Different types of calcium channels and secretion from bovine chromaffin cells

被引:49
作者
Lukyanetz, EA
Neher, E
机构
[1] AA Bogomolets Physiol Inst, UA-252601 Kiev, Ukraine
[2] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
关键词
Ca2+ channels; calcium-secretion coupling; chromaffin cells; conotoxins; dihydropyridines; exocytosis;
D O I
10.1046/j.1460-9568.1999.00707.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Bovine chromaffin cells possess several types of Ca2+ channels, and influx of Ca2+ is known to trigger secretion. However, discrepant information about the relative importance of the individual subtypes in secretion has been reported. We used whole-cell patch-clamp measurements in isolated cells in culture combined with fura-2 microfluorimetry and pharmacological manipulation to determine the dependence of secretion on different types of Ca2+ channels. We stimulated cells with relatively long depolarizing voltage-clamp pulses in a medium containing 60 mM CaCl2. We found that, within a certain range of pulse parameters, secretion as measured by membrane capacitance changes was mainly determined by the total cumulative charge of Ca2+ inflow and the basal [Ca2+] level preceding a stimulus. Blocking or reducing the contribution of specific types of Ca2+ channels using either 20 mu M nifedipine plus 10 mu M nimodipine or 1 mu M omega CTxGVIA (omega-conotoxin GVIA) or 2 mu M omega CTxMVIIC (omega-conotoxin MVIIC) reduced secretion in proportion to Ca2+ charge, irrespective of the toxin used. We conclude that for long-duration stimuli, which release a large fraction of the readily releasable pool of vesicles, it is not so important through which type of channels Ca2+ enters the cell. Release is determined by the total amount of Ca2+ entering and by the filling state of the readily releasable pool, which depends on basal [Ca2+] before the stimulus. This result does not preclude that other stimulation patterns may lead to responses in which subtype specificity of Ca2+ channels matters.
引用
收藏
页码:2865 / 2873
页数:9
相关论文
共 62 条
  • [1] BINDING OF OMEGA-CONOTOXIN TO RECEPTOR-SITES ASSOCIATED WITH THE VOLTAGE-SENSITIVE CALCIUM-CHANNEL
    ABE, T
    KOYANO, K
    SAISU, H
    NISHIUCHI, Y
    SAKAKIBARA, S
    [J]. NEUROSCIENCE LETTERS, 1986, 71 (02) : 203 - 208
  • [2] Opioid inhibition of Ca2+ channel subtypes in bovine chromaffin cells: Selectivity of action and voltage dependence
    Albillos, A
    Carbone, E
    Gandia, L
    Garcia, AG
    Pollo, A
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1996, 8 (08) : 1561 - 1570
  • [3] Re-evaluation of the P/Q Ca2+ channel components of Ba2+ currents in bovine chromaffin cells superfused with solutions containing low and high Ba2+ concentrations
    Albillos, A
    Garcia, AG
    Olivera, B
    Gandia, L
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1996, 432 (06): : 1030 - 1038
  • [4] CALCIUM-CHANNEL SUBTYPES IN CAT CHROMAFFIN CELLS
    ALBILLOS, A
    ARTALEJO, AR
    LOPEZ, MG
    GANDIA, L
    GARCIA, AG
    CARBONE, E
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1994, 477 (02): : 197 - 213
  • [5] 3 TYPES OF CA2+ CHANNEL TRIGGER SECRETION WITH DIFFERENT EFFICACIES IN CHROMAFFIN CELLS
    ARTALEJO, CR
    ADAMS, ME
    FOX, AP
    [J]. NATURE, 1994, 367 (6458) : 72 - 76
  • [6] 3 TYPES OF BOVINE CHROMAFFIN CELL CA-2+ CHANNELS - FACILITATION INCREASES THE OPENING PROBABILITY OF A 27-PS CHANNEL
    ARTALEJO, CR
    MOGUL, DJ
    PERLMAN, RL
    FOX, AP
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1991, 444 : 213 - 240
  • [7] CALCIUM REQUIREMENTS FOR SECRETION IN BOVINE CHROMAFFIN CELLS
    AUGUSTINE, GJ
    NEHER, E
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1992, 450 : 247 - 271
  • [8] IONIC CHANNELS OF THE INNER SEGMENT OF TIGER SALAMANDER CONE PHOTORECEPTORS
    BARNES, S
    HILLE, B
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1989, 94 (04) : 719 - 743
  • [9] SYNTAXIN - A SYNAPTIC PROTEIN IMPLICATED IN DOCKING OF SYNAPTIC VESICLES AT PRESYNAPTIC ACTIVE ZONES
    BENNETT, MK
    CALAKOS, N
    SCHELLER, RH
    [J]. SCIENCE, 1992, 257 (5067) : 255 - 259
  • [10] BURGOYNE RD, 1995, J PHYSIOL PHARMACOL, V46, P273