pubmed-article:6893989 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:6893989 | lifeskim:mentions | umls-concept:C0014597 | lld:lifeskim |
pubmed-article:6893989 | lifeskim:mentions | umls-concept:C0021853 | lld:lifeskim |
pubmed-article:6893989 | lifeskim:mentions | umls-concept:C0025979 | lld:lifeskim |
pubmed-article:6893989 | lifeskim:mentions | umls-concept:C0026049 | lld:lifeskim |
pubmed-article:6893989 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
pubmed-article:6893989 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:6893989 | pubmed:issue | 3 Pt 1 | lld:pubmed |
pubmed-article:6893989 | pubmed:dateCreated | 1981-4-24 | lld:pubmed |
pubmed-article:6893989 | pubmed:abstractText | The bundle of filaments within microvilli of intestinal epithelial cells contains five major proteins including actin, calmodulin, and subunits of 105-, 95-, and 70-kdaltons. It has been previously shown (Howe, C. L., M. S. Mooseker, and T. A. Graves. 1980. Brush-border calmodulin: a major component of the isolated microvillus core. J. Cell Biol. 85: 916-923) that the addition of Ca++ (> 10(-6) M) to microvillus cores causes a rapid, drastic, but at least partially reversible disruption of this actin filament bundle. High-speed centrifugation of microvillus cores treated with Ca++ indicates that several core proteins are solubilized, including 30-50% of the actin and calmodulin, along with much of the 95- and 70-kdalton subunits. Gel filtration of such Ca++ extracts in the presence and absence of Ca++ indicates that microvillar actin "solated" by Ca++ is in an oligomeric state probably complexed with the 95-kdalton subunit. Removal of Ca++ results in the reassembly of F-actin, probably still complexed with 95-kdalton subunit, as determined by gel filtration, cosedimentation, viscometry, and electron microscopy. The 95-kdalton subunit (95K) was purified from Ca++ extracts by DEAE-Sephadex chromatography and its interaction with actin characterized by viscometry, cosedimentation, and EM in the presence and absence of Ca++. In the presence, but not absence, of Ca++, 95K inhibits actin assembly (50% inhibition at 1:50-60 95K to actin) and also reduces the viscosity of F-actin solutions. Similarly, sedimentation of actin is inhibited by 95K, but a small, presumably oligomeric actin- 95K complex formed in the presence of Ca++ is pelletable after long-term centrifugation. In the absence of Ca++, 95K cosediments with F-actin. EM of 95K-actin mixtures reveals that 95K "breaks" actin into small, filamentous fragments in the presence of Ca++. Reassembly of filaments occurs once Ca++ is removed. In the absence of Ca++, 95K has no effect on filament structure and, at relatively high ratios (1:2-6) of 95K to actin, this core protein will aggregate actin filaments into bundles. | lld:pubmed |
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pubmed-article:6893989 | pubmed:language | eng | lld:pubmed |
pubmed-article:6893989 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6893989 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:6893989 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:6893989 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:6893989 | pubmed:month | Dec | lld:pubmed |
pubmed-article:6893989 | pubmed:issn | 0021-9525 | lld:pubmed |
pubmed-article:6893989 | pubmed:author | pubmed-author:MoosekerM SMS | lld:pubmed |
pubmed-article:6893989 | pubmed:author | pubmed-author:HoweC LCL | lld:pubmed |
pubmed-article:6893989 | pubmed:author | pubmed-author:FalchEE | lld:pubmed |
pubmed-article:6893989 | pubmed:author | pubmed-author:WhartonK AKA | lld:pubmed |
pubmed-article:6893989 | pubmed:author | pubmed-author:GravesT ATA | lld:pubmed |
pubmed-article:6893989 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:6893989 | pubmed:volume | 87 | lld:pubmed |
pubmed-article:6893989 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:6893989 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:6893989 | pubmed:pagination | 809-22 | lld:pubmed |
pubmed-article:6893989 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:6893989 | pubmed:meshHeading | pubmed-meshheading:6893989-... | lld:pubmed |
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pubmed-article:6893989 | pubmed:meshHeading | pubmed-meshheading:6893989-... | lld:pubmed |
pubmed-article:6893989 | pubmed:year | 1980 | lld:pubmed |
pubmed-article:6893989 | pubmed:articleTitle | Regulation of microvillus structure: calcium-dependent solation and cross-linking of actin filaments in the microvilli of intestinal epithelial cells. | lld:pubmed |
pubmed-article:6893989 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:6893989 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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