Ishihara Seiichiro, Kurosawa Haruna, Haga Hisashi
Department of Advanced Transdisciplinary Sciences, Faculty of Advanced Life Science, Hokkaido University, N10-W8, Kita-ku, Sapporo 060-0810, Japan.
Division of Soft Matter, Graduate School of Life Science, Hokkaido University, N10-W8, Kita-ku, Sapporo 060-0810, Japan.
Gels. 2023 Feb 10;9(2):148. doi: 10.3390/gels9020148.
The stiffness of extracellular matrices (ECMs) is critical for cellular functions. Therefore, modulating the stiffness of ECMs in vitro is necessary to investigate the role of stiffness in cellular phenomena. Collagen gels are widely used for cell culture matrices in vitro. However, modulation of the stiffness in collagen gels for cell culture is challenging owing to the limited knowledge of the method to increase the stiffness while maintaining low cytotoxicity. Here, we established a novel method to modulate collagen gel stiffness from 0.0292 to 12.5 kPa with low cytotoxicity. We prepared collagens with genipin, a low-cytotoxic crosslinker of amines, at different concentrations and successfully modulated the stiffness of the gels. In addition, on 10 mM genipin-mixed collagen gels (approximately 12.5 kPa), H1299 human lung cancer cells showed spreading morphology and nuclear localization of yes-associated protein (YAP), typical phenomena of cells on stiff ECMs. Mouse mesenchymal stromal cells on 10 mM genipin-mixed collagen gels differentiated to vascular smooth muscle cells. On the other hand, the cells on 0 mM genipin-mixed collagen gels (approximately 0.0292 kPa) differentiated to visceral smooth muscle cells. Our new method provides a novel way to prepare stiffness-modulated collagen gels with low cytotoxicity in cell culture.
细胞外基质(ECM)的硬度对细胞功能至关重要。因此,在体外调节ECM的硬度对于研究硬度在细胞现象中的作用是必要的。胶原蛋白凝胶广泛用于体外细胞培养基质。然而,由于在保持低细胞毒性的同时增加硬度的方法的知识有限,调节用于细胞培养的胶原蛋白凝胶的硬度具有挑战性。在这里,我们建立了一种新方法,可在低细胞毒性的情况下将胶原蛋白凝胶的硬度从0.0292调节到12.5 kPa。我们用京尼平(一种低细胞毒性的胺交联剂)制备了不同浓度的胶原蛋白,并成功调节了凝胶的硬度。此外,在10 mM京尼平混合的胶原蛋白凝胶(约12.5 kPa)上,H1299人肺癌细胞呈现出铺展形态和Yes相关蛋白(YAP)的核定位,这是细胞在坚硬ECM上的典型现象。10 mM京尼平混合的胶原蛋白凝胶上的小鼠间充质基质细胞分化为血管平滑肌细胞。另一方面,0 mM京尼平混合的胶原蛋白凝胶(约0.0292 kPa)上的细胞分化为内脏平滑肌细胞。我们的新方法为在细胞培养中制备具有低细胞毒性的硬度调节胶原蛋白凝胶提供了一种新途径。