Amer Luke D, Mahoney Melissa J, Bryant Stephanie J
1 Department of Chemical and Biological Engineering, University of Colorado , Boulder, Colorado.
Tissue Eng Part B Rev. 2014 Oct;20(5):455-67. doi: 10.1089/ten.TEB.2013.0462. Epub 2014 Apr 22.
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.
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。