Epithelial-mesenchymal interaction protects normal colonocytes from 4-HNE-induced phenotypic transformation

PLoS One. 2024 Apr 26;19(4):e0302932. doi: 10.1371/journal.pone.0302932. eCollection 2024.

Abstract

Introduction: Recent studies have shown that epithelial-stromal interactions could play a role in the development of colorectal cancer. Here, we investigated the role of fibroblasts in the transformation of normal colonocytes induced by 4-HNE.

Methods: Normal Co colonocytes and nF fibroblasts from the same mouse colon were exposed, in monoculture (m) or coculture (c), to 4-HNE (5 μM) twice weekly for 3 weeks. Gene expression was then analysed and the ability of Co colonocytes to grow in anchorage-independent conditions was tested in soft agar. Fibroblasts previously treated or not with 4-HNE were also seeded in culture inserts positioned above the agar layers to allow paracrine exchanges with colonocytes.

Results: First, 60% of the genes studied were modulated by coculture in Co colonocytes, with notably increased expression of BMP receptors. Furthermore, while 4-HNE increased the ability of monoculture-treated Co colonocytes to form colonies, this effect was not observed in coculture-treated Co colonocytes. Adding a selective BMPR1 inhibitor during the treatment phase abolished the protective effect of coculture. Conversely, addition of a BMP4 agonist to the medium of monoculture-treated Co colonocytes prevented phenotypic transformation by 4-HNE. Second, the presence of nF(m)-HNE fibroblasts during the soft agar assay increased the number and size of Co(m) colonocyte colonies, regardless of whether these cells had been previously treated with 4-HNE in monoculture. For soft agar assays performed with nF(c) and Co(c) cells initially treated in coculture, only the reassociation between Co(c)-HNE and nF(c)-HNE resulted in a small increase in the number of colonies.

Conclusions: During the exposure phase, the epithelial-mesenchymal interaction protected colonocytes from 4-HNE-induced phenotypic transformation via activation of the BMP pathway. This intercellular dialogue also limited the ability of fibroblasts to subsequently promote colonocyte-anchorage-independent growth. In contrast, fibroblasts pre-exposed to 4-HNE in monoculture strongly increased the ability of Co(m) colonocytes to form colonies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes* / pharmacology
  • Animals
  • Bone Morphogenetic Protein 4* / metabolism
  • Cell Transformation, Neoplastic / drug effects
  • Coculture Techniques*
  • Colon* / cytology
  • Colon* / drug effects
  • Colon* / metabolism
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Epithelial-Mesenchymal Transition* / drug effects
  • Fibroblasts* / drug effects
  • Fibroblasts* / metabolism
  • Mice
  • Phenotype

Substances

  • Bone Morphogenetic Protein 4
  • Aldehydes
  • 4-hydroxy-2-nonenal

Grants and funding

La Ligue Nationale Contre Le Cancer – comity 31/32”, France.