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在三维多孔藻酸盐支架中培养软骨细胞可增强细胞增殖、基质合成和基因表达。

Chondrocytes culture in three-dimensional porous alginate scaffolds enhanced cell proliferation, matrix synthesis and gene expression.

作者信息

Lin Yu-Ju, Yen Chi-Nan, Hu Yu-Chen, Wu Yung-Chih, Liao Chun-Jen, Chu I-Ming

机构信息

Chemical Engineering Department, National Tsing Hua University, Taiwan.

出版信息

J Biomed Mater Res A. 2009 Jan;88(1):23-33. doi: 10.1002/jbm.a.31841.

Abstract

For the limited availability of autologous chondrocytes, a cultured system for expansion in vitro until sufficient cells are obtained must be developed. These cells must maintain their chondrocyte phenotype in vitro as well as in vivo, following implantation to ensure that differentiated chondrocytes synthesize a normal hyaline cartilage matrix and not a fibro-cartilage matrix. This study uses porous three-dimensional (3-D) alginate scaffolds within a perfusion system to culture low-density (5 x 10(5) cells) primary porcine chondrocytes for 1-4 weeks to study their proliferation and differentiation. The results of RT-PCR reveal that most cells could maintain their differentiation state for up to 4 weeks of culturing. Chondrocytes proliferated to 3 x 10(7) cells after 4 weeks in culture. Alginate scaffolds induced the formation of chondrocyte clusters and stimulated the synthesis of matrix, which effects were evaluated using histology and electron microscopy. These findings demonstrate that culturing chondrocytes in alginate scaffolds may effectively prevent the dedifferentiation and improve autologous chondrocyte transplantation.

摘要

由于自体软骨细胞的来源有限,必须开发一种体外培养扩增系统,直至获得足够数量的细胞。这些细胞在体外以及体内植入后都必须保持其软骨细胞表型,以确保分化的软骨细胞合成正常的透明软骨基质,而非纤维软骨基质。本研究在灌注系统中使用多孔三维(3-D)海藻酸盐支架培养低密度(5×10⁵ 个细胞)的原代猪软骨细胞1至4周,以研究其增殖和分化情况。逆转录聚合酶链反应(RT-PCR)结果显示,大多数细胞在培养长达4周的时间内都能保持其分化状态。培养4周后,软骨细胞增殖至3×10⁷ 个细胞。海藻酸盐支架诱导形成软骨细胞簇,并刺激基质合成,使用组织学和电子显微镜对这些效应进行了评估。这些发现表明,在海藻酸盐支架中培养软骨细胞可有效防止去分化,并改善自体软骨细胞移植。

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