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用于正常和病变肾脏的组织工程三维体外模型。

Tissue-engineered three-dimensional in vitro models for normal and diseased kidney.

机构信息

Department of Biomedical Engineering, Tufts University, Medford, Massachusetts 02155, USA.

出版信息

Tissue Eng Part A. 2010 Sep;16(9):2821-31. doi: 10.1089/ten.tea.2009.0595.

Abstract

Morphogenesis of epithelial cells involves processes by which kidney shape and function are regulated. The lack of in vitro models that are sustainable for longer time periods and emulating complex intercellular interactions of the kidney have limited understanding about epithelial tissue morphogenesis and its aberrations in diseases such as autosomal dominant polycystic kidney disease (ADPKD). A sustainable three-dimensional (3D) coculture system for normal and diseased kidney tissues is reported here. Tubule- and ADPKD cyst-derived cells were cultured in extracellular matrix molecules infused into 3D porous silk scaffolds, and these cultures were subsequently extended into a perfusion bioreactor. The results indicated collagen-matrigel-mediated morphogenesis for both (normal and disease) cell types and also supported coculturing with fibroblasts. The structural and functional features of the kidney-like tissue structures were validated based on the distribution of E-cadherin, N-cadherin, Na+ K+ ATPase pump, and cellular uptake of the organic anion (6-carboxy fluorescein). Further, the structures were sustained for longer time periods using a perfusion bioreactor to demonstrate the potential utility of this 3D in vitro coculture system for ADPKD research, other epithelial tissue systems, and for in vitro drug screening.

摘要

上皮细胞的形态发生涉及到调节肾脏形状和功能的过程。缺乏能够持续更长时间并模拟肾脏复杂细胞间相互作用的体外模型,限制了我们对上皮组织形态发生及其在疾病(如常染色体显性多囊肾病(ADPKD))中的异常的理解。本文报道了一种用于正常和病变肾脏组织的可持续性三维(3D)共培养系统。将肾小管和 ADPKD 囊肿来源的细胞培养在注入 3D 多孔丝支架的细胞外基质分子中,然后将这些培养物扩展到灌注生物反应器中。结果表明,胶原-基质胶介导了(正常和疾病)两种细胞类型的形态发生,并且还支持与成纤维细胞的共培养。基于 E-钙粘蛋白、N-钙粘蛋白、Na+K+ATP 酶泵和有机阴离子(6-羧基荧光素)的细胞摄取,验证了类似肾脏组织结构的结构和功能特征。此外,通过使用灌注生物反应器来延长结构的持续时间,证明了这种 3D 体外共培养系统在 ADPKD 研究、其他上皮组织系统以及体外药物筛选中的潜在应用价值。

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