NPAS4 refines spatial and temporal firing in CA1 pyramidal neurons

NPAS4 is an activity-dependent transcription factor that, in CA1 of the hippocampus, regulates inhibitory synapses made onto the active pyramidal neuron. In principle, NPAS4 thereby allows the past activity of a neuron to influence how it encodes information, although this has not yet been demonstrated. Here, we generated a sparse, CA1-specific knockout (KO) of NPAS4 in the mouse hippocampus and used optogenetic tagging to identify KO neurons <i>in vivo</i> . Recordings from intermingled wild-type (WT) and KO neurons in awake behaving animals revealed that NPAS4 deletion degrades spatial representations and temporal precision of spiking: KO neurons exhibited larger place fields with reduced in-field firing and increased out-of-field firing, less stable place fields, reduced coupling to local field potential theta oscillations, and diminished phase precession. These findings demonstrate that NPAS4 plays a crucial role in refining the spatial and temporal properties of CA1 pyramidal neuron spikes, which themselves are thought to be fundamental building blocks of more complex processes such as learning and memory.

Authors

Institutions

Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-03-22
DOI
https://doi.org/10.64898/2026.03.22.713468
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

NPAS4 refines spatial and temporal firing in CA1 pyramidal neurons

Anja Payne, Brenda L. Bloodgood, Clare R. Quirk, Stefan Leutgeb et al.
bioRxiv (Cold Spring Harbor Laboratory)
Neuroscience and Neuropharmacology Research
article

NPAS4 refines spatial and temporal firing in CA1 pyramidal neurons

Anja Payne, Brenda L. Bloodgood, Clare R. Quirk, Stefan Leutgeb, Chiaki I. Santiago, Andrea L. Hartzell, Jill K. Leutgeb, Daniel A Heinz, Lara Louise Hagopian, Rolando Sceptre Ganasi
article en

Abstract

NPAS4 is an activity-dependent transcription factor that, in CA1 of the hippocampus, regulates inhibitory synapses made onto the active pyramidal neuron. In principle, NPAS4 thereby allows the past activity of a neuron to influence how it encodes information, although this has not yet been demonstrated. Here, we generated a sparse, CA1-specific knockout (KO) of NPAS4 in the mouse hippocampus and used optogenetic tagging to identify KO neurons <i>in vivo</i> . Recordings from intermingled wild-type (WT) and KO neurons in awake behaving animals revealed that NPAS4 deletion degrades spatial representations and temporal precision of spiking: KO neurons exhibited larger place fields with reduced in-field firing and increased out-of-field firing, less stable place fields, reduced coupling to local field potential theta oscillations, and diminished phase precession. These findings demonstrate that NPAS4 plays a crucial role in refining the spatial and temporal properties of CA1 pyramidal neuron spikes, which themselves are thought to be fundamental building blocks of more complex processes such as learning and memory.

bioRxiv (Cold Spring Harbor Laboratory)
University of California, San Francisco (US), Janelia Research Campus (US), Ionis Pharmaceuticals (United States) (US), UC San Diego Health System (US), University of California San Diego (US), UC Irvine Health (US), Neurocrine Biosciences (United States) (US)
Openalex Percentile: Top 12%
Neuroscience and Neuropharmacology Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.