Yazaki Yushin, Oyane Ayako, Araki Hiroko, Sogo Yu, Ito Atsuo, Yamazaki Atsushi, Tsurushima Hideo
Research Institute for Science and Engineering, Waseda University, 3-4-1 Ohkubo, Shinjuku, Tokyo, 169-8555, Japan; Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 4, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8562, Japan.
Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 4, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8562, Japan.
Sci Technol Adv Mater. 2012 Nov 8;13(6):064204. doi: 10.1088/1468-6996/13/6/064204. eCollection 2012 Dec.
Surface-mediated gene transfer systems using apatite (Ap)-based composite layers have received increased attention in tissue engineering applications owing to their safety, biocompatibility and relatively high efficiency. In this study, DNA-antibody-apatite composite layers (DA-Ap layers), in which DNA and antibody molecules are immobilized within a matrix of apatite nanocrystals, were fabricated using a biomimetic coating process. They were then assayed for their gene transfer capability for application in a specific cell-targeted gene transfer. A DA-Ap layer that was fabricated with an anti-CD49f antibody showed a higher gene transfer capability to the CD49f-positive CHO-K1 cells than a DNA-apatite composite layer (D-Ap layer). The antibody facilitated the gene transfer capability of the DA-Ap layer only to the specific cells that were expressing corresponding antigens. When the DA-Ap layer was fabricated with an anti-N-cadherin antibody, a higher gene transfer capability compared with the D-Ap layer was found in the N-cadherin-positive P19CL6 cells, but not in the N-cadherin-negative UV♀2 cells or in the P19CL6 cells that were pre-blocked with anti-N-cadherin. Therefore, the antigen-antibody binding that takes place at the cell-layer interface should be responsible for the higher gene transfer capability of the DA-Ap than D-Ap layer. These results suggest that the DA-Ap layer works as a mediator in a specific cell-targeted gene transfer system.
基于磷灰石(Ap)的复合层表面介导基因转移系统因其安全性、生物相容性和相对较高的效率,在组织工程应用中受到越来越多的关注。在本研究中,采用仿生涂层工艺制备了DNA-抗体-磷灰石复合层(DA-Ap层),其中DNA和抗体分子固定在磷灰石纳米晶体基质中。然后对其在特定细胞靶向基因转移中的应用进行基因转移能力检测。用抗CD49f抗体制备的DA-Ap层对CD49f阳性的CHO-K1细胞的基因转移能力高于DNA-磷灰石复合层(D-Ap层)。该抗体仅促进DA-Ap层对表达相应抗原的特定细胞的基因转移能力。当用抗N-钙黏着蛋白抗体制备DA-Ap层时,在N-钙黏着蛋白阳性的P19CL6细胞中发现其基因转移能力高于D-Ap层,但在N-钙黏着蛋白阴性的UV♀2细胞或用抗N-钙黏着蛋白预先封闭的P19CL6细胞中未发现。因此,细胞层界面发生的抗原-抗体结合应该是DA-Ap层比D-Ap层具有更高基因转移能力的原因。这些结果表明,DA-Ap层在特定细胞靶向基因转移系统中起介导作用。