Effects of rosightazone and high fat diet on lipase/esterase expression in adipose tissue

被引:36
作者
Shen, Wen-Jun [1 ]
Patel, Shailja
Yu, Zaixin
Jue, Dyron
Kraemer, Fredric B.
机构
[1] Stanford Univ, Div Endocrinol, Palo Alto, CA 94304 USA
[2] VA Palo Alto Hlth Care Syst, Palo Alto, CA 94304 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2007年 / 1771卷 / 02期
关键词
lipase; esterase; rosiglitazone; high fat diet;
D O I
10.1016/j.bbalip.2006.11.009
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 number of intracellular lipase/esterase have been reported in adipose tissue either by functional assays of activity or through proteomic analysis. In the current work, we have studied the relative expression level of 12 members of the lipase/esterase family that are found in white adipose tissue. We found that the relative mRNA levels of ATGL and HSL are the most abundant, being 2-3 fold greater than TGH or ADPN; whereas other intracellular neutral lipase/esterases were expressed at substantially lower levels. High fat feeding did not alter the mRNA expression levels of most lipase/esterases, but did reduce CGI-58 and WBSCR21. Likewise, rosiglitazone treatment did not alter the mRNA expression levels of most lipase/esterases, but did increase ATGL, TGH, CGI-58 and WBSCR21, while reducing ADPN. WAT from HSL-/- mice showed no compensatory increase in any lipase/esterases, rather mRNA levels of most lipase/esterases were reduced. In contrast, BAT from HSL-/- mice showed an increase in ATGL expression, as well as a decrease in ES-1, APEH and WBSCR21. Analysis of the immunoreactive protein levels of some of the lipases confirmed the results seen with mRNA. In conclusion, these data highlight the complexity of the regulation of the expression of intracellular neutral lipase/esterases involved in lipolysis. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
相关论文
共 46 条
[1]   Adiponutrin, a transmembrane protein corresponding to a novel dietary- and obesity-linked mRNA specifically expressed in the adipose lineage [J].
Baulande, S ;
Lasnier, F ;
Lucas, M ;
Pairault, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (36) :33336-33344
[2]   The lipolytic proteome of mouse adipose tissue [J].
Birner-Gruenberger, R ;
Susani-Etzerodt, H ;
Waldhuber, M ;
Riesenhuber, G ;
Schmidinger, H ;
Rechberger, G ;
Kollroser, M ;
Strauss, JG ;
Lass, A ;
Zimmermann, R ;
Haemmerle, G ;
Zechner, R ;
Hermetter, A .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (11) :1710-1717
[3]   Translocation of hormone-sensitive lipase and perilipin upon lipolytic stimulation of rat adipocytes [J].
Clifford, GM ;
Londos, C ;
Kraemer, FB ;
Vernon, RG ;
Yeaman, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (07) :5011-5015
[4]   Adipose tissue expression of the lipid droplet-associating proteins S3-12 and perilipin is controlled by peroxisome proliferator-activated receptor-γ [J].
Dalen, KT ;
Schoonjans, K ;
Ulven, SM ;
Weedon-Fekjaer, MS ;
Bentzen, TG ;
Koutnikova, H ;
Auwerx, J ;
Nebbl, HI .
DIABETES, 2004, 53 (05) :1243-1252
[5]   Effects of pioglitazone on adipose tissue remodeling within the setting of obesity and insulin resistance [J].
de Souza, CJ ;
Eckhardt, M ;
Gagen, K ;
Dong, M ;
Chen, W ;
Laurent, D ;
Burkey, BF .
DIABETES, 2001, 50 (08) :1863-1871
[6]   Peroxisome proliferator-activated receptor-γ transcriptionally up-regulates hormone-sensitive lipase via the involvement of specificity protein-1 [J].
Deng, T ;
Shan, S ;
Li, PP ;
Shen, ZF ;
Lu, XP ;
Cheng, J ;
Ning, ZQ .
ENDOCRINOLOGY, 2006, 147 (02) :875-884
[7]   Triacylglycerol hydrolase: role in intracellular lipid metabolism [J].
Dolinsky, VW ;
Gilham, D ;
Alam, M ;
Vance, DE ;
Lehner, R .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (13) :1633-1651
[8]   Regulation of triacylglycerol hydrolase expression by dietary fatty acids and peroxisomal proliferator-activated receptors [J].
Dolinsky, VW ;
Gilham, D ;
Hatch, GM ;
Agellon, LB ;
Lehner, R ;
Vance, DE .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2003, 1635 (01) :20-28
[9]   The cloning and expression of a murine triacylglycerol hydrolase cDNA and the structure of its corresponding gene [J].
Dolinsky, VW ;
Sipione, S ;
Lehner, R ;
Vance, DE .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2001, 1532 (03) :162-172
[10]  
Dumasia Rupal, 2005, Current Drug Targets - Cardiovascular & Haematological Disorders, V5, P377, DOI 10.2174/156800605774370362