TY - JOUR
T1 - Genetically engineered angiogenic cell sheets using magnetic force-based gene delivery and tissue fabrication techniques
AU - Akiyama, Hirokazu
AU - Ito, Akira
AU - Kawabe, Yoshinori
AU - Kamihira, Masamichi
N1 - Funding Information:
We thank Toda Kogyo Co. for kindly supplying the magnetite. We are also grateful to Mr. Y. Suenaga and Mr. S. Huang for technical assistances. One of the authors, Hirokazu Akiyama, is a research fellow of the Japan Society for the Promotion of Science (JSPS). This work was supported in part by Grants-in-Aid for Scientific Research (nos. 21686079 and 20034043) from JSPS.
PY - 2010/2
Y1 - 2010/2
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=72149134885&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=72149134885&partnerID=8YFLogxK
U2 - 10.1016/j.biomaterials.2009.11.017
DO - 10.1016/j.biomaterials.2009.11.017
M3 - Article
C2 - 19942286
AN - SCOPUS:72149134885
SN - 0142-9612
VL - 31
SP - 1251
EP - 1259
JO - Biomaterials
JF - Biomaterials
IS - 6
ER -