Cross-talk between liver and intestine in control of cholesterol and energy homeostasis

被引:38
作者
Groen, Albert K. [1 ,2 ]
Bloks, Vincent W. [1 ]
Verkade, Henkjan [1 ]
Kuipers, Folkert [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Pediat, NL-9700 AB Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, NL-9700 AB Groningen, Netherlands
关键词
Bile acids; Transintestinal cholesterol excretion; TICE; FGF15; Cholestasis; Reverse cholesterol transport; BILE-ACID SYNTHESIS; LOW-DENSITY-LIPOPROTEIN; BILIARY PHOSPHOLIPID SECRETION; GLUCAGON-LIKE PEPTIDE-1; X-RECEPTOR ACTIVATION; TRANSPORT IN-VIVO; RAT-LIVER; NEUTRAL STEROL; LINOLEIC-ACID; SR-BI;
D O I
10.1016/j.mam.2014.02.001
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
A major hurdle for organisms to dispose of cholesterol is the inability to degrade the sterol nucleus which constitutes the central part of the molecule. Synthesis of the sterol nucleus requires a complex, energy costly, metabolic pathway but also generates a diverse array of intermediates serving crucial roles in cellular energy metabolism and signal transduction. This may be the reason why this complex pathway has survived evolutionary pressure. The only way to get rid of substantial amounts of cholesterol is conversion into bile acid or direct excretion of the sterol in the feces. The lack of versatility in disposal mechanisms causes a lack of flexibility to regulate cholesterol homeostasis which may underlie the considerable human pathology linked to cholesterol removal from the body. Export of cholesterol from the body requires an intricate communication between intestine and the liver. The last decade this inter-organ cross talk has been focus of intense research leading to considerable new insight. This novel information on particular the cross-talk between liver and intestine and role of bile acids as signal transducing molecules forms the focus of this review. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:77 / 88
页数:12
相关论文
共 124 条
[1]   Identification of scavenger receptor SR-BI as a high density lipoprotein receptor [J].
Acton, S ;
Rigotti, A ;
Landschulz, KT ;
Xu, SZ ;
Hobbs, HH ;
Krieger, M .
SCIENCE, 1996, 271 (5248) :518-520
[2]   Reverse cholesterol transport in man: promotion of fecal steroid excretion by infusion of reconstituted HDL [J].
Angelin, B ;
Parini, P ;
Eriksson, M .
ATHEROSCLEROSIS SUPPLEMENTS, 2002, 3 (04) :23-30
[3]   Circulating Fibroblast Growth Factors as Metabolic Regulators-A Critical Appraisal [J].
Angelin, Bo ;
Larsson, Tobias E. ;
Rudling, Mats .
CELL METABOLISM, 2012, 16 (06) :693-705
[4]   ApoE promotes hepatic selective uptake but not RCT due to increased ABCA1-mediated cholesterol efflux to plasma [J].
Annema, Wijtske ;
Dikkers, Arne ;
de Boer, Jan Freark ;
Gautier, Thomas ;
Rensen, Patrick C. N. ;
Rader, Daniel J. ;
Tietge, Uwe J. F. .
JOURNAL OF LIPID RESEARCH, 2012, 53 (05) :929-940
[5]   Internalization of Modified Lipids by CD36 and SR-A Leads to Hepatic Inflammation and Lysosomal Cholesterol Storage in Kupffer Cells [J].
Bieghs, Veerle ;
Verheyen, Fons ;
van Gorp, Patrick J. ;
Hendrikx, Tim ;
Wouters, Kristiaan ;
Luetjohann, Dieter ;
Gijbels, Marion J. J. ;
Febbraio, Maria ;
Binder, Christoph J. ;
Hofker, Marten H. ;
Shiri-Sverdlov, Ronit .
PLOS ONE, 2012, 7 (03)
[6]   BIOLOGICAL SYNTHESIS OF CHOLESTEROL [J].
BLOCH, K .
SCIENCE, 1965, 150 (3692) :19-&
[7]   EXPRESSION AND DISTRIBUTION OF CHOLESTEROL 7-ALPHA-HYDROXYLASE IN RAT-LIVER [J].
BRASSIL, PJ ;
EDWARDS, RJ ;
DAVIES, DS .
BIOCHEMICAL PHARMACOLOGY, 1995, 50 (03) :311-316
[8]   STEROL EXCRETION AND CHOLESTEROL ABSORPTION IN DIABETICS AND NONDIABETICS WITH AND WITHOUT HYPERLIPIDEMIA [J].
BRIONES, ER ;
STEIGER, DL ;
PALUMBO, PJ ;
OFALLON, WM ;
LANGWORTHY, AL ;
ZIMMERMAN, BR ;
KOTTKE, BA .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1986, 44 (03) :353-361
[9]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[10]   A Reappraisal of the Mechanism by Which Plant Sterols Promote Neutral Sterol Loss in Mice [J].
Brufau, Gemma ;
Kuipers, Folkert ;
Lin, Yuguang ;
Trautwein, Elke A. ;
Groen, Albert K. .
PLOS ONE, 2011, 6 (06)