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  • 1
    Online Resource
    Online Resource
    Elsevier BV ; 1997
    In:  Journal of Biological Chemistry Vol. 272, No. 49 ( 1997-12), p. 30766-30773
    In: Journal of Biological Chemistry, Elsevier BV, Vol. 272, No. 49 ( 1997-12), p. 30766-30773
    Type of Medium: Online Resource
    ISSN: 0021-9258
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1997
    detail.hit.zdb_id: 2141744-1
    detail.hit.zdb_id: 1474604-9
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Elsevier BV ; 2006
    In:  Journal of Lipid Research Vol. 47, No. 3 ( 2006-03), p. 504-514
    In: Journal of Lipid Research, Elsevier BV, Vol. 47, No. 3 ( 2006-03), p. 504-514
    Type of Medium: Online Resource
    ISSN: 0022-2275
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2006
    detail.hit.zdb_id: 1466675-3
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 2009
    In:  Journal of Lipid Research Vol. 50 ( 2009-04), p. S132-S137
    In: Journal of Lipid Research, Elsevier BV, Vol. 50 ( 2009-04), p. S132-S137
    Type of Medium: Online Resource
    ISSN: 0022-2275
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2009
    detail.hit.zdb_id: 1466675-3
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  • 4
    Online Resource
    Online Resource
    Elsevier BV ; 2011
    In:  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease Vol. 1812, No. 9 ( 2011-09), p. 1121-1129
    In: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Elsevier BV, Vol. 1812, No. 9 ( 2011-09), p. 1121-1129
    Type of Medium: Online Resource
    ISSN: 0925-4439
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2011
    detail.hit.zdb_id: 2209528-7
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  • 5
    Online Resource
    Online Resource
    Canadian Science Publishing ; 1985
    In:  Canadian Journal of Biochemistry and Cell Biology Vol. 63, No. 8 ( 1985-08-01), p. 870-881
    In: Canadian Journal of Biochemistry and Cell Biology, Canadian Science Publishing, Vol. 63, No. 8 ( 1985-08-01), p. 870-881
    Abstract: An investigation of the role of phospholipids in lipoprotein assembly and secretion is important since phospholipids, particularly phosphatidylcholine, are prominent components of all plasma lipoproteins. The fatty acid composition of phosphatidylcholine is virtually identical in human very low (VLDL), low, and high density lipoproteins, which supports the idea that phosphatidylcholine exchanges freely among plasma lipoproteins. However, the fatty acid composition of phosphatidylcholine from cultured rat hepatocytes is different from that in the secreted lipoproteins. In addition, the composition of molecular species of phosphatidylcholine is quite different in the rat liver, plasma, and red cells.Phosphatidylcholine is made in liver by two alternate pathways, by the CDP-choline pathway and by the methylation of phosphatidylethanolamine. Regulation of phosphatidylcholine biosynthesis by the CDP-choline pathway in rat liver is well established. In most instances, the rate of phosphatidylcholine synthesis is governed by the activity of CTP:phosphocholine cytidylyltransferase, which is present in the cytosol and also associated with microsomes. The cytosolic enzyme is inactive but can be reversibly translocated to the microsomes, where it is active. Translocation of this enzyme to the microsomes can be achieved either by a dephosphorylation reaction or by the presence of fatty acids in the cytosol.Once synthesized, how is phosphatidylcholine assembled into lipoprotein particles? The sequence of assembly of phospholipids into VLDL has been investigated in several studies. In a pulse–chase experiment, there was an initial labelling (within 15 min of the pulse) of phospholipids in secreted VLDL, which probably reflected the rapid movement of the phospholipids from their site of synthesis (the endoplasmic reticulum) to the Golgi. There appears to be a rapid exchange of phospholipid between the Golgi membranes and contents. There was also a delayed labelling (after 30 min) of the phospholipids and triacylglycerols (from [ 3 H]glycerol) and the apoproteins (from [ 3 H]leucine) in the secreted VLDL. This lag was attributed to the time taken for the nascent VLDL particles to move from the lumen of the endoplasmic reticulum to the Golgi and into the medium.Is phosphatidylcholine biosynthesis required for lipoprotein secretion? This question was investigated in rats maintained on a choline-deficient diet for 10 days. The total amount of plasma phosphatidylcholine decreased by approximately 40% and the rats developed fatty livers. The mechanisms for these effects of choline deficiency have not been fully explained, although one might anticipate that a deficiency of choline would inhibit the synthesis of phosphatidylcholine via the CDP-choline pathway.In addition, the possibility was considered that the alternative pathway for phosphatidylcholine biosynthesis (the methylation of phosphatidylethanolamine) might be necessary for lipoprotein secretion. Inhibition of the methylation pathway for phosphatidylcholine synthesis by greater than 90% in cultured rat hepatocytes did not inhibit the secretion of phosphatidylcholine, phosphatidylethanolamine, or apoproteins of the lipoproteins in the culture medium.Since phosphatidylcholine, triacylglycerol, and cholesterol are required for lipoprotein assembly and secretion, there might be some coordination among the synthesis and secretion of phosphatidylcholine, triacylglycerol, and cholesterol. Such coordinate regulation has been observed. For example, fatty acids stimulate the synthesis and secretion of both triacylglycerol and phosphatidylcholine by cultured rat hepatocytes. In addition, glucagon and AMP inhibit fatty acid synthesis, phosphatidylcholine biosynthesis, and the secretion of both phosphatidylcholine and triacylglycerol. Surprisingly, insulin appears to inhibit lipoprotein secretion even though it promotes fatty acid and cholesterol biosynthesis. In other studies in which there was an increased supply of cholesterol and cholesterol esters in the diet of rats, the percent of cholesterol esters in the core of the secreted VLDL particles was increased. Moreover, cholesterol feeding increased the plasma concentrations of both phosphatidylcholine and cholesterol. Presumably, there was a coordination of the synthesis of phosphatidylcholine with the level of cholesterol in the cells and (or) plasma.We conclude that phosphatidylcholine biosynthesis is a critical component for the synthesis and secretion of lipoproteins from liver.
