Evidence map›Paper›PMID 40738390›Full record

ArticleExperimental eye research2025

Cellular responses to short-term intraocular pressure elevation in a porcine eye explant model.

Kelsey Ritter-Gordy, Sarah Quillen, Mary E Pease, Thomas V Johnson, Bryce Chiang, Harry A Quigley, Elizabeth C Kimball

Abstract read
In one paragraph

Article in Experimental eye research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Kelsey Ritter-GordyGlaucoma Center of Excellence, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sarah QuillenGlaucoma Center of Excellence, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: Squille1@jh.edu.
Mary E PeaseGlaucoma Center of Excellence, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Thomas V JohnsonGlaucoma Center of Excellence, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Bryce ChiangGlaucoma Center of Excellence, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Harry A QuigleyGlaucoma Center of Excellence, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Elizabeth C KimballGlaucoma Center of Excellence, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI JEFFREY MUMM · 1985 to 2026
$22.1M
PATHOGENESIS OF GLAUCOMATOUS OPTIC NERVE DAMAGER01EY002120 · NEI · JOHNS HOPKINS UNIVERSITY · PI QUIGLEY, HARRY ALAN · 1985 to 2025
$12.6M
Pathogenesis of Glaucomatous Optic Nerve DamageR56EY002120 · NEI · JOHNS HOPKINS UNIVERSITY · PI QUIGLEY, HARRY ALAN · 2008 to 2008
$369k
NEI NIH HHS P30 EY001765NEI NIH HHS R01 EY002120NEI NIH HHS R56 EY002120
6 · The paper itself

Abstract

Cost-effective glaucoma models are needed in animals whose optic nerve head lamina cribrosa (LC) is similar to the human, such as pigs. We studied responses to acute intraocular pressure (IOP) elevation in porcine eye explants in which eyes were cannulated to maintain IOP at 10 or 50 mmHg for 4, 16 or 24 h. Quantitative fluorescence imaging of amyloid precursor protein (APP) found localized axonal transport at the LC in explant tissue after IOP elevations for 4 and 16 h, as do primate glaucoma and human glaucoma eyes (both P ≤ 0.001, Mann Whitney). Immunofluorescent labeling identified which cells express molecules in the transforming growth factor β and integrin signaling pathways. Quantification of mechanosensitive pathway molecules was performed at 4 and 24 h on micro-dissected retina, prelamina, LC and optic nerve. LC RhoA increased at 24 h (P = 0.03, t-test), myelinated optic nerve ratio of p-cofilin to total cofilin increased at 4 h (P = 0.05, t-test), and LC p-Smad2/3 increased at 24 h (P = 0.01, t-test). Integrin β1 and vinculin decreased at 4 h in the LC (P = 0.004 and P = 0.04, respectively, t-tests). At 24 h, LC integrin β1 returned to baseline, while vinculin increased (P = 0.004). Explants demonstrate dynamic changes in axons and astrocytes during at least 24 h post mortem. Mechanosensitive signaling pathways can be studied in porcine eyes with large sample sizes at low cost.

Indexed as

GlaucomaIntraocular PressureOcular HypertensionOptic DiskAmyloid beta-Protein PrecursorAnimalsDisease Models, AnimalSignal TransductionSwineTransforming Growth Factor betaAmyloid beta-Protein PrecursorTransforming Growth Factor betaGlaucoma modelIntegrinIntraocular pressurePigRho kinase

Identifiers

PMID40738390
PMCPMC12653994

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.