Fatty acid transport proteins in disease: New insights from invertebrate models

被引:48
作者
Dourlen, Pierre [1 ]
Sujkowski, Alyson [2 ]
Wessells, Robert [2 ]
Mollereau, Bertrand [1 ]
机构
[1] Univ Lyon, Ecole Normale Super Lyon, CNRS, Lab Mol Biol Cell,UMR5239,Biosci Lyon Gerland UMS, Lyon, France
[2] Wayne State Univ, Sch Med, Dept Physiol, Detroit, MI 48201 USA
关键词
ACYL-COA SYNTHETASE; DIET-INDUCED OBESITY; ICHTHYOSIS PREMATURITY SYNDROME; MICROVESSEL ENDOTHELIAL-CELLS; HEPATIC LIPID HOMEOSTASIS; RETINOID VISUAL CYCLE; WORKING RAT-HEART; CAENORHABDITIS-ELEGANS; SACCHAROMYCES-CEREVISIAE; FATP4;
D O I
10.1016/j.plipres.2015.08.001
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
The dysregulation of lipid metabolism has been implicated in various diseases, including diabetes, cardiopathies, dermopathies, retinal and neurodegenerative diseases. Mouse models have provided insights into lipid metabolism. However, progress in the understanding of these pathologies is hampered by the multiplicity of essential cellular processes and genes that modulate lipid metabolism. Drosophila and Caenorhabditis elegans have emerged as simple genetic models to improve our understanding of these metabolic diseases. Recent studies have characterized fatty acid transport protein (fatp) mutants in Drosophila and C elegans, establishing new models of cardiomyopathy, retinal degeneration, fat storage disease and dermopathies. These models have generated novel insights into the physiological role of the Fatp protein family in vivo in multicellular organisms, and are likely to contribute substantially to progress in understanding the etiology of various metabolic disorders. Here, we describe and discuss the mechanisms underlying invertebrate fatp mutant models in the light of the current knowledge relating to FATPs and lipid disorders in vertebrates. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:30 / 40
页数:11
相关论文
共 137 条
[1]   Ceramidase expression facilitates membrane turnover a and endocytosis of rhodopsin in photoreceptors [J].
Acharya, U ;
Mowen, MB ;
Nagashima, K ;
Acharya, JK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (07) :1922-1926
[2]   Modulating sphingolipid biosynthetic pathway rescues photoreceptor degeneration [J].
Acharya, U ;
Patel, S ;
Koundakjian, E ;
Nagashima, K ;
Han, X ;
Acharya, JK .
SCIENCE, 2003, 299 (5613) :1740-1743
[3]   An update on molecular aspects of the non-syndromic ichthyoses [J].
Akiyama, Masashi ;
Shimizu, Hiroshi .
EXPERIMENTAL DERMATOLOGY, 2008, 17 (05) :373-382
[4]   SLC27 fatty acid transport proteins [J].
Anderson, Courtney M. ;
Stahl, Andreas .
MOLECULAR ASPECTS OF MEDICINE, 2013, 34 (2-3) :516-528
[5]   A Promoter Polymorphism in the Liver-specific Fatty Acid Transport Protein 5 is Associated with Features of the Metabolic Syndrome and Steatosis [J].
Auinger, A. ;
Valenti, L. ;
Pfeuffer, M. ;
Helwig, U. ;
Herrmann, J. ;
Fracanzani, A. L. ;
Dongiovanni, P. ;
Fargion, S. ;
Schrezenmeir, J. ;
Rubin, D. .
HORMONE AND METABOLIC RESEARCH, 2010, 42 (12) :854-859
[6]   Drosophila insulin-like peptide-6 (dilp6) expression from fat body extends lifespan and represses secretion of Drosophila insulin-like peptide-2 from the brain [J].
Bai, Hua ;
Kang, Ping ;
Tatar, Marc .
AGING CELL, 2012, 11 (06) :978-985
[7]   Diabetic larvae and obese flies -: Emerging studies of metabolism in Drosophila [J].
Baker, Keith D. ;
Thummel, Carl S. .
CELL METABOLISM, 2007, 6 (04) :257-266
[8]   Cellular and molecular events mediated by docosahexaenoic acid-derived neuroprotectin D1 signaling in photoreceptor cell survival and brain protection [J].
Bazan, Nicolas G. .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2009, 81 (2-3) :205-211
[9]   Dietary composition regulates Drosophila mobility and cardiac physiology [J].
Bazzell, Brian ;
Ginzberg, Sara ;
Healy, Lindsey ;
Wessells, R. J. .
JOURNAL OF EXPERIMENTAL BIOLOGY, 2013, 216 (05) :859-868
[10]   High-Fat-Diet-Induced Obesity and Heart Dysfunction Are Regulated by the TOR Pathway in Drosophila [J].
Birse, Ryan T. ;
Choi, Joan ;
Reardon, Kathryn ;
Rodriguez, Jessica ;
Graham, Suzanne ;
Diop, Soda ;
Ocorr, Karen ;
Bodmer, Rolf ;
Oldham, Sean .
CELL METABOLISM, 2010, 12 (05) :533-544