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Bio-inspired oligovitronectin-grafted surface for enhanced self-renewal and long-term maintenance of human pluripotent stem cells under feeder-free conditions

Authors
 Hyun-Ji Park  ;  Kisuk Yang  ;  Mun-Jung Kim  ;  Jiho Jang  ;  Mihyun Lee  ;  Dong-Wook Kim  ;  Haeshin Lee  ;  Seung-Woo Cho 
Citation
 BIOMATERIALS, Vol.50 : 127-139, 2015 
Journal Title
BIOMATERIALS
ISSN
 0142-9612 
Issue Date
2015
MeSH
Amino Acid Sequence ; Biomimetic Materials/pharmacology* ; Cell Communication/drug effects ; Cell Proliferation/drug effects ; Cell Self Renewal/drug effects* ; Cells, Cultured ; Clone Cells ; Embryo, Mammalian/cytology ; Embryo, Mammalian/drug effects ; Feeder Cells/cytology ; Feeder Cells/drug effects ; Focal Adhesions/drug effects ; Humans ; Indoles/chemistry ; Molecular Sequence Data ; Pluripotent Stem Cells/cytology* ; Pluripotent Stem Cells/drug effects* ; Polymers/chemistry ; Signal Transduction/drug effects ; Surface Properties ; Vitronectin/chemistry ; Vitronectin/pharmacology*
Keywords
Feeder-free maintenance ; Human pluripotent stem cells ; Material-independent surface coating ; Polydopamine ; Vitronectin peptide
Abstract
Current protocols for human pluripotent stem cell (hPSC) expansion require feeder cells or matrices from animal sources that have been the major obstacle to obtain clinical grade hPSCs due to safety issues, difficulty in quality control, and high expense. Thus, feeder-free, chemically defined synthetic platforms have been developed, but are mostly confined to typical polystyrene culture plates. Here, we report a chemically defined, material-independent, bio-inspired surface coating allowing for feeder-free expansion and maintenance of self-renewal and pluripotency of hPSCs on various polymer substrates and devices. Polydopamine (pDA)-mediated immobilization of vitronectin (VN) peptides results in surface functionalization of VN-dimer/pDA conjugates. The engineered surfaces facilitate adhesion, proliferation, and colony formation of hPSCs via enhanced focal adhesion, cell-cell interaction, and biophysical signals, providing a chemically defined, xeno-free culture system for clonal expansion and long-term maintenance of hPSCs. This surface engineering enables the application of clinically-relevant hPSCs to a variety of biomedical systems such as tissue-engineering scaffolds and medical devices.
Full Text
http://www.sciencedirect.com/science/article/pii/S0142961215000320
DOI
10.1016/j.biomaterials.2015.01.015
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Physiology (생리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Dong Wook(김동욱) ORCID logo https://orcid.org/0000-0002-5025-1532
Jang, Ji Ho(장지호) ORCID logo https://orcid.org/0000-0001-5551-3514
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/139556
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