Albrecht Dirk R, Underhill Gregory H, Wassermann Travis B, Sah Robert L, Bhatia Sangeeta N
Department of Bioengineering, University of California-San Diego, La Jolla, California 92037, USA.
Nat Methods. 2006 May;3(5):369-75. doi: 10.1038/nmeth873.
Successful application of living cells in regenerative medicine requires an understanding of how tissue structure relates to organ function. There is growing evidence that presentation of extracellular cues in a three-dimensional (3D) context can fundamentally alter cellular responses. Thus, microenvironment studies that previously were limited to adherent two-dimensional (2D) cultures may not be appropriate for many cell types. Here we present a method for the rapid formation of reproducible, high-resolution 3D cellular structures within a photopolymerizable hydrogel using dielectrophoretic forces. We demonstrate the parallel formation of >20,000 cell clusters of precise size and shape within a thin 2-cm(2) hydrogel and the maintenance of high cell viability and differentiated cell markers over 2 weeks. By modulating cell-cell interactions in 3D clusters, we present the first evidence that microscale tissue organization regulates bovine articular chondrocyte biosynthesis. This platform permits investigation of tissue architecture in other multicellular processes, from embryogenesis to regeneration to tumorigenesis.
活细胞在再生医学中的成功应用需要了解组织结构与器官功能之间的关系。越来越多的证据表明,在三维(3D)环境中呈现细胞外信号可以从根本上改变细胞反应。因此,以前仅限于贴壁二维(2D)培养的微环境研究可能不适用于许多细胞类型。在此,我们提出了一种利用介电泳力在可光聚合水凝胶中快速形成可重复、高分辨率3D细胞结构的方法。我们展示了在薄的2平方厘米水凝胶中平行形成超过20,000个精确大小和形状的细胞簇,并在2周内维持高细胞活力和分化细胞标记物。通过调节3D簇中的细胞-细胞相互作用,我们首次证明了微观组织组织调节牛关节软骨细胞生物合成。该平台允许研究从胚胎发生到再生再到肿瘤发生的其他多细胞过程中的组织结构。