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胶原生物矿化的体外模型。

In vitro models of collagen biomineralization.

机构信息

Laboratory of Materials and Interface Chemistry and Soft Matter CryoTEM Unit, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.

出版信息

J Struct Biol. 2013 Aug;183(2):258-69. doi: 10.1016/j.jsb.2013.04.003. Epub 2013 Apr 15.

Abstract

Over the last several years, significant progress has been made toward understanding the mechanisms involved in the mineralization of hard collagenous tissues, such as bone and dentin. Particularly notable are the identification of transient mineral phases that are precursors to carbonated hydroxyapatite, the identification and characterization of non-collagenous proteins that are involved in controlling mineralization, and significant improvements in our understanding of the structure of collagen. These advances not only represent a paradigm shift in the way collagen mineralization is viewed and understood, but have also brought new challenges to light. In this review, we discuss how recent in vitro models have addressed critical questions regarding the role of the non-collagenous proteins in controlling mineralization, the nature of the interactions between amorphous calcium phosphate and collagen during the early stages of mineralization, and the role of collagen in the mineralization process. We discuss the significance of these findings in expanding our understanding of collagen biomineralization, while addressing some of the limitations that are inherent to in vitro systems.

摘要

在过去的几年中,人们在理解硬胶原组织(如骨和牙本质)矿化所涉及的机制方面取得了重大进展。特别值得注意的是,鉴定出了碳酸羟基磷灰石的前体瞬态矿物相,鉴定和表征了参与控制矿化的非胶原蛋白质,以及对胶原结构的理解有了重大改进。这些进展不仅代表了人们看待和理解胶原矿化方式的范式转变,也带来了新的挑战。在这篇综述中,我们讨论了最近的体外模型如何解决关于非胶原蛋白质在控制矿化中的作用、无定形磷酸钙和胶原在矿化早期相互作用的本质,以及胶原在矿化过程中的作用等关键问题。我们讨论了这些发现对扩展我们对胶原生物矿化的理解的意义,同时解决了体外系统固有的一些局限性。

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