Activin A stimulates mouse macrophages to express APRIL via the Smad3 and ERK/CREB pathways

Immunol Lett. 2011 Oct 30;140(1-2):92-6. doi: 10.1016/j.imlet.2011.07.001. Epub 2011 Jul 18.

Abstract

A proliferation-inducing ligand (APRIL) is primarily expressed by macrophages and dendritic cells, and stimulates B cell proliferation, differentiation, survival, and Ig production. In the present study, we investigated the role and signaling mechanisms of activin A in APRIL expression by mouse macrophages. Activin A markedly enhanced APRIL expression in mouse macrophages at both the transcriptional and protein levels. Overexpression of dominant-negative (DN)-Smad3 and SB431542 abrogated activin-induced APRIL transcription. Furthermore, activin A induced Smad3 phosphorylation. These results indicate that activin A enhances APRIL expression through both activin receptor-like kinase 4 (ALK4) and Smad3. In a subsequent analysis of activin A signaling, it was found that PD98059, an extracellular signal-related kinase (ERK) inhibitor, eliminated activin A-induced APRIL expression. On the other hand, overexpression of cAMP responsive element-binding protein (CREB), a molecule downstream of ERK, augmented activin A-induced APRIL expression, and this effect could be abolished by PD98059. This finding that activin A induces ERK and CREB phosphorylation suggests that ERK and CREB act as intermediates in APRIL expression. Taken together, these results demonstrate that activin A can enhance APRIL expression through two different pathways, Smad3 and ERK/CREB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activins / pharmacology*
  • Animals
  • Benzamides / pharmacology
  • Cell Line
  • Cyclic AMP Response Element-Binding Protein / immunology
  • Cyclic AMP Response Element-Binding Protein / metabolism*
  • Dioxoles / pharmacology
  • Flavonoids / pharmacology
  • MAP Kinase Signaling System / immunology
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Macrophages / pathology
  • Mice
  • Mice, Inbred BALB C
  • Mutation / genetics
  • Smad3 Protein / metabolism*
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / genetics
  • Transgenes / genetics
  • Tumor Necrosis Factor Ligand Superfamily Member 13 / genetics
  • Tumor Necrosis Factor Ligand Superfamily Member 13 / immunology
  • Tumor Necrosis Factor Ligand Superfamily Member 13 / metabolism*

Substances

  • 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide
  • Benzamides
  • Cyclic AMP Response Element-Binding Protein
  • Dioxoles
  • Flavonoids
  • Smad3 Protein
  • Tumor Necrosis Factor Ligand Superfamily Member 13
  • activin A
  • Activins
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one