首页> 外文期刊>Experimental Hematology: Official Publication of the International Society for Experimental Hematology >Expansion of mouse hematopoietic progenitor cells in three-dimensional cocultures on frozen-thawed stromal cell layers formed within porous scaffolds
【24h】

Expansion of mouse hematopoietic progenitor cells in three-dimensional cocultures on frozen-thawed stromal cell layers formed within porous scaffolds

机译:三维共培养中小鼠造血祖细胞在多孔支架内形成的冻融基质细胞层上的扩增

获取原文
获取原文并翻译 | 示例
           

摘要

To establish a highly efficient method of ex vivo expansion of hematopoietic cells (HCs), three-dimensional (3D) cocultures of HCs and stromal cell lines were performed using porous polymer scaffolds. Hematopoietic cells derived from mouse fetal livers were expanded by two successive cultures without the use of exogenous cytokines, namely, 3D cultures of stromal cells (DAS 104-8 cell line) to form stromal layers within the scaffolds, and, subsequently, by cocultures of the HCs on the stromal cell layers for 2 weeks. To expand the HCs more conveniently, in some experiments the stromal layers formed within the scaffolds were frozen (3D freezing) before the cocultures, then stored and applied to the cocultures after thawing. When the HCs were cocultured on the stromal layers of the DAS 104-8 cells, primitive HCs (c-kit and CD34(+) cells) were expanded several fold during the cocultures. In contrast, the expansion of these primitive HCs was remarkably enhanced in the cocultures using the 3D frozen-thawed DAS 104-8 stromal layers (c-kit cells > fifteenfold and CD34(+) cells > thirtyfold), and these expansions were significantly higher than those without the 3D freezing. The expansions enhanced by cocultures on the 3D frozen-thawed stromal layers were also observed in the cocultures with another stromal cell line (DAS 104-4). Because 3D frozen-thawed stromal cell lines are easy to handle, 3D coculture of HCs on frozen-thawed stromal cell lines may be an effective and convenient method for expanding primitive HCs. Copyright (C) 2015 ISEH International Society for Experimental Hematology. Published by Elsevier Inc.
机译:为了建立高效的造血细胞(HCs)体外扩增方法,使用多孔聚合物支架进行HCs和基质细胞系的三维(3D)共培养。在不使用外源细胞因子的情况下,通过两次连续培养来扩增源自小鼠胎儿肝脏的造血细胞,即基质细胞的3D培养物(DAS 104-8细胞系)在支架内形成基质层,然后,通过共培养HCs在基质细胞层上放置2周。为了更方便地扩增HC,在某些实验中,将支架内形成的基质层在共培养之前进行冷冻(3D冷冻),然后保存并在解冻后应用于共培养。当HCs在DAS 104-8细胞的基质层上共培养时,原始HCs(c-kit和CD34(+)细胞)在共培养过程中扩展了数倍。相比之下,使用3D冻融的DAS 104-8基质层(c-kit细胞> 15倍,CD34(+)细胞> 30倍)在共培养物中显着增强了这些原始HC的扩增。比那些没有3D冻结的人在与另一种基质细胞系(DAS 104-4)的共培养物中,也观察到了在3D冻融的基质层上的共培养所增强的扩增。由于3D冻融基质细胞系易于处理,因此在冻融基质细胞系上进行HCs 3D共培养可能是扩增原始HCs的有效方法。 ISEH国际实验血液学会版权所有(C)2015。由Elsevier Inc.发布

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号