期刊文献+

藻酸盐凝胶三维培养条件下牛胰岛素-转铁蛋白-硒钠对兔关节软骨细胞表型的影响 被引量:4

Effects of Insulin-Transferrin-Selenium on the phenotype of rabbit articular chondrocytes cultured in three-dimensional alginate hydrogel
下载PDF
导出
摘要 目的探讨牛胰岛素-转铁蛋白-硒钠(ITS)对藻酸盐凝胶三维培养条件下兔关节软骨细胞表型的影响。方法分离培养兔关节软骨细胞,将单层培养的P2代细胞接种于藻酸盐凝胶中,分别在DMEM培养液中加入10%胎牛血清(FBS)、0.2%FBS+1%ITS、1%ITS即设为FBS组、ITS/FBS组,ITS组行DNA、蛋白聚糖(GAG)含量测定及组织化学检测。结果软骨细胞在藻酸盐凝胶中始终保持球形样外观,甲苯胺蓝染色及Ⅱ型胶原免疫组化染色呈阳性。3组GAG合成无显著性差异(P>0.05)。培养的第6天ITS组DNA含量低于FBS组(P<0.05),第12天低于ITS/FBS组和FBS组(P<0.05)。结论ITS可促进藻酸盐凝胶中软骨细胞的增殖,并保持其表型。 Objective To investigate the effects of Insulin-Transferrin-Selenium (ITS) on the phenotype of rabbit articular chondro cytes cultured in three-dimensional (3D) alginate hydrogel, Methods Chondrocytes isolated from articular cartilage of rabbit were replica ted in monolayer culture system to obtain the second passage of the cells, which were then suspended in sodium alginate solution for third passage culture. Chondrocyte-seeded alginate hydrogels were maintained in the following culture media: DMEM supplemented respectively with 10% FBS (fetal bovine serum), DMEM SUDulemented with 1% ITS and 0.2% FBS. or DMEM SuDolemented with 1% ITS.According to the media listed above, the cells were divided into three groups: FBS, ITS/FBS and ITS group. As designed, the cells were harvested from alginate hydrogels at different culture time, and the proliferation and phenotype of the harvested cells were evaluated by de tecting the content of DNA and glycosaminoglycans (GAG), and also histochemistry staining. Results Chondrocytes could retain their spheroidal morphology when cultured in alginate hydmgels. The cells harvested from hydrogels were positive for toluidine blue and type Ⅱcollagen immunohistochemistry. No significant difference was found in the synthesis of GAG in the three kinds of tested media ( P〉0.05). The DNA content in samples of ITS group was significantly lower than that of FBS group on day 6 ( P〈0.05), whereas it was significant ly lower than that of both ITS/FBS group and FBS group on day 12 (P〈0. 05). Conclusions In alginate hydrogels, ITS can stimulate the proliferation of articular chondrocytes and play a part in maintaining an excellent differentiation phenotype.
出处 《解放军医学杂志》 CAS CSCD 北大核心 2009年第2期159-162,共4页 Medical Journal of Chinese People's Liberation Army
关键词 牛胰岛素-转铁蛋白-亚硒酸盐 软骨细胞 关节 藻酸盐 insulin transferrireselenium chondrocytes joints alginates
  • 相关文献

参考文献9

  • 1Holmes TC. Novel peptide-based biomaterial scaffolds for tissue engineering. Trends Biotechnol, 2002, 20(1): 16. 被引量:1
  • 2Kisiday JD, Kurz B, Dimicco MA, et al. Evaluation of medium sup plemented with insulin transferrirvselenium for culture of primary bovine calf chondrocytes in three-dimensional hydrogel scaffolds. Tissue Eng, 2005, 11(5): 141. 被引量:1
  • 3Chua KH, Aminuddin BS, Fuzina NH, et al. Insulin-transferrin- selenium prevent human chondroeyte dedifferentiation and promote the formation of high quality tissue engineered human hyaline cartilage. Eur Cell Mater, 2005, 9:58. 被引量:1
  • 4薛庆善.细胞培养与分离的试验技术.北京:科学出版社,2001.494. 被引量:1
  • 5郭全义,卢世璧,张莉,袁玫,眭翔,许文静.藻酸钙凝胶为载体体外短期培养羊软骨细胞的生物学性状[J].中国临床康复,2006,10(1):61-63. 被引量:7
  • 6刘义,钱和.1,9-二甲基亚甲基蓝光度法测定海参糖胺聚糖[J].分析试验室,2005,24(6):59-61. 被引量:11
  • 7Kuriwaka M, Ochi M, Uchio Y, et al. Optimum combination of monolayer and three-dimensional cultures for cartilage-like tissue engineering. Tissue Eng, 2003, 9(1): 41. 被引量:1
  • 8Park SH, Park SR, Chung SI, et al. Thoughts and progress Artif Organs, 2005, 29(10): 838. 被引量:1
  • 9IJn YJ, Yen CN, Hu YC, et al. Chondrocytes culture in three-dimensional porous alginate scaffolds enhanced cdl proliferation, matrix synthesis and gene expression. J Biomed Mater Res Part A. [2008-02- 6]. http://www, intersdence, wiley, com/ jpages / 1549 3296/ suppmat. 被引量:1

二级参考文献23

  • 1Hunziker EB, Rosenberg LC. Repair of partial-thickness defects in articular cartilage: cell recruitment from the synovial membrane. J Bone Joint Surg Am 1996;78(5):721-33. 被引量:1
  • 2Schuman L, Buma P,Versleyen D, et al. Chondrocyte behaviour within different types of callagen gel in vitro. Biomaterials 1995;16(10):809-14. 被引量:1
  • 3van Susante JL, Buma P,Schuman L, et al.Resurfacing potential of heterologous chondrocytes suspended in fibrin glue in large full-thickness defects of femoral articular cartilage: an experimental study in the goat. Biomaterials 1999;20(13): 1167-75. 被引量:1
  • 4van Susante JLC, Buma P, van Osch GJVM, et al. Culture of chondrocytes in alginate and callagen cartier gels. Acta Orthop Scand 1995;66(5):549-56. 被引量:1
  • 5Minas T, Nehrer S. Current concepts in the treatment of articular cartilage defects. Orthopedics 1997;20 (6): 525-38. 被引量:1
  • 6Dell'Accio F, Vanlauwe J, Bellemans J, et al. Expanded phenotypically stable chondrocytes persist in the repair tissue and contribute to cartilage matrix formation and structural integration in a goat model of autalogous chondrocyte implantation. J Orthop Res 2003;21(1):123-31. 被引量:1
  • 7Mayne R. Cartilage callagens. What is their function, and are they invalved in articular disease? Arthritis Rheum 1989;32(3):241-6. 被引量:1
  • 8Schmid TM, Linsenmayer TF. Immunohistochemical localization of short chain cartilage callagen (type X) in avian tissues. J Cell Biol 1985;100(2):598-605. 被引量:1
  • 9Kuettner KE. Biochemistry of articular cartilage in health and disease. Clin Biochem 1992 25(3):155-63. 被引量:1
  • 10Zimmermann DR,Ruoslahti E.Multiple domains of the large fibroblast proteoglycan, versican. EMBO J 1989;8(10):2975-81. 被引量:1

共引文献16

同被引文献91

引证文献4

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部