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用于骨组织工程应用的模块化、血管化肥大软骨构建体

Modular, Vascularized Hypertrophic Cartilage Constructs for Bone Tissue Engineering Applications.

作者信息

Schott Nicholas G, Kaur Gurcharan, Coleman Rhima, Stegemann Jan P

出版信息

bioRxiv. 2024 Mar 1:2024.02.26.582166. doi: 10.1101/2024.02.26.582166.

DOI:10.1101/2024.02.26.582166
PMID:38464155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10925222/
Abstract

Insufficient vascularization is a main barrier to creating engineered bone grafts for treating large and ischemic defects. Modular tissue engineering approaches have promise in this application because of the ability to combine tissue types and to localize microenvironmental cues to drive desired cell function. In direct bone formation approaches, it is challenging to maintain sustained osteogenic activity, since vasculogenic cues can inhibit tissue mineralization. This study harnessed the physiological process of endochondral ossification to create multiphase tissues that allowed concomitant mineralization and vessel formation. Mesenchymal stromal cells in pellet culture were differentiated toward a cartilage phenotype, followed by induction to chondrocyte hypertrophy. Hypertrophic pellets exhibited increased alkaline phosphatase activity, calcium deposition, and osteogenic gene expression relative to chondrogenic pellets. In addition, hypertrophic pellets secreted and sequestered angiogenic factors, and supported new blood vessel formation by co-cultured endothelial cells and undifferentiated stromal cells. Multiphase constructs created by combining hypertrophic pellets and vascularizing microtissues and maintained in unsupplemented basal culture medium were shown to support robust vascularization and sustained tissue mineralization. These results demonstrate a new strategy to produce multiphase engineered constructs that concomitantly support the generation of mineralize and vascularized tissue in the absence of exogenous osteogenic or vasculogenic medium supplements.

摘要

血管化不足是制造用于治疗大面积缺血性骨缺损的工程化骨移植物的主要障碍。模块化组织工程方法在该应用中具有前景,因为它能够组合组织类型并定位微环境信号以驱动所需的细胞功能。在直接骨形成方法中,维持持续的成骨活性具有挑战性,因为血管生成信号会抑制组织矿化。本研究利用软骨内成骨的生理过程来创建多相组织,从而实现矿化和血管形成同步进行。将颗粒培养中的间充质基质细胞诱导分化为软骨表型,随后诱导其向软骨细胞肥大分化。相对于软骨生成颗粒,肥大颗粒表现出碱性磷酸酶活性增加、钙沉积增加和成骨基因表达增加。此外,肥大颗粒分泌并隔离血管生成因子,并通过与共培养的内皮细胞和未分化的基质细胞共同作用来支持新血管形成。通过将肥大颗粒与血管化微组织相结合并在无补充的基础培养基中培养而构建的多相结构,被证明能够支持强大的血管化和持续的组织矿化。这些结果证明了一种新策略,即生产多相工程构建体,在不添加外源性成骨或血管生成培养基的情况下,同时支持矿化组织和血管化组织的生成。