TGF-beta1 disrupts endotoxin signaling in microglial cells through Smad3 and MAPK pathways

J Immunol. 2004 Jul 15;173(2):962-8. doi: 10.4049/jimmunol.173.2.962.

Abstract

Human formyl peptide receptor-like 1 and its mouse homologue formyl peptide receptor 2 (FPR2) are G protein-coupled receptors used by a number of exogenous and host-derived chemotactic peptides, including the 42 aa form of beta amyloid peptide, a causative factor of Alzheimer's disease. Functional FPR2 was induced by bacterial LPS in murine microglial cells, the resident phagocytic cells that play a pivotal role in inflammatory and immunological diseases in the CNS. To identify agents that may suppress microglial cell activation under proinflammatory conditions, we investigated the effect of TGF-beta1 on the expression of functional FPR2 by microglial cells activated by LPS. TGF-beta1 dose-dependently inhibited the mRNA expression and function of FPR2 in LPS-activated microglial cells. The inhibitory effect of TGF-beta1 was mediated by Smad3, a key signaling molecule coupled to the TGF-beta receptor, and the transcription coactivator, p300. Also, TGF-beta1 activates MAPKs in microglial cells that became refractory to further stimulation by LPS. These effects of TGF-beta1 culminate in the inhibition of LPS-induced activation of NF-kappaB and the up-regulation of FPR2 in microglial cells. Thus, TGF-beta1 may exert a protective role in CNS diseases characterized by microglial cell activation by proinflammatory stimulants.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • DNA-Binding Proteins / metabolism*
  • E1A-Associated p300 Protein
  • Lipopolysaccharides / metabolism*
  • Mice
  • Microglia / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism*
  • NF-kappa B / metabolism
  • Nuclear Proteins / metabolism
  • Receptors, Formyl Peptide / metabolism
  • Smad3 Protein
  • Trans-Activators / metabolism*
  • Transforming Growth Factor beta / metabolism*
  • Transforming Growth Factor beta1

Substances

  • DNA-Binding Proteins
  • Lipopolysaccharides
  • NF-kappa B
  • Nuclear Proteins
  • Receptors, Formyl Peptide
  • Smad3 Protein
  • Smad3 protein, mouse
  • TGFB1 protein, human
  • Tgfb1 protein, mouse
  • Trans-Activators
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • formyl peptide receptor 2, mouse
  • E1A-Associated p300 Protein
  • Ep300 protein, mouse
  • Mitogen-Activated Protein Kinases