File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Simulation of cell proliferation in mouse oral epithelium, and the action of epidermal growth factor: Evidence for a high degree of synchronization of the stem cells

TitleSimulation of cell proliferation in mouse oral epithelium, and the action of epidermal growth factor: Evidence for a high degree of synchronization of the stem cells
Authors
KeywordsSimulation model
Epidermal growth factor
Circadian rhythm
Cell synchronization
Stem cells
Issue Date2002
Citation
Cell Proliferation, 2002, v. 35, n. SUPPL. 1, p. 68-77 How to Cite?
AbstractComputer simulation has been carried out to help to determine the cell-proliferative mechanisms underlying data gathered from a double-labelling experiment on the dorsal tongue of the mouse. Good fits to the data have been obtained by assuming that there is a high degree of synchrony in the stem cells, which have a 24-h cell cycle time, and that daughters of these cells undergo two further divisions, with mean cell cycle times of 48 h, before differentiating. This results in one-seventh of proliferative cells being stem cells, which ties in well with the concept of epidermal proliferative units. There is no need to assume that S-phase duration changes diurnally. The administration of epidermal growth factor seems to increase the degree of synchrony. In such systems, the influx to S-phase and the efflux from it have very sudden short peaks, which it is impossible to observe unless observations are taken very frequently. There are therefore implications for the designs of experiments that attempt to study diurnal rhythms or the effect of factors that disturb the normal proliferative pattern of cells.
Persistent Identifierhttp://hdl.handle.net/10722/249004
ISSN
2021 Impact Factor: 8.755
2020 SCImago Journal Rankings: 1.647
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAppleton, D. R.-
dc.contributor.authorThomson, P. J.-
dc.contributor.authorDonaghey, C. E.-
dc.contributor.authorPotten, C. S.-
dc.contributor.authorMcGurk, M.-
dc.date.accessioned2017-10-27T05:58:51Z-
dc.date.available2017-10-27T05:58:51Z-
dc.date.issued2002-
dc.identifier.citationCell Proliferation, 2002, v. 35, n. SUPPL. 1, p. 68-77-
dc.identifier.issn0960-7722-
dc.identifier.urihttp://hdl.handle.net/10722/249004-
dc.description.abstractComputer simulation has been carried out to help to determine the cell-proliferative mechanisms underlying data gathered from a double-labelling experiment on the dorsal tongue of the mouse. Good fits to the data have been obtained by assuming that there is a high degree of synchrony in the stem cells, which have a 24-h cell cycle time, and that daughters of these cells undergo two further divisions, with mean cell cycle times of 48 h, before differentiating. This results in one-seventh of proliferative cells being stem cells, which ties in well with the concept of epidermal proliferative units. There is no need to assume that S-phase duration changes diurnally. The administration of epidermal growth factor seems to increase the degree of synchrony. In such systems, the influx to S-phase and the efflux from it have very sudden short peaks, which it is impossible to observe unless observations are taken very frequently. There are therefore implications for the designs of experiments that attempt to study diurnal rhythms or the effect of factors that disturb the normal proliferative pattern of cells.-
dc.languageeng-
dc.relation.ispartofCell Proliferation-
dc.subjectSimulation model-
dc.subjectEpidermal growth factor-
dc.subjectCircadian rhythm-
dc.subjectCell synchronization-
dc.subjectStem cells-
dc.titleSimulation of cell proliferation in mouse oral epithelium, and the action of epidermal growth factor: Evidence for a high degree of synchronization of the stem cells-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1046/j.1365-2184.35.s1.7.x-
dc.identifier.pmid12139709-
dc.identifier.scopuseid_2-s2.0-0036367517-
dc.identifier.volume35-
dc.identifier.issueSUPPL. 1-
dc.identifier.spage68-
dc.identifier.epage77-
dc.identifier.isiWOS:000177033600008-
dc.identifier.issnl0960-7722-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats