Xin Yu, Ligorio Cosimo, O'brien Marie, Collins Richard, Dong Siyuan, Miller Aline F, Saiani Alberto, Gough Julie E
Department of Materials & Henry Royce Institute, School of Natural Sciences, Faculty of Science and Engineering, The University of Manchester, UK.
Department of Materials & Manchester Institute of Biotechnology, School of Natural Sciences, Faculty of Science and Engineering, The University of Manchester, UK.
J Mater Chem B. 2024 Dec 11;12(48):12553-12566. doi: 10.1039/d4tb01701c.
Supramolecular bioinspired self-assembling peptide hydrogel (SAPH) scaffolds represent a class of fully defined synthetic materials whose chemical and mechanical properties can be finely engineered. In this study, the relationship between SAPHs physicochemical properties and HepG2 cells viability, spheroid formation and function are discussed. We first report that negatively charged SAPHs promote hepatocyte proliferation and spheroids formation 3D culture while positively charged SAPHs lead to hepatocyte death irrespective of the hydrogel mechanical properties. More specifically HepG2 cultured in 3D in E(FKFE) negatively charged SAPH maintained a differentiated phenotype and assembled into well-defined spheroids with strong cell-cell interactions. Furthermore, HepG2 spheroids responded to acetaminophen exposure with upregulation of key CYP450 enzymes expression clearly showing their potential for drug toxicity testing. These findings demonstrate how fine-tuned functional SAPH scaffolds can be used to identify key scaffolds parameters affecting cells. In this case we demonstrated the potential of negatively charged SAPHs for the 3D culture of HepG2 with potential applications in drug screening.
超分子生物启发自组装肽水凝胶(SAPH)支架是一类完全确定的合成材料,其化学和机械性能可以进行精细设计。在本研究中,讨论了SAPH的物理化学性质与HepG2细胞活力、球体形成及功能之间的关系。我们首次报道,带负电荷的SAPH在三维培养中促进肝细胞增殖和球体形成,而带正电荷的SAPH则导致肝细胞死亡,与水凝胶的机械性能无关。更具体地说,在E(FKFE)带负电荷的SAPH中进行三维培养的HepG2保持分化表型,并组装成具有强细胞间相互作用的明确球体。此外,HepG2球体对乙酰氨基酚暴露有反应,关键CYP450酶表达上调,清楚地显示了它们在药物毒性测试中的潜力。这些发现证明了如何使用微调的功能性SAPH支架来确定影响细胞的关键支架参数。在这种情况下,我们展示了带负电荷的SAPH在HepG2三维培养中的潜力及其在药物筛选中的潜在应用。