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Peer-reviewedCC BY 4.0Frontiers in Neuroscience

Single-cell dataset of juvenile mouse neurons from the thalamic reticular nucleus: whole-cell patch-clamp electrophysiology

Abstract

This dataset provides single-cell whole-cell patch-clamp electrophysiology for 19 interneurons of the thalamic reticular nucleus (TRN) in juvenile mice. The recordings were obtained from male C57Bl/6J mice sampled within the developmental window of postnatal days 24 to 34. Acute horizontal brain slices were used, and visually targeted whole-cell recordings were performed in current-clamp mode. A standardized current-clamp stimulus battery was used identically across all cells to characterize their intrinsic electrophysiological properties—passive membrane behavior, action-potential threshold and waveform, suprathreshold firing patterns, and the hyperpolarization-evoked rebound-burst dynamics characteristic of reticular thalamic neurons. The release comprises 18,015 recorded sweeps and their full, un-decimated signal traces (400 million digitized samples), preserved in the community-standard NWB (icephys) format alongside the original Igor Pro source files, and indexed into tidy, queryable Apache Parquet tables—one record per recording session, one per sweep, and one per digitized sample—linked by a normalized recording identifier. Each recording includes animal metadata (postnatal age, body weight, strain, genotype, slice orientation, and recorded region) and its resting membrane potential. The dataset is released as a FAIR² Data Package under the Open Data Commons Attribution License v1.0 (ODC-By v1.0), with machine-readable metadata conforming to the MLCommons Croissant specification, QUDT units, and PROV-O provenance. It is intended for neuroscientists, computational modelers, and machine-learning researchers studying the intrinsic electrophysiology of TRN neurons.

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BibTeX
@article{pezzoli2026singlecell,
  title = {{Single-cell dataset of juvenile mouse neurons from the thalamic reticular nucleus: whole-cell patch-clamp electrophysiology}},
  author = {Maurizio Pezzoli and Rodrigo Perin and Henry Markram},
  journal = {Frontiers in Neuroscience},
  year = {2026},
  month = oct,
  doi = {10.3389/fnins.2026.1927631},
  url = {https://www.frontiersin.org/articles/10.3389/fnins.2026.1927631},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Single-cell dataset of juvenile mouse neurons from the thalamic reticular nucleus: whole-cell patch-clamp electrophysiology
AU  - Maurizio Pezzoli
AU  - Rodrigo Perin
AU  - Henry Markram
PY  - 2026
DA  - 2026/10/29
JO  - Frontiers in Neuroscience
DO  - 10.3389/fnins.2026.1927631
UR  - https://www.frontiersin.org/articles/10.3389/fnins.2026.1927631
AB  - This dataset provides single-cell whole-cell patch-clamp electrophysiology for 19 interneurons of the thalamic reticular nucleus (TRN) in juvenile mice. The recordings were obtained from male C57Bl/6J mice sampled within the developmental window of postnatal days 24 to 34. Acute horizontal brain slices were used, and visually targeted whole-cell recordings were performed in current-clamp mode. A standardized current-clamp stimulus battery was used identically across all cells to characterize their intrinsic electrophysiological properties—passive membrane behavior, action-potential threshold and waveform, suprathreshold firing patterns, and the hyperpolarization-evoked rebound-burst dynamics characteristic of reticular thalamic neurons. The release comprises 18,015 recorded sweeps and their full, un-decimated signal traces (400 million digitized samples), preserved in the community-standard NWB (icephys) format alongside the original Igor Pro source files, and indexed into tidy, queryable Apache Parquet tables—one record per recording session, one per sweep, and one per digitized sample—linked by a normalized recording identifier. Each recording includes animal metadata (postnatal age, body weight, strain, genotype, slice orientation, and recorded region) and its resting membrane potential. The dataset is released as a FAIR² Data Package under the Open Data Commons Attribution License v1.0 (ODC-By v1.0), with machine-readable metadata conforming to the MLCommons Croissant specification, QUDT units, and PROV-O provenance. It is intended for neuroscientists, computational modelers, and machine-learning researchers studying the intrinsic electrophysiology of TRN neurons.
SN  - 1662-453X
SN  - 1662-4548
ER  -