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Ultrastructure and quantification of synapses in the insect nervous system
1Neuroscience Institute, Life Sciences Centre, Dalhousie University, Halifax, Nova Scotia, Canada.
Journal of Neuroscience Methods
|October 21, 1996
Summary
Standard electron microscopy (EM) methods reveal synaptic junction organelles in insects. Serial sectioning clarifies junction profiles, identifying multiple-contact synapses and aiding neuropile organization studies.
Area of Science:
- Neuroscience
- Cell Biology
- Electron Microscopy
Background:
- Standard electron microscopy (EM) is effective for visualizing synaptic junction organelles in insect species.
- Synaptic profiles in single sections often represent a few morphological classes, necessitating serial section analysis for full understanding.
- Central synapses are frequently multiple-contact types, with variations in postsynaptic elements defining individual junctions.
Purpose of the Study:
- To elucidate the utility of standard EM methods in characterizing insect synaptic junctions.
- To establish protocols for identifying and classifying synaptic sites within neuropile.
- To provide methods for estimating synaptic contact numbers using EM data.
Main Methods:
- Utilizing standard electron microscopy (EM) for ultrastructural analysis of synaptic junctions.
- Employing serial sectioning techniques to reconstruct synaptic morphology and understand profile variations.
- Tracing neuronal processes (dendrite-axon continuity) to identify neuron of origin.
Main Results:
- Morphological stereotypy observed within synaptic classes, with variations explained by sectioning planes.
- Identification of multiple-contact synapses as a common feature in central nervous systems.
- Development of methods for estimating synaptic profiles and contacts from single and serial sections, accounting for section thickness and junction size.
Conclusions:
- Standard EM, particularly with serial sectioning, is crucial for comprehensive synaptic junction analysis in insects.
- Understanding profile variations from different sectioning planes aids in identifying synaptic sites and characterizing neuropile organization.
- Methods for quantifying synaptic contacts can be refined using EM data and correction formulae.