Nature Communications (Jun 2023)

A village in a dish model system for population-scale hiPSC studies

  • Drew R. Neavin,
  • Angela M. Steinmann,
  • Nona Farbehi,
  • Han Sheng Chiu,
  • Maciej S. Daniszewski,
  • Himanshi Arora,
  • Yasmin Bermudez,
  • Cátia Moutinho,
  • Chia-Ling Chan,
  • Monique Bax,
  • Mubarika Tyebally,
  • Vikkitharan Gnanasambandapillai,
  • Chuan E. Lam,
  • Uyen Nguyen,
  • Damián Hernández,
  • Grace E. Lidgerwood,
  • Robert M. Graham,
  • Alex W. Hewitt,
  • Alice Pébay,
  • Nathan J. Palpant,
  • Joseph E. Powell

DOI
https://doi.org/10.1038/s41467-023-38704-1
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 12

Abstract

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Abstract The mechanisms by which DNA alleles contribute to disease risk, drug response, and other human phenotypes are highly context-specific, varying across cell types and different conditions. Human induced pluripotent stem cells are uniquely suited to study these context-dependent effects but cell lines from hundreds or thousands of individuals are required. Village cultures, where multiple induced pluripotent stem lines are cultured and differentiated in a single dish, provide an elegant solution for scaling induced pluripotent stem experiments to the necessary sample sizes required for population-scale studies. Here, we show the utility of village models, demonstrating how cells can be assigned to an induced pluripotent stem line using single-cell sequencing and illustrating that the genetic, epigenetic or induced pluripotent stem line-specific effects explain a large percentage of gene expression variation for many genes. We demonstrate that village methods can effectively detect induced pluripotent stem line-specific effects, including sensitive dynamics of cell states.