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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0004112,
umls-concept:C0017262,
umls-concept:C0017337,
umls-concept:C0021747,
umls-concept:C0185117,
umls-concept:C0205421,
umls-concept:C0206116,
umls-concept:C0206256,
umls-concept:C1308752,
umls-concept:C1367714,
umls-concept:C1415900,
umls-concept:C1706327,
umls-concept:C2003941,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
1994-3-9
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pubmed:abstractText |
IFN-gamma is a potent macrophage activator and induces a number of early and delayed genes. crg-2, the presumed murine homologue of human IP-10, belongs to a family of proinflammatory chemokines and is induced as an immediate early gene in response to IFN-gamma in macrophages. In contrast, class II MHC or Ia genes which are essential for Ag presentation are induced as a delayed response to IFN-gamma. We studied the expression of crg-2 and compared it with Ia in astrocytes and microglia of the central nervous system since, like macrophages, these cells can also produce a number of cytokines, express Ia molecules, and present Ag. We showed that crg-2 mRNA was induced in astrocytes and microglia by IFN-gamma as well as a paramyxovirus, Newcastle disease virus (NDV). Crg-2 protein was detected in the cytoplasm and in the supernatants of IFN-gamma-treated astrocytes and microglia. IFN-gamma and NDV or UV irradiated-NDV (UV-NDV) also induced Ia mRNA in these cells. The kinetics of expression of crg-2 and Ia mRNA were compared in the same systems. While crg-2 mRNA appeared within 2 h and reached a maximum in 6 to 8 h, Ia mRNA was not detected before 8 h. Cycloheximide superinduced crg-2 mRNA induced by IFN-gamma or UV-NDV but it abolished Ia mRNA induction by the same stimuli. The induction of crg-2 in astrocytes and microglia likely contributes to the development of immune-mediated inflammation in response to viruses or in autoimmune diseases of the central nervous system.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CXCL10,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CXC,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Monokines,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
152
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1411-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:8301141-Animals,
pubmed-meshheading:8301141-Astrocytes,
pubmed-meshheading:8301141-Chemokine CXCL10,
pubmed-meshheading:8301141-Chemokines, CXC,
pubmed-meshheading:8301141-Cytokines,
pubmed-meshheading:8301141-Gene Expression,
pubmed-meshheading:8301141-Genes, Immediate-Early,
pubmed-meshheading:8301141-Histocompatibility Antigens Class II,
pubmed-meshheading:8301141-Interferon-gamma,
pubmed-meshheading:8301141-Microglia,
pubmed-meshheading:8301141-Monokines,
pubmed-meshheading:8301141-Newcastle disease virus,
pubmed-meshheading:8301141-RNA, Messenger,
pubmed-meshheading:8301141-Rats,
pubmed-meshheading:8301141-Rats, Inbred Lew,
pubmed-meshheading:8301141-Rats, Sprague-Dawley,
pubmed-meshheading:8301141-Time Factors
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pubmed:year |
1994
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pubmed:articleTitle |
IFN and virus-inducible expression of an immediate early gene, crg-2/IP-10, and a delayed gene, I-A alpha in astrocytes and microglia.
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pubmed:affiliation |
Department of Neurology, University of Maryland, School of Medicine, Baltimore 21201.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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