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骨形态发生蛋白模拟肽连接水凝胶对 3D 生物打印牙构建体中牙髓干细胞(DPSCs)分化的影响。

The effect of BMP-mimetic peptide tethering bioinks on the differentiation of dental pulp stem cells (DPSCs) in 3D bioprinted dental constructs.

机构信息

Wake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine, Winston-Salem, NC 27157, United States of America.

出版信息

Biofabrication. 2020 Jul 1;12(3):035029. doi: 10.1088/1758-5090/ab9492.

Abstract

The goal of this study was to use 3D bioprinting technology to create a bioengineered dental construct containing human dental pulp stem cells (hDPSCs). To accomplish this, we first developed a novel bone morphogenetic protein (BMP) peptide-tethering bioink formulation and examined its rheological properties, its printability, and the structural stability of the bioprinted construct. Second, we evaluated the survival and differentiation of hDPSCs in the bioprinted dental construct by measuring cell viability, proliferation, and gene expression, as well as histological and immunofluorescent analyses. Our results showed that the peptide conjugation into the gelatin methacrylate-based bioink formulation was successfully performed. We determined that greater than 50% of the peptides remained in the bioprinted construct after three weeks in vitro cell culture. Human DPSC viability was >90% in the bioprinted constructs immediately after the printing process. Alizarin Red staining showed that the BMP peptide construct group exhibited the highest calcification as compared to the growth medium, osteogenic medium, and non-BMP peptide construct groups. In addition, immunofluorescent and quantitative reverse transcription-polymerase chain reaction analyses showed robust expression of dentin sialophosphoprotein and osteocalcin in the BMP peptide dental constructs. Together, these results strongly suggested that BMP peptide-tethering bioink could accelerate the differentiation of hDPSCs in 3D bioprinted dental constructs.

摘要

本研究旨在利用 3D 生物打印技术构建包含人牙髓干细胞(hDPSCs)的工程化牙本质结构。为实现这一目标,我们首先开发了一种新型骨形态发生蛋白(BMP)肽偶联生物墨水配方,并对其流变性能、可打印性和生物打印结构的稳定性进行了研究。其次,我们通过测量细胞活力、增殖和基因表达以及组织学和免疫荧光分析,评估了 hDPSCs 在生物打印牙本质结构中的存活和分化情况。结果表明,肽成功地偶联到明胶甲基丙烯酸酯基生物墨水配方中。我们发现,在体外细胞培养 3 周后,仍有超过 50%的肽保留在生物打印结构中。生物打印结构中 hDPSC 的活力在打印后立即>90%。茜素红染色显示,与生长培养基、成骨培养基和非 BMP 肽构建体组相比,BMP 肽构建体组表现出最高的钙化。此外,免疫荧光和定量逆转录聚合酶链反应分析显示,BMP 肽牙本质构建体中牙本质涎磷蛋白和骨钙素的表达非常活跃。综上所述,这些结果强烈表明,BMP 肽偶联生物墨水可以加速 hDPSCs 在 3D 生物打印牙本质结构中的分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a313/7641314/2d28f48c73d2/nihms-1640930-f0001.jpg

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