Source:http://linkedlifedata.com/resource/pubmed/id/16202616
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2006-2-28
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pubmed:abstractText |
The aim of this study was to investigate the role of microglia in radiation-induced astrocyte gliosis. We found that a single dose of 15 Gy radiation to a whole rat brain increased immunostaining of glial fibrillary acidic protein in astrocytes 6 h later, and even more so 24 h later, indicating the initiation of gliosis. While irradiation of cultured rat astrocytes had little effect, irradiation of microglia-astrocyte mixed-cultures displayed altered astrocyte phenotype into more processed, which is another characteristic of gliosis. Experiments using microglia-conditioned media indicated this astrocyte change was due to factors released from irradiated microglia. Irradiation of cultured mouse microglial cells induced a dose-dependent increase in mRNA levels for cyclooxygenase-2 (COX-2), interleukin (IL)-1beta, IL-6, IL-18, tumor necrosis factor-alpha and interferon-gamma-inducible protein-10, which are usually associated with microglia activation. Consistent with these findings, irradiation of microglia activated NF-kappaB, a transcription factor that regulates microglial activation. Addition of prostaglandin E2 (PGE2: a metabolic product of the COX-2 enzyme) to primary cultured rat astrocytes resulted in phenotypic changes similar to those observed in mixed-culture experiments. Therefore, it appears that PGE(2) released from irradiated microglia is a key mediator of irradiation-induced gliosis or astrocyte phenotype change. These data suggest that radiation-induced microglial activation and resultant production of PGE2 seems to be associated with an underlying cause of inflammatory complications associated with radiation therapy for malignant gliomas.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Culture Media, Conditioned,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Glial Fibrillary Acidic Protein,
http://linkedlifedata.com/resource/pubmed/chemical/N-(2-cyclohexyloxy-4-nitrophenyl)met...,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrobenzenes,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfonamides
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0969-9961
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
457-67
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16202616-Animals,
pubmed-meshheading:16202616-Astrocytes,
pubmed-meshheading:16202616-Cells, Cultured,
pubmed-meshheading:16202616-Coculture Techniques,
pubmed-meshheading:16202616-Culture Media, Conditioned,
pubmed-meshheading:16202616-Cyclooxygenase 2,
pubmed-meshheading:16202616-Cyclooxygenase Inhibitors,
pubmed-meshheading:16202616-Dinoprostone,
pubmed-meshheading:16202616-Electrophoretic Mobility Shift Assay,
pubmed-meshheading:16202616-Glial Fibrillary Acidic Protein,
pubmed-meshheading:16202616-Gliosis,
pubmed-meshheading:16202616-Immunoblotting,
pubmed-meshheading:16202616-Immunohistochemistry,
pubmed-meshheading:16202616-Mice,
pubmed-meshheading:16202616-Microglia,
pubmed-meshheading:16202616-Nitrobenzenes,
pubmed-meshheading:16202616-RNA, Messenger,
pubmed-meshheading:16202616-Radiation, Ionizing,
pubmed-meshheading:16202616-Rats,
pubmed-meshheading:16202616-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:16202616-Sulfonamides
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pubmed:year |
2006
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pubmed:articleTitle |
Ionizing radiation induces astrocyte gliosis through microglia activation.
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pubmed:affiliation |
Research Institute, National Cancer Center, Goyang, Gyeonggi, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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