    Type of Medium: Online Resource
    ISSN: 0714-7511
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 1985
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  • 6
    Online Resource
    Online Resource
    Elsevier BV ; 2016
    In:  Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids Vol. 1861, No. 2 ( 2016-02), p. 119-129
    In: Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, Elsevier BV, Vol. 1861, No. 2 ( 2016-02), p. 119-129
    Type of Medium: Online Resource
    ISSN: 1388-1981
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 2209502-0
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  • 7
    Online Resource
    Online Resource
    Elsevier BV ; 2017
    In:  Biochimica et Biophysica Acta (BBA) - Biomembranes Vol. 1859, No. 9 ( 2017-09), p. 1558-1572
    In: Biochimica et Biophysica Acta (BBA) - Biomembranes, Elsevier BV, Vol. 1859, No. 9 ( 2017-09), p. 1558-1572
    Type of Medium: Online Resource
    ISSN: 0005-2736
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2017
    detail.hit.zdb_id: 2209384-9
    SSG: 12
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  • 8
    Online Resource
    Online Resource
    Wiley ; 2002
    In:  Journal of Neurochemistry Vol. 83, No. 5 ( 2002-12), p. 1154-1163
    In: Journal of Neurochemistry, Wiley, Vol. 83, No. 5 ( 2002-12), p. 1154-1163
    Abstract: Niemann–Pick type‐C (NPC) disease is characterized by a progressive loss of neurons and an accumulation of unesterified cholesterol within the endocytic pathway. Unlike other tissues, however, NPC1‐deficient brains do not accumulate cholesterol but whether or not NPC1‐deficient neurons accumulate cholesterol is not clear. Therefore, as most studies on cholesterol homeostasis in NPC1‐deficient cells have been performed in fibroblasts we have investigated cholesterol homeostasis in cultured murine sympathetic neurons lacking functional NPC1. These neurons did not display obvious abnormalities in growth or morphology and appeared to respond normally to nerve growth factor. Filipin staining revealed numerous cholesterol‐filled endosomes/lysosomes in NPC1‐deficient neurons and the mass of cholesterol in cell bodies was greater than in wild‐type neurons. Surprisingly, however, the cholesterol content of NPC1‐deficient and wild‐type neurons as a whole was the same. This apparent paradox was resolved when the cholesterol content of NPC1‐deficient distal axons was found to be less than of wild‐type axons. Cholesterol sequestration in cell bodies did not depend on exogenously supplied cholesterol since the cholesterol accumulated before birth and did not disperse when neurons were cultured without exogenous cholesterol. The altered cholesterol distribution between cell bodies and axons suggests that transport of cholesterol, particularly that synthesized endogenously, from cell bodies to distal axons is impaired in NPC1‐deficient neurons.
    Type of Medium: Online Resource
    ISSN: 0022-3042 , 1471-4159
    Language: English
    Publisher: Wiley
    Publication Date: 2002
    detail.hit.zdb_id: 2020528-4
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    Elsevier BV ; 2004
    In:  Journal of Biological Chemistry Vol. 279, No. 14 ( 2004-04), p. 14009-14015
    In: Journal of Biological Chemistry, Elsevier BV, Vol. 279, No. 14 ( 2004-04), p. 14009-14015
    Type of Medium: Online Resource
    ISSN: 0021-9258
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2004
    detail.hit.zdb_id: 2141744-1
    detail.hit.zdb_id: 1474604-9
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Wiley ; 1986
    In:  FEBS Letters Vol. 204, No. 2 ( 1986-08-18), p. 243-246
    In: FEBS Letters, Wiley, Vol. 204, No. 2 ( 1986-08-18), p. 243-246
    Abstract: We have examined the effect of inhibitors of methylation of phosphatidylethanolamine on lipoprotein secretion from cultured rat hepatocytes. The incorporation of [1‐ 3 H]ethanolamine into phosphatidylcholine of hepatocytes and secreted lipoproteins was inhibited by greater than 90% by the methylation inhibitors 3‐deazaadenosine and Neplanocin. In addition, these compounds strongly inhibited the incorporation of [3‐ 3 H]serine into the choline moiety of phosphatidylcholine of the hepatocytes, but had no effect on incorporation of [3‐ 3 H]serine into secreted phosphatidylcholine. The results suggest that a pool of phosphatidylcholine targeted for lipoprotein secretion originates from phosphatidylethanolamine made from serine and this methylation reaction has the unique property of being insensitive to 3‐deazaadenosine.
    Type of Medium: Online Resource
    ISSN: 0014-5793 , 1873-3468
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1986
    detail.hit.zdb_id: 1460391-3
    SSG: 12
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