Two components of transmitter release from the chick ciliary presynaptic terminal and their regulation by protein kinase C

被引:14
作者
Yawo, H [1 ]
机构
[1] Tohoku Univ, Sch Med, Dept Physiol & Pharmacol, Neurophysiol Div, Sendai, Miyagi 9808575, Japan
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1999年 / 516卷 / 02期
关键词
D O I
10.1111/j.1469-7793.1999.0461v.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. A study was made of the effects of phorbol ester (phorbol 12-myristate 13-acetate, PMA, 0.1 mu M) on the two components of evoked transmitter release, namely the fast synchronous and the slow asynchronous components, from the giant presynaptic terminal of the chick ciliary ganglion. The excitatory postsynaptic currents (EPSCs) were recorded under whole cell voltage clamp of the postsynaptic neuron. 2. The decay time constant of the slow component was prolonged by replacing Ca2+ with Sr2+ In 5 mM [Sr2+](o) the fast component decayed with a time constant of 2.6 +/- 1.4 ms whereas the slow component decayed with a time constant of 19 +/- 7 ms. 3. When stimulated with twin pulses with a short interpulse interval, the fast component of the second EPSC was often depressed whereas the slow component was usually facilitated. Both components were positively dependent on [Sr2+](o) in a,saturable manner, but the fast component approached its maximum at a lower [Sr2+](o) than the slow component. 4. PMA potentiated both the fast and slow components to a similar extent and with a similar time course. For each component, the effect of PMA was less potent at high [Sr2+](o) than at low [Sr2+](o). For either the fast or the slow component the PMA-induced potentiation was accompanied by a reduction in the paired-pulse ratio (PPR). 5. Despite the different dissociation constant for dextran-conjugated fura-2, the fluorescent ratio for intraterminal [Sr2+] ([Sr2+](i)) decayed to the baseline after the nerve-evoked increment with a time course similar to that for [Ca2+](i), suggesting that intraterminal Sr2+ is buffered less efficiently than Ca2+. PMA did not increase the [Sr2+](i) transients: produced by stimulation of the presynaptic oculomotor nerve. 6. It is suggested that protein kinase C (PKC) modulates both the fast and slow components through common molecular mechanisms that upregulate the Sr2+ sensitivity of the vesicle fusion probability.
引用
收藏
页码:461 / 470
页数:10
相关论文
共 29 条
  • [1] QUANTAL INDEPENDENCE AND UNIFORMITY OF PRESYNAPTIC RELEASE KINETICS AT FROG NEUROMUSCULAR JUNCTION
    BARRETT, EF
    STEVENS, CF
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1972, 227 (03): : 665 - 689
  • [2] KINETICS OF TRANSMITTER RELEASE AT FROG NEUROMUSCULAR JUNCTION
    BARRETT, EF
    STEVENS, CF
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1972, 227 (03): : 691 - 708
  • [3] Calcium current during a single action potential in a large presynaptic terminal of the rat brainstem
    Borst, JGG
    Sakmann, B
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1998, 506 (01): : 143 - 157
  • [4] Calcium influx and transmitter release in a fast CNS synapse
    Borst, JGG
    Sakmann, B
    [J]. NATURE, 1996, 383 (6599) : 431 - 434
  • [5] THE EFFECT OF POTASSIUM ON EXOCYTOSIS OF TRANSMITTER AT THE FROG NEUROMUSCULAR-JUNCTION
    CECCARELLI, B
    FESCE, R
    GROHOVAZ, F
    HAIMANN, C
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1988, 401 : 163 - 183
  • [6] Paired-pulse facilitation and depression at unitary synapses in rat hippocampus: Quantal fluctuation affects subsequent release
    Debanne, D
    Guerineau, NC
    Gahwiler, BH
    Thompson, SM
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1996, 491 (01): : 163 - 176
  • [7] CO-OPERATIVE ACTION OF CALCIUM IONS IN TRANSMITTER RELEASE AT NEUROMUSCULAR JUNCTION
    DODGE, FA
    RAHAMIMO.R
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1967, 193 (02): : 419 - &
  • [8] SYNAPTOTAGMIN-I - A MAJOR CA2+ SENSOR FOR TRANSMITTER RELEASE AT A CENTRAL SYNAPSE
    GEPPERT, M
    GODA, Y
    HAMMER, RE
    LI, C
    ROSAHL, TW
    STEVENS, CF
    SUDHOF, TC
    [J]. CELL, 1994, 79 (04) : 717 - 727
  • [9] 2 COMPONENTS OF TRANSMITTER RELEASE AT A CENTRAL SYNAPSE
    GODA, Y
    STEVENS, CF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) : 12942 - 12946
  • [10] GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440