Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2000-4-12
pubmed:abstractText
The densities of skeletal muscle intramembrane charge movement and macroscopic L-type Ca(2+) current have been shown to increase during prenatal development. In the present work, the electrophysiological characteristics of L-type Ca(2+) channels were analyzed over the embryonic period E14 to E19 using the whole-cell and cell-attached procedures. At the macroscopic level, the whole-cell L-type Ca(2+) conductance increased 100% between E14 and E19. This enhancement was accompanied by a small negative shift of the voltage dependence and a marked acceleration of the inactivation kinetics. At the single-channel level, the unitary conductance decreased significantly from 13.2 +/- 0.1 pS (n = 8) at E14 to 10.7 +/- 0.3 pS (n = 7) at E18 and the open probability was multiplied by 2. No significant change of the density of functional channels was observed during the same period. In contrast to the density of intramembrane charge movement, which, under the same conditions, has been shown to increase between 16 and 19 days, L-type Ca(2+) channels properties change mostly between 14 and 16 days. Taken together, these results suggest that the two functions of the dihydropyridine receptor are carried by two different proteins which could be differentially regulated by subunit composition and/or degree of phosphorylation.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-10332087, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-12991237, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-1437518, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-1663002, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-1712427, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-1716787, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-1864461, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-2157159, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-2423878, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-2434854, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-2458430, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-2849609, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-2903448, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-6088541, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-6317445, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-7539048, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-7971150, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8171118, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8210181, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8381753, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8576701, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8583415, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8598910, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8783073, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8804599, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-8913592, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-9049149, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-9278527, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-9649380, http://linkedlifedata.com/resource/pubmed/commentcorrection/10692316-9664036
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0006-3495
pubmed:author
pubmed:issnType
Print
pubmed:volume
78
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1282-92
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2000
pubmed:articleTitle
Functional expression of the L-type calcium channel in mice skeletal muscle during prenatal myogenesis.
pubmed:affiliation
Laboratoire de Physiologie des Eléments Excitables, UMR Centre National de la Recherche Scientifique 5578, UCB-Lyon 1, 69622 Villeurbanne Cedex, France. strube@physio.univ-lyon1.fr
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't