AI Article Synopsis

  • Human induced pluripotent stem cells (hiPSCs) can create various organoids, but their potential to contain specific stem cells was unclear until now.
  • Researchers discovered a subset of cells in hiPSC-derived corneal epithelial cell sheets that express ABCB5, a marker for corneal epithelial stem cells, indicating these cells can form new tissue.
  • These findings suggest that hiPSC-derived cell sheets enriched with ABCB5 could be used for vision recovery in people with stem cell deficiencies, marking a significant step in stem cell research and therapy.

Article Abstract

Human induced pluripotent stem cells (hiPSCs) can generate a multiplicity of organoids, yet no compelling evidence currently exists as to whether or not these contain tissue-specific, holoclone-forming stem cells. Here, we show that a subpopulation of cells in a hiPSC-derived corneal epithelial cell sheet is positive for ABCB5 (ATP-binding cassette, sub-family B, member 5), a functional marker of adult corneal epithelial stem cells. These cells possess remarkable holoclone-forming capabilities, which can be suppressed by an antibody-mediated ABCB5 blockade. The cell sheets are generated from ABCB5 hiPSCs that first emerge in 2D eye-like organoids around six weeks of differentiation and display corneal epithelial immunostaining characteristics and gene expression patterns, including sustained expression of ABCB5. The findings highlight the translational potential of ABCB5-enriched, hiPSC-derived corneal epithelial cell sheets to recover vision in stem cell-deficient human eyes and represent the first report of holoclone-forming stem cells being directly identified in an hiPSC-derived organoid.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233200PMC
http://dx.doi.org/10.1016/j.isci.2021.102688DOI Listing

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