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Microcarrier suspension cultures for high-density expansion and differentiation of human pluripotent stem cells to neural progenitor cells.

Publication ,  Journal Article
Bardy, J; Chen, AK; Lim, YM; Wu, S; Wei, S; Weiping, H; Chan, K; Reuveny, S; Oh, SKW
Published in: Tissue engineering. Part C, Methods
February 2013

Neural progenitor cells (NPCs) derived from human induced pluripotent stem cells (hiPSCs) can be differentiated to neural cells that model neurodegenerative diseases and be used in the screening of potential drugs to ameliorate the disease phenotype. Traditionally, NPCs are produced in 2D cultures, in low yields, using a laborious process that includes generation of embryonic bodies, plating, and colony selections. To simplify the process and generate large numbers of hiPSC-derived NPCs, we introduce a microcarrier (MC) system for the expansion of a hiPSC line and its subsequent differentiation to NPC, using iPS (IMR90) as a model cell line. In the expansion stage, a process of cell propagation in serum-free MC culture was developed first in static culture, which is then scaled up in stirred spinner flasks. A 7.7-fold expansion of iPS (IMR90) and cell yield of 1.3×10⁶ cells/mL in 7 days of static MC culture were achieved. These cells maintained expression of OCT 3/4 and TRA-1-60 and possessed a normal karyotype over 10 passages. A higher cell yield of 6.1×10⁶ cells/mL and 20-fold hiPSC expansion were attained using stirred spinner flasks (seeded from MC static cultures) and changing the medium-exchange regimen from once to twice a day. In the differentiation stage, NPCs were generated with 78%-85% efficiency from hiPSCs using a simple serum-free differentiation protocol. Finally, the integrated process of cell expansion and differentiation of hiPSCs into NPCs using an MC in spinner flasks yielded 333 NPCs per seeded hiPSC as compared to 53 in the classical 2D tissue culture protocol. Similar results were obtained with the HES-3 human embryonic stem cell line. These NPCs were further differentiated into βIII-tubulin⁺ neurons, GFAP⁺ astrocytes, and O4⁺ oligodendrocytes, showing that cells maintained their multilineage differentiation potential.

Duke Scholars

Published In

Tissue engineering. Part C, Methods

DOI

EISSN

1937-3392

ISSN

1937-3384

Publication Date

February 2013

Volume

19

Issue

2

Start / End Page

166 / 180

Related Subject Headings

  • Real-Time Polymerase Chain Reaction
  • Pluripotent Stem Cells
  • Neurons
  • Karyotyping
  • Immunohistochemistry
  • Humans
  • Flow Cytometry
  • Culture Media, Serum-Free
  • Cells, Cultured
  • Cell Division
 

Citation

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Bardy, J., Chen, A. K., Lim, Y. M., Wu, S., Wei, S., Weiping, H., … Oh, S. K. W. (2013). Microcarrier suspension cultures for high-density expansion and differentiation of human pluripotent stem cells to neural progenitor cells. Tissue Engineering. Part C, Methods, 19(2), 166–180. https://doi.org/10.1089/ten.tec.2012.0146
Bardy, Jo’an, Allen K. Chen, Yu Ming Lim, Selena Wu, Shunhui Wei, Han Weiping, Ken Chan, Shaul Reuveny, and Steve K. W. Oh. “Microcarrier suspension cultures for high-density expansion and differentiation of human pluripotent stem cells to neural progenitor cells.Tissue Engineering. Part C, Methods 19, no. 2 (February 2013): 166–80. https://doi.org/10.1089/ten.tec.2012.0146.
Bardy J, Chen AK, Lim YM, Wu S, Wei S, Weiping H, et al. Microcarrier suspension cultures for high-density expansion and differentiation of human pluripotent stem cells to neural progenitor cells. Tissue engineering Part C, Methods. 2013 Feb;19(2):166–80.
Bardy, Jo’an, et al. “Microcarrier suspension cultures for high-density expansion and differentiation of human pluripotent stem cells to neural progenitor cells.Tissue Engineering. Part C, Methods, vol. 19, no. 2, Feb. 2013, pp. 166–80. Epmc, doi:10.1089/ten.tec.2012.0146.
Bardy J, Chen AK, Lim YM, Wu S, Wei S, Weiping H, Chan K, Reuveny S, Oh SKW. Microcarrier suspension cultures for high-density expansion and differentiation of human pluripotent stem cells to neural progenitor cells. Tissue engineering Part C, Methods. 2013 Feb;19(2):166–180.

Published In

Tissue engineering. Part C, Methods

DOI

EISSN

1937-3392

ISSN

1937-3384

Publication Date

February 2013

Volume

19

Issue

2

Start / End Page

166 / 180

Related Subject Headings

  • Real-Time Polymerase Chain Reaction
  • Pluripotent Stem Cells
  • Neurons
  • Karyotyping
  • Immunohistochemistry
  • Humans
  • Flow Cytometry
  • Culture Media, Serum-Free
  • Cells, Cultured
  • Cell Division