Taking cues from the extracellular matrix to design bone-mimetic regenerative scaffolds

被引:52
作者
Curry, Andrew S. [1 ]
Pensa, Nicholas W. [1 ]
Barlow, Abby M. [2 ]
Bellis, Susan L. [1 ,2 ]
机构
[1] Univ Alabama Birmingham, Dept Biomed Engn, 1918 Univ Blvd, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Cell Dev & Integrat Biol, 1918 Univ Blvd, Birmingham, AL 35294 USA
关键词
Bone; Scaffold; Biomimetic; Growth factor; Extracellular matrix; Regenerative medicine; GROWTH FACTOR-BB; COLLAGEN-BINDING DOMAIN; LENGTH POLYGLUTAMATE DOMAINS; ENDOTHELIAL-CELL ACTIVATION; EXTRACTION SOCKET DEFECTS; FACTOR FUSION PROTEIN; MARROW STROMAL CELLS; MORPHOGENETIC PROTEIN-2; CALCIUM-PHOSPHATE; IN-VIVO;
D O I
10.1016/j.matbio.2016.02.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is an ongoing need for effective materials that can replace autologous bone grafts in the clinical treatment of bone injuries and deficiencies. In recent years, research efforts have shifted away from a focus on inert biomaterials to favor scaffolds that mimic the biochemistry and structure of the native bone extracellular matrix (ECM). The expectation is that such scaffolds will integrate with host tissue and actively promote osseous healing. To further enhance the osteoinductivity of bone graft substitutes, ECM-mimetic scaffolds are being engineered with a range of growth factors (GFs). The technologies used to generate GF-modified scaffolds are often inspired by natural processes that regulate the association between endogenous ECMs and GFs. The purpose of this review is to summarize research centered on the development of regenerative scaffolds that replicate the fundamental collagen-hydroxyapatite structure of native bone ECM, and the functionalization of these scaffolds with GFs that stimulate critical events in osteogenesis. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:397 / 412
页数:16
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