类有机物
间质细胞
细胞生物学
骨细胞
骨细胞
干细胞
基质(化学分析)
细胞分化
骨组织
体内
材料科学
体外
生物
生物医学工程
解剖
成骨细胞
医学
癌症研究
生物化学
基因
生物技术
复合材料
作者
Anat Akiva,J. Melke,Sana Ansari,Nalan Liv,Robin van der Meijden,Merijn van Erp,Feihu Zhao,Merula Stout,Wouter H. Nijhuis,Cecilia de Heus,Claudia Muñiz Ortera,Job Fermie,Judith Klumperman,Keita Ito,Nico A. J. M. Sommerdijk,Sandra Hofmann
标识
DOI:10.1002/adfm.202010524
摘要
Abstract Bone formation (osteogenesis) is a complex process in which cellular differentiation and the generation of a mineralized organic matrix are synchronized to produce a hybrid hierarchical architecture. To study the mechanisms of osteogenesis in health and disease, there is a great need for functional model systems that capture in parallel, both cellular and matrix formation processes. Stem cell‐based organoids are promising as functional, self‐organizing 3D in vitro models for studying the physiology and pathology of various tissues. However, for human bone, no such functional model system is yet available. This study reports the in vitro differentiation of human bone marrow stromal cells into a functional 3D self‐organizing co‐culture of osteoblasts and osteocytes, creating an organoid for early stage bone (woven bone) formation. It demonstrates the formation of an organoid where osteocytes are embedded within the collagen matrix that is produced by the osteoblasts and mineralized under biological control. Alike in in vivo osteocytes, the embedded osteocytes show network formation and communication via expression of sclerostin. The current system forms the most complete 3D living in vitro model system to investigate osteogenesis, both in physiological and pathological situations, as well as under the influence of external triggers (mechanical stimulation, drug administration).
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