Contributions of mitochondria to animal physiology: from homeostatic sensor to calcium signalling and cell death

被引:501
作者
Duchen, MR [1 ]
机构
[1] UCL, Dept Physiol, London WC1E 6BT, England
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1999年 / 516卷 / 01期
关键词
D O I
10.1111/j.1469-7793.1999.001aa.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Over recent years, it has become clear that mitochondria play a central role in many key aspects of animal physiology and pathophysiology. Their central and ubiquitous task is clearly the production of ATP. Nevertheless, they also play subtle roles in glucose homeostasis, acting as the sensor for substrate supply in the transduction pathway that promotes insulin secretion by the pancreatic beta-cell and that modulates the excitability of the hypothalamic glucose-sensitive neurons involved in appetite control. Mitochondria may also act as sensors of availability of oxygen, the other major mitochondrial substrate, in the regulation of respiration. Mitochondria take up calcium, and the high capacity mitochondrial calcium uptake pathway provides a mechanism that couples energy demand to increased ATP production through the calcium-dependent upregulation of mitochondrial enzyme activity. Mitochondrial calcium accumulation may also have a substantial impact on the spatiotemporal dynamics of cellular calcium signals, with subtle differences of detail in different cell types. Recent work has also revealed the centrality of mitochondrial dysfunction as an irreversible step in the pathway to both necrotic and apoptotic cell death. This review looks at recent developments in these rapidly evolving areas of cell physiology in an attempt to draw together disparate areas of research into it common theme.
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页码:1 / 17
页数:17
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共 112 条
  • [31] DUCHEN MR, 1992, J PHYSL, V450, P31
  • [32] ACTIVATION OF MITOCHONDRIAL OXIDATIVE-METABOLISM BY CALCIUM-IONS IN LIMULUS VENTRAL PHOTORECEPTOR
    FEIN, A
    TSACOPOULOS, M
    [J]. NATURE, 1988, 331 (6155) : 437 - 440
  • [33] Leptin and the regulation of body weight in mammals
    Friedman, JM
    Halaas, JL
    [J]. NATURE, 1998, 395 (6704) : 763 - 770
  • [34] FRIEL DD, 1994, J NEUROSCI, V14, P4007
  • [35] Recent developments in the molecular genetics of mitochondrial disorders
    Graeber, MB
    Müller, U
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 153 (02) : 251 - 263
  • [36] Rickettsia, typhus and the mitochondrial connection
    Gray, MW
    [J]. NATURE, 1998, 396 (6707) : 109 - 110
  • [37] Mitochondria and apoptosis
    Green, DR
    Reed, JC
    [J]. SCIENCE, 1998, 281 (5381) : 1309 - 1312
  • [38] MITOCHONDRIAL NONSPECIFIC PORES REMAIN CLOSED DURING CARDIAC ISCHEMIA, BUT OPEN UPON REPERFUSION
    GRIFFITHS, EJ
    HALESTRAP, AP
    [J]. BIOCHEMICAL JOURNAL, 1995, 307 : 93 - 98
  • [39] The Ca2+ transport mechanisms of mitochondria and Ca2+ uptake from physiological-type Ca2+ transients
    Gunter, TE
    Buntinas, L
    Sparagna, GC
    Gunter, KK
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1998, 1366 (1-2): : 5 - 15
  • [40] Type III InsP3 receptor channel stays open in the presence of increased calcium
    Hagar, RE
    Burgstahler, AD
    Nathanson, MH
    Ehrlich, BE
    [J]. NATURE, 1998, 396 (6706) : 81 - 84