Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2-3
pubmed:dateCreated
2004-1-19
pubmed:abstractText
Bile salts (BS) inhibit the secretion of apolipoprotein B (apoB) and triacylglycerol (TG) in primary rat, mouse and human hepatocytes and in mice in vivo. We investigated whether lipidation of apoB into a lipoprotein particle is required for this inhibitory action of BS. The sodium/taurocholate co-transporting polypeptide (Ntcp) was co-expressed in McArdle-RH7777 (McA-RH7777) cells stably expressing the full-length human apoB100 (h-apoB100, secreted as TG-rich lipoprotein particles) or carboxyl-truncated human apoB18 (h-apoB18, secreted in lipid-free form). The doubly transfected cell lines (h-apoB/r-Ntcp) effectively accumulated taurocholic acid (TC). TC incubation decreased the secretion of endogenous rat apoB100 (-50%) and h-apoB18 (-35%), but did not affect secretion of rat apoA-I. Pulse-chase experiments (35S-methionine) indicated that the impaired secretion of radiolabeled h-apoB18 and h-apoB100 was associated with accelerated intracellular degradation. The calpain protease inhibitor N-acetyl-leucyl-leucyl-norleucinal (ALLN) partially inhibited intracellular apoB degradation but did not affect the amount of either h-apoB18 or h-apoB100 secreted into the medium, indicating that inhibition of apoB secretion by TC is not due to calpain-dependent proteasomal degradation. We conclude that TC does not inhibit apoB secretion by interference with its lipidation, but rather involves a mechanism dependent on the N-terminal end of apoB.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Apolipoprotein A-I, http://linkedlifedata.com/resource/pubmed/chemical/Apolipoprotein B-100, http://linkedlifedata.com/resource/pubmed/chemical/Apolipoproteins B, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cysteine Proteinase Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Leupeptins, http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins, VLDL, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Organic Anion Transporters..., http://linkedlifedata.com/resource/pubmed/chemical/Symporters, http://linkedlifedata.com/resource/pubmed/chemical/Taurocholic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides, http://linkedlifedata.com/resource/pubmed/chemical/acetylleucyl-leucyl-norleucinal, http://linkedlifedata.com/resource/pubmed/chemical/sodium-bile acid cotransporter, http://linkedlifedata.com/resource/pubmed/chemical/very low density lipoprotein...
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0006-3002
pubmed:author
pubmed:issnType
Print
pubmed:day
30
pubmed:volume
1635
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
93-103
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:14729072-Animals, pubmed-meshheading:14729072-Apolipoprotein A-I, pubmed-meshheading:14729072-Apolipoprotein B-100, pubmed-meshheading:14729072-Apolipoproteins B, pubmed-meshheading:14729072-Carrier Proteins, pubmed-meshheading:14729072-Cell Line, Tumor, pubmed-meshheading:14729072-Cysteine Proteinase Inhibitors, pubmed-meshheading:14729072-Hepatocytes, pubmed-meshheading:14729072-Leupeptins, pubmed-meshheading:14729072-Lipoproteins, VLDL, pubmed-meshheading:14729072-Liver Neoplasms, Experimental, pubmed-meshheading:14729072-Membrane Transport Proteins, pubmed-meshheading:14729072-Organic Anion Transporters, Sodium-Dependent, pubmed-meshheading:14729072-Rats, pubmed-meshheading:14729072-Symporters, pubmed-meshheading:14729072-Taurocholic Acid, pubmed-meshheading:14729072-Time Factors, pubmed-meshheading:14729072-Transfection, pubmed-meshheading:14729072-Triglycerides
pubmed:year
2003
pubmed:articleTitle
Inhibition of apolipoprotein B secretion by taurocholate is controlled by the N-terminal end of the protein in rat hepatoma McArdle-RH7777 cells.
pubmed:affiliation
Department of Pediatrics, Groningen University Institute for Drug Exploration, Pediatric Gastroenterology, Academic Hospital, The Netherlands.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't