OSCR

Chronic Stress Induces Retinal Ganglion Cell Degeneration Featuring Reduced Density, Altered Intrinsic Electrophysiology, and Light Responses.

Overview

Authors: Manfei Huo1, Meizhen Zhu1, Yuqing Wu1, Zeyuan Ding1,2, Siqi Li1, Yanli Ran1
ORCID iDs: Yanli Ran
  1. Key Laboratory of Preclinical Study for New Drugs of Gansu Province, Institute of Physiology, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China
  2. The School of Life Sciences, Lanzhou University, Lanzhou 730000, China
Institutions: Lanzhou University (China)
Journal: Biology, volume 15, issue 17, article 1446
Dates: received 24 June 2026; accepted 21 August 2026; published online 24 August 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.3390/biology15171446 · PMID 42737879 · PMCID PMC13565546 · OpenAlex W7204145253
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: depression (population), cellular / molecular (subfield)
Methods: Statistics, Connectivity, Physiology & signal measures
Keywords: depression, blood perfusion, retinal ganglion cells, intrinsic properties, light responses
Topic: Retinal Development and Disorders (Molecular Biology, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Funding: Lanzhou University (561120203); National Natural Science Foundation of China (32200810)
Citations: not cited yet (Europe PMC); 55 references in the paper

Abstract

Depression is often associated with functional disturbances in the visual system. However, the fundamental features underlying these visual system aberrations in depression remain to be fully elucidated. In particular, in the first stage of visual processing, how different retinal output neuron types change their intrinsic properties and output features in response to specific light stimulation remains unclear. Here, by adopting a mouse model of depression induced by chronic unpredictable stress (CUS), we found that depression is associated with reduced blood perfusion in the retinal inner plexiform layer (IPL). The hypoperfusion in the IPL is paralleled by a remarkable reduction of retinal ganglion cell (RGC) density, with more cell loss in ipRGCs than in the general RGCs. The surviving RGCs—particularly, ipRGCs—changed their intrinsic electrical properties, exhibiting decreased membrane input resistance, more depolarized resting membrane potential, and altered spiking properties. Additionally, these cells showed stimulus-size-dependent increases in light-evoked responses. Together, our findings demonstrate that depression is associated with the retinal IPL hypoperfusion and RGC impairments (particularly ipRGCs) and suggest retinal layer- and RGC-type-specific susceptibilities, furthering our understanding of retinal pathophysiology in depression.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data Availability Statement

All data presented in this study is available at https://doi.org/10.5281/zenodo.20822064.

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 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 6 authors, 5 keywords, 2 funders, 55 references.

Cite

This paper

Huo, M., Zhu, M., Wu, Y., Ding, Z., Li, S., & Ran, Y. (2026). Chronic Stress Induces Retinal Ganglion Cell Degeneration Featuring Reduced Density, Altered Intrinsic Electrophysiology, and Light Responses. Biology, 15(17), 1446. https://doi.org/10.3390/biology15171446

BibTeX

@article{huo2026chronic,
author = {Huo, Manfei and Zhu, Meizhen and Wu, Yuqing and Ding, Zeyuan and Li, Siqi and Ran, Yanli},
title = {{Chronic Stress Induces Retinal Ganglion Cell Degeneration Featuring Reduced Density, Altered Intrinsic Electrophysiology, and Light Responses}},
journal = {Biology},
year = {2026},
month = aug,
volume = {15},
number = {17},
pages = {1446},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
issn = {2079-7737},
doi = {10.3390/biology15171446},
url = {https://doi.org/10.3390/biology15171446},
pmid = {42737879},
pmcid = {PMC13565546}
}

RIS

TY - JOUR
AU - Huo, Manfei
AU - Zhu, Meizhen
AU - Wu, Yuqing
AU - Ding, Zeyuan
AU - Li, Siqi
AU - Ran, Yanli
TI - Chronic Stress Induces Retinal Ganglion Cell Degeneration Featuring Reduced Density, Altered Intrinsic Electrophysiology, and Light Responses
T2 - Biology
J2 - Biology (Basel)
PY - 2026
DA - 2026/08/24
VL - 15
IS - 17
SP - 1446
SN - 2079-7737
PB - Multidisciplinary Digital Publishing Institute (MDPI)
DO - 10.3390/biology15171446
UR - https://doi.org/10.3390/biology15171446
LA - en
ER -

CSL-JSON

{
"id": "10.3390/biology15171446",
"type": "article-journal",
"title": "Chronic Stress Induces Retinal Ganglion Cell Degeneration Featuring Reduced Density, Altered Intrinsic Electrophysiology, and Light Responses",
"container-title": "Biology",
"author": [
{
"family": "Huo",
"given": "Manfei"
},
{
"family": "Zhu",
"given": "Meizhen"
},
{
"family": "Wu",
"given": "Yuqing"
},
{
"family": "Ding",
"given": "Zeyuan"
},
{
"family": "Li",
"given": "Siqi"
},
{
"family": "Ran",
"given": "Yanli"
}
],
"container-title-short": "Biology (Basel)",
"volume": "15",
"issue": "17",
"page": "1446",
"DOI": "10.3390/biology15171446",
"PMID": "42737879",
"PMCID": "PMC13565546",
"ISSN": "2079-7737",
"publisher": "Multidisciplinary Digital Publishing Institute (MDPI)",
"URL": "https://doi.org/10.3390/biology15171446",
"language": "en",
"issued": {
"date-parts": [
[
2026,
8,
24
]
]
}
}

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.2026.116842
Intrinsic electrical diversity of PV<sup>+</sup> retinal ganglion cells.
Journal: iScience
In common: 4 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 methods
In common: 4 references
[3] doi:10.1186/s12888-026-08216-5 [code]
Habenular structural-functional dysconnectivity in bipolar disorder: evidence from multimodal imaging and transcriptomic integration.
Journal: BMC psychiatry
In common: cellular / molecular, 3 references
[4] doi:10.1016/j.isci.2026.117088 [code]
Spatial biases in visual feature representation of mouse dorsal lateral geniculate nucleus boutons.
Journal: iScience
In common: 3 references
[5] doi:10.1126/sciadv.aed0772 [code]
Deep learning reveals a neurocomputational mechanism predicting depression risk in adolescents.
Journal: Science advances
In common: depression, 2 references
[6] doi:10.1126/sciadv.aeg3223 [code]
The extreme diversity of retinal amacrine cells has deep evolutionary roots.
Journal: Science advances
In common: cellular / molecular, 2 references
[7] doi:10.1007/s11920-026-01671-7 [code]
Light Exposure as a Modifiable Determinant of Mental Health.
Journal: Current psychiatry reports
In common: 2 references
[8] doi:10.1093/pnasnexus/pgag224 [code]
Preserving predictive information under biologically plausible compression.
Journal: PNAS nexus
In common: 2 references
[9] doi:10.1159/000553608
The Mechanism of Carboxypeptidase E Regulating NLRP3 Inflammasome Signaling in the Pathogenesis of Depression-Like Behaviors in Mice.
Journal: Neuroimmunomodulation
In common: depression, cellular / molecular, 1 reference
[10] doi:10.3389/fphar.2026.1895800
NDP-MSH rescues LPS-induced neuroinflammation, synaptic deficits, and depressive-like behaviors in mice: involvement of MC1R-cAMP/PKA signaling.
Journal: Frontiers in pharmacology
In common: depression, cellular / molecular, 1 reference

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.

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.