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TPL2-mediated activation of ERK1 and ERK2 regulates the processing of pre-TNF in LPS-stimulated macrophages
Simon Rousseau1,*,
Matoula Papoutsopoulou2,
Antony Symons2,
Dorthe Cook3,
John M. Lucocq4,
Alan R. Prescott4,
Anne O'Garra3,
Steven C. Ley2, and
Philip Cohen1,*
1 MRC Protein Phosphorylation Unit, College of Life Sciences, University of Dundee, Dow Street, Dundee, DD1 5EH, UK 2 Division of Immune Cell Biology, National Institute for Medical Research, Mill Hill, London, NW7 1AA, UK 3 Division of Immunoregulation, National Institute for Medical Research, Mill Hill, London, NW7 1AA, UK 4 Division of Cell Biology and Immunology, College of Life Sciences, University of Dundee, Dow Street, Dundee, DD1 5EH, UK
* Authors for correspondence (e-mails: s.rousseau{at}dundee.ac.uk; p.cohen{at}dundee.ac.uk)
Abstract:
Activation of the TPL2-MKK1/2-ERK1/2 signalling pathway is essentialfor lipopolysaccharide (LPS)-stimulated production of TNF inmacrophages. Here, we demonstrate that, unexpectedly, TPL2-deficientor MKK1-inhibited macrophages produce near normal levels ofpre-TNF when TLR2, TLR4 and TLR6 are activated by their respectiveagonists, but fail to secrete TNF. We show that LPS stimulatesthe appearance of pre-TNF at the cell surface and that thisis prevented by inhibition of MAPK kinases 1 and 2 (MKK1/2)or in TPL2-deficient macrophages. However, the transport ofpre-TNF from the Golgi to the plasma membrane is unaffectedby inhibition of the TPL2-MKK1/2-ERK1/2 pathway. Finally, weshow that TACE, the protease that cleaves pre-TNF to secretedTNF, is phosphorylated by ERK1 and ERK2 (ERK1/2) at Thr735 inLPS-stimulated macrophages. Therefore, although TACE activityper se is not required for the LPS-stimulated cell surface expressionof pre-TNF, the phosphorylation of this protease might contributeto, or be required for, the cell surface expression of the pre-TNF–TACEcomplex.
Key Words: COT TNF MAP kinase TACE TLR
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[DOI: 10.1126/stke.12ec15] |Abstract »
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