Zinc-transporter genes in human visceral and subcutaneous adipocytes: Lean versus obese

被引:71
作者
Smidt, Kamille
Pedersen, Steen B.
Brock, Birgitte
Schmitz, Ole
Fisker, Sanne
Bendix, Jorgen
Wogensen, Lise
Rungby, Jorgen
机构
[1] Aarhus Univ Hosp, Dept Endocrinol C, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Endocrinol M, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ Hosp, Dept Surg L, DK-8000 Aarhus C, Denmark
[4] Aarhus Univ Hosp, NBG, Res Lab Biochem Pathol, DK-8000 Aarhus C, Denmark
[5] Aarhus Univ, Dept Pharmacol, DK-8000 Aarhus C, Denmark
关键词
zinc; zinc-transporters; adipocytes; obesity;
D O I
10.1016/j.mce.2006.10.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Zinc ions influence adipose tissue metabolism by regulating leptin secretion and by promoting free fatty acid release and glucose uptake. The mechanisms controlling zinc metabolism in adipose tissue are unknown. We therefore examined the gene-expression levels of a number of zinc-transporting proteins in adipose tissue, comparing subcutaneous fat with visceral fat from lean and obese humans. Both ZnT-proteins responsible for zinc transport from cytosol to extracellular compartments and intracellular vesicles and Zip-proteins responsible for zinc transport to the cytoplasm were expressed in all samples. This suggests that zinc metabolism in adipocytes is actively controlled by zinc-transporters. The expression levels were different in lean and obese subjects suggesting a role for these proteins in obesity. Furthermore, the expression levels were different from subcutaneous fat to intra-abdominal fat suggesting that the metabolic activity in adipocytes is to some extent dependent upon zinc and the activity of zinc-transporting proteins or vice versa. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:68 / 73
页数:6
相关论文
共 28 条
[1]   Chronic treatment with 5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside increases insulin-stimulated glucose uptake and GLUT4 translocation in rat skeletal muscles in a fiber type-specific manner [J].
Buhl, ES ;
Jessen, N ;
Schmitz, O ;
Pedersen, SB ;
Pedersen, O ;
Holman, GD ;
Lund, S .
DIABETES, 2001, 50 (01) :12-17
[2]   Zinc status in plasma of obese individuals during glucose administration [J].
Chen, MD ;
Lin, PY ;
Sheu, WHH .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1997, 60 (1-2) :123-129
[3]   ZINC IN HAIR AND SERUM OF OBESE INDIVIDUALS IN TAIWAN [J].
CHEN, MD ;
LIN, PY ;
LIN, WH ;
CHENG, V .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1988, 48 (05) :1307-1309
[4]   Zinc may be a mediator of leptin production in humans [J].
Chen, MD ;
Song, YM ;
Lin, PY .
LIFE SCIENCES, 2000, 66 (22) :2143-2149
[5]   Identification and cloning of a β-cell-specific zinc transporter, ZnT-8, localized into insulin secretory granules [J].
Chimienti, F ;
Devergnas, S ;
Favier, A ;
Seve, M .
DIABETES, 2004, 53 (09) :2330-2337
[6]   Elimination of zinc from synaptic vesicles in the intact mouse brain by disruption of the ZnT3 gene [J].
Cole, TB ;
Wenzel, HJ ;
Kafer, KE ;
Schwartzkroin, PA ;
Palmiter, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1716-1721
[7]   INSULIN-LIKE EFFECT OF ZINC ON ADIPOCYTES [J].
COULSTON, L ;
DANDONA, P .
DIABETES, 1980, 29 (08) :665-667
[8]   Differential responses of visceral and subcutaneous fat depots to nutrients [J].
Einstein, FH ;
Atzmon, G ;
Yang, XM ;
Ma, XH ;
Rincon, M ;
Rudin, E ;
Muzumdar, R ;
Barzilai, N .
DIABETES, 2005, 54 (03) :672-678
[9]   Functional characterization of a novel mammalian zinc transporter, ZnT6 [J].
Huang, LP ;
Kirschke, CP ;
Gitschier, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (29) :26389-26395
[10]   A novel gene involved in zinc transport is deficient in the lethal milk mouse [J].
Huang, LP ;
Gitschier, J .
NATURE GENETICS, 1997, 17 (03) :292-297