TY - JOUR
T1 - Folate receptor-specific cell-cell adhesion by using a folate-modified peptide-based anchor
AU - Nagai, Hiroko
AU - Hatanaka, Wataru
AU - Matsuda, Masayoshi
AU - Kishimura, Akihiro
AU - Katayama, Yoshiki
AU - Mori, Takeshi
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Number JP17K19204. Hatanaka thanks the Japan Society for the Promotion of Science and the Program for Leading Graduate Schools for fellowship.
Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2019/7/24
Y1 - 2019/7/24
N2 - We report here a folate-modified membrane anchor for cell surface modification to induce cell adhesion to target cells. The membrane anchor region, which was consisted of cationic lysine residues and palmitoyl group-modified residues, was modified with folate through an oligoethlene glycol linker. The peptide anchor was modified on to the cell membrane by using β-cyclodextrin as a solubilizer of the peptide anchor. After modification, the peptide anchor disappeared from the cell membrane via endocytotic uptake or dissociation from the cell membrane. However, the endocytosed peptide was represented on the cell surface via recycling endosome pathway. The obtained folate-modified cells successfully adhered on to target cells which expressed folate receptor α via ligand-receptor specific interaction and adhesion continued at least 4 hours.
AB - We report here a folate-modified membrane anchor for cell surface modification to induce cell adhesion to target cells. The membrane anchor region, which was consisted of cationic lysine residues and palmitoyl group-modified residues, was modified with folate through an oligoethlene glycol linker. The peptide anchor was modified on to the cell membrane by using β-cyclodextrin as a solubilizer of the peptide anchor. After modification, the peptide anchor disappeared from the cell membrane via endocytotic uptake or dissociation from the cell membrane. However, the endocytosed peptide was represented on the cell surface via recycling endosome pathway. The obtained folate-modified cells successfully adhered on to target cells which expressed folate receptor α via ligand-receptor specific interaction and adhesion continued at least 4 hours.
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U2 - 10.1080/09205063.2019.1616975
DO - 10.1080/09205063.2019.1616975
M3 - Article
C2 - 31064276
AN - SCOPUS:85066156158
SN - 0920-5063
VL - 30
SP - 983
EP - 993
JO - Journal of Biomaterials Science, Polymer Edition
JF - Journal of Biomaterials Science, Polymer Edition
IS - 11
ER -