Genetically engineered angiogenic cell sheets using magnetic force-based gene delivery and tissue fabrication techniques

被引:72
作者
Akiyama, Hirokazu [1 ]
Ito, Akira [1 ]
Kawabe, Yoshinori [1 ]
Kamihira, Masamichi [1 ]
机构
[1] Kyushu Univ, Dept Chem Engn, Fac Engn, Nishi Ku, Fukuoka 8190395, Japan
关键词
Magnetite cationic liposome; VEGF; Magnetofection; Cell sheet; Vascularization; Tissue engineering; SKELETAL-MUSCLE TISSUE; CATIONIC LIPOSOMES; IN-VITRO; VEGF; NANOPARTICLES; VASCULARIZATION; CONSTRUCTION; TRANSDUCTION; VASCULATURE; EXPRESSION;
D O I
10.1016/j.biomaterials.2009.11.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A major limitation in tissue engineering is the insufficient formation of blood vessels in implanted tissues, resulting in reduced cell density and graft size. We report here the fabrication of angiogenic cell sheets using a combination of two magnetic force-based techniques which use magnetite cationic liposomes (MCLs), magnetofection and magnetic cell accumulation. A retroviral vector encoding an expression cassette of vascular endothelial growth factor (VEGF) was labeled with MCLs, to magnetically attract the particles onto a monolayer of mouse myoblast C2C12 cells, for gene delivery. MCL-mediated infection increased transduction efficiency by 6.7-fold compared with the conventional method. During the fabrication of the tissue constructs, MCL-labeled cells were accumulated in the presence of a magnetic field to promote the spontaneous formation of a multilayered cell sheet. VEGF gene-engineered C2C12 (C2C12/VEGF) cell sheets, constructed using both magnetic force-based techniques, were subcutaneously transplanted into nude mice. Histological analyses revealed that on day 14 the C2C12/VEGF cell sheet grafts had produced thick tissues, with a high-cell density, and promoted vascularization. This suggests that the method described here represents a powerful strategy in tissue engineering. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1251 / 1259
页数:9
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