Distribution of Ca2+ channels on frog motor nerve terminals revealed by fluorescent omega-conotoxin
- PMID: 1707093
- PMCID: PMC6575372
- DOI: 10.1523/JNEUROSCI.11-04-01032.1991
Distribution of Ca2+ channels on frog motor nerve terminals revealed by fluorescent omega-conotoxin
Abstract
Tetramethylrhodamine-conjugated omega-conotoxin was used as a fluorescent stain (Jones et al., 1989) to determine the spatial distribution of voltage-gated Ca2+ channels along frog motor nerve terminals. Like native omega-conotoxin, the fluorescent toxin blocked neuromuscular transmission irreversibly. The fluorescent staining was confined to the neuromuscular junction and consisted of a series of narrow bands (in face views) or dots (in side views) approximately 1 micron apart. This characteristic staining pattern was prevented by pretreatment with omega-conotoxin and by prior denervation for 5-7 d. Combined fluorescence and phase-contrast optics indicated that the stain was on the synaptic rather than the nonsynaptic side of the nerve terminal. The bands and dots of stain proved to be in spatial register with the postsynaptic junctional folds, as revealed by combined staining of ACh receptors. It is concluded that the voltage-gated Ca2+ channels on frog motor nerve terminals are concentrated at active zones. The findings are consistent with the suggestion (Heuser et al., 1974; Pumplin et al., 1981) that the large intramembraneous particles seen at freeze-fractured active zones are voltage-gated Ca2+ channels.
Similar articles
-
Calcium channels and calcium-gated potassium channels at the frog neuromuscular junction.J Physiol Paris. 1993;87(1):15-24. doi: 10.1016/0928-4257(93)90020-t. J Physiol Paris. 1993. PMID: 7508311
-
Multiple types of Ca2+ channels in mouse motor nerve terminals.Eur J Neurosci. 1997 Apr;9(4):817-23. doi: 10.1111/j.1460-9568.1997.tb01431.x. Eur J Neurosci. 1997. PMID: 9153589
-
Inhibition by neosurugatoxin and omega-conotoxin of acetylcholine release and muscle and neuronal nicotinic receptors in mouse neuromuscular junction.Neuroscience. 1992;48(3):727-35. doi: 10.1016/0306-4522(92)90416-y. Neuroscience. 1992. PMID: 1318519
-
Omega-conotoxin does not block the verapamil-sensitive calcium channels at mouse motor nerve terminals.Neurosci Lett. 1987 Nov 23;82(2):177-80. doi: 10.1016/0304-3940(87)90125-x. Neurosci Lett. 1987. PMID: 2447536
-
A review on conotoxins targeting ion channels and acetylcholine receptors of the vertebrate neuromuscular junction.Acta Physiol Pharmacol Ther Latinoam. 1999;49(4):257-67. Acta Physiol Pharmacol Ther Latinoam. 1999. PMID: 10797869 Review.
Cited by
-
Determinants of the time course of facilitation at the granule cell to Purkinje cell synapse.J Neurosci. 1996 Sep 15;16(18):5661-71. doi: 10.1523/JNEUROSCI.16-18-05661.1996. J Neurosci. 1996. PMID: 8795622 Free PMC article.
-
Presynaptic calcium dynamics and transmitter release evoked by single action potentials at mammalian central synapses.Biophys J. 1997 Feb;72(2 Pt 1):637-51. doi: 10.1016/s0006-3495(97)78702-2. Biophys J. 1997. PMID: 9017193 Free PMC article.
-
Mechanisms controlling the trafficking, localization, and abundance of presynaptic Ca2+ channels.Front Mol Neurosci. 2023 Jan 13;15:1116729. doi: 10.3389/fnmol.2022.1116729. eCollection 2022. Front Mol Neurosci. 2023. PMID: 36710932 Free PMC article. Review.
-
Synaptic Vesicles Having Large Contact Areas with the Presynaptic Membrane are Preferentially Hemifused at Active Zones of Frog Neuromuscular Junctions Fixed during Synaptic Activity.Int J Mol Sci. 2019 May 31;20(11):2692. doi: 10.3390/ijms20112692. Int J Mol Sci. 2019. PMID: 31159267 Free PMC article. Review.
-
Depolarization-induced Ca2+ entry preferentially evokes release of large quanta in the developing Xenopus neuromuscular junction.J Neurophysiol. 2010 Nov;104(5):2730-40. doi: 10.1152/jn.01041.2009. Epub 2010 Sep 15. J Neurophysiol. 2010. PMID: 20844112 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous