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单层或三维条件下培养的耳软骨细胞和鼻中隔软骨细胞用于软骨组织工程的能力。

Aptitude of auricular and nasoseptal chondrocytes cultured under a monolayer or three-dimensional condition for cartilage tissue engineering.

作者信息

Asawa Yukiyo, Ogasawara Toru, Takahashi Tsuguharu, Yamaoka Hisayo, Nishizawa Satoru, Matsudaira Ko, Mori Yoshiyuki, Takato Tsuyoshi, Hoshi Kazuto

机构信息

Department of Cartilage and Bone Regeneration (Fujisoft), Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

Tissue Eng Part A. 2009 May;15(5):1109-18. doi: 10.1089/ten.tea.2007.0218.

Abstract

To elucidate the characterizations of chondrocytes originating from auricular cartilage (donors: 10-15 years) and nasoseptal one (20-23 years), we evaluated proliferation or matrix synthesis of both cells cultured under monolayer and collagen type I (COL1) three-dimensional (3D) conditions. Three passages were needed until cell numbers of auricular chondrocytes in the 3D culture increased 1000-fold, although those in monolayer culture or nasoseptal monolayer and 3D cells reached a 1000-fold increase at four passages. When we cultured the tissue-engineered cartilage pellets made of the chondrocytes proliferated at 1000-fold increase, the pellets of monolayer cells maintained their sizes during the culture period. However, those of nasoseptal 3D cells began to shrink at day 1 and became approximately one-tenth in size at day 21. The downsizing of pellets may result from the upregulation of tumor necrosis factor (TNF)-alpha or the related proteinases, including matrix metalloproteinases (MMPs)-1, -2, and -3, and cathepsin B, suggesting that the nasoseptal chondrocytes, which are physiologically separated from COL1, may be hardly adapted for the COL1 3D proliferation condition. Ideally, these characteristics would have been compared between the chondrocytes from donors that are completely matched in ages. However, according to our data using closely matched ones, the auricular chondrocytes seemed to more rapidly proliferate and produce less proteinases during this 3D culture than the nasoseptal ones.

摘要

为阐明源自耳软骨(供体年龄:10 - 15岁)和鼻中隔软骨(20 - 23岁)的软骨细胞的特征,我们评估了在单层培养和I型胶原(COL1)三维(3D)条件下培养的这两种细胞的增殖或基质合成情况。三维培养中,耳软骨细胞数量增加1000倍需要传代三次,而单层培养的耳软骨细胞或鼻中隔单层及三维培养的细胞在传代四次时达到1000倍的增长。当我们培养由增殖1000倍的软骨细胞制成的组织工程软骨微球时,单层培养细胞的微球在培养期间保持其大小。然而,鼻中隔三维培养细胞的微球在第1天开始缩小,在第21天尺寸约变为原来的十分之一。微球缩小可能是由于肿瘤坏死因子(TNF)-α或相关蛋白酶上调所致,这些蛋白酶包括基质金属蛋白酶(MMPs)-1、-2和-3以及组织蛋白酶B,这表明生理上与COL1分离的鼻中隔软骨细胞可能难以适应COL1三维增殖条件。理想情况下,这些特征应在年龄完全匹配的供体来源的软骨细胞之间进行比较。然而,根据我们使用年龄相近供体的数据,在这种三维培养中,耳软骨细胞似乎比鼻中隔软骨细胞增殖更快且产生的蛋白酶更少。

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