MAPK phosphatase 1 inhibition of p38α within lung myofibroblasts is essential for spontaneous fibrosis resolution

J Clin Invest. 2024 Mar 21;134(10):e172826. doi: 10.1172/JCI172826.

Abstract

Fibrosis following tissue injury is distinguished from normal repair by the accumulation of pathogenic and apoptosis-resistant myofibroblasts (MFs), which arise primarily by differentiation from resident fibroblasts. Endogenous molecular brakes that promote MF dedifferentiation and clearance during spontaneous resolution of experimental lung fibrosis may provide insights that could inform and improve the treatment of progressive pulmonary fibrosis in patients. MAPK phosphatase 1 (MKP1) influences the cellular phenotype and fate through precise and timely regulation of MAPK activity within various cell types and tissues, yet its role in lung fibroblasts and pulmonary fibrosis has not been explored. Using gain- and loss-of-function studies, we found that MKP1 promoted lung MF dedifferentiation and restored the sensitivity of these cells to apoptosis - effects determined to be mainly dependent on MKP1's dephosphorylation of p38α MAPK (p38α). Fibroblast-specific deletion of MKP1 following peak bleomycin-induced lung fibrosis largely abrogated its subsequent spontaneous resolution. Such resolution was restored by treating these transgenic mice with the p38α inhibitor VX-702. We conclude that MKP1 is a critical antifibrotic brake whose inhibition of pathogenic p38α in lung fibroblasts is necessary for fibrosis resolution following lung injury.

Keywords: Cell biology; Fibrosis; Molecular biology; Protein kinases; Pulmonology.

MeSH terms

  • Animals
  • Apoptosis
  • Bleomycin / toxicity
  • Dual Specificity Phosphatase 1* / genetics
  • Dual Specificity Phosphatase 1* / metabolism
  • Humans
  • Lung* / metabolism
  • Lung* / pathology
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Mitogen-Activated Protein Kinase 14* / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 14* / genetics
  • Mitogen-Activated Protein Kinase 14* / metabolism
  • Myofibroblasts* / enzymology
  • Myofibroblasts* / metabolism
  • Myofibroblasts* / pathology
  • Pulmonary Fibrosis* / chemically induced
  • Pulmonary Fibrosis* / enzymology
  • Pulmonary Fibrosis* / genetics
  • Pulmonary Fibrosis* / metabolism
  • Pulmonary Fibrosis* / pathology