Abstract
Electrical activity regulates the manner in which neurons mature and form connections to each other. However, it remains unclear whether increased single-cell activity is sufficient to alter the development of synaptic connectivity of that neuron or whether a global increase in circuit activity is necessary. To address this question, we genetically increased neuronal excitability of in vivo individual adult-born neurons in the mouse dentate gyrus via expression of a voltage-gated bacterial sodium channel. We observed that increasing the excitability of new neurons in an otherwise unperturbed circuit leads to changes in both their input and axonal synapses. Furthermore, the activity-dependent transcription factor Npas4 is necessary for the changes in the input synapses of these neurons, but it is not involved in changes to their axonal synapses. Our results reveal that an increase in cell-intrinsic activity during maturation is sufficient to alter the synaptic connectivity of a neuron with the hippocampal circuit and that Npas4 is required for activity-dependent changes in input synapses.
Publication types
-
Research Support, N.I.H., Extramural
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Bacterial Proteins / genetics
-
Bacterial Proteins / metabolism
-
Basic Helix-Loop-Helix Transcription Factors / genetics
-
Basic Helix-Loop-Helix Transcription Factors / metabolism*
-
Dentate Gyrus / cytology*
-
Dentate Gyrus / metabolism*
-
Disks Large Homolog 4 Protein
-
Electric Stimulation
-
Excitatory Postsynaptic Potentials / drug effects
-
Excitatory Postsynaptic Potentials / physiology*
-
Female
-
Gene Expression Regulation / physiology
-
Genetic Vectors / metabolism
-
Green Fluorescent Proteins / genetics
-
Green Fluorescent Proteins / metabolism
-
Guanylate Kinases / genetics
-
Guanylate Kinases / metabolism
-
In Vitro Techniques
-
K Cl- Cotransporters
-
Luminescent Proteins / genetics
-
Luminescent Proteins / metabolism
-
Membrane Proteins / genetics
-
Membrane Proteins / metabolism
-
Mice
-
Mice, Inbred C57BL
-
Mice, Transgenic
-
Microscopy, Confocal
-
Mutation / genetics
-
Nerve Net / physiology
-
Neurons / physiology*
-
Patch-Clamp Techniques
-
Receptors, N-Methyl-D-Aspartate / genetics
-
Receptors, N-Methyl-D-Aspartate / metabolism
-
Red Fluorescent Protein
-
Sodium Channel Blockers / pharmacology
-
Sodium Channels / genetics
-
Sodium Channels / metabolism
-
Symporters / genetics
-
Symporters / metabolism
-
Synapses / genetics
-
Synapses / physiology*
-
Tetrodotoxin / pharmacology
-
Vesicular Inhibitory Amino Acid Transport Proteins / metabolism
Substances
-
Bacterial Proteins
-
Basic Helix-Loop-Helix Transcription Factors
-
Disks Large Homolog 4 Protein
-
Dlg4 protein, mouse
-
Luminescent Proteins
-
Membrane Proteins
-
NMDA receptor A1
-
NaChBac protein, bacteria
-
Npas4 protein, mouse
-
Receptors, N-Methyl-D-Aspartate
-
Sodium Channel Blockers
-
Sodium Channels
-
Symporters
-
Vesicular Inhibitory Amino Acid Transport Proteins
-
Viaat protein, mouse
-
enhanced green fluorescent protein
-
Green Fluorescent Proteins
-
Tetrodotoxin
-
Guanylate Kinases