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Fabrication of a 3-dimensional cardiac tissue using a modular tissue engineering approach.

机译:使用模块化组织工程方法制造3维心脏组织。

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摘要

Implantation of engineered cardiac tissue may restore lost cardiac function to damaged myocardium. We propose that functional cardiac tissue can be fabricated using a modular, vascularized tissue engineering approach developed in our laboratory. In this study, rat aortic endothelial cells (RAEC) were coated onto sub-millimetre size modules embedded with cardiomyocyte-enriched neonatal rat heart cells (CM) and assembled into a contractile, macroporous sheet-like construct.;The fate of modular cardiac tissues in vivo was examined using two implantation strategies based on a syngeneic animal model. Co-culture modules (CM and EC) were either injected into the peri-infarct zone of the heart, or fabricated into a patch form and implanted over a right ventricular free wall defect. In both models, donor EC were involved in the formation of blood vessels-like structures, which appeared to have connected with the host vasculature. Co-culture implants had a higher overall vessel density compared to CM-only implants, but only in the absence of Matrigel(TM). Moreover, donor CM organized into striated muscle-like structures, at least when Matrigel(TM) was removed from the matrix. Together these results suggest that modular cardiac tissue can survive and develop into native-like structures when implanted in vivo and the potential of the modular approach as a platform for building 3-D vascularised cardiac tissue should be explored in greater depth.;Cell morphologies, contractility and responsiveness to electrical stimulus were examined to evaluate the function of the resulting modular construct. CM embedded modules contracted spontaneously at day 7 post-fabrication and remained viable in vitro at day 14. Modules cultured in 10% bovine serum were more contractile and responsive to external stimulus compared to 10% FBS medium cultured modules. VE-cadherin staining showed a confluent layer of RAEC on CM embedded co-culture modules at day 7. Co-culture modules were also contractilie, but when compared to CM only modules their electrical responsiveness was slightly diminished. Modules assembled into macroporous sheets retained their characteristics at day 10 post-assembly. Micrographs from histological sections revealed the existence of muscle bundles near the perimeter of modules and at inter-module junctions.
机译:工程化心脏组织的植入可能会使受损的心肌恢复丧失的心脏功能。我们建议可以使用我们实验室开发的模块化血管化组织工程方法来制造功能性心脏组织。在这项研究中,将大鼠主动脉内皮细胞(RAEC)涂在嵌入了富含心肌细胞的新生大鼠心脏细胞(CM)的亚毫米大小的模块上,并组装成可收缩的大孔片状构建体。使用基于同系动物模型的两种植入策略检查体内。共培养模块(CM和EC)要么被注入心脏的梗死周围区域,要么被制成贴片形式并植入右心室游离壁缺损处。在这两种模型中,供体EC都参与了血管样结构的形成,似乎与宿主脉管系统有关。与仅CM植入物相比,共培养植入物具有更高的总血管密度,但仅在没有MatrigelTM的情况下。此外,至少当从基质中除去Matrigel TM时,供体CM组织成条纹状的肌肉样结构。这些结果共同表明,模块化的心脏组织在体内植入后可以存活并发展成天然结构,因此应更深入地探讨模块化方法作为构建3-D血管化心脏组织的平台的潜力。检查收缩性和对电刺激的反应性,以评估所得模块化结构的功能。 CM嵌入式模块在制造后的第7天自然收缩,并在第14天在体外保持活力。与10%FBS培养基培养的模块相比,在10%牛血清中培养的模块更具收缩性和对外部刺激的反应。 VE-钙黏着蛋白染色在第7天显示在CM嵌入式共培养模块上有一个RAEC汇合层,共培养模块也收缩,但与仅CM相比,它们的电响应性略有下降。组装成大孔板的模块在组装后第10天保持其特性。组织学切片的显微照片显示,在模块周围和模块间连接处存在肌肉束。

著录项

  • 作者

    Leung, Brendan Martin.;

  • 作者单位

    University of Toronto (Canada).;

  • 授予单位 University of Toronto (Canada).;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 0 p.
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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