Salvador Tânia, Oliveira Mariana B, Mano João F
Department of Chemistry, CICECO-Aveiro Institute of Materials, University of Aveiro, Campus Universitário de Santiago, Aveiro, 3810-193, Portugal.
Adv Healthc Mater. 2020 Oct;9(20):e2000543. doi: 10.1002/adhm.202000543. Epub 2020 Sep 9.
The popularity of cell-laden injectable hydrogels has steeply increased due to their compatibility with minimally invasive surgical procedures. However, the diffusion of indispensable molecules for cell survival through bulk hydrogel structures, particularly oxygen, is often limited to micrometric distances, often hampering cell viability or uniform tissue formation in constructs with clinically relevant sizes. The introduction of micropores in hydrogels or the use of oxygen-generating materials has enabled combining advantages of porous 3D scaffolds with the injectability properties of in situ-solidifying hydrogels. Here, cell-laden injectable gelatin methacryloyl (GelMA) foams are fabricated using a single polymer formulation. Air bubbles are introduced into GelMA solutions using a simple-to-implement method based on pulling/pushing the solution through a syringe. Human mesenchymal stem cells derived from the adipose tissue (hASCs) cultured in bulk hydrogels (diameter c.a. 5 mm) show low permanence in the core of the materials and stain for factors associated to hypoxia (hypoxia-inducible factor-1 alpha (HIF-1α)) after 7 days of culture. In opposition, cells cultured in optimized foams do not stain for HIF-1α, show high permanence, homogeneous viability, and consistent phenotype in the whole depth of the biomaterials, while secreting increased amounts of regenerative growth factors to the surrounding medium.
由于与微创手术程序的兼容性,载细胞可注射水凝胶的受欢迎程度急剧上升。然而,细胞存活所必需的分子通过大块水凝胶结构的扩散,尤其是氧气,通常仅限于微米级距离,这常常妨碍具有临床相关尺寸的构建物中的细胞活力或均匀组织形成。在水凝胶中引入微孔或使用产氧材料能够将多孔3D支架的优点与原位固化水凝胶的可注射性相结合。在此,使用单一聚合物配方制备了载细胞可注射甲基丙烯酰化明胶(GelMA)泡沫。基于通过注射器推拉溶液的简单方法,将气泡引入GelMA溶液中。在大块水凝胶(直径约5mm)中培养的源自脂肪组织的人间充质干细胞(hASCs)在材料核心显示出低持久性,并在培养7天后对与缺氧相关的因子(缺氧诱导因子-1α(HIF-1α))染色。相反,在优化的泡沫中培养的细胞不显示HIF-1α染色,在生物材料的整个深度显示出高持久性、均匀的活力和一致的表型,同时向周围培养基分泌增加量的再生生长因子。