Conjugated linoleic acid supplementation caused reduction of perilipin1 and aberrant lipolysis in epididymal adipose tissue

被引:14
作者
Cai, Demin [2 ]
Li, Hongji [1 ]
Zhou, Bo [2 ]
Han, Liqiang [1 ]
Zhang, Xiaomei [2 ]
Yang, Guoyu [1 ]
Yang, Guoqing [2 ]
机构
[1] Henan Agr Univ, Minist Agr, Key Lab Anim Biochem & Nutr, Zhengzhou 450002, Henan Province, Peoples R China
[2] Henan Agr Univ, Coll Anim Sci & Vet Med, Zhengzhou 450002, Henan Province, Peoples R China
关键词
Conjugated linoleic acids; Perilipin1; expression; promoter; Lipolysis; ACTIVATED RECEPTOR-GAMMA; 3T3-L1; ADIPOCYTES; LIPID-METABOLISM; TNF-ALPHA; MICE; LIPODYSTROPHY; TRANS-10; ISOMER; GENE; MECHANISMS;
D O I
10.1016/j.bbrc.2012.05.038
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
Perilipin1, a coat protein of lipid droplet, plays a key role in adipocyte lipolysis and fat formation of adipose tissues. However, it is not clear how the expression of perilipin1 is affected in the decreased white adipose tissues (WAT) of mice treated with dietary supplement of conjugated linoleic acids (CLA). Here we obtained lipodystrophic mice by dietary administration of CLA which exhibited reduced epididymal (EPI) WAT, aberrant adipocytes and decreased expression of leptin in this tissue. We found both transcription and translation of perilipin1 was suppressed significantly in EPI WAT of CLA-treated mice compared to that of control mice. The gene expression of negative regulator tumor necrosis factor alpha (TNF alpha) and the positive regulator Peroxisome Proliferator-Activated Receptor-gamma (PPAR gamma) of perilipin1 was up-regulated and down-regulated, respectively. In cultured 3T3-L1 cells the promoter activity of perilipin1 was dramatically inhibited in the presence of CLA. Using ex vivo experiment we found that the basal lipolysis was elevated but the hormone-stimulated lipolysis blunted in adipose explants of CLA-treated mice compared to that of control mice, suggesting that the reduction of perilipin1 in white adipose tissues may at least in part contribute to CLA-mediated alternation of lipolysis of WAT. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:621 / 626
页数:6
相关论文
共 26 条
[1]   Perilipin, a critical regulator of fat storage and breakdown, is a target gene of estrogen receptor-related receptor α [J].
Akter, Mst. Hasina ;
Yamaguchi, Tomohiro ;
Hirose, Fumiko ;
Osumi, Takashi .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 368 (03) :563-568
[2]  
[Anonymous], FEBS LETT
[3]   The peroxisome proliferator-activated receptor γ regulates expression of the perilipin gene in adipocytes [J].
Arimura, N ;
Horiba, T ;
Imagawa, M ;
Shimizu, M ;
Sato, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) :10070-10076
[4]   Dietary conjugated linoleic acid in health: Physiological effects and mechanisms of action [J].
Belury, MA .
ANNUAL REVIEW OF NUTRITION, 2002, 22 :505-531
[5]   Biological effects of conjugated linoleic acids in health and disease [J].
Bhattacharya, Arunabh ;
Banu, Jameela ;
Rahman, Mizanur ;
Causey, Jennifer ;
Fernandes, Gabriel .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2006, 17 (12) :789-810
[6]   The perilipin family of structural lipid droplet proteins: stabilization of lipid droplets and control of lipolysis [J].
Brasaemle, Dawn L. .
JOURNAL OF LIPID RESEARCH, 2007, 48 (12) :2547-2559
[7]   Isomer-specific regulation of metabolism and PPARγ signaling by CLA in human preadipocytes [J].
Brown, JM ;
Boysen, MS ;
Jensen, SS ;
Morrison, RF ;
Storkson, J ;
Lea-Currie, R ;
Pariza, M ;
Mandrup, S ;
McIntosh, MK .
JOURNAL OF LIPID RESEARCH, 2003, 44 (07) :1287-1300
[8]   Trans-10,cis-12 CLA increases adipocyte lipolysis and alters lipid droplet-associated proteins:: role of mTOR and ERK signaling [J].
Chung, SY ;
Brown, JM ;
Sandberg, MB ;
McIntosh, M .
JOURNAL OF LIPID RESEARCH, 2005, 46 (05) :885-895
[9]   ANTICARCINOGENS FROM FRIED GROUND-BEEF - HEAT-ALTERED DERIVATIVES OF LINOLEIC-ACID [J].
HA, YL ;
GRIMM, NK ;
PARIZA, MW .
CARCINOGENESIS, 1987, 8 (12) :1881-1887
[10]   Adipose depletion and apoptosis induced by trans-10, cis-12 conjugated linoleic acid in mice [J].
Hargrave, KM ;
Li, CL ;
Meyer, BJ ;
Kachman, SD ;
Hartzell, DL ;
Della-Fera, MA ;
Miner, JL ;
Baile, CA .
OBESITY RESEARCH, 2002, 10 (12) :1284-1290