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pubmed-article:15866482pubmed:abstractTextThe scavenger receptor class B, type I (SR-BI) mediates the cellular selective uptake of cholesteryl esters and other lipids from high-density lipoproteins (HDL) and low-density lipoproteins (LDL). This process, unlike classical receptor-mediated endocytosis, does not result in lipoprotein degradation. Instead, the lipid depleted particles are released into the medium. Here we show that selective lipid uptake mediated by murine SR-BI can be uncoupled from the endocytosis of HDL or LDL particles. We found that blocking selective lipid uptake by incubating cells with the small chemical inhibitors BLT-1 or BLT-4 did not affect endocytosis of HDL. Similarly, blocking endocytosis by hyperosmotic sucrose or K+ depletion did not prevent selective lipid uptake from HDL or LDL. These findings suggest that mSR-BI-mediated selective uptake occurs at the cell surface upon the association of lipoproteins with mSR-BI and does not require endocytosis of HDL or LDL particles.lld:pubmed
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pubmed-article:15866482pubmed:articleTitleEndocytosis is not required for the selective lipid uptake mediated by murine SR-BI.lld:pubmed
pubmed-article:15866482pubmed:affiliationDepartment of Cell Biology, Harvard Medical School and The CBR Institute for Biomedical Research, 200 Longwood Avenue, Room 134, Boston, MA 02115, USA.lld:pubmed
pubmed-article:15866482pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15866482pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:15866482pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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