Fatty acids do not activate UCP2 in pancreatic beta cells: comparison with UCP1

被引:14
|
作者
Galetti, Sandrine [1 ]
Sarre, Alexandre [1 ]
Perreten, Helene [1 ]
Produit-Zengaffinen, Nathalie [1 ]
Muzzin, Patrick [1 ]
Assimacopoulos-Jeannet, Francoise [1 ]
机构
[1] Univ Geneva, Fac Med, Dept Cell Physiol & Metab, CH-1211 Geneva 4, Switzerland
来源
基金
瑞士国家科学基金会;
关键词
UCP2; UCP1; INS-1; cells; Fatty acid-induced uncoupling; Mitochondria; STIMULATED INSULIN-SECRETION; MITOCHONDRIAL UNCOUPLING PROTEINS; PROTON LEAK; OXIDATIVE-PHOSPHORYLATION; NITRIC-OXIDE; HIGH GLUCOSE; OVEREXPRESSION; EXPRESSION; INDUCTION; THERMOGENESIS;
D O I
10.1007/s00424-008-0548-8
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
UCP2 is expressed in pancreatic beta cells where its postulated uncoupling activity will modulate glucose-induced changes in ATP/ADP ratio and insulin secretion. The consequences of UCP2 over/underexpression on beta-cell function has mainly been studied in the basal state; however, a UCP has no uncoupling activity unless stimulated by fatty acids and/or reactive oxygen species. Here, UCP2 was overexpressed in INS-1 cells and parameters reflecting mitochondrial coupling measured in the basal state and after stimulation by fatty acids. For comparison, UCP1 was expressed to similar levels and the same parameters measured. Neither UCP1 expression nor UCP2 overexpression modified basal or glucose-stimulated metabolic changes. Upon addition of fatty acids, UCP1-expressing cells displayed the expected mitochondrial uncoupling effect, while UCP2 did not elicit any measurable change in mitochondrial function. Taken together, our data demonstrate that, in pancreatic beta-cells, UCP2 has no uncoupling activity in the basal state or after fatty acid stimulation.
引用
收藏
页码:931 / 940
页数:10
相关论文
共 50 条
  • [1] Fatty acids do not activate UCP2 in pancreatic beta cells: comparison with UCP1
    Sandrine Galetti
    Alexandre Sarre
    Hélène Perreten
    Nathalie Produit-Zengaffinen
    Patrick Muzzin
    Françoise Assimacopoulos-Jeannet
    Pflügers Archiv - European Journal of Physiology, 2009, 457
  • [2] Retinoids activate proton transport by the uncoupling proteins UCP1 and UCP2
    Rial, E
    González-Barroso, M
    Fleury, C
    Iturrizaga, S
    Sanchis, D
    Jiménez-Jiménez, J
    Ricquier, D
    Goubern, M
    Bouillaud, F
    EMBO JOURNAL, 1999, 18 (21): : 5827 - 5833
  • [3] UCP1, UCP2 and UCP3: Are they true uncouplers of respiration?
    F Bouillaud
    International Journal of Obesity, 1999, 23 : S19 - S23
  • [4] UCP1, UCP2 and UCP3: Are they true uncouplers of respiration?
    Bouillaud, F
    INTERNATIONAL JOURNAL OF OBESITY, 1999, 23 (Suppl 6) : S19 - S23
  • [5] Thermogenic responses in brown fat cells are fully UCP1-dependent - UCP2 or UCP3 do not substitute for UCP1 in adrenergically or fatty acid-induced thermogenesis
    Matthias, A
    Ohlson, KBE
    Fredriksson, JM
    Jacobsson, A
    Nedergaard, J
    Cannon, B
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (33) : 25073 - 25081
  • [6] The uncoupling protein homologues: UCP1, UCP2, UCP3, StUCP and AtUCP
    Ricquier, D
    Bouillaud, F
    BIOCHEMICAL JOURNAL, 2000, 345 : 161 - 179
  • [7] Structure-function relationships in UCP1, UCP2 and chimeras - EPR analysis and retinoic acid activation of UCP2
    Chomiki, N
    Voss, JC
    Warden, CH
    EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (04): : 903 - 913
  • [8] Physiological regulation of the transport activity in the uncoupling proteins UCP1 and UCP2
    Rial, E
    González-Barroso, MM
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2001, 1504 (01): : 70 - 81
  • [9] UCP1: The Original Uncoupling Protein—and Perhaps the Only One? New Perspectives on UCP1, UCP2, and UCP3 in the Light of the Bioenergetics of the UCP1-Ablated Mice
    Jan Nedergaard
    Anita Matthias
    Valeria Golozoubova
    Anders Jacobsson
    Barbara Cannon
    Journal of Bioenergetics and Biomembranes, 1999, 31 : 475 - 491
  • [10] Chimeric proteins between UCP1 and UCP3: The middle third of UCP1 is necessary and sufficient for activation by fatty acids
    Hagen, T
    Lowell, BB
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 276 (02) : 642 - 648