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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1979-7-25
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pubmed:abstractText |
The (high-affinity receptor)-mediated uptake of homologous low-density (low-rho) lipoproteins by cultured human arterial smooth muscle cells or human skin fibroblasts is controlled by the sialic acid content of low-rho lipoprotein particles. This conclusion is derived from the following results. 1. Gangliosides incubated with native low-rho lipoproteins associate with low-rho lipoprotein particles. Low-rho lipoproteins modified by associated GLac1, GGtet1, and GGtet2b + GGtet3 gangliosides are internalized by arterial smooth muscle cells at a rate up to 80% lower than native low-rho lipoproteins or those preincubated with desialized gangliosides. 2. The inhibitory effect of gangliosides is specific for high affinity uptake and not detectable on skin fibroblasts deficient in low-rho-lipoprotein receptor. 3. Desialyzed low-rho lipoproteins are internalized by smooth muscle cells up to 100% faster than native low-rho lipoproteins, the enhancement of uptake corresponding to the degree of desialization.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0014-2956
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
2
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pubmed:volume |
93
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
51-5
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pubmed:dateRevised |
2007-7-23
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pubmed:meshHeading |
pubmed-meshheading:220045-Aorta,
pubmed-meshheading:220045-Biological Transport,
pubmed-meshheading:220045-Cells, Cultured,
pubmed-meshheading:220045-Fibroblasts,
pubmed-meshheading:220045-Gangliosides,
pubmed-meshheading:220045-Humans,
pubmed-meshheading:220045-Kinetics,
pubmed-meshheading:220045-Lipoproteins, LDL,
pubmed-meshheading:220045-Muscle, Smooth,
pubmed-meshheading:220045-Protein Binding,
pubmed-meshheading:220045-Sialic Acids,
pubmed-meshheading:220045-Skin
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pubmed:year |
1979
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pubmed:articleTitle |
Sialic-acid content of low-density lipoproteins controls their binding and uptake by cultured cells.
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pubmed:publicationType |
Journal Article
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