TY - JOUR
T1 - Control of Cell-Substrate Binding Related to Cell Proliferation Cycle Status Using a Cytocompatible Phospholipid Polymer Bearing Phenylboronic Acid Groups
AU - Ishihara, Kazuhiko
AU - Abe, Masashi
AU - Fukazawa, Kyoko
AU - Konno, Tomohiro
N1 - Funding Information:
The authors wish to thank Dr. Yuuki Inoue, Department of Materials Engineering, The University of Tokyo, for his kind support of this research. Part of this research was funded by the Ministry of Education, Culture, Sports, Science, and Technology of Japan as a Grant‐in‐Aid for Scientific Research on Innovative Areas “‘Nanomedicine Molecular Science”’ (No.2306).
Funding Information:
The authors wish to thank Dr. Yuuki Inoue, Department of Materials Engineering, The University of Tokyo, for his kind support of this research. Part of this research was funded by the Ministry of Education, Culture, Sports, Science, and Technology of Japan as a Grant-in-Aid for Scientific Research on Innovative Areas “‘Nanomedicine Molecular Science”’ (No.2306).
Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/4
Y1 - 2021/4
N2 - To provide high-quality cellular raw materials for cell engineering and pharmaceutical engineering, a polymer substrate is prepared for cell separation focusing on the cell proliferation cycle. There are many types of sugar chains on cell membranes, which function as signaling molecules to control interactions with the exterior of the cell; their abundance changes during the cell-proliferation cycle. In this study, a phenylboronic acid group, which has affinity for sugar chains, is introduced into a polymer containing a phosphorylcholine group that does not induce cell activation. On the surface of this polymer, human promyelocytic leukemia cells can adhere. The adhesion rate is increased by pretreating the substrate with an alkaline solution. Moreover, cell adhesion is dependent on the sugar additive in the culture medium. Therefore, cell adhesion is governed by reactions between the sugar chain on the cell membrane and the phenylboronic acid groups on the substrate. It is revealed that the adhesion rate changes depending on the expression level of sugar chains related to the cell-proliferation cycle. Based on this, it may be proposed a cell proliferation cycle-specific separation process using the polymer substrate based on cell adhesion depending on sugar chain density.
AB - To provide high-quality cellular raw materials for cell engineering and pharmaceutical engineering, a polymer substrate is prepared for cell separation focusing on the cell proliferation cycle. There are many types of sugar chains on cell membranes, which function as signaling molecules to control interactions with the exterior of the cell; their abundance changes during the cell-proliferation cycle. In this study, a phenylboronic acid group, which has affinity for sugar chains, is introduced into a polymer containing a phosphorylcholine group that does not induce cell activation. On the surface of this polymer, human promyelocytic leukemia cells can adhere. The adhesion rate is increased by pretreating the substrate with an alkaline solution. Moreover, cell adhesion is dependent on the sugar additive in the culture medium. Therefore, cell adhesion is governed by reactions between the sugar chain on the cell membrane and the phenylboronic acid groups on the substrate. It is revealed that the adhesion rate changes depending on the expression level of sugar chains related to the cell-proliferation cycle. Based on this, it may be proposed a cell proliferation cycle-specific separation process using the polymer substrate based on cell adhesion depending on sugar chain density.
KW - 2-methacryloyloxyethyl phosphorylcholine polymer
KW - cell engineering
KW - cell separation
KW - cell-proliferation cycle
KW - p-vinylphenylboronic acid group
KW - surface functionality
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U2 - 10.1002/mabi.202000341
DO - 10.1002/mabi.202000341
M3 - Article
C2 - 33502108
AN - SCOPUS:85099943701
SN - 1616-5187
VL - 21
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
IS - 4
M1 - 2000341
ER -