Biomineralization of bone: a fresh view of the roles of non-collagenous proteins

被引:79
作者
Gorski, Jeffrey Paul [1 ,2 ]
机构
[1] Univ Missouri, Sch Dent, Dept Oral Biol, Kansas City, MO 64108 USA
[2] Univ Missouri, Ctr Excellence Study Musculoskeletal & Dent Tissu, Kansas City, MO 64108 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2011年 / 16卷
关键词
Biomineralization; PHEX; Phospho; 1; Bone sialoprotein; DMP1; Type XI collagen; Fetuin; MATRIX EXTRACELLULAR PHOSPHOGLYCOPROTEIN; LINKED GLYCOPROTEINS SIBLINGS; PHOSPHATE-REGULATING GENE; MEPE-ASARM-PEPTIDES; COMPLEXES IN-VITRO; ACIDIC GLYCOPROTEIN-75; CALCIUM-PHOSPHATE; OSTEOBLAST DIFFERENTIATION; GROWTH-PLATE; FETUIN-A;
D O I
10.2741/3875
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The impact of genetics has dramatically affected our understanding of the functions of non-collagenous proteins. Specifically, mutations and knockouts have defined their cellular spectrum of actions. However, the biochemical mechanisms mediated by non-collagenous proteins in biomineralization remain elusive. It is likely that this understanding will require more focused functional testing at the protein, cell, and tissue level. Although initially viewed as rather redundant and static acidic calcium binding proteins, it is now clear that non-collagenous proteins in mineralizing tissues represent diverse entities capable of forming multiple protein-protein nteractions which act in positive and negative ways to regulate the process of bone mineralization. Several new examples from the author's laboratory are provided which illustrate this theme including an apparent activating effect of hydroxyapatite crystals on metalloproteinases. This review emphasizes the view that secreted non-collagenous proteins in mineralizing bone actively participate in the mineralization process and ultimately control where and how much mineral crystal is deposited, as well as determining the quality and biomechanical properties of the mineralized matrix produced.
引用
收藏
页码:2598 / 2621
页数:24
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