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pubmed-article:1875451pubmed:abstractTextMacrophages were incubated with 125I-VLDL for 5 h in presence or absence of lipoprotein lipase (LPL) inhibitor, benzene boronic acid (BBA). Both the uptake and degradation of 125I-VLDL by macrophages were saturable, and the uptake and degradation curves were virtually identical. When macrophages were incubated with 125I-VLDL for 10 h in presence of BBA, the uptake and degradation of 125I-VLDL were still saturable. However, in absence of BBA, the uptake and degradation were no longer saturable. The results suggest that with macrophages incubated with VLDL for a shorter period, VLDL was taken up predominantly via receptor pathway, with a longer period of incubation, LPL played a striking role in uptake of VLDL.lld:pubmed
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pubmed-article:1875451pubmed:authorpubmed-author:WangC FCFlld:pubmed
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pubmed-article:1875451pubmed:authorpubmed-author:JiangW GWGlld:pubmed
pubmed-article:1875451pubmed:authorpubmed-author:WangH XHXlld:pubmed
pubmed-article:1875451pubmed:authorpubmed-author:FengZ CZClld:pubmed
pubmed-article:1875451pubmed:authorpubmed-author:ZhongY QYQlld:pubmed
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pubmed-article:1875451pubmed:pagination39-44lld:pubmed
pubmed-article:1875451pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:1875451pubmed:articleTitleRelationship of VLDL receptor and LPL in metabolism of VLDL by macrophage.lld:pubmed
pubmed-article:1875451pubmed:affiliationDepartment of Biochemistry, Tongji Medical University, Wuhan.lld:pubmed
pubmed-article:1875451pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1875451pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed