首页> 外文OA文献 >Treatment with platelet lysate induces endothelial differentiation of bone marrow mesenchymal stem cells under fluid shear stress
【2h】

Treatment with platelet lysate induces endothelial differentiation of bone marrow mesenchymal stem cells under fluid shear stress

机译:血小板裂解液处理可在流体切应力作用下诱导骨髓间充质干细胞的内皮细胞分化

摘要

By considering stem cell-based therapies as a new hope for the treatment of some tragic diseases, marrow stromal cells or marrow mesenchymal stem cells (MSCs) were considered as a suitable and safe multipotential cell source for this new therapeutic approach. For this purpose, many investigations have been performed on differentiation of MSCs toward specific cell lines to overcome the demand for providing the organ specific cells for cell therapy or preparation of engineered tissues. In the present study, differentiation of MSCs to endothelial cells (ECs) by mechanical and chemical stimulation was evaluated. Fluid shear stress (FSS) was used as mechanical inducer, while platelet lysate (PL) and estradiol (E) were used as chemical induction factors. MSCs were placed under FSS with different forces (2, 5 and 10 dyn/cm²) for different periods (6, 12 and 24 hours). In some groups, PL and E were added to the culture media to evaluate their effect on expression of EC specific markers. This investigation revealed that FSS with low tension (2.5-5 dyn/cm²) for a long time (24 hours) or high tension (10 dyn/cm²) in short time (6 hours) in the presence of PL could differentiate MSCs toward ECs. The presence of PL was necessary for initiation of endothelial differentiation, and in the absence of PL, there was not any expression of CD34 and Cadherin5 (Cdh5)among cells. Adding E to the culture medium did not change the rate of endothelial differentiation under FSS. Generated endothelial progenitors could produce von Willebrand factor (vWF) after two weeks culture and also they formed tubular structures after culture on matrigel.
机译:通过考虑将基于干细胞的疗法作为治疗某些悲剧性疾病的新希望,骨髓基质细胞或骨髓间充质干细胞(MSC)被认为是这种新治疗方法的合适且安全的多能细胞来源。为此目的,已经进行了许多关于MSC向特定细胞系分化的研究,以克服提供器官特异性细胞用于细胞治疗或工程组织制备的需求。在本研究中,评估了通过机械和化学刺激将MSC分化为内皮细胞(EC)。流体剪切应力(FSS)用作机械诱导剂,而血小板溶解产物(PL)和雌二醇(E)用作化学诱导因子。将MSCs以不同的力(2、5和10 dyn / cm 2)置于FSS下不同的时间(6、12和24小时)。在某些组中,将PL和E添加到培养基中以评估它们对EC特异性标志物表达的影响。该调查表明,在存在PL的情况下,长时间(24小时)低张力(2.5-5 dyn /cm²)或短时间内(6小时)高张力(10 dyn /cm²)的FSS可以使MSC分化为EC 。 PL的存在是启动内皮细胞分化所必需的,而在PL不存在的情况下,细胞中CD34和Cadherin5(Cdh5)均无任何表达。在培养基中添加E不会改变FSS下内皮分化的速率。培养的两周后,生成的内皮祖细胞可以产生血管性假血友病因子(vWF),并且在基质胶上培养后,它们也形成管状结构。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

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