TY - JOUR
T1 - Thermoresponsive polymer-modified microfibers for cell separations
AU - Nagase, Kenichi
AU - Sakurada, Yoichi
AU - Onizuka, Satoru
AU - Iwata, Takanori
AU - Yamato, Masayuki
AU - Takeda, Naoya
AU - Okano, Teruo
N1 - Funding Information:
Part of this research was supported by the “Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program),” initiated by the Council for Science and Technology Policy of the Japan Society for the Promotion of Science (JSPS), Creation of Innovation Centers For Advanced Interdisciplinary Research Areas Program in the Project for Developing Innovation Systems “Cell Sheet Tissue Engineering Center (CSTEC)” from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, and a Grant-in-aid for Scientific Research (No. 26420714 for KN) from the Japan Society for the Promotion of Science (JSPS), SENTAN from the Japan Science and Technology Agency (JST) and A3 Foresight Program “Nano-Biomaterials and Delivery Strategies in Regenerative Medicine for Intractable Diseases” from JSPS. The MEXT-Supported Program for the Strategic Research Foundation at Private Universities is also acknowledged for financial support (S1201006 for NT).
Funding Information:
Part of this research was supported by the ?Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program),? initiated by the Council for Science and Technology Policy of the Japan Society for the Promotion of Science (JSPS), Creation of Innovation Centers For Advanced Interdisciplinary Research Areas Program in the Project for Developing Innovation Systems ?Cell Sheet Tissue Engineering Center (CSTEC)? from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, and a Grant-in-aid for Scientific Research (No. 26420714 for KN) from the Japan Society for the Promotion of Science (JSPS), SENTAN from the Japan Science and Technology Agency (JST) and A3 Foresight Program ?Nano-Biomaterials and Delivery Strategies in Regenerative Medicine for Intractable Diseases? from JSPS. The MEXT-Supported Program for the Strategic Research Foundation at Private Universities is also acknowledged for financial support (S1201006 for NT).
Publisher Copyright:
© 2017 Acta Materialia Inc.
PY - 2017/4/15
Y1 - 2017/4/15
N2 - Thermoresponsive polymer-modified microfibers were prepared through electrospinning of poly(4-vinylbenzyl chloride) (PVBC) and subsequent surface-initiated atom transfer radical polymerization for grafting poly(N-isopropylacrylamide) (PIPAAm). Electrospinning conditions were optimized to produce large-diameter (20 μm) PVBC microfibers. The amount of PIPAAm grafted on the microfibers was controlled via the IPAAm monomer concentration. The microfibers exhibited thermally controlled cell separation by selective adhesion of normal human dermal fibroblasts in a mixed cell suspension that also contained human umbilical vein endothelial cells. In addition, adipose-derived stem cells (ADSCs) exhibited thermally modulated cell adhesion and detachment, while adhesion of other ADSC-related cells was low. Thus, ADSCs could be separated from a mixture of adipose tissue-derived cells simply by changing the temperature. Overall, the PIPAAm-modified microfibers are potentially applicable as temperature-modulated cell separation materials. Statement of Significance Thermoresponsive poly(N-isopropylacrylamide) (PIPAAm) polymer-modified poly(4-vinylbenzyl chloride) (PVBC) microfibers were prepared via electrospinning of PVBC, followed by surface-initiated ATRP. They formed effective thermally-modulated cell separation materials with large surface areas. Cells adhered and extended along the modified microfibers; this was not observed on previously reported PIPAAm-modified flat substrates. The cellular adhesion enabled separation of fibroblast cells, as well as that of adipose-derived mesenchymal stem cells, from mixtures of similar cells. Thus, the temperature-controlled thermoresponsive microfibers would be potentially useful as cell separation materials.
AB - Thermoresponsive polymer-modified microfibers were prepared through electrospinning of poly(4-vinylbenzyl chloride) (PVBC) and subsequent surface-initiated atom transfer radical polymerization for grafting poly(N-isopropylacrylamide) (PIPAAm). Electrospinning conditions were optimized to produce large-diameter (20 μm) PVBC microfibers. The amount of PIPAAm grafted on the microfibers was controlled via the IPAAm monomer concentration. The microfibers exhibited thermally controlled cell separation by selective adhesion of normal human dermal fibroblasts in a mixed cell suspension that also contained human umbilical vein endothelial cells. In addition, adipose-derived stem cells (ADSCs) exhibited thermally modulated cell adhesion and detachment, while adhesion of other ADSC-related cells was low. Thus, ADSCs could be separated from a mixture of adipose tissue-derived cells simply by changing the temperature. Overall, the PIPAAm-modified microfibers are potentially applicable as temperature-modulated cell separation materials. Statement of Significance Thermoresponsive poly(N-isopropylacrylamide) (PIPAAm) polymer-modified poly(4-vinylbenzyl chloride) (PVBC) microfibers were prepared via electrospinning of PVBC, followed by surface-initiated ATRP. They formed effective thermally-modulated cell separation materials with large surface areas. Cells adhered and extended along the modified microfibers; this was not observed on previously reported PIPAAm-modified flat substrates. The cellular adhesion enabled separation of fibroblast cells, as well as that of adipose-derived mesenchymal stem cells, from mixtures of similar cells. Thus, the temperature-controlled thermoresponsive microfibers would be potentially useful as cell separation materials.
KW - Cell separation
KW - Electrospun microfiber
KW - Polymer brush
KW - Regenerative medicine
KW - Stimuli responsive polymer
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U2 - 10.1016/j.actbio.2017.02.033
DO - 10.1016/j.actbio.2017.02.033
M3 - Article
C2 - 28219809
AN - SCOPUS:85014074252
SN - 1742-7061
VL - 53
SP - 81
EP - 92
JO - Acta Biomaterialia
JF - Acta Biomaterialia
ER -