Intrinsic electrical diversity of PV<sup>+</sup> retinal ganglion cells.
Overview
Abstract
Mouse retinal ganglion cells (RGCs) transform visual signals into spiking outputs and are known as a heterogeneous cell population. We combined electrophysiological recordings and anatomical analyses to characterize parvalbumin-positive (PV+) RGC subtypes, including ON-OFF direction selective (OODS), ON transient small receptive field (ON tr SmRF), OFF transient medium receptive field (OFF tr MeRF), and the OFF transient small receptive field (OFF tr SmRF) RGC. Intrinsic properties such as input resistance, maximum depolarization rate, and maximum rebound firing rate distinguished five functional subtypes, including one previously unmatched population. Analysis of axonal morphology revealed subtype-specific differences in axon initial segment (AIS) length and diameter. OFF tr MeRF RGCs display shortest AISs and smallest proximal axon diameter, correlating with unique near-threshold spikelets. Following axotomy, loss of the AIS reduced maximum firing rates and altered spike properties. Our results demonstrate substantial biophysical diversity among a subset of PV+ RGCs, complementing previously described differences.
Reproduced under the paper's license (CC BY), from the paper cited above.
Code
The paper says that its authors' code is available on request: it was not published with the paper, so there is nothing to verify.
The paper's code and data availability statement is in the Data section.
Tracing map
A tracing map links a paper to the code its authors published: this paper has none (its code is available on request), so it has no map.
Data
No dataset and no data link were found in the paper.
Data and code availability
Data: All data reported in this paper will be shared by the lead contact upon request.
Code: All code used in this study has been deposited at TU Wien Research Data Repository and is publicly available at https://
Additional information: Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 3, 28 September 2026
- Authors: added Paul Werginz (0000-0002-3441-3167); removed Paul Werginz
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 3 authors, 4 keywords, 1 funder, 46 references, 4 RRIDs.
Cite
This paper
Király, V., Zeck, G., & Werginz, P. (2026). Intrinsic electrical diversity of PV&
BibTeX
@article{kiraly2026intri
author = {Király, Viktória and Zeck, Günther and Werginz, Paul},
title = {{Intrinsic electrical diversity of PV\&
journal = {iScience},
year = {2026},
month = aug,
volume = {29},
number = {8},
pages = {116842},
publisher = {Elsevier},
issn = {2589-0042},
doi = {10.1016/
url = {https://
pmid = {42631048},
pmcid = {PMC13495337}
}
RIS
TY - JOUR
AU - Király, Viktória
AU - Zeck, Günther
AU - Werginz, Paul
TI - Intrinsic electrical diversity of PV&
T2 - iScience
J2 - iScience
PY - 2026
DA - 2026/
VL - 29
IS - 8
SP - 116842
SN - 2589-0042
PB - Elsevier
DO - 10.1016/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1016/
"type": "article-journal",
"title": "Intrinsic electrical diversity of PV&
"container-title": "iScience",
"author": [
{
"family": "Király",
"given": "Viktória"
},
{
"family": "Zeck",
"given": "Günther"
},
{
"family": "Werginz",
"given": "Paul"
}
],
"container-title-short":
"volume": "29",
"issue": "8",
"page": "116842",
"DOI": "10.1016/
"PMID": "42631048",
"PMCID": "PMC13495337",
"ISSN": "2589-0042",
"publisher": "Elsevier",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
8,
13
]
]
}
}
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1016/j.isci.2026.117088 [code]
- Spatial biases in visual feature representation of mouse dorsal lateral geniculate nucleus boutons.Journal: iScienceIn common: 5 references
- [2] doi:10.1016/j.crmeth.2026.101308 [code]
- Projection targeting with phototagging to study the structure and function of retinal ganglion cells.Journal: Cell reports methodsIn common: 5 references
- [3] doi:10.3389/fncel.2026.1690466
- Purkinje cell-specific loss of Neurofascin and Ankyrin G causes disruption of axon initial segments, neurodegeneration, and cerebellar ataxia.Journal: Frontiers in cellular neuroscienceIn common: 4 references
- [4] doi:10.3390/biology15171446
- Chronic Stress Induces Retinal Ganglion Cell Degeneration Featuring Reduced Density, Altered Intrinsic Electrophysiology, and Light Responses.Journal: BiologyIn common: 4 references
- [5] doi:10.1038/s41598-026-49531-x [code]
- Population-scale analysis of frequency-dependent calcium dynamics in retinal ganglion cells under electric field stimulation.Journal: Scientific reportsIn common: 2 references
- [6] doi:10.1038/s41467-026-77800-w [code]
- Learning reorganizes dendritic and stabilizes axon initial segment inhibitory synapses in CA1 pyramidal neurons.Journal: Nature communicationsIn common: 2 references
- [7] doi:10.1126/sciadv.aee4940 [code]
- Neuron-derived SPP1 instructs microglia to limit degeneration.Journal: Science advancesIn common: 2 references
- [8] doi:10.1371/journal.pbio.3003789 [code]
- Encoding performance of cortical neurons critically depends on their morphological and neurophysiological properties.Journal: PLoS biologyIn common: 2 references
- [9] doi:10.1038/s44319-026-00786-5
- Age-related decline in nuclear envelope LINC complex drives neuronal aging via axon initial segment dysfunction.Journal: EMBO reportsIn common: 2 references
- [10] doi:10.1093/pnasnexus/pgag224 [code]
- Preserving predictive information under biologically plausible compression.Journal: PNAS nexusIn common: 2 references
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
