Media composition modulates human embryonic stem cell morphology and may influence preferential lineage differentiation potential

PLoS One. 2019 Mar 19;14(3):e0213678. doi: 10.1371/journal.pone.0213678. eCollection 2019.

Abstract

Undifferentiated human embryonic stem cells have a distinct morphology (hESC). Changes in cell morphology during culture can be indicative of differentiation. hESC, maintained in diverse medias, demonstrated alterations in morphological parameters and subsequent alterations in underlying transcript expression and lineage differentiation. Analysis of morphological parameters showed distinct and significant differences between the undefined, less defined and Xeno-free medias while still maintaining pluripotency markers. This suggested that the less defined media may be creating dynamic instability in the cytoskeleton, with the cytoskeleton becoming more stabilised in the Xeno-free media as demonstrated by smaller and rounder cells. Examination of early lineage markers during undirected differentiation using d5 embryoid bodies demonstrated increased mesodermal lineage preference as compared to endodermal or ectoderm in cells originally cultured in Xeno-free media. Undefined media showed preference for mesoderm and ectoderm lineages, while less defined media (BSA present) demonstrated no preference. These data reveal that culture media may produce fundamental changes in cell morphology which are reflected in early lineage differentiation choice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Culture Techniques
  • Cell Differentiation*
  • Cell Line
  • Cell Lineage*
  • Cluster Analysis
  • Culture Media / chemistry*
  • Cytoskeleton / metabolism
  • Ectoderm / cytology
  • Embryoid Bodies
  • Endoderm / cytology
  • Gene Expression Profiling
  • Human Embryonic Stem Cells / cytology*
  • Humans
  • Mesoderm / cytology
  • Microscopy, Fluorescence
  • Pluripotent Stem Cells / cytology*
  • Transcription, Genetic

Substances

  • Culture Media

Grants and funding

The PPG and LH would like to acknowledge funding from Stem Cells Australia, an Australian Research Council Strategic Initiative in Stem Cell Science (SR110001002). PPG, LH and XC would like to acknowledge funding from the JEM Research Foundation philanthropic funding, The Merchant Charitable Foundation and the University of Queensland for their support and funding of this work. MG and PPG acknowledge this research utilised the facilities, and the scientific and technical assistance of the National Biologics Facility (NBF) at The University of Queensland. NBF is supported by Therapeutic Innovation Australia (TIA). TIA is supported by the Australian Government through the National Collaborative Research Infrastructure Strategy (NCRIS) program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.