Collagen Scaffolds in Bone Sialoprotein-Mediated Bone Regeneration

被引:60
|
作者
Kruger, Thomas E. [1 ]
Miller, Andrew H. [1 ]
Wang, Jinxi [1 ,2 ]
机构
[1] Univ Kansas, Med Ctr, Dept Orthoped Surg, Harrington Lab Mol Orthoped, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Biochem & Mol Biol, Kansas City, KS 66160 USA
来源
基金
美国国家卫生研究院;
关键词
OSTEOBLAST DIFFERENTIATION; MATRIX MINERALIZATION; BINDING-SITES; RGD-MOTIFS; PROTEIN; CELLS; OSTEOGENESIS; ADHESION; DOMAIN; IDENTIFICATION;
D O I
10.1155/2013/812718
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Decades of research in bioengineering have resulted in the development of many types of 3-dimentional (3D) scaffolds for use as drug delivery systems (DDS) and for tissue regeneration. Scaffolds may be comprised of different natural fibers and synthetic polymers as well as ceramics in order to exert the most beneficial attributes including biocompatibility, biodegradability, structural integrity, cell infiltration and attachment, and neovascularization. Type I collagen scaffolds meet most of these criteria. In addition, type I collagen binds integrins through RGD and non-RGD sites which facilitates cell migration, attachment, and proliferation. Type I collagen scaffolds can be used for bone tissue repair when they are coated with osteogenic proteins such as bone morphogenic protein (BMP) and bone sialoprotein (BSP). BSP, a small integrin-binding ligand N-linked glycoprotein (SIBLING), has osteogenic properties and plays an essential role in bone formation. BSP also mediates mineral deposition, binds type I collagen with high affinity, and binds alpha v beta(3) and alpha v beta(5) integrins which mediate cell signaling. This paper reviews the emerging evidence demonstrating the efficacy of BSP-collagen scaffolds in bone regeneration.
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页数:6
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