文章摘要
李丹1 冯锐成1 张丽新1 郭方琪2 梁洋1 滕春波1.通过G418 处理离体纯化小鼠胰腺上皮细胞[J].,2011,11(12):2242-2246
通过G418 处理离体纯化小鼠胰腺上皮细胞
Purification of Pancreatic Epithelial Cells Treated with G418 in Vitro
  
DOI:
中文关键词: G418  成纤维细胞  胰腺上皮细胞
英文关键词: G418  Fibroblasts  Pancreatic epithelial cells
基金项目:国家自然科学基金项目资助(30670304)
作者单位
李丹1 冯锐成1 张丽新1 郭方琪2 梁洋1 滕春波1 东北林业大学生命科学学院发育生物学研究室 
摘要点击次数: 622
全文下载次数: 974
中文摘要:
      目的:探索一种能有效去除成纤维细胞,筛选有较强增殖能力上皮细胞的方法。方法:本研究利用成纤维细胞对G418 敏感 的特性,在成体小鼠胰腺细胞分离后,采用悬浮细胞直接接种到含30μg/mL G418 的培养基中,或细胞贴壁生长汇合至50-70%后 用30 至100μg/mL 之间不同浓度G418 处理24h、48h 或72h 两种方案进行上皮细胞的纯化。结果:在直接接种法培养处理中, 存活的大部分细胞为成纤维细胞,上皮细胞的生长受到抑制,无法得到纯化的胰腺上皮集落;而在细胞贴壁生长汇合至50-70%后 经G418 处理,成纤维细胞随着处理浓度的增加死亡率也在逐渐上升,其中50μg/mL G418 处理72 小时对去除成纤维细胞效果最 佳。结论:G418 处理能够有效去除成纤维细胞,分离纯化出一群在离体条件下具有强增殖能力、形成大上皮细胞集落的细胞。该 分离纯化方法为今后进一步研究成体胰腺干/ 祖细胞增殖与分化调控机制等问题奠定基础。
英文摘要:
      Objective: To eliminate the fibroblasts and purify epithelial cells from adult mouse pancreas in vitro. Methods: Based on the sensitivity of fibroblasts to G418, this study designed two schemes:Scheme 1 was that the isolated single cells from pancreas were cultured directly in media with 30μg/mL G418, and Scheme 2 was that the isolated single cells were cultured to 50-70% aggregation, and then they were treated with G418 at concentrations from 30 to 100 μg/mL of G418 for 24h, 48h or 72h. Results: The results showed that the growth of the epithelial cells was inhibited in scheme 1, but that of the fibroblasts was little affected. However, after the pancreatic cell grew 50-70% aggregation in scheme 2, G418 treatment could eliminate the fibroblasts, and the death ratio of fibroblasts increase with the elevation of G418 concentration. Among them, 50 μg/mL G418 treatment for 72h was optimal to kill fibroblasts and preserve epithelial cells. Conclutions: G418 treatment could effectively purify a pancreatic epithelial cells with strong proliferative and colonyforming capability, thus provide a pathway for further studies on the proliferation and differentiation of adult pancreas stem/progenitor cells.
查看全文   查看/发表评论  下载PDF阅读器
关闭