Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3 Pt 1
pubmed:dateCreated
1981-4-24
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.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-1030705, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-1033184, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-11222, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-1202021, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-14179458, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-14907713, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-152766, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-18683, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-287075, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-365871, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-370125, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-379865, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-4253329, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-4254541, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-42649, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-492320, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-4944636, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-5344150, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-5432063, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-568144, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-568557, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-569662, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-574874, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-6892606, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-6893051, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-6893424, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-6987245, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-6998986, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-7400215, http://linkedlifedata.com/resource/pubmed/commentcorrection/6893989-783170
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0021-9525
pubmed:author
pubmed:issnType
Print
pubmed:volume
87
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
809-22
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1980
pubmed:articleTitle
Regulation of microvillus structure: calcium-dependent solation and cross-linking of actin filaments in the microvilli of intestinal epithelial cells.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.