软骨细胞生物打印后细胞活力分析

合集下载
  1. 1、下载文档前请自行甄别文档内容的完整性,平台不提供额外的编辑、内容补充、找答案等附加服务。
  2. 2、"仅部分预览"的文档,不可在线预览部分如存在完整性等问题,可反馈申请退款(可完整预览的文档不适用该条件!)。
  3. 3、如文档侵犯您的权益,请联系客服反馈,我们会尽快为您处理(人工客服工作时间:9:00-18:30)。

软骨细胞生物打印后细胞活力分析
曲淼;沈聪聪;侯亦康;许佑荣;柴岗;高晓燕
【期刊名称】《组织工程与重建外科杂志》
【年(卷),期】2014(000)001
【摘要】目的:初步确立软骨细胞的二维生物打印方法,实现对细胞喷射过程的控制并保持打印后的细胞活力。

方法取原代软骨细胞,常规培养至第2代。

实验分2组:打印组,快速成型组织打印机进行二维细胞打印,X轴间隔300μm, Y 轴间隔1500μm,激光共聚焦显微镜观察,经生物打印后培养2 h,Live/Dead viability Kit测定细胞活力,激光共聚焦显微镜观察细胞荧光染色情况;对照组除细胞悬液不行打印,其余操作同打印组。

结果打印组细胞激光共聚焦显微镜观察,“细胞墨滴”在二维组织中均匀分布,满足二维设计细胞打印的要求,每个“细胞墨滴”含细胞15~35个。

细胞活力测试显示,打印组细胞活力与对照组无明显区别。

结论通过生物打印技术可实现软骨细胞在二维平面上的定向、定量规则分布,为进一步的细胞三维打印乃至器官打印体系奠定基础。

%Objective To establish a two-dimensional biological printing technique of chondrocytes so as to control the cell transfer process and keep cell viability after printing. Methods Primary chondrocytes were obtained from auricles of 8-week-old piglets and then were regularly sub-cultured to passage 2 (P2). The experiment was divided into 2 groups:printing group and control group. In printing group, P2 chondrocytes were transferred by rapid prototype biological printer (interval in x-axis 300 μm, interval in y-axis 1 500 μm), and were then cultured for 2 hours, afterwards cell viability was detected
by Live/Dead viability Kit and cell fluorescence was observed by laser scanning confocal microscope; In control group, all steps were the same as printing group except that cell suspension received no printing. Results Laser scanning confocal microscope observation on the cells in printing group revealed the “cell ink droplets”. They were distributed regularly and evenly in the two-dimensional layer and each contained 15-35 cells, meeting the requirement of designing two-dimensional cell printing. The cells in printing group went through cell viability test, laser scanning confocal microscope observation showed that it was no significant difference between the control group and the printing groups in terms of cell viability. Conclusion Biological printing technique can realize the oriented, quantificational and regular distribution of chondrocytes in the two-dimensional plane and lays the foundation for the construction of three-dimensional cell printing or even organ printing system.
【总页数】3页(P11-13)
【作者】曲淼;沈聪聪;侯亦康;许佑荣;柴岗;高晓燕
【作者单位】200011 上海市上海交通大学医学院附属第九人民医院整复外科,上海市组织工程研究重点实验室;200011 上海市上海交通大学医学院附属第九人民医院整复外科,上海市组织工程研究重点实验室;200011 上海市上海交通大学医学院附属第九人民医院整复外科,上海市组织工程研究重点实验室;200011 上海市上海交通大学医学院附属第九人民医院整复外科,上海市组织工程研究重点实验室;200011 上海市上海交通大学医学院附属第九人民医院整复外科,上海市组织工程研究重点实验室;201318 上海市上海市周浦医院
【正文语种】中文
【中图分类】R319
【相关文献】
1.丝裂霉素C处理后鼠胚成纤维细胞活力分析 [J], 余树民;王晗;窦忠英
2.软骨细胞培养及其冻存复苏后的生物学特性比较 [J], 孙和炎;卜海富;王明丽;卢晓林;张学瑜;汪正宇
3.3D打印联合生物材料在下颌阻生第三磨牙完整拔除后修复下颌第一磨牙缺失的效果探讨 [J], 黄凯良;林丽;梁善钦
4.3D打印脊柱后凸模型体外模拟截骨在脊柱后凸畸形矫形手术的应用效果分析[J], 任鹏飞;矫健航;张善勇;王洋;吴敏飞
5.原发性骨性关节炎膝关节软骨细胞差异表达circRNA、miRNA筛选和生物学功能及其相互作用分析 [J], 王莹; 郭雄; 王民; 杨益民; 任志伟; 尹思
因版权原因,仅展示原文概要,查看原文内容请购买。

相关文档
最新文档