| Literature DB >> 24647229 |
Guadalupe Sabio1, Roger J Davis2.
Abstract
The binding of tumour necrosis factor α (TNFα) to cell surface receptors engages multiple signal transduction pathways, including three groups of mitogen-activated protein (MAP) kinases: extracellular-signal-regulated kinases (ERKs); the cJun NH2-terminal kinases (JNKs); and the p38 MAP kinases. These MAP kinase signalling pathways induce a secondary response by increasing the expression of several inflammatory cytokines (including TNFα) that contribute to the biological activity of TNFα. MAP kinases therefore function both upstream and down-stream of signalling by TNFα receptors. Here we review mechanisms that mediate these actions of MAP kinases during the response to TNFα.Entities:
Keywords: ERK; JNK; MAP kinase; TNF; p38 MAP kinase
Mesh:
Substances:
Year: 2014 PMID: 24647229 PMCID: PMC4099309 DOI: 10.1016/j.smim.2014.02.009
Source DB: PubMed Journal: Semin Immunol ISSN: 1044-5323 Impact factor: 11.130