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用于韧带再生的高度取向纤维支架的多类型动态培养

Multiple-type dynamic culture of highly oriented fiber scaffold for ligament regeneration.

作者信息

Mizutani Naoki, Kawato Hitoshi, Maeda Yuko, Takebayashi Takafumi, Miyamoto Keiichi, Horiuchi Takashi

机构信息

Division of Chemistry for Materials, Faculty of Engineering, Graduate School of Mie University, 1577 Kurima-Machiyacho, Tsu, Mie, 514-8507, Japan.

出版信息

J Artif Organs. 2013 Mar;16(1):49-58. doi: 10.1007/s10047-012-0665-1. Epub 2012 Oct 25.

Abstract

The ruptured anterior cruciate ligament does not heal spontaneously as it has a low capacity for healing. Therefore, the development of new healing techniques employing tissue engineering is vital. As a potentially new approach for ligament regeneration, this study used a highly oriented fiber scaffold made of elastin and collagen (the mean diameters were 1.7 ± 0.4 μm and 0.5 ± 1.4 μm, respectively), which comprise the extracellular matrix of the ligament. In addition, a multiple-type dynamic culture consisting of a combination of pressure and twist stimulation was performed to examine the influence of mechanical force on the functional maintenance of ligament cells and on the differentiation of ligament cells to osteoblast-like cells. Our results show that a pressure stimulation and elastin A upregulated the expression of alkaline phosphatase (ALP) (a marker of osteogenic differentiation) and promoted the osteogenic differentiation of ligament cells. In addition, the twist stimulation upregulated the expression of type III collagen (the main component of ligament tissue). Furthermore, the combination of pressure and twist stimulation promoted the expression of type III collagen and ALP protein depending on the portion of scaffold.

摘要

前交叉韧带断裂后无法自行愈合,因为其愈合能力较低。因此,开发采用组织工程的新愈合技术至关重要。作为韧带再生的一种潜在新方法,本研究使用了一种由弹性蛋白和胶原蛋白制成的高度定向纤维支架(平均直径分别为1.7±0.4μm和0.5±1.4μm),它们构成了韧带的细胞外基质。此外,进行了由压力和扭转刺激组合而成的多类型动态培养,以研究机械力对韧带细胞功能维持以及韧带细胞向成骨样细胞分化的影响。我们的结果表明,压力刺激和弹性蛋白A上调了碱性磷酸酶(ALP,成骨分化的标志物)的表达,并促进了韧带细胞的成骨分化。此外,扭转刺激上调了III型胶原蛋白(韧带组织的主要成分)的表达。此外,压力和扭转刺激的组合根据支架部分促进了III型胶原蛋白和ALP蛋白的表达。

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