The Novel mTOR Complex 1/2 Inhibitor P529 Inhibits Human Lung Myofibroblast Differentiation

J Cell Biochem. 2017 Aug;118(8):2241-2249. doi: 10.1002/jcb.25878. Epub 2017 Apr 18.

Abstract

Idiopathic pulmonary fibrosis is a progressive and deadly disorder with very few therapeutic options. Palomid 529 (8-(1-hydroxyethyl)-2-methoxy-3-(4-methoxybenzyloxy)-benzo[c]chromen-6-one; P529) is a novel dual inhibitor of mechanistic target of rapamycin complex 1/2 (mTORC1/2). In these studies, we investigated the effect of P529 on TGF-β-dependent signaling and myofibroblast differentiation. TGF-β-induced phosphorylation of the mTORC1 targets, p70 S6 kinase 1 (S6K1), and eukaryotic translation initiation factor 4E binding protein 1 (4E-BP1), were both dose dependently inhibited by P529 in human lung fibroblasts with maximal inhibition occurring between 10 and 20 μM. mTORC2-mediated phosphorylation of Akt at the S473 site was partially inhibited with a similar dose dependency, as was TGF-β-induced myofibroblast differentiation. Protein levels of TGF-β-induced fibronectin and collagen were similarly decreased by P529. At this dose, there was also inhibition of mRNA transcript levels for Col1 and α-SMA, suggesting inhibition of transcriptional activation. However, there was no effect of P529 on canonical TGF-β-induced Smad signaling, as assessed by receptor-associated Smad2/3 phosphorylation, Smad2/3/4 translocation, or Smad-driven gene expression, as assessed by Smad-binding element driven luciferase. Conversely, activation of mTORC1/2 signaling was dependent on TGF-β type I receptor (ALK5) signaling and on Smad2/3 expression. P529 treatment disrupted TGF-β-induced actin stress fiber formation during myofibroblast differentiation, the deposition of new extracellular fibronectin matrix, and linear wound closure by fibroblasts. Likewise, mTOR knockdown inhibited TGF-β-induced myofibroblast differentiation. In conclusion, P529 inhibits TGF-β-induced myofibroblast differentiation, actin stress fiber formation, and matrix protein expression and deposition. Inhibition of mTORC1/2 by P529 may be a promising approach to inhibit in vivo fibrosis. J. Cell. Biochem. 118: 2241-2249, 2017. © 2017 Wiley Periodicals, Inc.

Keywords: ACTIN CYTOSKELETON; FIBRONECTIN DEPOSITION; MYOFIBROBLAST; P529; PULMONARY FIBROSIS; Smad; TGF-β; mTOR; mTORC1; mTORC2.

MeSH terms

  • Actins / metabolism
  • Adaptor Proteins, Signal Transducing / metabolism
  • Benzopyrans / pharmacology*
  • Blotting, Western
  • Cell Cycle Proteins
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Collagen / metabolism
  • Fibronectins / metabolism
  • Humans
  • Mechanistic Target of Rapamycin Complex 1 / antagonists & inhibitors*
  • Mechanistic Target of Rapamycin Complex 1 / metabolism*
  • Mechanistic Target of Rapamycin Complex 2 / antagonists & inhibitors*
  • Mechanistic Target of Rapamycin Complex 2 / metabolism*
  • Myofibroblasts / cytology
  • Myofibroblasts / drug effects*
  • Phosphoproteins / metabolism
  • Phosphorylation / drug effects
  • Protein Serine-Threonine Kinases / metabolism
  • Receptor, Transforming Growth Factor-beta Type I
  • Receptors, Transforming Growth Factor beta / metabolism
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism
  • Survival of Motor Neuron 1 Protein / metabolism
  • Transforming Growth Factor beta / pharmacology

Substances

  • Actins
  • Adaptor Proteins, Signal Transducing
  • Benzopyrans
  • Cell Cycle Proteins
  • EIF4EBP1 protein, human
  • Fibronectins
  • Phosphoproteins
  • Receptors, Transforming Growth Factor beta
  • Survival of Motor Neuron 1 Protein
  • Transforming Growth Factor beta
  • Collagen
  • Mechanistic Target of Rapamycin Complex 1
  • Mechanistic Target of Rapamycin Complex 2
  • Protein Serine-Threonine Kinases
  • Ribosomal Protein S6 Kinases, 70-kDa
  • ribosomal protein S6 kinase, 70kD, polypeptide 1
  • Receptor, Transforming Growth Factor-beta Type I
  • TGFBR1 protein, human
  • palomid 529