Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-1-5
pubmed:abstractText
This study characterizes Hsp70 induction in human smooth muscle cells (SMC) by herbimycin A and cyclopentenone prostaglandins. The magnitude of Hsp70 induction by cyclopentenone prostaglandins was 8- to 10-fold higher than induction by herbimycin A. Hsp70 induction by delta12PGJ2 was first observed at 10 microM, rose to 4000-5000 ng/mL within one log unit and a maximum response was not observed; concentrations of delta12PGJ2 higher than 30 microM were toxic to the cells. A maximum response with herbimycin A (500 ng/mL) was reached at 0.05 microM and maintained to 1 microM without toxicity. Both, delta12PGJ2 and herbimycin A, were inhibited by dithiothreitol (DTT, 100 microM) at lower concentrations and became less sensitive to inhibition at higher concentrations. Hsp70 induction after incubation of SMC with delta12PGJ2 followed by addition of herbimycin A was significantly higher than Hsp70 induction after incubation with herbimycin A followed by addition of delta12PGJ2. When cells were incubated with [3H]-PGJ2, followed by protein denaturation, substantial radioactivity remained protein-bound suggesting that the prostaglandin must be covalently bound. Covalent binding was largely insensitive to DTT. Maximal Hsp70 induction was observed after 5 minutes of exposure of the cells to herbimycin A followed by a 20 hour recovery period in agent-free medium. Cells required 3-4 hours of exposure to delta12PGJ2 followed by a 20 hour recovery period in order to see high Hsp70 induction. Binding of the heat shock factor (HSF) to the heat shock element (HSE) in the presence of herbimycin A or delta12PGJ2, and the effects of DTT, mirrored the results of Hsp70 induction. The results suggest that probable differences between the 2 agents are at the level of the signal transduction prior to HSF activation.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-1631114, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-1656993, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-2070817, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-2427013, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-2783121, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-2813398, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-3211126, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-3302206, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-6157190, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-7559801, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-7622464, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-7760364, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-7988663, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-7988667, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-7988673, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-8102520, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-8131836, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-8609226, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-8856973, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-8856984, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-8943275, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-9649501, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-9686751, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-9702196, http://linkedlifedata.com/resource/pubmed/commentcorrection/11147963-9743115
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/9-deoxy-9,10-didehydro-12,13-didehyd..., http://linkedlifedata.com/resource/pubmed/chemical/9-deoxy-delta-9-prostaglandin D2, http://linkedlifedata.com/resource/pubmed/chemical/Anti-Bacterial Agents, http://linkedlifedata.com/resource/pubmed/chemical/Antiviral Agents, http://linkedlifedata.com/resource/pubmed/chemical/Benzoquinones, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Dithiothreitol, http://linkedlifedata.com/resource/pubmed/chemical/HSP70 Heat-Shock Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lactams, Macrocyclic, http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandin D2, http://linkedlifedata.com/resource/pubmed/chemical/Quinones, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/heat shock transcription factor, http://linkedlifedata.com/resource/pubmed/chemical/herbimycin
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1355-8145
pubmed:author
pubmed:issnType
Print
pubmed:volume
5
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
121-31
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2000
pubmed:articleTitle
Induction of heat shock protein 70 by herbimycin A and cyclopentenone prostaglandins in smooth muscle cells.
pubmed:affiliation
Department of Cardiovascular Biology, Rh ne Poulenc Rorer Central Research, Collegeville, PA 19426, USA.
pubmed:publicationType
Journal Article