Miyamoto Yoshitaka, Koshidaka Yumie, Noguchi Hirofumi, Oishi Koichi, Saito Hiroaki, Yukawa Hiroshi, Kaji Noritada, Ikeya Takeshi, Suzuki Satoshi, Iwata Hisashi, Baba Yoshinobu, Murase Katsutoshi, Hayashi Shuji
Department of Advanced Medicine in Biotechnology and Robotics, Nagoya University Graduate School of Medicine , Showa-ku, Nagoya , Japan.
† Department of Surgery, Clinical Research Center, Chiba-East Hospital, National Hospital Organization , Chiba , Japan.
Cell Med. 2013 May 14;5(2-3):89-96. doi: 10.3727/215517913X666530. eCollection 2013 Nov 10.
Magnetic resonance imaging (MRI) using magnetic nanoparticles has been used to diagnose vascular diseases as well as to monitor transplanted cells and tissues. In this study, we synthesized magnetic iron oxide nanoparticles (TMADM-03), electrically charged by the presence of a cationic end-group substitution of dextran, and observed these nanoparticles inside three-dimensional models of HepG2 spheroids, which mimic tissues. Patterned cell array glass disks were prepared to visualize the presence of TMADM-03 uptaken by HepG2 spheroids using transmission electron microscopy (TEM). The HepG2 cells (2 × 10(5) cells) were inoculated onto Cell-able™ 12-well plates. After 48 h of culture, the cells were incubated with 75 µg Fe/ml TMADM-03 in culture medium for 24 h. To investigate the cellular function of the HepG2 spheroids, the albumin secretion was evaluated by an ELISA. The albumin secretion after incubation for 24 h was reduced compared with the secretion prior to the addition of TMADM-03. TEM image samples were prepared in a planar direction or a vertical direction to the HepG2 spheroids on patterned cell array glass disks. The incorporation of TMADM-03 inside the HepG2 spheroids was confirmed. In addition, TMADM-03 could be observed in the deeper layers of the spheroids, and this was localized in the lysosomes. These data suggest that the novel magnetic iron oxide nanoparticles invade three-dimensional HepG2 spheroids.
使用磁性纳米颗粒的磁共振成像(MRI)已被用于诊断血管疾病以及监测移植的细胞和组织。在本研究中,我们合成了磁性氧化铁纳米颗粒(TMADM - 03),其因葡聚糖阳离子端基取代而带电,并在模仿组织的HepG2球体三维模型中观察这些纳米颗粒。制备了图案化细胞阵列玻璃盘,以使用透射电子显微镜(TEM)可视化HepG2球体摄取的TMADM - 03的存在。将HepG2细胞(2×10⁵个细胞)接种到Cell - able™ 12孔板上。培养48小时后,将细胞在含有75μg Fe/ml TMADM - 03的培养基中孵育24小时。为了研究HepG2球体的细胞功能,通过酶联免疫吸附测定(ELISA)评估白蛋白分泌。与添加TMADM - 03之前的分泌相比,孵育24小时后的白蛋白分泌减少。在图案化细胞阵列玻璃盘上,在与HepG2球体平面方向或垂直方向制备TEM图像样本。证实了TMADM - 03在HepG2球体内的掺入。此外,在球体的较深层中可以观察到TMADM - 03,并且其定位于溶酶体中。这些数据表明新型磁性氧化铁纳米颗粒侵入三维HepG2球体。