文章摘要
刘鑫成,孟星星,祝 瑞,张煜珅,成西侠,范宏斌.使用透明质酸钠复合海藻酸钠水凝胶球3D培养软骨细胞抑制细胞去分化的研究[J].,2017,17(16):3049-3053
使用透明质酸钠复合海藻酸钠水凝胶球3D培养软骨细胞抑制细胞去分化的研究
The Application of Sodium Alginate Hydrogel Beads with Hyaluronic Acid in the Three-dimensional Culture of Chondrocytes to Inhibit the Dedifferentiation of Chondrocytes
投稿时间:2016-10-22  修订日期:2016-11-10
DOI:10.13241/j.cnki.pmb.2017.16.012
中文关键词: 软骨细胞  透明质酸钠  海藻酸钠  水凝胶  3D培养
英文关键词: Chondrocytes  Sodium alginate  Alginate  Hydrogel  Three-dimensional culture
基金项目:国家自然科学基金项目(31170936, 31470936)
作者单位E-mail
刘鑫成 第四军医大学西京医院骨科 陕西 西安 710032 xincheng__liu@163.com 
孟星星 第四军医大学航空航天卫生学教研室 陕西 西安 710032  
祝 瑞 空军工程大学理学院 陕西 西安 710051  
张煜珅 第四军医大学西京医院骨科 陕西 西安 710032  
成西侠 第四军医大学西京医院骨科 陕西 西安 710032  
范宏斌 第四军医大学西京医院骨科 陕西 西安 710032  
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中文摘要:
      摘要 目的:验证海藻酸钠(Alginate, Alg)水凝胶球添加透明质酸钠(Sodium hyaluronate, HA)后,对大鼠膝软骨细胞体外3D培养时软骨细胞去分化的抑制情况。方法:用Ⅱ型胶原酶消化法获取2周龄SD大鼠膝关节原代软骨细胞,体外培养传代至P2。细胞分为2组,1组用2%海藻酸钠水凝胶球3D培养(Alg组),另一组用2%海藻酸钠+1%透明质酸钠的水凝胶球3D培养(Alg/HA组),采用正交法制作海藻酸钠水凝胶球。培养14天后,两组各取水凝胶球进行死活细胞染色观察细胞状态。其他水凝胶球收集后用4%多聚甲醛固定,30%蔗糖溶液脱水,OCT(Optimal cutting temperature compound)包埋剂包埋切片,采用苏木精 - 伊红染色法(Hematoxylin-eosin staining, HE染色)、甲苯胺蓝染色观察软骨细胞形态;采用阿利新蓝染色观察对比糖胺聚糖(Glycosaminoglycan, GAG)含量;采用免疫荧光染色对比Ⅱ型胶原(Collagen type Ⅱ, Col Ⅱ)含量;采用蛋白质免疫印迹法(Western blot)检测软骨细胞Col Ⅱ和聚蛋白多糖(Aggrecan, ACAN)的表达情况。结果:死活细胞染色显示两组水凝球内软骨细胞状态良好,几乎无死细胞;阿利新蓝染色显示Alg/HA组与Alg组相比软骨细胞分泌更多的GAG;免疫荧光染色显示Alg/HA组比Alg组软骨细胞内含更多的Ⅱ型胶原;Western blot显示Alg/HA组软骨细胞比Alg组Col Ⅱ的蛋白表达更多。结论:含透明质酸钠的海藻酸钠水凝胶可以更好地维持软骨细胞的表型,抑制软骨细胞去分化。
英文摘要:
      ABSTRACT Objective: To verify the inhibitory effect of sodium alginate hydrogel beads with hyaluronic acid on the dedifferentiation of chondrocytes in vitro. Methods: Chondrocytes were obtained from knee articular of 2-week-old SD rat with type Ⅱ collagenase digestion method and cultured in vitro. P2 cells were divided into 2 groups. One was cultivated within 2% sodium alginate beads 3D culture (Alg group), another was cultivated within 2% sodium alginate + 1% sodium hyaluronate beads 3D culture (Alg/HA group). 14 days later, part of the beads were stained by live/dead cell staining, and others were harvested, fixed by 4% poly formaldehyde, OCT(Optimal cutting temperature compound) embedded and frozenly sectioned. Hematoxylin - eosin staining(HE staining) was used to observe the morphology of chondrocytes in the beads; Alcian blue staining was used for observation and comparison of glycosaminoglycan (GAG) content in chondrocytes. The immunofluorescence staining was used for comparison of type Ⅱ collagen (Col Ⅱ) content. Western blot was used to detect the expression of Col Ⅱ. Results: Live/ dead cell staining showed that there were few dead chondrocytes in 2 groups of alginate beads. Alcian blue staining showed that chondrocytes in Alg/HA group secreted more GAG than those in Alg group. Immunofluorescence showed that chondrocytes in Alg/HA group produced more Col Ⅱ than those in Alg group. Western blot showed that the Col Ⅱ expression of chondrocytes in Alg/HA group was higher than that in Alg groups. Conclusion: Alginate beads with sodium hyaluronate could maintain the chondrogenic phenotype and inhibit the dedifferentiation of chondrocytes better.
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