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Protein transport between crayfish lateral giant axons.
T A Viancour1, R A Sheller, G D Bittner
1University of Maryland, Department of Biological Sciences, Catonsville 21228.
Brain Research
|January 26, 1988
Summary
Proteins can move between crayfish axons via exocytosis and endocytosis. This axon-to-axon transport mechanism, observed with horseradish peroxidase (HRP), may aid severed axon survival.
Area of Science:
- Neuroscience
- Cell Biology
- Biochemistry
Background:
- Segmental lateral giant axons (SLGAs) in crayfish provide a model for studying axonal transport.
- Understanding protein movement between neurons is crucial for neural plasticity and repair.
Purpose of the Study:
- To investigate if functionally intact proteins can move between adjacent axons under physiological conditions.
- To elucidate the mechanism of axon-to-axon protein transport.
Main Methods:
- Iontophoretic injection of horseradish peroxidase (HRP) into single SLGAs in crayfish.
- Localization of HRP using a non-cytotoxic procedure requiring intact enzymatic activity.
- Analysis of HRP localization in adjacent SLGAs and associated structures.
- Assessment of HRP transfer under varying calcium concentrations and measurement of synaptic electrical resistance.
Main Results:
- Horseradish peroxidase (HRP) frequently transferred between injected and adjacent SLGAs.
- HRP transfer occurred more frequently in the caudal direction than rostral.
- Ultrastructural analysis revealed HRP associated with vesicles at septate junctions and in the perijunctional extracellular space.
- HRP transfer was significantly reduced in low-calcium saline, suggesting a calcium-dependent mechanism.
- No difference in synaptic electrical resistance was observed between sites with and without HRP transfer.
Conclusions:
- Axon-to-axon protein transport occurs via exocytosis from the injected axon and endocytosis by the adjacent axon.
- This mechanism is calcium-dependent and involves vesicular transport across septate junctions.
- Such protein transfer may contribute to the long-term survival of severed axon segments.