Evidence map›Paper›PMID 32797200›Full record

ArticleInvestigative ophthalmology & visual science2020

Autophagy in the Aging and Experimental Ocular Hypertensive Mouse Model.

April Nettesheim, Angela Dixon, Myoung Sup Shim, Aislyn Coyne, Molly Walsh, Paloma B Liton

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.8field-weighted citation impact, top 5% of its field
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

25 citing papers in PubMed, 34 citations in OpenAlex.

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  14. Review
  15. Autophagy in Human Retinal Neurons in Glaucoma.Bulletin of experimental biology and medicine · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. Mitophagy in the aging nervous system.Frontiers in cell and developmental biology · 2022
    Review
  20. Review
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

6 authors at 1 institution in 1 country.

April NettesheimDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Angela DixonDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Myoung Sup ShimDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Aislyn CoyneDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Molly WalshDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Paloma B LitonDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Duke University · US

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
Autophagy and Mechanotransduction in the Trabecular MeshworkR01EY026885 · NEI · DUKE UNIVERSITY · PI Paloma Liton · 2016 to 2026
$4.7M
Lysosomal Enzymes in Outflow Pathway Physiology and PathophysiologyR01EY027733 · NEI · DUKE UNIVERSITY · PI LITON, PALOMA · 2017 to 2020
$1.8M
NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY026885NEI NIH HHS R01 EY027733
6 · The paper itself

Abstract

Purpose: To investigate autophagy in the outflow pathway and ganglion cell layer in the aging and ocular hypertensive mouse. Methods: Both 4-month-old and 18-month-old C57BL/6J and GFP-LC3 mice were subjected to unilateral injection of hypertonic saline into a limbal vein, causing sclerosis of the outflow pathway and subsequent elevation of intraocular pressure (IOP). IOP was measured on a weekly basis using a rebound tonometer. Protein expression levels of LC3B, Lamp1, and p62 were evaluated by western blot and/or immunofluorescence. Retinal ganglion cell (RGC) count was performed in whole retinal flat mounts using an anti-Brn3a antibody. Optic nerves were fixed with 4% paraformaldehyde and resin-embedded for axon counts and electron microscopy. Results: In contrast to 18-month-old mice, which developed sustained elevated IOP with a single injection, 4-month-old mice were refractory to high elevations of IOP. Interestingly, both the percentage of animals that developed elevated IOP and the mean ∆IOP were significantly higher in the transgenic mice compared to C57BL/6J. Immunofluorescence and western blot analysis showed dysregulated autophagy in the iridocorneal and retina tissues from 18-month-old mice compared to 4-month-old ones. Moreover, the LC3-II/LC3-I ratio correlated with IOP. As expected, injected hypertensive eyes displayed axonal degeneration and RGC death. RGC and axon loss were significantly exacerbated with aging, especially when combined with GFP-LC3 expression. Autophagic structures were observed in the degenerating axons. Conclusions: Our results indicate dysregulation of autophagy in the trabecular meshwork and retinal tissues with aging and suggest that such dysregulation of autophagy contributes to neurodegeneration in glaucoma.

Indexed as

AgingAutophagyAnimalsBlotting, WesternDisease Models, AnimalFemaleFluorescent Antibody TechniqueGreen Fluorescent ProteinsIntraocular PressureMaleMiceMice, Inbred C57BLMice, TransgenicOcular HypertensionOptic NerveRetinal Ganglion CellsGreen Fluorescent Proteins

Identifiers

PMID32797200
PMCPMC7441338
OpenAlexW3049006941

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.