The importance of redox shuttles to pancreatic β-cell energy metabolism and function

被引:39
作者
Bender, K.
Newsholme, P. [1 ]
Brennan, L.
Maechler, P.
机构
[1] Univ Coll Dublin, Conway Inst, Sch Biomol & Biomed Sci, Dublin 4, Ireland
[2] Univ Geneva, Med Ctr, Dept Cell Physiol & Metab, CH-1211 Geneva, Switzerland
关键词
Aralar1; beta-cell; energy metabolism; malate-aspartate shuttle; mitochondrion; redox shuttle;
D O I
10.1042/BST0340811
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The coupling of cytosolic glycolytic NADH production with the mitochondrial electron transport chain is crucial for pancreatic beta-cell function and energy metabolism. The activity of lactate dehydrogenase in the beta-cell is low, thus glycolysis-derived electrons are transported towards the mitochondrial matrix by a NADH shuttle system, which in turn regenerates cytosolic NAD(+). Mitochondrial electron transport then produce!; ATP, the main coupling factor for insulin secretion. Aralarl, a Ca2+-sensitive member of the malate-aspartate shuttle expressed in beta-cells, has been found to play a significant role in nutrient-stimulated insulin secretion and beta-cell function. increased capacity of Aralarl enhances the responsiveness of the cell to glucose. Conversely, inhibition of the malate-aspartate shuttle results in impaired glucose metabolism and insulin secretion. Current research investigates potentiating or attenuating activities of various amino acids on insulin secretion, mitochondrial membrane potential and NADH production in Aralar1-overexpressing beta-cells. This work may provide evidence for a central role of Aralarl in the regulation of nutrient metabolism in the beta-cells.
引用
收藏
页码:811 / 814
页数:4
相关论文
共 21 条
  • [11] Mazurek S, 1999, J CELL PHYSIOL, V181, P136
  • [12] ROLE OF CALCIUM-IONS IN REGULATION OF MAMMALIAN INTRAMITOCHONDRIAL METABOLISM
    MCCORMACK, JG
    HALESTRAP, AP
    DENTON, RM
    [J]. PHYSIOLOGICAL REVIEWS, 1990, 70 (02) : 391 - 425
  • [13] Neuronal and astrocytic shuttle mechanisms for cytosolic-mitochondrial transfer of reducing equivalents: Current evidence and pharmacological tools
    McKenna, MC
    Waagepetersen, HS
    Schousboe, A
    Sonnewald, U
    [J]. BIOCHEMICAL PHARMACOLOGY, 2006, 71 (04) : 399 - 407
  • [14] Newsholme EA., 1983, BIOCH MED SCI
  • [15] The pancreatic beta-cell as a fuel sensor: An electrophysiologist's viewpoint
    Rorsman, P
    [J]. DIABETOLOGIA, 1997, 40 (05) : 487 - 495
  • [16] The malate-aspartate NADH shuttle member Aralar1 determines glucose metabolic fate, mitochondrial activity, and insulin secretion in beta cells
    Rubi, B
    del Arco, A
    Bartley, C
    Satrustegui, J
    Maechler, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (53) : 55659 - 55666
  • [17] REGULATION OF MITOCHONDRIAL GLYCEROL-PHOSPHATE DEHYDROGENASE BY CA-2+ WITHIN ELECTROPERMEABILIZED INSULIN-SECRETING CELLS (INS-1)
    RUTTER, GA
    PRALONG, WF
    WOLLHEIM, CB
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1175 (01) : 107 - 113
  • [18] SCHURR A, 1999, SCIENCE, V287, P931
  • [19] SEKINE N, 1994, J BIOL CHEM, V269, P4895
  • [20] Evidence of enhancement of malate-aspartate shuttle activity in β cells of streptozotocin-induced non-insulin-dependent diabetic rats
    Song, DK
    Ahn, YH
    Bae, H
    Park, WK
    Hong, YS
    Ho, WK
    Earm, YE
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (01): : 92 - 96