Literature DB >> 10194330

Intestinal absorption of dietary cholesteryl ester is decreased but retinyl ester absorption is normal in carboxyl ester lipase knockout mice.

W Weng1, L Li, A M van Bennekum, S H Potter, E H Harrison, W S Blaner, J L Breslow, E A Fisher.   

Abstract

Carboxyl ester lipase (CEL; EC 3.1.1.13) hydrolyzes cholesteryl esters and retinyl esters in vitro. In vivo, pancreatic CEL is thought to liberate cholesterol and retinol from their esters prior to absorption in the intestine. CEL is also a major lipase in the breast milk of many mammals, including humans and mice, and is thought to participate in the processing of triglycerides to provide energy for growth and development while the pancreas of the neonate matures. Other suggested roles for CEL include the direct facilitation of the intestinal absorption of free cholesterol and the modification of plasma lipoproteins. Mice with different CEL genotypes [wild type (WT), knockout (CELKO), heterozygote] were generated to study the functions of CEL in a physiological system. Mice grew and developed normally, independent of the CEL genotype of the pup or nursing mother. Consistent with this was the normal absorption of triglyceride in CELKO mice. The absorption of free cholesterol was also not significantly different between CELKO (87 +/- 26%, mean +/- SD) and WT littermates (76 +/- 10%). Compared to WT mice, however, CELKO mice absorbed only about 50% of the cholesterol provided as cholesteryl ester (CE). There was no evidence for the direct intestinal uptake of CE or for intestinal bacterial enzymes that hydrolyze it, suggesting that another enzyme besides CEL can hydrolyze dietary CE in mice. Surprisingly, CELKO and WT mice absorbed similar amounts of retinol provided as retinyl ester (RE). RE hydrolysis, however, was required for absorption, implying that CEL was not the responsible enzyme. The changes in plasma lipid and lipoprotein levels to diets with increasing lipid content were similar in mice of all three CEL genotypes. Overall, the data indicate that in the mouse, other enzymes besides CEL participate in the hydrolysis of dietary cholesteryl esters, retinyl esters, and triglycerides.

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Year:  1999        PMID: 10194330     DOI: 10.1021/bi981679a

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  32 in total

1.  Pancreatic function in carboxyl-ester lipase knockout mice.

Authors:  Mette Vesterhus; Helge Raeder; Amarnath J Kurpad; Dan Kawamori; Anders Molven; Rohit N Kulkarni; C Ronald Kahn; Pål Rasmus Njølstad
Journal:  Pancreatology       Date:  2010-08-19       Impact factor: 3.996

Review 2.  Human pancreatic digestive enzymes.

Authors:  David C Whitcomb; Mark E Lowe
Journal:  Dig Dis Sci       Date:  2007-01-05       Impact factor: 3.199

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Authors:  Tony Y Wang; Min Liu; Piero Portincasa; David Q-H Wang
Journal:  Eur J Clin Invest       Date:  2013-09-18       Impact factor: 4.686

4.  Plasma carboxyl ester lipase activity modulates apolipoprotein B-containing lipoprotein metabolism in a transgenic mouse model.

Authors:  Ling Li; Wei Weng; Earl H Harrison; Edward A Fisher
Journal:  Metabolism       Date:  2008-10       Impact factor: 8.694

Review 5.  Mechanisms involved in the intestinal absorption of dietary vitamin A and provitamin A carotenoids.

Authors:  Earl H Harrison
Journal:  Biochim Biophys Acta       Date:  2011-06-12

Review 6.  Retinoids: Potent regulators of metabolism.

Authors:  Pierre-Jacques Brun; Kryscilla Jian Zhang Yang; Seung-Ah Lee; Jason J Yuen; William S Blaner
Journal:  Biofactors       Date:  2012-12-22       Impact factor: 6.113

Review 7.  Complexity of vitamin E metabolism.

Authors:  Lisa Schmölz; Marc Birringer; Stefan Lorkowski; Maria Wallert
Journal:  World J Biol Chem       Date:  2016-02-26

8.  A single dose of c9,t11 or t10,c12 conjugated linoleic acid isomers perturbs vitamin A metabolism in mice.

Authors:  Elena Giordano; Sebastiano Banni; Loredana Quadro
Journal:  Nutr Res       Date:  2011-11       Impact factor: 3.315

9.  Lectin-like Ox-LDL receptor is expressed in human INT-407 intestinal cells: involvement in the transcytosis of pancreatic bile salt-dependent lipase.

Authors:  Nadine Bruneau; Stéphane Richard; Françoise Silvy; Alain Verine; Dominique Lombardo
Journal:  Mol Biol Cell       Date:  2003-04-04       Impact factor: 4.138

10.  Branched Fatty Acid Esters of Hydroxy Fatty Acids Are Preferred Substrates of the MODY8 Protein Carboxyl Ester Lipase.

Authors:  Matthew J Kolar; Siddhesh S Kamat; William H Parsons; Edwin A Homan; Tim Maher; Odile D Peroni; Ismail Syed; Karianne Fjeld; Anders Molven; Barbara B Kahn; Benjamin F Cravatt; Alan Saghatelian
Journal:  Biochemistry       Date:  2016-08-10       Impact factor: 3.162

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