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J Neurophysiol 94: 4544-4553, 2005. First published August 17, 2005; doi:10.1152/jn.01193.2004
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Imaging of Ca2+ Dynamics Within the Presynaptic Terminals of Salamander Rod Photoreceptors

Ernest C. Steele, Jr.1, Xiaoming Chen1, P. Michael Iuvone2 and Peter R. MacLeish1

1Department of Anatomy and Neurobiology, Neuroscience Institute, Morehouse School of Medicine and 2Department of Pharmacology, Emory University School of Medicine, Atlanta, Georgia

Submitted 19 November 2004; accepted in final form 7 August 2005

Although the overall importance of Ca2+ as a mediator of cell signaling and neurotransmitter release has long been appreciated, the details of Ca2+ dynamics within the inner segments of vertebrate rod photoreceptors are just beginning to be elucidated. Even less is known regarding Ca2+ dynamics within the rod presynaptic terminal compartment. Using fura-2 to report changes in intracellular Ca2+, we imaged the responses of enzymatically dissociated salamander rod photoreceptors retaining intact axons and presynaptic terminals stimulated with a brief depolarizing puff of KCl (30 mM pipette concentration). In the vast majority of cells, the response was a large increase in Ca2+ levels in the terminal compartment, but not in the soma. In contrast, rods exhibited a substantial elevation in somatic Ca2+ levels when depolarized with a brief puff of 100 mM KCl (pipette concentration). These data are consistent with previously reported differences in Ca2+ buffering mechanisms within the somatic and terminal compartments. Additionally, they may reflect the presence of Ca2+ channels having distinct properties within the membranes of the two compartments. Consistent with this hypothesis, fluorescent immunocytochemistry using an antibody against the L-type Ca2+ channel Cav1.2 ({alpha}1C) subunit and semiquantitative confocal microscopy revealed a high concentration of immunoreactivity in the membranes of terminals of intact rods compared with the somata. Further investigations using enzymatically dissociated preparations of intact rod photoreceptors retaining their presynaptic terminals will allow further testing of these and other hypotheses regarding the compartmentalized regulation of Ca2+ dynamics within rod photoreceptors.


Address for reprint requests and other correspondence: E. C. Steele, 720 Westview Drive SW, Atlanta, GA 30310 (E-mail: esteele{at}msm.edu)




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P. R. MacLeish and C. A. Nurse
Ion Channel Compartments in Photoreceptors: Evidence From Salamander Rods With Intact and Ablated Terminals
J Neurophysiol, July 1, 2007; 98(1): 86 - 95.
[Abstract] [Full Text] [PDF]




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