TY - JOUR
T1 - The effect of RGD peptide-conjugated magnetite cationic liposomes on cell growth and cell sheet harvesting
AU - Ito, Akira
AU - Ino, Kousuke
AU - Kobayashi, Takeshi
AU - Honda, Hiroyuki
N1 - Funding Information:
The authors would like to thank Toda Kogyo Co. for supplying the magnetite and Dr. Yoshiko Miura (Nagoya University) for comments regarding RGD-MCL preparation. This work was supported in part by the 21st Century COE Program ‘Nature-Guided Materials Processing’ and by a Grant-in-Aid for Scientific Research (No. 15760587) of the Ministry of Education, Sports, Science and Technology, Japan.
PY - 2005/11
Y1 - 2005/11
N2 - Tissue engineering requires novel technologies for establishing 3D constructs, and the layered method of culturing cell sheets (cell sheet engineering) is one potentially useful approach. In the present study, we investigated whether coating the culture surface with RGD (Arg-Gly-Asp) peptide-conjugated magnetite cationic liposomes (RGD-MCLs) was able to facilitate cell growth, cell sheet construction and cell sheet harvest using magnetic force without enzymatic treatment. To promote cell attachment, an RGD-motif-containing peptide was coupled to the phospholipid of our original magnetite cationic liposomes (MCLs). The RGD-MCLs were added to a commercially available 24-well ultra-low-attachment plate the surface of which comprised a covalently bound hydrogel layer that was hydrophilic and neutrally charged. A magnet was placed on the underside of the well in order to attract the RGD-MCLs to the surface of the well, and then NIH/3T3 cells were seeded into the well. Cells adhered to the bottom of the culture surface, which was coated with RGD-MCLs, and the cells spread and proliferated to confluency. After incubation, the magnet was removed and the cells were detached from the bottom of the plates, forming a contiguous cell sheet. Because the sheets contained magnetite nanoparticles, they could be harvested using a magnet inserted into the well. These results suggest that this novel methodology using RGD-MCLs and magnetic force, which we have termed 'magnetic force-based tissue engineering (Mag-TE)', is a promising approach for tissue engineering.
AB - Tissue engineering requires novel technologies for establishing 3D constructs, and the layered method of culturing cell sheets (cell sheet engineering) is one potentially useful approach. In the present study, we investigated whether coating the culture surface with RGD (Arg-Gly-Asp) peptide-conjugated magnetite cationic liposomes (RGD-MCLs) was able to facilitate cell growth, cell sheet construction and cell sheet harvest using magnetic force without enzymatic treatment. To promote cell attachment, an RGD-motif-containing peptide was coupled to the phospholipid of our original magnetite cationic liposomes (MCLs). The RGD-MCLs were added to a commercially available 24-well ultra-low-attachment plate the surface of which comprised a covalently bound hydrogel layer that was hydrophilic and neutrally charged. A magnet was placed on the underside of the well in order to attract the RGD-MCLs to the surface of the well, and then NIH/3T3 cells were seeded into the well. Cells adhered to the bottom of the culture surface, which was coated with RGD-MCLs, and the cells spread and proliferated to confluency. After incubation, the magnet was removed and the cells were detached from the bottom of the plates, forming a contiguous cell sheet. Because the sheets contained magnetite nanoparticles, they could be harvested using a magnet inserted into the well. These results suggest that this novel methodology using RGD-MCLs and magnetic force, which we have termed 'magnetic force-based tissue engineering (Mag-TE)', is a promising approach for tissue engineering.
KW - Cell culture
KW - Liposomes
KW - Magnetite nanoparticles
KW - RGD peptide
KW - Tissue engineering
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U2 - 10.1016/j.biomaterials.2005.03.039
DO - 10.1016/j.biomaterials.2005.03.039
M3 - Article
C2 - 15899515
AN - SCOPUS:20444474657
SN - 0142-9612
VL - 26
SP - 6185
EP - 6193
JO - Biomaterials
JF - Biomaterials
IS - 31
ER -