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The kinase TPL2 activates ERK and p38 signaling to promote neutrophilic inflammation.

Kate SengerVictoria C PhamEugene VarfolomeevJason A HackneyCesar A CorzoJenna L CollierVivian Wing Chong LauZhiyu HuangKajal HamidzhadehPatrick CaplaziIvan PengA Francesca SetiadiRoss FrancisAndres Paler-MartinezYoungsu C KwonVladimir Ramirez-CarrozziYonglian SunPatricia W GriggMerone Roose-GirmaSurinder JeetKai H BarckAnna PhamNaruhisa OtaConnie HaJeremy StinsonJoseph GuilloryLucinda TamZora ModrusanClaire EmsonBrent S McKenzieMichael J TownsendRichard A D CaranoSøren WarmingDomagoj VucicJason DeVossWyne P LeeJennie R LillAli A Zarrin
Published in: Science signaling (2017)
Tumor progression locus 2 (TPL2; also known as MAP3K8) is a mitogen-activated protein kinase (MAPK) kinase kinase (MAP3K) that phosphorylates the MAPK kinases MEK1 and MEK2 (MEK1/2), which, in turn, activate the MAPKs extracellular signal-regulated kinase 1 (ERK1) and ERK2 (ERK1/2) in macrophages stimulated through the interleukin-1 receptor (IL-1R), Toll-like receptors (TLRs), or the tumor necrosis factor receptor (TNFR). We describe a conserved and critical role for TPL2 in mediating the effector functions of neutrophils through the activation of the p38 MAPK signaling pathway. Gene expression profiling and functional studies of neutrophils and monocytes revealed a MEK1/2-independent branch point downstream of TPL2 in neutrophils. Biochemical analyses identified the MAPK kinases MEK3 and MEK6 and the MAPKs p38α and p38δ as downstream effectors of TPL2 in these cells. Genetic ablation of the catalytic activity of TPL2 or therapeutic intervention with a TPL2-specific inhibitor reduced the production of inflammatory mediators by neutrophils in response to stimulation with the TLR4 agonist lipopolysaccharide (LPS) in vitro, as well as in rodent models of inflammatory disease. Together, these data suggest that TPL2 is a drug target that activates not only MEK1/2-dependent but also MEK3/6-dependent signaling to promote inflammatory responses.
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