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Immunohistochemical and Calcium Imaging Methods in Wholemount Rat Retina
Published on: October 13, 2014
Differential distribution of synaptotagmin immunoreactivity among synapses in the goldfish, salamander, and mouse
Ruth Heidelberger1, Meng M Wang, David M Sherry
1Department of Neurobiology and Anatomy and the W.M. Keck Center for the Neurobiology of Learning and Memory, University of Texas-Houston Medical School, Houston, USA.
Insights
Synaptotagmin I, a calcium sensor, shows varied localization in goldfish retinal synapses. Different antibodies reveal distinct forms of synaptotagmin in conventional, bipolar cell, and photoreceptor terminals.
Area of Science:
- Neuroscience
- Cell Biology
- Molecular Biology
Background:
- Synaptotagmin I is considered the primary calcium sensor for exocytosis at conventional synapses.
- Phasic release at ribbon synapses in goldfish Mb1 bipolar cells suggests a different or modified calcium sensor due to lower calcium affinity.
Purpose of the Study:
- To investigate the presence and localization of synaptotagmin in goldfish retinal synapses using specific antibodies.
- To determine if synaptotagmin I functions as the calcium sensor in ribbon synapses.
Main Methods:
- Immunolabeling of goldfish retina with three distinct synaptotagmin antibodies.
- Western blotting of goldfish and mouse retinal membranes to confirm antibody specificity.
- Comparative analysis of synaptotagmin labeling in goldfish, salamander, and mouse retinas.
Main Results:
- Two antibodies specifically labeled the 65-kDa synaptotagmin protein on western blots.
- The first antibody labeled conventional synapses but not ribbon synapses of Mb1 bipolar cells or photoreceptors.
- The second antibody did not label any synapses in the goldfish retina, while a third antibody labeled photoreceptor terminals.
- Species-specific differences in synaptotagmin epitope labeling were observed across retinas.
Conclusions:
- Synaptotagmin appears in at least three distinct forms within goldfish retinal synapses.
- These forms are differentially localized to conventional, bipolar cell, and photoreceptor terminals.
- Variations may reflect differences in synaptotagmin isoforms, post-translational modifications, or binding partners.
Abstract:
Synaptotagmin I is the leading candidate for the calcium sensor that triggers exocytosis at conventional synapses. However, physiological characterization of the calcium sensor for phasic release at the ribbon-style synapses of the goldfish Mb1 bipolar cell demonstrates a lower than predicted affinity for calcium, suggesting that a modified or different sensor triggers exocytosis at this synapse. We examined synaptotagmin immunolabeling in goldfish retina using two different antibodies directed against synaptotagmin epitopes that specifically labeled the expected 65-kDa protein on western blots of goldfish and mouse retinal membranes. The first antiserum strongly labeled conventional synapses in the inner plexiform layer (IPL), but did not label the ribbon-style synapse-containing synaptic terminals of goldfish Mb1 bipolar cells or photoreceptors. The second antibody also specifically labeled the expected 65-kDa protein on western blots but did not label any synapses in the goldfish retina. A third synaptotagmin antibody that performed poorly on western blots selectively labeled goldfish photoreceptor terminals. These results suggest that synaptotagmin may exist in at least three distinct "forms" in goldfish retinal synapses. These forms, which are differentially localized to conventional synapses, bipolar cell, and photoreceptor terminals, may represent differences in isoform, posttranslational modifications, epitope availability, and protein-binding partners. Labeling with these antibodies in the salamander and mouse retina revealed species-specific differences, indicating that synaptotagmin epitopes can vary across species as well as among synapses.
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