Quantitative expression patterns of peroxisome proliferator-activated receptor-β/δ (PPARβ/δ) protein in mice

被引:134
作者
Girroir, Elizabeth E. [1 ]
Hollingshead, Holly E. [1 ,2 ]
He, Pengfei [1 ]
Zhu, Bokai [1 ]
Perdew, Gary H. [1 ]
Peters, Jeffrey M. [1 ,2 ]
机构
[1] Penn State Univ, Ctr Mol Toxicol & Carcinogenesis, Dept Vet & Biomed Sci, University Pk, PA 16802 USA
[2] Penn State Univ, Grad Program Biochem Microbiol & Mol biol, University Pk, PA 16802 USA
关键词
peroxisome proliferator-activated receptor beta/delta; antibody; expression; biochemistry;
D O I
10.1016/j.bbrc.2008.04.086
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The expression patterns of PPAR beta/delta have been described, but the majority of these data are based on mRNA data. To date, there are no reports that have quantitatively examined the expression of PPAR beta/delta protein in mouse tissues. In the present study, a highly specific PPAR beta/delta antibody was developed, characterized, and used to examine tissue expression patterns of PPAR beta/delta. As compared to commercially available anti-PPAR beta/delta antibodies, one of six polyclonal anti-PPAR beta/delta antibodies developed was significantly more effective for immunoprecipitation of in vitro-translated PPAR beta/delta. This antibody was used for quantitative Western blot analysis using radioactive detection methods. Expression of PPAR beta/delta was highest in colon, small intestine, liver, and keratinocytes as compared to other tissues including heart, spleen, skeletal muscle, lung, brain, and thymus. Interestingly, PPAR beta/delta expression was localized in the nucleus and RXR alpha can be co-immunoprecipitated with nuclear PPAR beta/delta. Results from these studies demonstrate that PPAR beta/delta expression is highest in intestinal epithelium, liver, and keratinocytes, consistent with significant biological roles in these tissues. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:456 / 461
页数:6
相关论文
共 17 条
[1]
Differential expression of peroxisome proliferator-activated receptor-α, -β, and -γ during rat embryonic development [J].
Braissant, O ;
Wahli, W .
ENDOCRINOLOGY, 1998, 139 (06) :2748-2754
[2]
Differential expression of peroxisome proliferator-activated receptors (PPARs): Tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat [J].
Braissant, O ;
Foufelle, F ;
Scotto, C ;
Dauca, M ;
Wahli, W .
ENDOCRINOLOGY, 1996, 137 (01) :354-366
[3]
The role of peroxisome proliferator-activated receptor-β/δ in epithelial cell growth and differentiation [J].
Burdick, AD ;
Kim, DJ ;
Peraza, MA ;
Gonzalez, FJ ;
Peters, JM .
CELLULAR SIGNALLING, 2006, 18 (01) :9-20
[4]
Rat PPARs: Quantitative analysis in adult rat tissues and regulation in fasting and refeeding [J].
Escher, P ;
Braissant, O ;
Basu-Modak, S ;
Michalik, L ;
Wahli, W ;
Desvergne, B .
ENDOCRINOLOGY, 2001, 142 (10) :4195-4202
[5]
Reevaluation of the PPAR-β/δ ligand binding domain model reveals why it exhibits the activated form [J].
Fyffe, SA ;
Alphey, MS ;
Buetow, L ;
Smith, TK ;
Ferguson, MAJ ;
Sorensen, MD ;
Björkling, F ;
Hunter, WN .
MOLECULAR CELL, 2006, 21 (01) :1-2
[6]
Regulatory functions of PPARβ in metabolism:: Implications for the treatment of metabolic syndrome [J].
Grimaldi, Paul A. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2007, 1771 (08) :983-990
[7]
Corepressors selectively control the transcriptional activity of PPARγ in adipocytes [J].
Guan, HP ;
Ishizuka, T ;
Chui, PC ;
Lehrke, M ;
Lazar, MA .
GENES & DEVELOPMENT, 2005, 19 (04) :453-461
[8]
HIGASHIYAMA H, 2007, CELL BIOL, V127, P485
[9]
CHROMOSOMAL LOCALIZATION, INDUCIBILITY, TISSUE-SPECIFIC EXPRESSION AND STRAIN DIFFERENCES IN 3 MURINE PEROXISOME-PROLIFERATOR-ACTIVATED-RECEPTOR GENES [J].
JONES, PS ;
SAVORY, R ;
BARRATT, P ;
BELL, AR ;
GRAY, TJB ;
JENKINS, NA ;
GILBERT, DJ ;
COPELAND, NG ;
BELL, DR .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 233 (01) :219-226
[10]
Peroxisome proliferator-activated receptor-β/δ inhibits epidermal cell proliferation by down-regulation of kinase activity [J].
Kim, DJ ;
Murray, IA ;
Burns, AM ;
Gonzalez, FJ ;
Perdew, GH ;
Peters, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (10) :9519-9527