Colon organoid formation and cryptogenesis are stimulated by growth factors secreted from myofibroblasts

PLoS One. 2018 Jun 21;13(6):e0199412. doi: 10.1371/journal.pone.0199412. eCollection 2018.

Abstract

Although small intestinal epithelial stem cells form crypts when using intestinal culture conditions, colon stem cells usually form colonospheres. Colon mesenchymal cell feeder layers can stimulate colon crypts to form organoids and produce crypts. We have investigated whether conditioned medium from colon mesenchymal cells can also stimulate colonosphere and organoid cryptogenesis. We prepared conditioned medium (CM) from WEHI-YH2 cells (mouse colon myofibroblasts); the CM stimulated both colonosphere formation and organoid cryptogenesis in vitro. The colon organoid-stimulating factors in WEHI-YH2 CM are inactivated by heating and trypsin digestion and proteins can be concentrated by ultrafiltration. Both the colonosphere- and organoid cryptogenesis- stimulatory effects of the CM are independent of canonical Wnt and Notch signaling. In contrast, bone morphogenetic protein 4 (BMP4) abolishes colonosphere formation and organoid cryptogenesis. The Transforming Growth Factor beta (TGFβ) Type I receptor kinase inhibitor (A83-01) stimulates colonosphere formation, whereas the Epidermal Growth Factor receptor (EGFR) kinase inhibitor (AG1478) reduces the formation of colonospheres, but in the presence of EGF, a "just-right" concentration of AG1478 increases colon organoid cryptogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Colon / drug effects
  • Colon / growth & development*
  • Culture Media, Conditioned / pharmacology
  • Feeder Cells / cytology
  • Intercellular Signaling Peptides and Proteins / pharmacology*
  • Mice, Inbred C57BL
  • Microvilli / drug effects
  • Microvilli / metabolism*
  • Myofibroblasts / drug effects
  • Myofibroblasts / metabolism*
  • Organoids / drug effects
  • Organoids / growth & development*
  • Receptors, Notch / metabolism
  • Signal Transduction / drug effects
  • Spheroids, Cellular / cytology
  • Spheroids, Cellular / drug effects
  • Spheroids, Cellular / metabolism
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Wnt Proteins / metabolism

Substances

  • Biomarkers
  • Culture Media, Conditioned
  • Intercellular Signaling Peptides and Proteins
  • Receptors, Notch
  • Wnt Proteins

Grants and funding

This work was supported by the Ludwig Institute for Cancer Research, the National Health and Medical Research Council (NHMRC) Project Grant GNT1029628 and, Program Grant #487922, and funds from the Operational Infrastructure Support Program provided by the Victorian Government, Australia. The funders had no role on the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The manuscript is solely the responsibility of the institutions and individual authors and does not reflect the views of the NHMRC. H.Y.K.Y was supported by the Melbourne International Research Scholarship and Melbourne International Fee Remission Scholarship.