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Maintenance and differentiation of human ES cells on polyvinylidene fluoride scaffolds immobilized with a vitronectin-derived peptide

Authors
Park, Sang EunYeon, Gyu-BumGoo, Hui-GwanSeo, Dong SikDayem, Ahmed A.Lee, Kyung EunPark, Hyun-MeeCho, Ssang-GooKim, Dae-Sung
Issue Date
May-2021
Publisher
WILEY
Keywords
cardiac differentiation; human embryonic stem cells; long-term culture; polyvinylidene fluoride; scaffolds
Citation
JOURNAL OF CELLULAR PHYSIOLOGY, v.236, no.5, pp.3510 - 3520
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CELLULAR PHYSIOLOGY
Volume
236
Number
5
Start Page
3510
End Page
3520
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/49412
DOI
10.1002/jcp.30095
ISSN
0021-9541
Abstract
Polyvinylidene fluoride (PVDF) is biocompatible, easy to fabricate, and has piezoelectric properties; it has been used for many biomedical applications including stem cell engineering. However, long-term cultivation of human embryonic stem cells (hESCs) and their differentiation toward cardiac lineages on PVDF have not been investigated. Herein, PVDF nanoscaled membrane scaffolds were fabricated by electrospinning; a vitronectin-derived peptide-mussel adhesive protein fusion (VNm) was immobilized on the scaffolds. hESCs cultured on the VNm-coated PVDF scaffold (VNm-PVDF scaffold) were stably expanded for more than 10 passages while maintaining the expression of pluripotency markers and genomic integrity. Under cardiac differentiation conditions, hESCs on the VNm-PVDF scaffold generated more spontaneously beating colonies and showed the upregulation of cardiac-related genes, compared with those cultured on Matrigel and VNm alone. Thus, VNm-PVDF scaffolds may be suitable for the long-term culture of hESCs and their differentiation into cardiac cells, thus expanding their application in regenerative medicine.
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