Effects of obesity and weight loss on the expression of proteins involved in fatty acid metabolism in human adipose tissue

被引:32
作者
Fisher, RM [1 ]
Hoffstedt, J
Hotamisligil, GS
Thörne, A
Rydén, M
机构
[1] Karolinska Hosp, King Gustaf V Res Inst, Atherosclerosis Res Unit, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, Huddinge Univ Hosp, Dept Med, Stockholm, Sweden
[3] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA USA
[4] Huddinge Univ Hosp, Karolinska Inst, Dept Surg, Stockholm, Sweden
基金
美国国家卫生研究院;
关键词
adipocyte lipid binding protein; keratinocyte lipid binding protein; fatty acid translocase; adipose tissue; obesity;
D O I
10.1038/sj.ijo.0802110
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE: Disturbances in adipocyte lipolysis in obesity may contribute to elevated circulating non-esterified fatty acid (NEFA) concentrations and insulin resistance. In experimental models, NEFA metabolism is influenced by adipocyte proteins such as adipocyte and keratinocyte lipid binding proteins (aP2/ALBP and mall/KLBP) and fatty acid translocase (CD36). We investigated the effect of obesity and weight loss on the expression of these proteins in human subcutaneous adipose tissue. STUDY DESIGN AND SUBJECTS: Subcutaneous adipose tissue was obtained from 12 obese (body mass index (BMI) 42.4 +/- 1.6 kg/m(2)) and 12 lean (23.4 +/- 0.6 kg/m(2)) subjects. The obese subjects underwent gastric banding and biopsies were taken again after 2 y following a significant weight reduction (BMI 32.8 +/- 1.4 kg/m(2)). Adipose tissue proteins were quantified by Western blotting. RESULTS: Differential expression of ALBP, KLBP and CD36 was observed in lean and weight-reduced subjects compared with obese individuals. This resulted in a significantly lower ALBP/KLBP ratio in lean and weight-reduced individuals compared to obese subjects. Furthermore there was a significant influence of gender on this ratio. Moreover, the commonly used internal standard protein actin was expressed significantly higher in lean compared to obese individuals. CONCLUSION: The relative content of ALBP and KLBP in human adipose tissue changes with obesity, weight loss and gender indicating differential regulation. Differing responses in the expression patterns of adipose tissue proteins capable of binding NEFAs in response to weight changes suggest a potential importance in the development of obesity-associated complications.
引用
收藏
页码:1379 / 1385
页数:7
相关论文
共 28 条
[1]   Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats [J].
Aitman, TJ ;
Glazier, AM ;
Wallace, CA ;
Cooper, LD ;
Norsworthy, PJ ;
Wahid, FN ;
Al-Majali, KM ;
Trembling, PM ;
Mann, CJ ;
Shoulders, CC ;
Graf, D ;
St Lezin, E ;
Kurtz, TW ;
Kren, V ;
Pravenec, M ;
Ibrahimi, A ;
Abumrad, NA ;
Stanton, LW ;
Scott, J .
NATURE GENETICS, 1999, 21 (01) :76-83
[2]  
ARNER P, 1991, J LIPID RES, V32, P423
[3]  
ARNER P, 1995, INT J OBESITY, V19, P435
[4]   Hunting for human obesity genes? Look in the adipose tissue! [J].
Arner, P .
INTERNATIONAL JOURNAL OF OBESITY, 2000, 24 (Suppl 4) :S57-S62
[5]  
ARNER P, 1996, DIABETES REV, V4, P450
[6]   Role of fatty acids in the pathogenesis of insulin resistance and NIDDM [J].
Boden, G .
DIABETES, 1997, 46 (01) :3-10
[7]   Defective uptake and utilization of long chain fatty acids in muscle and adipose tissues of CD36 knockout mice [J].
Coburn, CT ;
Knapp, FF ;
Febbraio, M ;
Beets, AL ;
Silverstein, RL ;
Abumrad, NA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (42) :32523-32529
[8]  
Coe NR, 1999, J LIPID RES, V40, P967
[9]   Physiological properties and functions of intracellular fatty acid-binding proteins [J].
Coe, NR ;
Bernlohr, DA .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1998, 1391 (03) :287-306
[10]  
Elizalde M, 2000, J LIPID RES, V41, P1244