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Activation of Akt/PDK signaling in macrophages upon binding of receptor-recognized forms of alpha2-macroglobulin to its cellular receptor: effect of silencing the CREB gene.

Publication ,  Journal Article
Misra, UK; Pizzo, SV
Published in: J Cell Biochem
November 15, 2004

Macrophage binding of receptor-recognized forms of alpha2-macrogobulin (alpha2M*) significantly increases cAMP, CREB, and activated CREB. We have now examined the participation of the PI 3-kinase/PDK/Akt/p70s6k signaling cascade in alpha2M*-induced cellular proliferation and also studied the role of CREB in these events. Exposure of cells to alpha2M* caused an approximately 2-fold increase in CREB and its phosphorylation at Ser133, phosphorylation of the regulatory subunit of PI 3-kinase, Akt phosphorylation at Ser473 or Thr308, and phosphorylated 70s6k. Silencing of the CREB gene with dsRNA homologous in sequence to the target gene, markedly reduced the levels of CREB mRNA activation of CREB, PI 3-kinase, Akt, and p70s6k in alpha2M*-stimulated macrophages. We conclude that in murine peritoneal macrophages, alpha2M*-induced increase of cAMP is involved in cellular proliferation and this process is mediated by the PI 3-kinase signaling cascade.

Duke Scholars

Published In

J Cell Biochem

DOI

ISSN

0730-2312

Publication Date

November 15, 2004

Volume

93

Issue

5

Start / End Page

1020 / 1032

Location

United States

Related Subject Headings

  • alpha-Macroglobulins
  • Wortmannin
  • Signal Transduction
  • Proto-Oncogene Proteins c-akt
  • Proto-Oncogene Proteins
  • Protein Subunits
  • Protein Serine-Threonine Kinases
  • Protein Binding
  • Phosphorylation
  • Phosphoinositide-3 Kinase Inhibitors
 
Journal cover image

Published In

J Cell Biochem

DOI

ISSN

0730-2312

Publication Date

November 15, 2004

Volume

93

Issue

5

Start / End Page

1020 / 1032

Location

United States

Related Subject Headings

  • alpha-Macroglobulins
  • Wortmannin
  • Signal Transduction
  • Proto-Oncogene Proteins c-akt
  • Proto-Oncogene Proteins
  • Protein Subunits
  • Protein Serine-Threonine Kinases
  • Protein Binding
  • Phosphorylation
  • Phosphoinositide-3 Kinase Inhibitors