Related Experiment Videos
Synaptically released acetylcholine evokes Ca2+ elevations in astrocytes in hippocampal slices
Alfonso Araque1, Eduardo D Martín, Gertrudis Perea
1Instituto Cajal, Consejo Superior de Investigaciones Cientificas, Madrid 28002, Spain. araque@cajal.csic.es
Summary
Astrocytes in the rat hippocampus respond to acetylcholine released by nerve fibers. This synaptic signaling involves muscarinic receptors and intracellular calcium mobilization, highlighting neuron-astrocyte communication.
Area of Science:
- Neuroscience
- Cellular Neuroscience
- Astrocyte Biology
Background:
- Bidirectional communication between glial cells and neurons is increasingly recognized.
- Astrocytes, a type of glial cell, play crucial roles in brain function.
- Cholinergic signaling is vital for various cognitive processes.
Purpose of the Study:
- To investigate whether rat hippocampal astrocytes respond to synaptically released acetylcholine.
- To elucidate the mechanisms underlying astrocyte responses to cholinergic input.
Main Methods:
- Whole-cell recordings of membrane currents and intracellular calcium levels in hippocampal astrocytes.
- Stimulation of cholinergic afferents in brain slices.
- Application of pharmacological agents including tetrodotoxin, Cd2+, 4-aminopyridine, glutamate transporter antagonists, and atropine.
Main Results:
- Synaptic stimulation evoked long-lasting inward currents and increased intracellular calcium in astrocytes.
- These responses were dependent on synaptically released neurotransmitters and involved electrogenic glutamate transporter activity.
- Calcium elevations were mediated by muscarinic cholinergic receptors and involved intracellular calcium mobilization.
- Subcellular domains within astrocytes exhibited independent calcium variations.
Conclusions:
- Rat hippocampal astrocytes are responsive to synaptically released acetylcholine.
- Cholinergic neuron-astrocyte signaling occurs via muscarinic receptors, leading to intracellular calcium release.
- Astrocytes are targets of axonal inputs, indicating a role in synaptic integration.