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Expansion of human mesenchymal stem cells on poly(vinyl alcohol) microcarriers.

Authors
  • Kaneko, Masahiro1
  • Sato, Airi2
  • Ayano, Satoru3
  • Fujita, Akio3
  • Kobayashi, Goro3
  • Ito, Akira4
  • 1 Department of Chemical Systems Engineering, School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan. , (Japan)
  • 2 College of Bioscience and Biotechnology, Chubu University, 1200 Matsumoto, Kasugai, Aichi 487-8501, Japan. , (Japan)
  • 3 Research and Development Division, Kuraray Co., Ltd., 41 Miyukigaoka, Tsukuba, Ibaraki 305-0841, Japan. , (Japan)
  • 4 Department of Chemical Systems Engineering, School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan. Electronic address: [email protected]. , (Japan)
Type
Published Article
Journal
Journal of Bioscience and Bioengineering
Publisher
Elsevier
Publication Date
Nov 01, 2023
Volume
136
Issue
5
Pages
407–414
Identifiers
DOI: 10.1016/j.jbiosc.2023.08.003
PMID: 37657971
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

Microcarriers provide a high surface-area-to-volume ratio that can realize high yields of cell products, including human mesenchymal stem cells (hMSCs). Here, we report a novel poly(vinyl alcohol) (PVA)-based microcarrier for hMSC expansion in suspension culture. PVA microcarriers were prepared as collagen-coated PVA hydrogels 181 μm in size and a high surface-area-to-weight ratio of 2945 cm2/g. The PVA microcarriers supported a 2.6-fold expansion of hMSCs in a 30-mL single-use stirred bioreactor after a 7 d culture period, comparable to that of commercially available microcarriers. Interestingly, we observed that hMSCs on PVA microcarriers adhered to adjacent microcarriers, resulting in the aggregation of hMSC-PVA microcarriers. Therefore, we conducted a long-term expansion culture using a bead-to-bead cell transfer method with PVA microcarriers. Fresh microcarriers were added to the cell-populated microcarriers in the bioreactor on days 7 and 14. hMSCs on PVA microcarriers continued to grow for 21 d using the bead-to-bead cell transfer method. Furthermore, magnetic PVA (PVA-mag) microcarriers were developed by loading magnetic nanoparticles into PVA microcarriers, and we demonstrated that these PVA-mag microcarriers enabled cell recovery by magnetic separation. These results suggest that these PVA microcarriers can contribute to the large-scale culture of hMSCs for regenerative medicine and cell therapy. Copyright © 2023 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.

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