rdf:type |
|
lifeskim:mentions |
umls-concept:C0007765,
umls-concept:C0010837,
umls-concept:C0011065,
umls-concept:C0027882,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0041904,
umls-concept:C0162638,
umls-concept:C0567416,
umls-concept:C1704259,
umls-concept:C1705987
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pubmed:issue |
2-3
|
pubmed:dateCreated |
2001-4-6
|
pubmed:abstractText |
Cerebellar granule neurons can be maintained in culture in a medium containing high serum and depolarising levels of KCl. When serum is removed and the KCl levels lowered from 25 to 5 mM, the cells undergo apoptosis. Apoptosis can be prevented by inhibitors of transcription or translation, suggesting a need for macromolecular synthesis in the apoptotic process. Using quantitative reverse transcription-polymerase chain reaction the levels of mRNA for a range of genes postulated to be important in apoptosis have been examined. Elevated levels of caspase 3, c-Jun, and Fas ligand were found, in addition to a corresponding increase in c-Jun protein and activation of caspase-3. These results suggest that cerebellar granule neurons upregulate components of both death receptor-mediated and the mitochondrial-mediated death pathways.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Casp3 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3,
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/Fas Ligand Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-jun,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Tnfsf6 protein, rat
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
|
pubmed:issn |
0304-3940
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
20
|
pubmed:volume |
302
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
113-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11290400-Animals,
pubmed-meshheading:11290400-Animals, Newborn,
pubmed-meshheading:11290400-Apoptosis,
pubmed-meshheading:11290400-Caspase 3,
pubmed-meshheading:11290400-Caspases,
pubmed-meshheading:11290400-Cells, Cultured,
pubmed-meshheading:11290400-Cerebellar Cortex,
pubmed-meshheading:11290400-Fas Ligand Protein,
pubmed-meshheading:11290400-Gene Expression Regulation,
pubmed-meshheading:11290400-Male,
pubmed-meshheading:11290400-Membrane Glycoproteins,
pubmed-meshheading:11290400-Neurons,
pubmed-meshheading:11290400-Proto-Oncogene Proteins c-jun,
pubmed-meshheading:11290400-RNA, Messenger,
pubmed-meshheading:11290400-Rats,
pubmed-meshheading:11290400-Rats, Sprague-Dawley,
pubmed-meshheading:11290400-Signal Transduction,
pubmed-meshheading:11290400-Up-Regulation
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pubmed:year |
2001
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pubmed:articleTitle |
Upregulation of death pathway molecules in rat cerebellar granule neurons undergoing apoptosis.
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pubmed:affiliation |
Anatomical Neuropharmacology Unit, Medical Research Council, OX1 3TH, Oxford, UK.
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pubmed:publicationType |
Journal Article
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