首页> 外文期刊>Journal of Medical Colleges of PLA >Experimental study on the induction of bone marrow stromal cells differentiating into cardiomyocyte-like cells with cardiomyocytes in vitro
【24h】

Experimental study on the induction of bone marrow stromal cells differentiating into cardiomyocyte-like cells with cardiomyocytes in vitro

机译:体外诱导心肌细胞诱导骨髓基质细胞分化为心肌样细胞的实验研究

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: To investigate the feasibility of bone marrow stromal cells (BMSCs) differentiating into cardiomyocyte-like cells in heterogeneous cardiomyocytes microenvironment in vitro. Methods: Mouse GFP-BMSCs were isolated by centrifugation through a Ficoll step gradient and purified by plating culture and depletion of the non-adherent cells. Neonatal rat cardiomyocytes (CMs) were isolated by enzymatic dissociation from hearts of 1-to 2-day-old Sprague-Dawley (SD) rats and differentially plated to remove fibroblasts. Mouse GFP-BMSCs were cocultured with neonatal rat CMs through direct and indirect contact, respectively. Cardiomyogenic differentiation of BMSCs was evaluated by immunostaining with anti-α-actin monoclonal antibody and observing synchronous contraction with adjacent CMs by phase contrast microphotography. Results: On day 7 of coculture, GFP-BMSCs (CMs : BMSCs = 4 : 1) attached to non-fluorescent contracting cells (rat-derived CMs) showed myotube-like formation and started to contract synchronously with adjacent cardiomyocytes. About 10% of the fluorescent GFP-BMSCs were cardiomyocyte-like cells as determined by cell morphology and positive actin staining. Conclusion:Direct cell-to-cell interaction with CMs is crucial for cardiomyogenic differentiation of BMSCs in heterogeneous CMs microenvironment in vitro. This provides a novel inducing pathway for directional differentiation of cardiovascular tissue engineering seed cells.
机译:目的:探讨异种心肌细胞微环境中骨髓基质细胞(BMSCs)分化为心肌样细胞的可行性。方法:通过Ficoll梯度梯度离心分离小鼠GFP-BMSCs,并通过平板培养和去除非粘附细胞进行纯化。通过酶解从1至2天大的Sprague-Dawley(SD)大鼠心脏中分离出新生大鼠心肌细胞(CMs),并进行差异接种以去除成纤维细胞。通过直接和间接接触,将小鼠GFP-BMSC分别与新生大鼠CM共培养。通过用抗α-肌动蛋白单克隆抗体免疫染色并通过相差显微镜观察与相邻CM的同步收缩来评估BMSC的心肌发生分化。结果:在共培养的第7天,附着于非荧光收缩细胞(大鼠来源的CM)的GFP-BMSC(CMs:BMSCs = 4:1)显示出肌管样形成,并开始与相邻的心肌细胞同步收缩。通过细胞形态学和阳性肌动蛋白染色确定,大约10%的荧光GFP-BMSC是心肌样细胞。结论:在异质CMs微环境中,与CMs的直接细胞间相互作用对于BMSCs的心肌分化至关重要。这为心血管组织工程种子细胞的定向分化提供了新颖的诱导途径。

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