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厚多功能心脏贴片的模块化组装。

Modular assembly of thick multifunctional cardiac patches.

作者信息

Fleischer Sharon, Shapira Assaf, Feiner Ron, Dvir Tal

机构信息

The Laboratory for Tissue Engineering and Regenerative Medicine, Department of Molecular Microbiology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 69978, Israel.

Center for Nanoscience and Nanotechnology, Tel Aviv University, Tel Aviv 69978, Israel.

出版信息

Proc Natl Acad Sci U S A. 2017 Feb 21;114(8):1898-1903. doi: 10.1073/pnas.1615728114. Epub 2017 Feb 6.

Abstract

In cardiac tissue engineering cells are seeded within porous biomaterial scaffolds to create functional cardiac patches. Here, we report on a bottom-up approach to assemble a modular tissue consisting of multiple layers with distinct structures and functions. Albumin electrospun fiber scaffolds were laser-patterned to create microgrooves for engineering aligned cardiac tissues exhibiting anisotropic electrical signal propagation. Microchannels were patterned within the scaffolds and seeded with endothelial cells to form closed lumens. Moreover, cage-like structures were patterned within the scaffolds and accommodated poly(lactic-co-glycolic acid) (PLGA) microparticulate systems that controlled the release of VEGF, which promotes vascularization, or dexamethasone, an anti-inflammatory agent. The structure, morphology, and function of each layer were characterized, and the tissue layers were grown separately in their optimal conditions. Before transplantation the tissue and microparticulate layers were integrated by an ECM-based biological glue to form thick 3D cardiac patches. Finally, the patches were transplanted in rats, and their vascularization was assessed. Because of the simple modularity of this approach, we believe that it could be used in the future to assemble other multicellular, thick, 3D, functional tissues.

摘要

在心脏组织工程中,细胞被接种到多孔生物材料支架内,以构建功能性心脏补片。在此,我们报告一种自下而上的方法,用于组装由具有不同结构和功能的多层组成的模块化组织。对白蛋白静电纺丝纤维支架进行激光图案化处理,以制造微槽,用于构建具有各向异性电信号传播特性的排列整齐的心脏组织。在支架内制作微通道,并接种内皮细胞以形成封闭的管腔。此外,在支架内制作笼状结构,并容纳聚乳酸-乙醇酸共聚物(PLGA)微粒系统,该系统可控制促进血管生成的VEGF或抗炎剂地塞米松的释放。对每一层的结构、形态和功能进行了表征,并在其最佳条件下分别培养组织层。在移植前,通过基于细胞外基质的生物胶水将组织层和微粒层整合在一起,形成厚的三维心脏补片。最后,将补片移植到大鼠体内,并评估其血管生成情况。由于这种方法具有简单的模块化特点,我们相信它未来可用于组装其他多细胞、厚的三维功能性组织。

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