ERK-mediated curvature feedback regulates branching morphogenesis in lung epithelial tissue

Curr Biol. 2024 Feb 26;34(4):683-696.e6. doi: 10.1016/j.cub.2023.12.049. Epub 2024 Jan 15.

Abstract

Intricate branching patterns emerge in internal organs due to the recurrent occurrence of simple deformations in epithelial tissues. During murine lung development, epithelial cells in distal tips of the single tube require fibroblast growth factor (FGF) signals emanating from their surrounding mesenchyme to form repetitive tip bifurcations. However, it remains unknown how the cells employ FGF signaling to convert their behaviors to achieve the recursive branching processes. Here, we show a mechano-chemical regulatory system underlying lung branching morphogenesis, orchestrated by extracellular signal-regulated kinase (ERK) as a downstream driver of FGF signaling. We found that tissue-scale curvature regulated ERK activity in the lung epithelium using two-photon live cell imaging and mechanical perturbations. ERK activation occurs specifically in epithelial tissues exhibiting positive curvature, regardless of whether the change in curvature was attributable to morphogenesis or perturbations. Moreover, ERK activation accelerates actin polymerization preferentially at the apical side of cells, mechanically contributing to the extension of the apical membrane, culminating in a reduction of epithelial tissue curvature. These results indicate the existence of a negative feedback loop between tissue curvature and ERK activity that transcends spatial scales. Our mathematical model confirms that this regulatory mechanism is sufficient to generate the recursive branching processes. Taken together, we propose that ERK orchestrates a curvature feedback loop pivotal to the self-organized patterning of tissues.

Keywords: ERK; FRET biosensor; curvature; live-cell imaging; lung development; mathematical model; mechano-chemical feedback; mechanobiology; self-organization; tissue morphogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Epithelium / metabolism
  • Extracellular Signal-Regulated MAP Kinases* / genetics
  • Extracellular Signal-Regulated MAP Kinases* / metabolism
  • Feedback
  • Fibroblast Growth Factors / metabolism
  • Lung*
  • Mesoderm
  • Mice
  • Morphogenesis / physiology

Substances

  • Extracellular Signal-Regulated MAP Kinases
  • Fibroblast Growth Factors