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Low-oxygen and knock-out serum maintain stemness in human retinal progenitor cells

  • Deepti Singh
  • Pierre C. Dromel
  • Michael YoungEmail author
Original Article

Abstract

Using stem and progenitor cells to treat retinal disorders holds great promise. Using defined culture conditions to maintain the desires phenotype is of utmost clinical importance. We cultured human retinal progenitor cells (hRPCs) in different conditions: such as normoxia (20% oxygen), and hypoxia (5% oxygen) with and without knock-out serum replacement (KOSR) to evaluate its effect on these cells. KOSR is known nutrient supplement often used to replace bovine serum for culturing embryonic or pluripotent stem cells, especially those destined for clinical applications. The purpose of this study was to identify the impact of different environmental and chemical cues to determine if this alters the fate of these cells. Our results indicate that cells cultured with or without KOSR do not show significant differences in viability, but that the oxygen tension can significantly change their viability (higher in hypoxia than normoxia). However, cells with KOSR in hypoxia condition expressed significantly higher stemness markers such as C-myc and Oct4 (31.20% and 13.44% respectively) in comparison to hRPCs cultured in KOSR at normoxia (12.07% and 4.05%). Furthermore, levels of markers for retinal commitment such as rhodopsin were significantly lower in the KOSR supplemented cells in hypoxia culture compared to normoxia. KOSR is known to improve proliferation and maintain stemness of embryonic cells and our experiments suggest that hRPCs maintain their proliferation and stemness characteristics in hypoxia with KOSR supplement. Normoxia, however, results in mature cell marker expression, suggesting a profound effect of oxygen tension on these cells.

Keywords

Human retinal progenitor cells Flow cytometer Stemness Hypoxia 

Notes

Acknowledgements

P.D would like to acknowledge the funding for his Ph.D. and his Ph.D. advisor Dr. Myron Spector for his inputs throughout the project and D.S would like to acknowledge “The DeGunzberg OcularRegeneration fund” for the support provided to complete this study.

Funding

This study was funded by The DeGunzberg OcularRegeneration fund (Grant Number 533133).

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

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Copyright information

© Springer Nature B.V. 2020

Authors and Affiliations

  1. 1.Schepens Eye Research Institute of Massachusetts Ear and EyeHarvard Medical SchoolBostonUSA
  2. 2.Department of Materials Science and EngineeringMassachusetts Institute of TechnologyCambridgeUSA

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