Mechanism for nicotine-induced up-regulation of Wnt signaling in human alveolar interstitial fibroblasts

Exp Lung Res. 2011 Apr;37(3):144-54. doi: 10.3109/01902148.2010.490288. Epub 2010 Dec 6.

Abstract

Nicotine exposure alters normal homeostatic pulmonary epithelial-mesenchymal paracrine signaling pathways, resulting in alveolar interstitial fibroblast (AIF)-to-myofibroblast (MYF) transdifferentiation. Since the AIF versus MYF phenotype is determined by the expression of peroxisome proliferator-activated receptor γ (PPARγ) and Wingless/Int (Wnt) signaling, respectively, the authors hypothesized that nicotine-induced AIF-to-MYF transdifferentiation is characterized by the down-regulation of PPARγ, and the up-regulation of the Wnt signaling pathway. As nicotine is known to activate protein kinase C (PKC) signaling, the authors also hypothesized that in AIFs, nicotine-induced up-regulation of Wnt signaling might be due to PKC activation. Embryonic human lung fibroblasts (WI38 cells) were treated with nicotine (1 × 10(-6) M) for either 30 minutes or 24 hours, with or without 30-minute pretreatment with calphostin C (1 × 10(-7) M), a pan-PKC inhibitor. Then the authors examined the activation of PKC (p-PKC) and Wnt signaling (p-GSK-3β, β-catenin, LEF-1, and fibronectin). Furthermore, activation of nicotinic acetylcholine receptor (nAChR)-α3 and -α7 and whether a PPARγ agonist, rosiglitazone (RGZ), blocks nicotine-mediated Wnt activation were examined. Following nicotine stimulation, there was clear evidence for nAChR-α3 and -α7 up-regulation, accompanied by the activation of PKC and Wnt signaling, which was further accompanied by significant changes in the expression of the downstream targets of Wnt signaling at 24 hours. Nicotine-mediated Wnt activation was almost completely blocked by pretreatment with either calphostin C or RGZ, indicating the central involvement of PKC activation and Wnt/PPARγ interaction in nicotine-induced up-regulation of Wnt signaling, and hence AIF-to-MYF transdifferentiation, providing novel preventive/therapeutic targets for nicotine-induced lung injury.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cell Line
  • Cell Transdifferentiation / drug effects
  • Cell Transdifferentiation / physiology
  • DNA Primers / genetics
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Humans
  • Naphthalenes / pharmacology
  • Nicotine / toxicity*
  • PPAR gamma / metabolism
  • Protein Kinase C / metabolism
  • Pulmonary Alveoli / drug effects*
  • Pulmonary Alveoli / metabolism*
  • Pulmonary Alveoli / pathology
  • Receptors, Nicotinic / metabolism
  • Rosiglitazone
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Thiazolidinediones / pharmacology
  • Up-Regulation / drug effects
  • Wnt Proteins / metabolism*
  • alpha7 Nicotinic Acetylcholine Receptor
  • beta Catenin / metabolism

Substances

  • CTNNB1 protein, human
  • Chrna7 protein, human
  • DNA Primers
  • Naphthalenes
  • PPAR gamma
  • Receptors, Nicotinic
  • Thiazolidinediones
  • Wnt Proteins
  • alpha7 Nicotinic Acetylcholine Receptor
  • beta Catenin
  • Rosiglitazone
  • Nicotine
  • Protein Kinase C
  • calphostin C