Uncoupling proteins 2 and 3 - Potential regulators of mitochondrial energy metabolism

被引:362
作者
Boss, O [1 ]
Hagen, T [1 ]
Lowell, BB [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Harvard Med Sch, Div Endocrinol, Dept Med, Boston, MA 02215 USA
关键词
D O I
10.2337/diabetes.49.2.143
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mitochondria use energy derived from fuel combustion to create a proton electrochemical gradient across the mitochondrial inner membrane. This intermediate form of energy is then used by ATP synthase to synthesize ATP Uncoupling protein-1 (UCP1) is a brown fat-specific mitochondrial inner membrane protein with proton transport activity. UCP1 catalyzes a highly regulated proton leak, converting energy stored within the mitochondrial proton electrochemical potential gradient to heat. This uncouples fuel oxidation from conversion of ADP to ATP. In rodents, UCP1 activity and brown fat contribute importantly to whole-body energy expenditure. Recently, two additional mitochondrial carriers with high similarity to UCP1 were molecularly cloned. In contrast to UCP1, UCP1 is expressed widely, and UCP3 is expressed preferentially in skeletal muscle. Biochemical studies indicate that UCP2 and UCP3, like UCP1, have uncoupling activity. While UCP1 is known to play an important role in regulating heat production during cold exposure, the biological functions of UCP2 and UCP3 are unknown. Possible functions include 1) control of adaptive thermogenesis in response to cold exposure and diet, 2) control of reactive oxygen species production by mitochondria, 3) regulation of ATP synthesis, and 4) regulation of fatty acid oxidation. This article will survey present knowledge regarding UCP1, UCP2, and UCP3, and review proposed functions for the two new uncoupling proteins.
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页码:143 / 156
页数:14
相关论文
共 182 条
[51]  
Fumeron F, 1996, INT J OBESITY, V20, P1051
[52]   The mechanism of proton transport mediated by mitochondrial uncoupling proteins [J].
Garlid, KD ;
Jaburek, M ;
Jezek, P .
FEBS LETTERS, 1998, 438 (1-2) :10-14
[53]   On the mechanism of fatty acid-induced proton transport by mitochondrial uncoupling protein [J].
Garlid, KD ;
Orosz, DE ;
Modriansky, M ;
Vassanelli, S ;
Jezek, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (05) :2615-2620
[54]   Cloning and characterization of an uncoupling protein homolog - A potential molecular mediator of human thermogenesis [J].
Gimeno, RE ;
Dembski, M ;
Weng, X ;
Deng, NH ;
Shyjan, AW ;
Gimeno, CJ ;
Iris, F ;
Ellis, SJ ;
Woolf, EA ;
Tartaglia, LA .
DIABETES, 1997, 46 (05) :900-906
[55]   Leptin, but not a β3-adrenergic agonist, upregulates muscle uncoupling protein-3 messenger RNA expression:: short-term thermogenic interactions [J].
Gómez-Ambrosi, J ;
Frühbeck, G ;
Martínez, JA .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (6-7) :992-997
[56]   Uncoupling protein-3 is a mediator of thermogenesis regulated by thyroid hormone, beta 3-adrenergic agonists, and leptin [J].
Gong, DW ;
He, YF ;
Karas, M ;
Reitman, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (39) :24129-24132
[57]   The uncoupling protein UCP1 does not increase the proton conductance of the inner mitochondrial membrane by functioning as a fatty acid anion transporter [J].
Gonzalez-Barroso, MM ;
Fleury, C ;
Bouillaud, F ;
Nicholls, DG ;
Rial, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) :15528-15532
[58]   Assessment of uncoupling activity of the human uncoupling protein 3 short form and three mutants of the uncoupling protein gene using a yeast heterologous expression system [J].
Hagen, T ;
Zhang, CY ;
Slieker, LJ ;
Chung, WK ;
Leibel, RL ;
Lowell, BB .
FEBS LETTERS, 1999, 454 (03) :201-206
[59]   WEIGHT-REDUCING EFFECTS OF THE PLASMA-PROTEIN ENCODED BY THE OBESE GENE [J].
HALAAS, JL ;
GAJIWALA, KS ;
MAFFEI, M ;
COHEN, SL ;
CHAIT, BT ;
RABINOWITZ, D ;
LALLONE, RL ;
BURLEY, SK ;
FRIEDMAN, JM .
SCIENCE, 1995, 269 (5223) :543-546
[60]   Role of the sympathetic nervous system and insulin in enhancing glucose uptake in peripheral tissues after intrahypothalamic injection of leptin in rats [J].
Haque, MS ;
Minokoshi, Y ;
Hamai, M ;
Iwai, M ;
Horiuchi, M ;
Shimazu, T .
DIABETES, 1999, 48 (09) :1706-1712