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<p>Differentiation of limbal stem cells (LSCs) from human pluripotent stem cells (hPSCs) shows promise for treating bilateral limbal stem cell deficiency. However, variation in hPSCs can compromise cell production protocols and increase unwanted heterogeneity. We hypothesize that intrinsic differences among hPSC lines affect their efficiency and consistency in LSC differentiation. Several hPSC lines were differentiated towards LSCs, and the process was analyzed in different timepoints using real-time qPCR (RT-qPCR) and immunofluorescence (IF) to assess differentiation efficiency. Flow cytometry (FC) was also used to quantify protein expression in the differentiated LSCs. Interestingly, variations in BMP4, LEF1, PAX6, and TGFB1 gene expressions, key factors in corneal epithelium induction, were high even in well-differentiating hPSC lines. Some batches failed to upregulate PAX6 and developed a fibroblastic, mesenchymal morphology, associated with elevated TGFB1 expression. This elevation correlated with fewer cells expressing LSC markers in later differentiation stages. FC results showed similar protein expression variation between lines and batches. These findings highlight the need for further optimization and quality control to ensure reliable production of homogeneous starting material for LSC differentiation.</p>

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Exploring the impact of human pluripotent stem cell heterogeneity on corneal limbal stem cell differentiation outcomes

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月18日

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  • Sonja Harjuntausta,
  • Meri Vattulainen,
  • Soile Nymark,
  • Heli Skottman

摘要

Differentiation of limbal stem cells (LSCs) from human pluripotent stem cells (hPSCs) shows promise for treating bilateral limbal stem cell deficiency. However, variation in hPSCs can compromise cell production protocols and increase unwanted heterogeneity. We hypothesize that intrinsic differences among hPSC lines affect their efficiency and consistency in LSC differentiation. Several hPSC lines were differentiated towards LSCs, and the process was analyzed in different timepoints using real-time qPCR (RT-qPCR) and immunofluorescence (IF) to assess differentiation efficiency. Flow cytometry (FC) was also used to quantify protein expression in the differentiated LSCs. Interestingly, variations in BMP4, LEF1, PAX6, and TGFB1 gene expressions, key factors in corneal epithelium induction, were high even in well-differentiating hPSC lines. Some batches failed to upregulate PAX6 and developed a fibroblastic, mesenchymal morphology, associated with elevated TGFB1 expression. This elevation correlated with fewer cells expressing LSC markers in later differentiation stages. FC results showed similar protein expression variation between lines and batches. These findings highlight the need for further optimization and quality control to ensure reliable production of homogeneous starting material for LSC differentiation.