pubmed-article:6540272 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:6540272 | lifeskim:mentions | umls-concept:C0029246 | lld:lifeskim |
pubmed-article:6540272 | lifeskim:mentions | umls-concept:C0014257 | lld:lifeskim |
pubmed-article:6540272 | lifeskim:mentions | umls-concept:C0034963 | lld:lifeskim |
pubmed-article:6540272 | lifeskim:mentions | umls-concept:C1166758 | lld:lifeskim |
pubmed-article:6540272 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
pubmed-article:6540272 | pubmed:dateCreated | 1984-9-14 | lld:pubmed |
pubmed-article:6540272 | pubmed:abstractText | The pattern of early cell movement after an experimental 'wound' and the organization of actin in stationary and moving cultured endothelial cells have been studied by means of: time-lapse photography; indirect immunofluorescence using anti-actin antibodies with and without pretreatment with the actin destabilizing factor present in human plasma; and differential centrifugation and densitometric analysis of stained sodium dodecylsulphate/polyacrylamide gels in order to evaluate the total and relative amounts of G and F-actin. Up to 5 h after a single scratch, movement consists of a coordinate spreading and translocation of a band of about 10 cells from the wound edge. Compared to stationary cells, moving endothelial cells show: no significant changes in the intensity and distribution of immunofluorescent staining with anti-actin antibodies, but an increased sensitivity of cytoplasmic actin, including stress fibres, to the actin-destabilizing factor purified from human plasma; and no significant change in the total amount of actin, but a decreased relative amount of F-actin and a corresponding increased relative amount of G-actin. We conclude that endothelial cell movement in vitro is accompanied by a rapid change in the state of actin organization characterized by an overall decrease in cytoplasmic F-actin. | lld:pubmed |
pubmed-article:6540272 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6540272 | pubmed:language | eng | lld:pubmed |
pubmed-article:6540272 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6540272 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:6540272 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:6540272 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6540272 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:6540272 | pubmed:month | Mar | lld:pubmed |
pubmed-article:6540272 | pubmed:issn | 0021-9533 | lld:pubmed |
pubmed-article:6540272 | pubmed:author | pubmed-author:GabbianiGG | lld:pubmed |
pubmed-article:6540272 | pubmed:author | pubmed-author:SchwartzS MSM | lld:pubmed |
pubmed-article:6540272 | pubmed:author | pubmed-author:HeimarkR LRL | lld:pubmed |
pubmed-article:6540272 | pubmed:author | pubmed-author:GabbianiFF | lld:pubmed |
pubmed-article:6540272 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:6540272 | pubmed:volume | 66 | lld:pubmed |
pubmed-article:6540272 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:6540272 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:6540272 | pubmed:pagination | 39-50 | lld:pubmed |
pubmed-article:6540272 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
pubmed-article:6540272 | pubmed:meshHeading | pubmed-meshheading:6540272-... | lld:pubmed |
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pubmed-article:6540272 | pubmed:meshHeading | pubmed-meshheading:6540272-... | lld:pubmed |
pubmed-article:6540272 | pubmed:year | 1984 | lld:pubmed |
pubmed-article:6540272 | pubmed:articleTitle | Organization of actin cytoskeleton during early endothelial regeneration in vitro. | lld:pubmed |
pubmed-article:6540272 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:6540272 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:6540272 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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