|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Received August 6, 2001
Accepted after revision November 14, 2001
1 Respiratory and Neuroscience Research Groups, Faculty of Medicine, University of Calgary, 3330-Hospital Drive, NW, Calgary, Alberta, Canada T2N 4N1
2 Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9
3 Department of Cell Biology and Anatomy, Faculty of Medicine, The University of Calgary, Calgary, Alberta, Canada T2N 4N1
* To whom correspondence should be addressed. E-mail: nisyed{at}acs.ucalgary.ca.
Calcium (Ca2+) channel clustering at specific presynaptic sites is a hallmark of mature synapses. However, the spatial distribution patterns of Ca2+ channels at newly formed synapses have not yet been demonstrated. Similarly, it is unclear whether Ca2+ 'hotspots' often observed at the presynaptic sites are indeed target cell contact specific and represent a specialized mechanism by which Ca2+ channels are targeted to select synaptic sites. Utilizing both soma-soma paired (synapsed) and single neurons from the mollusk Lymnaea, we have tested the hypothesis that differential gradients of voltage-dependent Ca2+ signals develop in presynaptic neuron at its contact point with the postsynaptic neuron; and that these Ca2+ hotspots are target cell contact specific. Fura-2 imaging, or two-photon laser scanning microscopy of Calcium Green, was coupled with electrophysiological techniques to demonstrate that voltage-induced Ca2+ gradients (hotspots) develop in the presynaptic cell at its contact point with the postsynaptic neuron, but not in unpaired single cells. The incidence of Ca2+ hotspots coincided with the appearance of synaptic transmission between the paired cells, and these gradients were target cell contact specific. In contrast, the voltage-induced Ca2+ signal in unpaired neurons was uniformly distributed throughout the somata; a similar pattern of Ca2+ gradient was observed in the presynaptic neuron when it was soma-soma paired with a non-synaptic partner cell. Moreover, voltage clamp recording techniques, in conjunction with a fast, optical differential perfusion system, were used to demonstrate that the total whole-cell Ca2+ (or Ba2+) current density in single and paired cells was not significantly different. However, the amplitude of Ba2+ current was significantly higher in the presynaptic cell at its contact side with the postsynaptic neurons, compared with non-contacted regions. In summary, this study demonstrates that voltage-induced Ca2+ hotspots develop in the presynaptic cell, concomitant with the appearance of synaptic transmission between the soma-soma paired cells. The appearance of Ca2+ gradients in presynaptic neurons is target cell contact specific and is probably due to a spatial redistribution of existing channels during synaptogenesis.
This article has been cited by other articles:
![]() |
S. Onizuka, T. Kasaba, and M. Takasaki The Effect of Lidocaine on Cholinergic Neurotransmission in an Identified Reconstructed Synapse Anesth. Analg., October 1, 2008; 107(4): 1236 - 1242. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Hui, G.-H. Fei, B. J. Saab, J. Su, J. C. Roder, and Z.-P. Feng Neuronal calcium sensor-1 modulation of optimal calcium level for neurite outgrowth Development, December 15, 2007; 134(24): 4479 - 4489. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Gardzinski, D. W. K. Lee, G.-H. Fei, K. Hui, G. J. Huang, H.-S. Sun, and Z.-P. Feng The role of synaptotagmin I C2A calcium-binding domain in synaptic vesicle clustering during synapse formation J. Physiol., May 15, 2007; 581(1): 75 - 90. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Wiersma-Meems, J. Van Minnen, and N. I. Syed Synapse Formation and Plasticity: The Roles of Local Protein Synthesis Neuroscientist, June 1, 2005; 11(3): 228 - 237. [Abstract] [PDF] |
||||
![]() |
S. Onizuka, T. Kasaba, T. Hamakawa, and M. Takasaki Lidocaine Excites Both Pre- and Postsynaptic Neurons of Reconstructed Respiratory Pattern Generator in Lymnaea stagnalis Anesth. Analg., January 1, 2005; 100(1): 175 - 182. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. J. Woodall, H. Naruo, D. J. Prince, Z. P. Feng, W. Winlow, M. Takasaki, and N. I. Syed Anesthetic Treatment Blocks Synaptogenesis But Not Neuronal Regeneration of Cultured Lymnaea Neurons J Neurophysiol, October 1, 2003; 90(4): 2232 - 2239. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. D. Spafford, L. Chen, Z.-P. Feng, A. B. Smit, and G. W. Zamponi Expression and Modulation of an Invertebrate Presynaptic Calcium Channel {alpha}1 Subunit Homolog J. Biol. Chem., June 6, 2003; 278(23): 21178 - 21187. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Meems, D. Munno, J. van Minnen, and N. I. Syed Synapse Formation Between Isolated Axons Requires Presynaptic Soma and Redistribution of Postsynaptic AChRs J Neurophysiol, May 1, 2003; 89(5): 2611 - 2619. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. D. Spafford, D. W. Munno, P. van Nierop, Z.-P. Feng, S. E. Jarvis, W. J. Gallin, A. B. Smit, G. W. Zamponi, and N. I. Syed Calcium Channel Structural Determinants of Synaptic Transmission between Identified Invertebrate Neurons J. Biol. Chem., January 31, 2003; 278(6): 4258 - 4267. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |