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

被引:107
作者
Weng, W
Li, L
van Bennekum, AM
Potter, SH
Harrison, EH
Blaner, WS
Breslow, JL
Fisher, EA
机构
[1] CUNY Mt Sinai Sch Med, Inst Cardiovasc, Lab Lipoprot Res, New York, NY 10029 USA
[2] CUNY Mt Sinai Sch Med, Dept Med, New York, NY 10029 USA
[3] Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA
[4] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[5] Med Coll Penn & Hahnemann Univ, Sch Med, Dept Biochem, Philadelphia, PA 19129 USA
关键词
D O I
10.1021/bi981679a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4143 / 4149
页数:7
相关论文
共 52 条
[1]   INTESTINAL EXPRESSION OF HUMAN APOLIPOPROTEIN A-IV IN TRANSGENIC MICE FAILS TO INFLUENCE DIETARY-LIPID ABSORPTION OR FEEDING-BEHAVIOR [J].
AALTOSETALA, K ;
BISGAIER, CL ;
HO, A ;
KIEFT, KA ;
TRABER, MG ;
KAYDEN, HJ ;
RAMAKRISHNAN, R ;
WALSH, A ;
ESSENBURG, AD ;
BRESLOW, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (04) :1776-1786
[2]  
ALEMI B, 1981, PEDIATRICS, V68, P484
[3]  
BELL CC, 1968, P SOC EXP BIOL MED, V128, P575
[4]  
BHAKDI S, 1995, J EXP MED, V182, P1959, DOI 10.1084/jem.182.6.1959
[5]   THE ROLE OF CHOLESTERYL ESTER HYDROLYSIS AND SYNTHESIS IN CHOLESTEROL TRANSPORT ACROSS RAT INTESTINAL MUCOSAL MEMBRANE A NEW CONCEPT [J].
BHAT, SG ;
BROCKMAN, HL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 109 (02) :486-492
[6]   BILE SALT-STIMULATED LIPASE IN HUMAN-MILK AND CARBOXYL ESTER HYDROLASE IN PANCREATIC-JUICE - ARE THEY IDENTICAL ENZYMES [J].
BLACKBERG, L ;
LOMBARDO, D ;
HERNELL, O ;
GUY, O ;
OLIVECRONA, T .
FEBS LETTERS, 1981, 136 (02) :284-288
[7]  
BLANER WS, 1987, EUR J BIOCHEM, V164, P973
[8]  
BOSNER MS, 1989, J BIOL CHEM, V264, P20261
[9]   PLASMA-CHOLESTEROL ESTERASE LEVEL IS A DETERMINANT FOR AN ATHEROGENIC LIPOPROTEIN PROFILE IN NORMOLIPIDEMIC HUMAN-SUBJECTS [J].
BRODTEPPLEY, J ;
WHITE, P ;
JENKINS, S ;
HUI, DY .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1272 (02) :69-72
[10]   IDENTITY OF A CYTOSOLIC NEUTRAL CHOLESTEROL ESTERASE IN RAT-LIVER WITH THE BILE-SALT STIMULATED CHOLESTEROL ESTERASE IN PANCREAS [J].
CAMULLI, ED ;
LINKE, MJ ;
BROCKMAN, HL ;
HUI, DY .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1005 (02) :177-182