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本文引用的文献

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Perfusion-decellularized pancreas as a natural 3D scaffold for pancreatic tissue and whole organ engineering.去细胞化的胰腺作为胰腺组织和整个器官工程的天然 3D 支架。
Biomaterials. 2013 Sep;34(28):6760-72. doi: 10.1016/j.biomaterials.2013.05.066. Epub 2013 Jun 17.
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Multicenter Australian trial of islet transplantation: improving accessibility and outcomes.澳大利亚多中心胰岛移植试验:提高可及性和结果。
Am J Transplant. 2013 Jul;13(7):1850-8. doi: 10.1111/ajt.12250. Epub 2013 May 13.
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The generation of pancreatic β-cell spheroids in a simulated microgravity culture system.在模拟微重力培养系统中生成胰腺β细胞球体。
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Macro- or microencapsulation of pig islets to cure type 1 diabetes.猪胰岛的宏观或微观包封治疗 1 型糖尿病。
World J Gastroenterol. 2012 Dec 21;18(47):6885-93. doi: 10.3748/wjg.v18.i47.6885.
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Potential role of mesenchymal stromal cells in pancreatic islet transplantation.间充质基质细胞在胰岛移植中的潜在作用。
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Pancreatic islet basement membrane loss and remodeling after mouse islet isolation and transplantation: impact for allograft rejection.胰岛分离和移植后小鼠胰岛基底膜丢失和重塑:同种异体移植排斥的影响。
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Regulation of endodermal differentiation of human embryonic stem cells through integrin-ECM interactions.通过整合素-细胞外基质相互作用调控人胚胎干细胞的内胚层分化。
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The prospect of induced pluripotent stem cells for diabetes mellitus treatment.诱导多能干细胞治疗糖尿病的前景。
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基于细胞的1型糖尿病治疗的组织工程方法。

Tissue engineering approaches to cell-based type 1 diabetes therapy.

作者信息

Amer Luke D, Mahoney Melissa J, Bryant Stephanie J

机构信息

1 Department of Chemical and Biological Engineering, University of Colorado , Boulder, Colorado.

出版信息

Tissue Eng Part B Rev. 2014 Oct;20(5):455-67. doi: 10.1089/ten.TEB.2013.0462. Epub 2014 Apr 22.

DOI:10.1089/ten.TEB.2013.0462
PMID:24417705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4185974/
Abstract

Type 1 diabetes mellitus is an autoimmune disease resulting from the destruction of insulin-producing pancreatic β-cells. Cell-based therapies, involving the transplantation of functional β-cells into diabetic patients, have been explored as a potential long-term treatment for this condition; however, success is limited. A tissue engineering approach of culturing insulin-producing cells with extracellular matrix (ECM) molecules in three-dimensional (3D) constructs has the potential to enhance the efficacy of cell-based therapies for diabetes. When cultured in 3D environments, insulin-producing cells are often more viable and secrete more insulin than those in two dimensions. The addition of ECM molecules to the culture environments, depending on the specific type of molecule, can further enhance the viability and insulin secretion. This review addresses the different cell sources that can be utilized as β-cell replacements, the essential ECM molecules for the survival of these cells, and the 3D culture techniques that have been used to benefit cell function.

摘要

1型糖尿病是一种自身免疫性疾病,由产生胰岛素的胰腺β细胞被破坏所致。基于细胞的疗法,即将功能性β细胞移植到糖尿病患者体内,已被探索作为这种疾病的一种潜在长期治疗方法;然而,成效有限。一种在三维(3D)构建物中用细胞外基质(ECM)分子培养产生胰岛素细胞的组织工程方法,有潜力提高基于细胞的糖尿病治疗的疗效。当在3D环境中培养时,产生胰岛素的细胞通常比在二维环境中的细胞更具活力,且分泌更多胰岛素。根据分子的具体类型,向培养环境中添加ECM分子可进一步提高细胞活力和胰岛素分泌。本综述探讨了可用作β细胞替代物的不同细胞来源、这些细胞存活所必需的ECM分子,以及已用于促进细胞功能的3D培养技术。