增加胶原支架中透明质酸含量对软骨细胞和间充质干细胞软骨形成表型维持的影响

Andrew C. Muran , Benjamin C. Schaffler , Andrew Wong , Eric Neufeld , Pooja Swami , Mark Pianka , Daniel Grande
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引用次数: 1

摘要

引言在关节软骨中,透明质酸(HA)已被证明可以增加软骨细胞的粘附、分化和增殖,并且其添加到三维(3D)支架中已被证明在体外可以改善软骨细胞表型。目的本研究的目的是确定(1)增加胶原支架中的HA水平是否能以剂量依赖的方式更好地维持软骨细胞的软骨形成表型;(2)注入HA的胶原支架是否能促进间充质干细胞(MSCs)在3D胶原/HA支架中分化为软骨细胞。方法将牛软骨细胞和大鼠间充质干细胞接种在2%或6%胶原/HA支架上,或不接种支架作为对照。在第6、12和18天收获细胞。实时聚合酶链式反应用于测量I型和II型胶原、SOX-9和聚集蛋白聚糖的表达。结果第18天,两组软骨细胞中I型和II型胶原的表达均增加。对于MSCs,在第18天,2%和6%支架组的I型胶原表达增加,聚集蛋白聚糖表达增加,2%HA组的SOX-9表达增加。结论尽管HA组对II型胶原产生的影响没有显著的剂量依赖性变化,但在第18天,与单层对照相比,两个HA支架组的II型胶原表达均显著增加。未来的实验应该延长时间点来阐明这些作用,并且应该使用人类软骨细胞和MSCs来确定生物学适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of increasing hyaluronic acid content in collagen scaffolds on the maintenance of chondrogenic phenotype in chondrocytes and mesenchymal stem cells

Introduction

In articular cartilage, hyaluronic acid (HA) has been shown to increase adhesion, differentiation, and proliferation of cartilage cells, and its addition to three-dimensional (3D) scaffolds has been shown to improve chondrocyte phenotype in vitro.

Objectives

The purpose of this study was to determine (1) whether increasing the HA levels in collagen scaffolds leads to better maintenance of the chondrogenic phenotype in chondrocytes in a dose-dependent manner and (2) whether collagen scaffolds infused with HA promote the differentiation of mesenchymal stem cells (MSCs) into chondrocytes within 3D collagen/HA scaffolds.

Methods

Bovine chondrocytes and rat MSCs were seeded onto 2% or 6% collagen/HA scaffolds, or no scaffold for controls. Cells were harvested at days 6, 12 and 18. Real-time polymerase chain reaction was used to measure expression of Type I and Type II collagen, SOX-9, and aggrecan.

Results

Expression of Type I and II collagen was increased at day 18 in the chondrocytes of both groups. For the MSCs, at day 18 there was increased expression of Type I collagen and increased expression of aggrecan in both the 2 and 6% scaffold groups, plus increased SOX-9 expression in the 2% HA group.

Conclusions

Though there was no significant dose-dependent change between the HA groups in their effects on Type II collagen production, both HA scaffold groups showed significantly increased expression of Type II collagen as compared to monolayer controls at 18 days. Future experiments should extend timepoints to elucidate these effects and human chondrocytes and MSCs should be used to determine biological applicability.

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