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用于关节软骨组织工程的与明胶/透明质酸/硫酸软骨素-6-硫酸盐三元共聚物混合的纤维蛋白胶:实时聚合酶链反应结果

Fibrin glue mixed with gelatin/hyaluronic acid/chondroitin-6-sulfate tri-copolymer for articular cartilage tissue engineering: the results of real-time polymerase chain reaction.

作者信息

Chou Cheng-Hung, Cheng Winston T K, Kuo Tzong-Fu, Sun Jui-Sheng, Lin Feng-Huei, Tsai Jui-Che

机构信息

Institute of Biomedical Engineering, College of Medicine, National Taiwan University, Taipei 100, Taiwan.

出版信息

J Biomed Mater Res A. 2007 Sep 1;82(3):757-67. doi: 10.1002/jbm.a.31186.

Abstract

Autologous fibrin glue has been demonstrated as a potential scaffold with very good biocompatibility for neocartilage formation. However, fibrin glue has been reported not to provide enough mechanical strength, but with many growth factors to interfere the tissue growth. Gelatin/hyaluronic acid/chondroitin-6-sulfate (GHC6S) tri-copolymer sponge has been prepared as scaffold for cartilage tissue engineering and showed very good results, but problems of cell seeding and cell distribution troubled the researchers. In this study, GHC6S particles would be added into the fibrin glue to provide better mechanical strength, better cell distribution, and easier cell seeding, which would be expected to improve cartilage regeneration in vitro. Porcine cryo-precipitated fibrinogen and thrombin prepared from prothrombin activated by 10% CaCl(2) solution were used in two groups. One is the fibrin glue group in which porcine chondrocytes were mixed with thrombin-fibrinogen solution, which was then converted into fibrin glue. The other is GHC6S-fibrin glue in which GHC6S particles were added into the thrombin-fibrinogen solution with porcine chondrocytes. After culturing for 1-2 weeks, the chondrocytes cultured in GHC6S-fibrin glue showed a round shape with distinct lacuna structure and showed positive in S-100 protein immunohistochemical stain. The related gene expressions of tissue inhibitor of metalloproteinases-1, matrix metalloproteinase-2, MT1-MMP, aggrecan, decorin, type I, II, X collagen, interleukin-1 beta, transforming growth factor-beta 1 (TGF-beta1), and Fas-associating death domain were checked by real-time PCR. The results indicated that the chondrocytes cultured in GHC6S-fibrin glue would effectively promote extracellular matrix (ECM) secretion and inhibit ECM degradation. The evidence could support that GHC6S-fibrin glue would be a promising scaffold for articular cartilage tissue engineering.

摘要

自体纤维蛋白胶已被证明是一种具有良好生物相容性的潜在支架,可用于新软骨形成。然而,据报道纤维蛋白胶不能提供足够的机械强度,且含有许多干扰组织生长的生长因子。明胶/透明质酸/硫酸软骨素-6-硫酸盐(GHC6S)三元共聚物海绵已被制备用作软骨组织工程的支架,并显示出非常好的效果,但细胞接种和细胞分布问题困扰着研究人员。在本研究中,将GHC6S颗粒添加到纤维蛋白胶中,以提供更好的机械强度、更好的细胞分布和更易于细胞接种,有望改善体外软骨再生。两组使用了由10%氯化钙溶液激活凝血酶制备的猪冷冻沉淀纤维蛋白原和凝血酶。一组是纤维蛋白胶组,将猪软骨细胞与凝血酶-纤维蛋白原溶液混合,然后转化为纤维蛋白胶。另一组是GHC6S-纤维蛋白胶组,将GHC6S颗粒添加到含有猪软骨细胞的凝血酶-纤维蛋白原溶液中。培养1-2周后,在GHC6S-纤维蛋白胶中培养的软骨细胞呈圆形,具有明显的陷窝结构,S-100蛋白免疫组织化学染色呈阳性。通过实时PCR检测金属蛋白酶组织抑制剂-1、基质金属蛋白酶-2、MT1-MMP、聚集蛋白聚糖、核心蛋白聚糖、I型、II型、X型胶原蛋白、白细胞介素-1β、转化生长因子-β1(TGF-β1)和Fas相关死亡结构域的相关基因表达。结果表明,在GHC6S-纤维蛋白胶中培养的软骨细胞可有效促进细胞外基质(ECM)分泌并抑制ECM降解。该证据支持GHC6S-纤维蛋白胶将是一种有前途的关节软骨组织工程支架。

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