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Cot/tpl2-MKK1/2-Erk1/2 controls mTORC1-mediated mRNA translation in Toll-like receptor-activated macrophages

Cot/tpl2-MKK1/2-Erk1/2 controls mTORC1-mediated mRNA translation in Toll-like receptor-activated macrophages

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Authors

  • Marta Lopez-Pelaez
  • Stefano Fumagalli
  • Carlos Sanz
  • Clara Herrero
  • Susana Guerra
  • Margarita Fernandez
  • Susana Alemany (Lead / Corresponding author)

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Original languageEnglish
Pages2982-2992
Number of pages11
JournalMolecular Biology of the Cell
Journal publication date2012
Volume23
Issue15
DOIs
StatePublished

Abstract

Cot/tpl2 is the only MAP3K that activates MKK1/2-Erk1/2 in Toll-like receptor- activated macrophages. Here we show that Cot/tpl2 regulates RSK, S6 ribosomal protein, and 4E-BP phosphorylation after stimulation of bone marrow-derived macrophages with lipopolysaccharide (LPS), poly I:C, or zymosan. The dissociation of the 4E-BP-eIF4E complex, a key event in the cap-dependent mRNA translation initiation, is dramatically reduced in LPS-stimulated Cot/tpl2-knockout (KO) macrophages versus LPS-stimulated wild-type (Wt) macrophages. Accordingly, after LPS activation, increased cap-dependent translation is observed in Wt macrophages but not in Cot/tpl2 KO macrophages. In agreement with these data, Cot/ tpl2 increases the polysomal recruitment of the 5 TOP eEF1a and eEF2 mRNAs, as well as of inflammatory mediator gene-encoding mRNAs, such as tumor necrosis factora (TNFa), interleukin-6 (IL-6), and KC in LPS-stimulated macrophages. In addition, Cot/tpl2 deficiency also reduces total TNFa, IL-6, and KC mRNA expression in LPS-stimulated macrophages, which is concomitant with a decrease in their mRNA half-lives. Macrophages require rapid fine control of translation to provide an accurate and not self-damaging response to host infection, and our data show that Cot/tpl2 controls inflammatory mediator gene-encoding mRNA translation in Toll-like receptor-activated macrophages. © 2012 López-Pelaéz et al.

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