Ma Hongmeng, Xu Lilin, Wu Shengjie, Wang Songdi, Li Jie, Ai Sifan, Yang Zhuangzhuang, Mo Rigen, Lin Lei, Li Yan, Wang Shusen, Gao Jie, Li Chen, Kong Deling
State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, and College of Life Sciences, Nankai University, Tianjin, 300071, China.
Research Institute of Transplant Medicine, Organ Transplant Center, Tianjin First Central Hospital, Nankai University, Tianjin, China.
Bioact Mater. 2024 Jul 8;41:1-14. doi: 10.1016/j.bioactmat.2024.07.007. eCollection 2024 Nov.
Although several synthetic hydrogels with defined stiffness have been developed to facilitate the proliferation and maintenance of human pluripotent stem cells (hPSCs), the influence of biochemical cues in lineage-specific differentiation and functional cluster formation has been rarely reported. Here, we present the application of Supragel, a supramolecular hydrogel formed by synthesized biotinylated peptides, for islet-like cluster differentiation. We observed that Supragel, with a peptide concentration of 5 mg/mL promoted spontaneous hPSCs formation into uniform clusters, which is mainly attributable to a supporting stiffness of ∼1.5 kPa as provided by the Supragel matrix. Supragel was also found to interact with the hPSCs and facilitate endodermal and subsequent insulin-secreting cell differentiation, partially through its components: the sequences of RGD and YIGSR that interacts with cell membrane molecules of integrin receptor. Compared to Matrigel and suspension culturing conditions, more efficient differentiation of the hPSCs was also observed at the stages 3 and 4, as well as the final stage toward generation of insulin-secreting cells. This could be explained by 1) suitable average size of the hPSCs clusters cultured on Supragel; 2) appropriate level of cell adhesive sites provided by Supragel during differentiation. It is worth noting that the Supragel culture system was more tolerance in terms of the initial seeding densities and less demanding, since a standard static cell culture condition was sufficient for the entire differentiation process. Our observations demonstrate a positive role of Supragel for hPSCs differentiation into islet-like cells, with additional potential in facilitating germ layer differentiation.
尽管已经开发出几种具有确定刚度的合成水凝胶来促进人类多能干细胞(hPSC)的增殖和维持,但关于生化信号在谱系特异性分化和功能簇形成中的影响却鲜有报道。在此,我们展示了Supragel的应用,Supragel是一种由合成的生物素化肽形成的超分子水凝胶,用于胰岛样簇的分化。我们观察到,肽浓度为5 mg/mL的Supragel促进hPSC自发形成均匀的簇,这主要归因于Supragel基质提供的约1.5 kPa的支撑刚度。还发现Supragel与hPSC相互作用,并部分通过其成分:与整合素受体细胞膜分子相互作用的RGD和YIGSR序列,促进内胚层及随后的胰岛素分泌细胞分化。与基质胶和悬浮培养条件相比,在第3和第4阶段以及向胰岛素分泌细胞生成的最后阶段,也观察到hPSC更有效的分化。这可以通过以下几点来解释:1)在Supragel上培养的hPSC簇的合适平均大小;2)Supragel在分化过程中提供的适当水平的细胞粘附位点。值得注意的是,Supragel培养系统在初始接种密度方面更具耐受性且要求较低,因为标准的静态细胞培养条件足以满足整个分化过程。我们的观察结果表明Supragel在hPSC分化为胰岛样细胞方面具有积极作用,在促进胚层分化方面还有额外的潜力。