAL INTERNATIONAL CONFERENCE OF THE IEEE ENGINEERING IN MEDICINE AND BIOLOGY SOCIETY (EMBC) | 2011年
关键词
TISSUE-ENGINEERED BONE; MESENCHYMAL STEM-CELLS; IN-VIVO; OSTEOGENESIS; ANGIOGENESIS; PROMOTION; POROSITY;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bone tissue engineering offers perhaps the most attractive treatment option for bone repair/regeneration as it eliminates complications of other bone grafting options (i.e., availability and immunogenicity issues of autografts and allografts, respectively). However, scaffold-based bone tissue engineering is largely limited by inadequate vascaularization, and as a result, bone formation is often restricted to the construct's periphery. In this study, we offer a two-pronged approach to overcome periphery-limited bone and vascular formation. We have developed optimally designed, mechanically strong, biodegradable scaffolds with increased porosity and interconnectivity. We have also identified and isolated superior, clinically-relevant cell populations (peripheral blood-derived endothelial progenitor cells (EPCs), and bone marrow-derived mesenchymal stem cells (MSCs)). In combination, we have developed a synthetic graft system suitable for the regeneration of vascularized bone.
引用
收藏
页码:2464 / 2467
页数:4
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