Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139.
Sci Rep. 2013 Oct 4;3:2863. doi: 10.1038/srep02863.
Diabetes is caused by the loss or dysfunction of insulin-secreting β-cells in the pancreas. β-cells reduce their mass and lose insulin-producing ability in vitro, likely due to insufficient cell-cell and cell-extracellular matrix (ECM) interactions as β-cells lose their native microenvironment. Herein, we built an ex-vivo cell microenvironment by culturing primary β-cells in direct contact with 'synthetic neighbors', cell-sized soft polymer microbeads that were modified with cell-cell signaling factors as well as components from pancreatic-tissue-specific ECMs. This biomimetic 3D microenvironment was able to promote native cell-cell and cell-ECM interactions. We obtained sustained maintenance of β-cell function in vitro enhanced cell viability from the few days usually observed in 2D culture to periods exceeding three weeks, with enhanced β-cell stability and insulin production. Our approach can be extended to create a general 3D culture platform for other cell types.
糖尿病是由胰腺中胰岛素分泌β细胞的缺失或功能障碍引起的。β细胞在体外减少其质量并丧失产生胰岛素的能力,这可能是由于β细胞失去其天然微环境时,细胞-细胞和细胞-细胞外基质(ECM)的相互作用不足所致。在此,我们通过将原代β细胞与“合成邻居”直接培养来构建体外细胞微环境,“合成邻居”是经过细胞间信号因子以及来自胰腺组织特异性 ECM 成分修饰的细胞大小的软聚合物微珠。这种仿生 3D 微环境能够促进天然的细胞-细胞和细胞-细胞外基质的相互作用。我们获得了体外β细胞功能的持续维持,与通常在 2D 培养中观察到的几天相比,细胞活力超过了三周,β细胞稳定性和胰岛素产生得到增强。我们的方法可以扩展到为其他细胞类型创建通用的 3D 培养平台。