Suppr超能文献

通过在支架上培养 TATVHL 肽移植的软骨细胞来进行软骨再生。

Cartilage regeneration by culturing chondrocytes in scaffolds grafted with TATVHL peptide.

机构信息

Department of Chemical Engineering National Chung Cheng University Chia-Yi, Taiwan, Republic of China.

出版信息

Colloids Surf B Biointerfaces. 2012 May 1;93:235-40. doi: 10.1016/j.colsurfb.2012.01.012. Epub 2012 Jan 21.

Abstract

Formation of neocartilage is a critical issue in contemporary regenerative medicine. This study presents the generation of tissue engineering cartilage in TATVHL peptide-grafted scaffolds. Bovine knee chondrocytes were seeded in TATVHL peptide-grafted scaffolds and cultured in a spinner bioreactor. The results revealed that surface TATVHL peptide enhanced the adhesion of bovine knee chondrocytes in scaffolds. However, an increase in the concentration of TATVHL peptide in scaffolds (up to 20 μg/mL) did not cause an evident variation in the cell viability. Surface TATVHL peptide was effective in promoting the quantity of cartilaginous components in constructs after dynamic cultivation. Biochemical assay, scanning electron microscope images, and histological staining demonstrated that surface TATVHL peptide accelerated the proliferation of bovine knee chondrocytes in constructs. In addition, the secretion of glycosaminoglycans and production of collagen in TATVHL peptide-grafted constructs were faster than those in TATVHL peptide-free constructs. TATVHL peptide can be a promising bioactive molecule to improve chondrogenesis in porous biomaterials.

摘要

软骨组织的形成是当代再生医学的一个关键问题。本研究介绍了在 TATVHL 肽接枝支架中生成组织工程软骨。将牛膝关节软骨细胞接种在 TATVHL 肽接枝支架中,并在旋转生物反应器中培养。结果表明,表面 TATVHL 肽增强了牛膝关节软骨细胞在支架中的黏附性。然而,支架中 TATVHL 肽浓度的增加(高达 20μg/mL)并没有导致细胞活力的明显变化。表面 TATVHL 肽在动态培养后对构建体中软骨成分的数量有促进作用。生化分析、扫描电子显微镜图像和组织学染色表明,表面 TATVHL 肽加速了构建体中牛膝关节软骨细胞的增殖。此外,TATVHL 肽接枝构建体中糖胺聚糖和胶原蛋白的分泌速度快于 TATVHL 肽无构建体。TATVHL 肽可以成为一种有前途的生物活性分子,以改善多孔生物材料中的软骨生成。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验