Maeda Eijiro, Tsutsumi Takehiro, Kitamura Nobuto, Kurokawa Takayuki, Ping Gong Jian, Yasuda Kazunori, Ohashi Toshiro
Laboratory of Micro and Nanomechanics, Division of Human Mechanical Systems and Design, Graduate School of Engineering, Hokkaido University, N13 W8, Kita-ku, Sapporo, Hokkaido 060-8628, Japan.
Laboratory of Micro and Nanomechanics, Division of Human Mechanical Systems and Design, Graduate School of Engineering, Hokkaido University, N13 W8, Kita-ku, Sapporo, Hokkaido 060-8628, Japan.
J Biomech. 2014 Oct 17;47(13):3408-14. doi: 10.1016/j.jbiomech.2014.07.021. Epub 2014 Jul 30.
A double-network (DN) gel, which was composed of poly(2-acrylamido-2-methylpropanesulfonic acid) and poly(N,N'-dimethyl acrylamide) (PAMPS/PDMAAm), has the potential to induce chondrogenesis both in vitro and in vivo. The present study investigated the biomechanical and biological responses of chondrogenic progenitor ATDC5 cells cultured on the DN gel. ATDC5 cells were cultured on a polystyrene surface without insulin (Culture 1) and with insulin (Culture 2), and on the DN gel without insulin (Culture 3). The cultured cells were evaluated using micropipette aspiration for cell Young's modulus and qPCR for gene expression of chondrogenic and actin organization markers on days 3, 7 and 14. On day 3, the cells in Culture 3 formed nodules, in which the cells exhibited an actin cortical layer inside them, and gene expression of type-II collagen, aggrecan, and SOX9 was significantly higher in Culture 3 than Cultures 1 and 2 (p<0.05). Young's modulus in Culture 3 was significantly higher than that in Culture 1 throughout the testing period (p<0.05) and that in Culture 2 on day 14 (p<0.01). There was continuous expression of actin organization markers in Culture 3. This study highlights that the cells on the DN gel increased the modulus and mRNA expression of chondrogenic markers at an earlier time point with a greater magnitude compared to those on the polystyrene surface with insulin. This study also demonstrates a possible strong interrelation among alteration of cell mechanical properties, changes in actin organization and the induction of chondrogenic differentiation.
一种由聚(2-丙烯酰胺-2-甲基丙烷磺酸)和聚(N,N'-二甲基丙烯酰胺)(PAMPS/PDMAAm)组成的双网络(DN)凝胶在体外和体内均具有诱导软骨形成的潜力。本研究调查了在DN凝胶上培养的软骨形成祖细胞ATDC5的生物力学和生物学反应。将ATDC5细胞分别培养在无胰岛素的聚苯乙烯表面(培养1)、有胰岛素的聚苯乙烯表面(培养2)以及无胰岛素的DN凝胶上(培养3)。在第3、7和14天,使用微量移液器抽吸法评估培养细胞的细胞杨氏模量,并通过qPCR检测软骨形成和肌动蛋白组织标志物的基因表达。在第3天,培养3中的细胞形成结节,其中细胞内部呈现出肌动蛋白皮质层,并且培养3中II型胶原蛋白、聚集蛋白聚糖和SOX9的基因表达显著高于培养1和培养2(p<0.05)。在整个测试期间,培养3的杨氏模量显著高于培养1(p<0.05),在第14天显著高于培养2(p<0.01)。培养3中肌动蛋白组织标志物持续表达。本研究强调,与在有胰岛素的聚苯乙烯表面培养的细胞相比,在DN凝胶上培养的细胞在更早的时间点以更大的幅度增加了软骨形成标志物的模量和mRNA表达。本研究还证明了细胞力学性质的改变、肌动蛋白组织的变化与软骨形成分化诱导之间可能存在密切的相互关系。