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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1984-10-24
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pubmed:abstractText |
By using density-gradient fractionation and high-voltage free-flow electrophoresis, human platelet membranes were separated into highly purified subfractions of surface (SM) and intracellular (IM) origin. Associated exclusively with the IM fraction is an ATP-dependent Ca2+ uptake that, in the absence of oxalate, reaches steady-state levels in 5-10 min. When Ca2+-EGTA buffers were used to control the external Ca2+ concentrations (range 0.1-50 microM) there was an increase in the intravesicle steady-state level of Ca2+ up to 10 microM external Ca2+ concentration. Above this level the intravesicle space becomes saturated at a concentration between 10 and 20 nmol of Ca2+ X (mg of protein)-1. The ionophore A23187 promotes a rapid and almost total release of the sequestered Ca2+ (greater than 90%, t1/2 1-2 min). The presence of oxalate in the external medium greatly enhances the Ca2+ accumulation to levels as high as 200 nmol X (mg of protein)-1, but the uptake process is more variable and rarely reaches steady-state level even after 2 h incubation. Moreover, accumulation in the presence of oxalate effects ionophore release with less than 80% depletion in 45-60 min. These findings, taken together with the known presence in the platelet of a wide variety of functional and metabolic processes triggered by this cation, suggest that the platelet IM has a key role in controlling cytosolic Ca2+ concentrations.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/6433901-14179458,
http://linkedlifedata.com/resource/pubmed/commentcorrection/6433901-6260785,
http://linkedlifedata.com/resource/pubmed/commentcorrection/6433901-6621685,
http://linkedlifedata.com/resource/pubmed/commentcorrection/6433901-6806123,
http://linkedlifedata.com/resource/pubmed/commentcorrection/6433901-6812567
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Calcimycin,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Oxalates,
http://linkedlifedata.com/resource/pubmed/chemical/Oxalic Acid
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0264-6021
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
222
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
413-7
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:6433901-Adenosine Triphosphate,
pubmed-meshheading:6433901-Blood Platelets,
pubmed-meshheading:6433901-Calcimycin,
pubmed-meshheading:6433901-Calcium,
pubmed-meshheading:6433901-Cell Fractionation,
pubmed-meshheading:6433901-Cell Membrane,
pubmed-meshheading:6433901-Centrifugation, Density Gradient,
pubmed-meshheading:6433901-Electrophoresis,
pubmed-meshheading:6433901-Humans,
pubmed-meshheading:6433901-Intracellular Membranes,
pubmed-meshheading:6433901-Oxalates,
pubmed-meshheading:6433901-Oxalic Acid
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pubmed:year |
1984
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pubmed:articleTitle |
Characterization of the calcium-sequestering process associated with human platelet intracellular membranes isolated by free-flow electrophoresis.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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