Department of Biomaterials, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Advanced Research Center for Oral & Craniofacial Sciences, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Tissue Eng Part B Rev. 2022 Feb;28(1):246-255. doi: 10.1089/ten.TEB.2020.0352. Epub 2021 Mar 29.
Bone regeneration was one of the earliest fields to develop in the context of tissue regeneration, and currently, repair of small-sized bone defects has reached a high success rate. Future researches are expected to incorporate more advanced techniques toward achieving rapid bone repair and modulation of the regenerated bone quality. For these purposes, it is important to have a more integrative understanding of the mechanisms of bone formation and maturation from multiple perspectives and to incorporate these new concepts into the development and designing of novel materials and techniques for bone regeneration. This review focuses on the analysis of the earliest stages of bone tissue development from the biology, material science, and engineering perspectives for a more integrative understanding of bone formation and maturation, and for the development of novel biology-based engineering approaches for tissue synthesis . More specifically, the authors describe the systematic methodology that allowed the understanding of the different nucleation sites in intramembranous and endochondral ossification, the space-making process for mineral formation and growth, as well as the process of apatite crystal cluster growth in the presence of suppressing biomolecules. Impact Statement A detailed understanding of the developmental process of bone tissue leads to the acquisition of useful information for the bone tissue fabrication. This review summarizes the study of the calcification process of the calvaria and epiphyses from an engineering perspective and provides useful information for the realization of bone tissue biofabrication. Here, we describe the new mechanism of space formation for mineralization such as rupture of chondrocytes and disruption of cell-cell adhesion. We also describe the roles of nucleation site such as cell membrane nanofragments and matrix vesicles.
骨再生是组织再生最早发展的领域之一,目前,修复小面积骨缺损的成功率已经很高。未来的研究有望结合更多先进技术,实现快速骨修复和调节再生骨质量。为此,从多个角度更综合地理解骨形成和成熟的机制,并将这些新概念纳入骨再生的新型材料和技术的开发和设计中是很重要的。本综述重点从生物学、材料科学和工程学的角度分析骨组织发育的早期阶段,以更综合地理解骨形成和成熟,并开发用于组织合成的新型基于生物学的工程方法。更具体地说,作者描述了一种系统的方法,该方法可以理解膜内和软骨内成骨中不同的成核位点、矿物质形成和生长的空间形成过程,以及在抑制生物分子存在的情况下磷灰石晶体团簇生长的过程。
引言
详细了解骨组织的发育过程有助于获取骨组织制造的有用信息。本综述从工程学的角度总结了颅骨和骨骺钙化过程的研究,并为实现骨组织的生物制造提供了有用的信息。在这里,我们描述了矿物质形成的新空间形成机制,如软骨细胞破裂和细胞-细胞黏附的破坏。我们还描述了成核位点的作用,如细胞膜纳米片段和基质小泡。