10. Bone Mineralization

L. Bonewald, S. Dallas, J. Gorski
{"title":"10. Bone Mineralization","authors":"L. Bonewald, S. Dallas, J. Gorski","doi":"10.1101/087969825.53.277","DOIUrl":null,"url":null,"abstract":"The mechanisms by which mineralized tissues such as bone acquire and regulate their mineral component are complex. The process of mineralization can be divided into the establishment of a primed, mineralizable matrix in which de novo mineral nucleation can occur, followed by the growth, expansion, and maturation of crystals. Perturbations in any of these events can result in bone disease and fragility. Elucidating the cellular and molecular mechanisms has been difficult because biomineralization is a combination of a physico-chemical process and a biological one. For example, phosphate participates directly in the formation of the hydroxyapatite crystals but recent studies have shown that phosphate can also directly regulate gene expression. This chapter summarizes current opinion within the field on key issues related to mineralization, such as whether mineralization is an active (cell-mediated) or a passive (physico-chemical) process and the role of cell-derived organelles/vesicles in mineralization. The molecular mediators and regulators of mineralization are reviewed and the question of whether there are unique mechanisms of mineralization in different types of bone tissue is addressed. Even though bone mineral density is currently the standard for predicting bone fragility, it is important to not only understand the inorganic component of bone, but also the organic component, as individuals with similar bone densities can have different susceptibility to fracture. These less clear properties of the skeleton that contribute to bone strength remain the focus of much investigation. THE CELLS RESPONSIBLE FOR BONE FORMATION AND MINERALIZATION Cells in the osteoblast/osteocyte lineage are responsible for bone formation...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"60 1","pages":"277-295"},"PeriodicalIF":0.0000,"publicationDate":"2009-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor Monograph Archive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/087969825.53.277","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The mechanisms by which mineralized tissues such as bone acquire and regulate their mineral component are complex. The process of mineralization can be divided into the establishment of a primed, mineralizable matrix in which de novo mineral nucleation can occur, followed by the growth, expansion, and maturation of crystals. Perturbations in any of these events can result in bone disease and fragility. Elucidating the cellular and molecular mechanisms has been difficult because biomineralization is a combination of a physico-chemical process and a biological one. For example, phosphate participates directly in the formation of the hydroxyapatite crystals but recent studies have shown that phosphate can also directly regulate gene expression. This chapter summarizes current opinion within the field on key issues related to mineralization, such as whether mineralization is an active (cell-mediated) or a passive (physico-chemical) process and the role of cell-derived organelles/vesicles in mineralization. The molecular mediators and regulators of mineralization are reviewed and the question of whether there are unique mechanisms of mineralization in different types of bone tissue is addressed. Even though bone mineral density is currently the standard for predicting bone fragility, it is important to not only understand the inorganic component of bone, but also the organic component, as individuals with similar bone densities can have different susceptibility to fracture. These less clear properties of the skeleton that contribute to bone strength remain the focus of much investigation. THE CELLS RESPONSIBLE FOR BONE FORMATION AND MINERALIZATION Cells in the osteoblast/osteocyte lineage are responsible for bone formation...
10. 骨矿化
矿化组织如骨获得和调节其矿物成分的机制是复杂的。矿化过程可分为两个阶段:初始的、可矿化的基质的建立,在这个基质中可以发生新的矿物成核,然后是晶体的生长、膨胀和成熟。这些事件中的任何扰动都可能导致骨骼疾病和脆弱。由于生物矿化是一个物理化学过程和生物学过程的结合,阐明其细胞和分子机制一直很困难。例如,磷酸盐直接参与羟基磷灰石晶体的形成,但最近的研究表明,磷酸盐也可以直接调节基因表达。本章总结了目前该领域对矿化相关关键问题的看法,例如矿化是主动的(细胞介导的)还是被动的(物理化学)过程,以及细胞来源的细胞器/囊泡在矿化中的作用。本文综述了矿化的分子介质和调节因子,并对不同类型骨组织中是否存在独特的矿化机制进行了讨论。尽管骨矿物质密度是目前预测骨脆弱性的标准,但重要的是不仅要了解骨的无机成分,还要了解有机成分,因为骨密度相似的个体对骨折的易感性可能不同。这些对骨骼强度有贡献的不太清楚的特性仍然是许多研究的焦点。负责骨形成和矿化的细胞成骨细胞/骨细胞谱系中的细胞负责骨形成…
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信