pubmed-article:10490613 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10490613 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
pubmed-article:10490613 | lifeskim:mentions | umls-concept:C0040649 | lld:lifeskim |
pubmed-article:10490613 | lifeskim:mentions | umls-concept:C1155209 | lld:lifeskim |
pubmed-article:10490613 | lifeskim:mentions | umls-concept:C0086982 | lld:lifeskim |
pubmed-article:10490613 | lifeskim:mentions | umls-concept:C1257759 | lld:lifeskim |
pubmed-article:10490613 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:10490613 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:10490613 | pubmed:dateCreated | 2000-2-3 | lld:pubmed |
pubmed-article:10490613 | pubmed:abstractText | A hallmark of inflammation is the burst-like formation of certain proteins, initiated by cellular stress and proinflammatory cytokines like interleukin 1 (IL-1) and tumor necrosis factor, stimuli which simultaneously activate different mitogen-activated protein (MAP) kinases and NF-kappaB. Cooperation of these signaling pathways to induce formation of IL-8, a prototype chemokine which causes leukocyte migration and activation, was investigated by expressing active and inactive forms of protein kinases. Constitutively active MAP kinase kinase 7 (MKK7), an activator of the stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK) pathway, induced IL-8 synthesis and transcription from a minimal IL-8 promoter. Furthermore, MKK7 synergized in both effects with NF-kappaB-inducing kinase (NIK). Activation of the IL-8 promoter by either of the kinases required functional NF-kappaB and AP-1 sites. While NIK and MKK7 did not affect degradation of IL-8 mRNA, an active form of MKK6, which selectively activates p38 MAP kinase, induced marked stabilization of the transcript and further increased IL-8 protein formation induced by NIK plus MKK7. Consistently, the MAP kinase kinase kinase MEKK1, which can activate NF-kappaB, SAPK/JNK, and p38 MAP kinases, most potently induced IL-8 formation. These results provide evidence that maximal IL-8 gene expression requires the coordinate action of at least three different signal transduction pathways which cooperate to induce mRNA synthesis and suppress mRNA degradation. | lld:pubmed |
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pubmed-article:10490613 | pubmed:language | eng | lld:pubmed |
pubmed-article:10490613 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10490613 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10490613 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:10490613 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10490613 | pubmed:month | Oct | lld:pubmed |
pubmed-article:10490613 | pubmed:issn | 0270-7306 | lld:pubmed |
pubmed-article:10490613 | pubmed:author | pubmed-author:WallaceAA | lld:pubmed |
pubmed-article:10490613 | pubmed:author | pubmed-author:HoffmannEE | lld:pubmed |
pubmed-article:10490613 | pubmed:author | pubmed-author:HollandPP | lld:pubmed |
pubmed-article:10490613 | pubmed:author | pubmed-author:CooperJ AJA | lld:pubmed |
pubmed-article:10490613 | pubmed:author | pubmed-author:ReschKK | lld:pubmed |
pubmed-article:10490613 | pubmed:author | pubmed-author:HoltmannHH | lld:pubmed |