首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >An atelocollagen honeycomb-shaped scaffold with a membrane seal (ACHMS-scaffold) for the culture of annulus fibrosus cells from an intervertebral disc.
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An atelocollagen honeycomb-shaped scaffold with a membrane seal (ACHMS-scaffold) for the culture of annulus fibrosus cells from an intervertebral disc.

机译:带有膜密封件(ACHMS支架)的蜂窝状胶原蜂窝状支架,用于培养来自椎间盘的纤维环细胞。

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摘要

The aim of this study was to investigate the possibility of using the atelocollagen honeycomb-shaped scaffold with a membrane seal (ACHMS-scaffold) for the culture of annulus fibrosus (AF) cells in tissue engineering procedures of intervertebral disc repair. AF cells from the intervertebral discs of Japanese white rabbits were cultured for up to 3 weeks in the ACHMS-scaffold to allow a high density, three-dimensional culture. Although the DNA content in the scaffold increased at a lower rate than in the monolayer culture, scanning electron microscopy data showed that the scaffold was filled with the grown AF cells and produced extracellular matrix on day 21. The amount of type II collagen and its mRNA expression by the scaffold cultured cells were determined using Western blotting and Northern blotting analyses, respectively, and remained at a higher level than in the monolayer cultured cells. Furthermore, glycosaminoglycan (GAG) accumulation in the scaffold culture was at a higher level than in the monolayer culture. Western blot analysis for extracted proteoglycans from the scaffold culture also exhibited a much higher proteoglycan accumulation than the monolayer culture. These results indicate that the AF cells are able to grow and remain phenotypically stable in the scaffold.
机译:这项研究的目的是调查在椎间盘修复的组织工程程序中,使用带膜密封件的Atelocollagen蜂窝状支架(ACHMS-scaffold)培养纤维环(AF)细胞的可能性。来自日本白兔椎间盘的AF细胞在ACHMS支架中培养长达3周,以进行高密度的三维培养。尽管支架中的DNA含量以比单层培养低的速率增加,但扫描电子显微镜数据显示支架在第21天充满了生长的AF细胞并产生了细胞外基质。II型胶原及其mRNA的量分别使用蛋白质印迹和Northern印迹分析确定支架培养细胞的表达,并保持在比单层培养细胞更高的水平。此外,支架培养物中的糖胺聚糖(GAG)积累水平高于单层培养物中的水平。从支架培养物中提取的蛋白聚糖的蛋白质印迹分析也显示出比单层培养物高得多的蛋白聚糖积累。这些结果表明AF细胞能够在支架中生长并在表型上保持稳定。

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