Mechanism of Bone Mineralization

被引:178
作者
Murshed, Monzur [1 ,2 ,3 ]
机构
[1] McGill Univ, Fac Dent, Montreal, PQ H3A 1G1, Canada
[2] McGill Univ, Div Expt Med, Dept Med, Montreal, PQ H4A 3J1, Canada
[3] Shriners Hosp Children, Montreal, PQ H4A 0A9, Canada
来源
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE | 2018年 / 8卷 / 12期
关键词
AMORPHOUS CALCIUM-PHOSPHATE; MATRIX GLA PROTEIN; NONSPECIFIC ALKALINE-PHOSPHATASE; GROWTH-PLATE; VITAMIN-D; MOUSE MODEL; CALCIFICATION; SKELETAL; COLLAGEN; GENE;
D O I
10.1101/cshperspect.a031229
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mineralized "hard" tissues of the skeleton possess unique biomechanical properties to support the body weight and movement and act as a source of essential minerals required for critical body functions. For a long time, extracellular matrix (ECM) mineralization in the vertebrate skeleton was considered as a passive process. However, the explosion of genetic studies during the past decades has established that this process is essentially controlled by multiple genetic pathways. These pathways regulate the homeostasis of ionic calcium and inorganic phosphate-two mineral components required for bone mineral formation, the synthesis of mineral scaffolding ECM, and the maintainence of the levels of the inhibitory organic and inorganic molecules controlling the process of mineral crystal formation and its growth. More recently, intracellular enzyme regulators of skeletal tissue mineralization have been identified. The current review will discuss the key determinants of ECM mineralization in bone and propose a unified model explaining this process.
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页数:11
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