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Isolation of Sensory Neurons of Aplysia californica for Patch Clamp Recordings of Glutamatergic Currents
Published on: July 10, 2013
Interleukin-2 inhibits the GABA-induced Cl- current in identified Aplysia neurons
1Department of Physiology, Shimane Medical University, Izumo, Japan.
Insights
Recombinant human interleukin-2 (rhIL-2) suppressed gamma-aminobutyric acid (GABA)-induced currents in Aplysia neurons. This immunomodulator effect on the nervous system was reversible and specific to active rhIL-2.
Area of Science:
- Neuroscience
- Immunology
- Marine Biology
Background:
- Interleukin-2 (IL-2) is an immunomodulator.
- Gamma-aminobutyric acid (GABA) is a primary inhibitory neurotransmitter in the nervous system.
- The effects of IL-2 on neuronal function are not fully understood.
Purpose of the Study:
- To investigate the effects of recombinant human interleukin-2 (rhIL-2) on GABA-induced currents in identified Aplysia neurons.
- To determine if rhIL-2 modulates neurotransmission in the marine mollusc Aplysia kurodai.
Main Methods:
- Conventional voltage-clamp technique.
- Pressure ejection of GABA and rhIL-2.
- Recording from identified neurons (R9 and R12) of Aplysia kurodai.
Main Results:
- Extracellular application of rhIL-2 (10-40 U/ml) significantly reduced GABA-induced Cl- currents.
- The observed suppression was fully reversible upon removal of rhIL-2.
- Heat-inactivated rhIL-2 had no effect, indicating the biological activity of rhIL-2 is responsible for the modulation.
Conclusions:
- Recombinant human interleukin-2 (rhIL-2) can modulate GABA-induced responses in the Aplysia nervous system.
- IL-2 may play a role in regulating neuronal excitability and synaptic transmission.
- These findings suggest a potential link between the immune system and nervous system function.
Abstract:
The effects of extracellularly applied recombinant human interleukin-2 (rhIL-2) on the gamma-aminobutyric acid (GABA)-induced Cl- current recorded from identified neurons (R9 and R12) of Aplysia kurodai were investigated with conventional voltage-clamp and pressure ejection techniques. Bath-applied rhIL-2 (10-40 U/ml) reduced the GABA-induced current in the neurons without affecting resting membrane conductance and the holding current. The suppressing effect of rhIL-2 on the current was completely reversible. Heat-inactivated rhIL-2 was without effect. These results suggest that the immunomodulator IL-2 can modulate the GABA-induced response in the nervous system.
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