Emergence of brown adipocytes in white fat in mice is under genetic control - Effects on body weight and adiposity

被引:523
作者
Guerra, C [1 ]
Koza, RA [1 ]
Yamashita, H [1 ]
Walsh, K [1 ]
Kozak, LP [1 ]
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
mitochondrial uncoupling protein; recombinant inbred strains; beta 3-adrenergic agonist; cold exposure; obesity;
D O I
10.1172/JCI3155
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The mRNA levels for the mitochondrial uncoupling protein (UCP1) in fat tissues of A/J and C57BL/6J inbred strains of mice varied in a regional-specific manner after stimulation of adrenergic signaling by cold exposure or treatment with a beta 3-adrenergic agonist, While the differences between strains were minimal in interscapular brown fat, large differences occurred in white fat tissues, particularly in retroperitoneal fat. Among the AXE recombinant inbred strains, the Ucp1 mRNA levels varied up to 130-fold. This large induction at the mRNA level was accompanied by a corresponding increase in brown adipocytes as revealed by immunohistology with anti-UCP1 antibodies. A high capacity to induce brown fat in areas of traditional white fat had no impact on the ability to gain weight in response to high fat and sucrose diets, but did correlate with the loss of weight in response to treatment with a beta 3-adrenergic agonist (CL 316,243), This genetic variation in mice provides an experimental approach to identify genes controlling the induction of brown adipocytes in white fat tissues.
引用
收藏
页码:412 / 420
页数:9
相关论文
共 39 条
[31]   Transgenic mice overexpressing the beta 1-adrenergic receptor in adipose tissue are resistant to obesity [J].
Soloveva, V ;
Graves, RA ;
Rasenick, MM ;
Spiegelman, BM ;
Ross, SR .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (01) :27-38
[32]   CONTROL OF EXPRESSION OF INSULIN RESISTANCE AND HYPERGLYCEMIA BY DIFFERENT GENETIC-FACTORS IN DIABETIC C57BL/6J MICE [J].
SURWIT, RS ;
SELDIN, MF ;
KUHN, CM ;
COCHRANE, C ;
FEINGLOS, MN .
DIABETES, 1991, 40 (01) :82-87
[33]   DIET-INDUCED TYPE-II DIABETES IN C57BL/6J MICE [J].
SURWIT, RS ;
KUHN, CM ;
COCHRANE, C ;
MCCUBBIN, JA ;
FEINGLOS, MN .
DIABETES, 1988, 37 (09) :1163-1167
[34]   TARGETED DISRUPTION OF THE BETA(3)-ADRENERGIC RECEPTOR GENE [J].
SUSULIC, VS ;
FREDERICH, RC ;
LAWITTS, J ;
TOZZO, E ;
KAHN, BB ;
HARPER, ME ;
HIMMSHAGEN, J ;
FLIER, JS ;
LOWELL, BB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29483-29492
[35]   Activation of the nuclear receptor peroxisome proliferator-activated gamma promotes brown adipocyte differentiation [J].
Tai, TAC ;
Jennermann, C ;
Brown, KK ;
Oliver, BB ;
MacGinnitie, MA ;
Wilkison, WO ;
Brown, HR ;
Lehmann, JM ;
Kliewer, SA ;
Morris, DC ;
Graves, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) :29909-29914
[36]  
Taylor B. A., 1981, Genetic variants and strains of the laboratory mouse., P397
[37]   Thermoregulatory and metabolic phenotypes of mice lacking noradrenaline and adrenaline [J].
Thomas, SA ;
Palmiter, RD .
NATURE, 1997, 387 (6628) :94-97
[38]   UCP3: An uncoupling protein homologue expressed preferentially and abundantly in skeletal muscle and brown adipose tissue [J].
VidalPuig, A ;
Solanes, G ;
Grujic, D ;
Flier, JS ;
Lowell, BB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 235 (01) :79-82
[39]   BROWN ADIPOSE-TISSUE IN THE PARAMETRIAL FAT PAD OF THE MOUSE [J].
YOUNG, P ;
ARCH, JRS ;
ASHWELL, M .
FEBS LETTERS, 1984, 167 (01) :10-14