Accelerated Limbal Epithelial Differentiation of Human Induced Pluripotent Stem Cells Using a Defined Keratinocyte Serum-Free Medium
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Purpose
Treatment of bilateral limbal stem cell deficiency (LSCD) is challenging due to the limited autologous stem cell sources. This study aimed to differentiate human induced pluripotent stem cells (hiPSCs) into limbal epithelial stem cells (LESCs) using a defined keratinocyte serum-free medium (DKSFM).
Methods
A fully characterized hiPSC line was committed to ectodermal differentiation using Essential 6 (E6) medium supplemented with 10 µM Y-27632 (Day 1), 10 µM SB-505124 plus 50 ng/ml bFGF (Day 2) and 25 ng/ml BMP-4 (Days 3 and 4). Differentiation was continued in DKSFM for an additional 21 days. Quantitative PCR (qPCR) and/or immunocytochemistry (ICC) for pluripotency, proliferation, LESC, and corneal epithelial markers were performed on samples collected at days 5, 10, 15, and 25 (D5 to D25) and compared with undifferentiated hiPSCs (UD).
Results
qPCR revealed a significant decrease in the expression of OCT4 and NANOG and a significant increase in ABCG2 and TP63 following ectodermal induction (i.e., D5), compared with UD (P < 0.05). The expression levels of Ki67 , ABCG2 , TP63 , and CK14 were significantly higher at D10, compared with D5 and D25 (P < 0.05). The ratio of p63α-positive cells was 71% and 56% in D10 and D15 cells, respectively (P < 0.05).
Discussion
Our method resulted in a limited but rapid differentiation of hiPSCs into LESC-like cells. The LESC-like cells appeared as early as 5 days following ectodermal induction and their population peaked after 10 days. Upon further optimization and validation, DKSFM can be used for rapid limbal epithelial differentiation of hiPSCs.
