An allied reprogramming, selection, expansion and differentiation platform for creating hiPSC on microcarriers

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An allied reprogramming, selection, expansion and differentiation platform for creating hiPSC on microcarriers
Title:
An allied reprogramming, selection, expansion and differentiation platform for creating hiPSC on microcarriers
Journal Title:
Cell Proliferation
Publication Date:
19 May 2022
Citation:
Lam, A. T. L., Ho, V., Vassilev, S., Reuveny, S., & Oh, S. K. W. (2022). An Allied reprogramming, selection, expansion and differentiation platform for creating hiPSC on microcarriers. Cell Proliferation. Portico. https://doi.org/10.1111/cpr.13256
Abstract:
Objectives: Induced pluripotent stem cells (iPSCs) generated by monolayer cultures is plagued by low efficiencies, high levels of manipulation and operator unpredictability. We have developed a platform, reprogramming, expansion, and differentiation on Microcarriers, to solve these challenges. Materials and Methods: Five sources of human somatic cells were reprogrammed, selected, expanded and differentiated in microcarriers suspension cultures. Results: Improvement of transduction efficiencies up to 2 times was observed. Accelerated reprogramming in microcarrier cultures was 7 days faster than mono-layer, providing between 30 and 50-fold more clones to choose from fibroblasts, peripheral blood mononuclear cells, T cells and CD34+stem cells. This was observed to be due to an earlier induction of genes (β-catenin, E-cadherin and EpCAM) on day 4 versus monolayer cultures which occurred on days 14 or later. Following that, faster induction and earlier stabilization of pluripotency genes occurred during the maturation phase of reprogramming. Integrated expansion without trypsinization and efficient differentiation, without embryoid bodies formation, to the three germ-layers, cardiomyocytes and haematopoietic stem cells were further demonstrated. Conclusions: Our method can solve the inherent problems of conventional mono-layer cultures. It is highly efficient, cell dissociation free, can be operated with lower labor, and allows testing of differentiation efficiency without trypsinization and generation of embryoid bodies. It is also amenable to automation for processing more samples in a small footprint, alleviating many challenges of manual monolayer selection.
License type:
Attribution 4.0 International (CC BY 4.0)
Funding Info:
This research / project is supported by the Agency for Science, Technology and Research - Joint Council Office grant
Grant Reference no. : 1331AFG075
Description:
ISSN:
0960-7722
1365-2184