rdf:type |
|
lifeskim:mentions |
umls-concept:C0003315,
umls-concept:C0007634,
umls-concept:C0030685,
umls-concept:C0123759,
umls-concept:C0391871,
umls-concept:C0680255,
umls-concept:C0752312,
umls-concept:C1283071,
umls-concept:C1879547,
umls-concept:C1963578,
umls-concept:C2587213
|
pubmed:issue |
24
|
pubmed:dateCreated |
2000-1-27
|
pubmed:abstractText |
Activation of antigen-presenting cells (APCs) by invariant constituents of pathogens such as lipopolysaccharide (LPS) or bacterial DNA (CpG-DNA) initiates immune responses. We have analyzed the mitogen-activated protein kinase (MAPK) pathways triggered by CpG-DNA and their significance for cytokine production in two subsets of APCs, i.e. macrophages and dendritic cells (DCs). We found that CpG-DNA induced extracellular signal-regulated kinase (ERK) activity in macrophages in a classic MEK-dependent way. This pathway up-regulated tumor necrosis factor production but down-regulated interleukin (IL)-12 production. However, in DCs, which produce large amounts of IL-12, CpG-DNA and LPS failed to induce ERK activity. Consistent with a specific negative regulatory role for ERK in macrophages, chemical activation of this pathway in DCs suppressed CpG-DNA-induced IL-12 production. Overall, these results imply that differential activation of MAP kinase pathways is a basic mechanism by which distinct subsets of innate immune cells regulate their effector functions.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0261-4189
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
6973-82
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:10601019-Animals,
pubmed-meshheading:10601019-Antigen-Presenting Cells,
pubmed-meshheading:10601019-Bone Marrow Cells,
pubmed-meshheading:10601019-Cell Line,
pubmed-meshheading:10601019-Cells, Cultured,
pubmed-meshheading:10601019-Dendritic Cells,
pubmed-meshheading:10601019-Dinucleoside Phosphates,
pubmed-meshheading:10601019-Gene Expression Regulation,
pubmed-meshheading:10601019-Interleukin-12,
pubmed-meshheading:10601019-Lipopolysaccharides,
pubmed-meshheading:10601019-Luciferases,
pubmed-meshheading:10601019-Macrophages,
pubmed-meshheading:10601019-Mice,
pubmed-meshheading:10601019-Mice, Inbred C57BL,
pubmed-meshheading:10601019-Mitogen-Activated Protein Kinases,
pubmed-meshheading:10601019-Oligodeoxyribonucleotides,
pubmed-meshheading:10601019-Recombinant Proteins,
pubmed-meshheading:10601019-Thionucleotides,
pubmed-meshheading:10601019-Transfection,
pubmed-meshheading:10601019-Tumor Necrosis Factor-alpha
|
pubmed:year |
1999
|
pubmed:articleTitle |
Cell type-specific activation of mitogen-activated protein kinases by CpG-DNA controls interleukin-12 release from antigen-presenting cells.
|
pubmed:affiliation |
Institute of Medical Microbiology, Technische Universität München, Trogerstrasse 9, D-81675 Munich.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|