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用于再生牙科的细胞负载支架 3D 生物打印的牙本质衍生水凝胶生物墨水。

A dentin-derived hydrogel bioink for 3D bioprinting of cell laden scaffolds for regenerative dentistry.

机构信息

Division of Biomaterials and Biomechanics, Department of Restorative Dentistry, OHSU School of Dentistry, Portland, OR, United States of America.

出版信息

Biofabrication. 2018 Jan 10;10(2):024101. doi: 10.1088/1758-5090/aa9b4e.

DOI:10.1088/1758-5090/aa9b4e
PMID:29320372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5796756/
Abstract

Recent studies in tissue engineering have adopted extracellular matrix (ECM) derived scaffolds as natural and cytocompatible microenvironments for tissue regeneration. The dentin matrix, specifically, has been shown to be associated with a host of soluble and insoluble signaling molecules that can promote odontogenesis. Here, we have developed a novel bioink, blending printable alginate (3% w/v) hydrogels with the soluble and insoluble fractions of the dentin matrix. We have optimized the printing parameters and the concentrations of the individual components of the bioink for print accuracy, cell viability and odontogenic potential. We find that, while viscosity, and hence printability of the bioinks, was greater in the formulations containing higher concentrations of alginate, a higher proportion of insoluble dentin matrix proteins significantly improved cell viability; where a 1:1 ratio of alginate and dentin (1:1 Alg-Dent) was most suitable. We further demonstrate high retention of the soluble dentin molecules within the 1:1 Alg-Dent hydrogel blends, evidencing renewed interactions between these molecules and the dentin matrix post crosslinking. Moreover, at concentrations of 100 μg ml, these soluble dentin molecules significantly enhanced odontogenic differentiation of stem cells from the apical papilla encapsulated in bioprinted hydrogels. In summary, the proposed novel bioinks have demonstrable cytocompatibility and natural odontogenic capacity, which can be a used to reproducibly fabricate scaffolds with complex three-dimensional microarchitectures for regenerative dentistry in the future.

摘要

最近的组织工程研究采用细胞外基质(ECM)衍生的支架作为组织再生的天然和细胞相容的微环境。牙本质基质特别显示与一系列可溶性和不溶性信号分子相关,这些信号分子可以促进牙发生。在这里,我们开发了一种新型生物墨水,将可打印的藻酸盐(3%w/v)水凝胶与牙本质基质的可溶性和不溶性部分混合。我们优化了打印参数和生物墨水的各个成分的浓度,以提高打印精度、细胞活力和牙原性潜力。我们发现,虽然生物墨水的粘度,因此打印性能在含有更高浓度藻酸盐的配方中更大,但更高比例的不溶性牙本质基质蛋白显着提高了细胞活力;藻酸盐和牙本质的比例为 1:1(1:1Alg-Dent)最为合适。我们进一步证明了可溶性牙本质分子在 1:1Alg-Dent 水凝胶混合物中的高保留率,证明了这些分子与交联后牙本质基质之间的重新相互作用。此外,在浓度为 100μg/ml 时,这些可溶性牙本质分子显着增强了包埋在生物打印水凝胶中的根尖乳头干细胞的成牙分化。总之,所提出的新型生物墨水具有可证明的细胞相容性和天然牙原性能力,可用于未来可重复制造具有复杂三维微观结构的支架,用于再生牙科。

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