Evidence map›Paper›PMID 25755083›Full record

ArticleDisease models & mechanisms2015

Neurodegeneration severity can be predicted from early microglia alterations monitored in vivo in a mouse model of chronic glaucoma.

Alejandra Bosco, Cesar O Romero, Kevin T Breen, Alexis A Chagovetz, Michael R Steele, Balamurali K Ambati, Monica L Vetter

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

112 citing papers in PubMed, 157 citations in OpenAlex.

  1. Article
  2. Review
  3. Neuroinflammation in glaucoma: a myriad of cellular pathways and players.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. The P2X7 Receptor Regulates IL-1β Secretion in the Human Retina.International journal of molecular sciences · 2025
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Role of Microglia in Glaucomatous Pathology.Advances in experimental medicine and biology · 2025
    Review
  19. Frontiers in ophthalmology · 2025
    Review
  20. Article

52 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Alejandra BoscoDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132, USA alejandra.bosco@neuro.utah.edu.
Cesar O RomeroDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132, USA.
Kevin T BreenDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132, USA.
Alexis A ChagovetzDepartment of Human Genetics, University of Utah, Salt Lake City, UT 84132, USA.
Michael R SteeleDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132, USA.
Balamurali K AmbatiDepartment of Ophthalmology and Visual Sciences, University of Utah, Salt Lake City, UT 84132, USA.
Monica L VetterDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132, USA.
University of Utah · US

Funding

University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI PAUL STEVEN BERNSTEIN · 2005 to 2026
$14.6M
The Role of Soluble Flt-1 and Raver2 in Ocular Vascular DemarcationsR01EY017950 · NEI · UNIVERSITY OF UTAH · PI AMBATI, BALAMURALI K · 2008 to 2021
$5.2M
Intraceptor Interference of VEGF PathwaysR01EY017182 · NEI · UNIVERSITY OF UTAH · PI AMBATI, BALAMURALI K · 2007 to 2017
$3.6M
The role of microglia in experimental glaucomaR01EY020878 · NEI · UNIVERSITY OF UTAH · PI VETTER, MONICA L · 2010 to 2014
$1.6M
Inhibitory regulation of microglia in glaucomaR01EY023621 · NEI · UNIVERSITY OF UTAH · PI VETTER, MONICA L · 2013 to 2016
$1.2M
NEI NIH HHS 5P30EY014800NEI NIH HHS P30 EY014800NEI NIH HHS R01 EY017182NEI NIH HHS R01EY017182NEI NIH HHS R01 EY017950NEI NIH HHS R01EY017950NEI NIH HHS R01 EY020878NEI NIH HHS R01EY020878NEI NIH HHS R01 EY023621NEI NIH HHS R01EY023621NIGMS NIH HHS R01GM09815
6 · The paper itself

Abstract

Microglia serve key homeostatic roles, and respond to neuronal perturbation and decline with a high spatiotemporal resolution. The course of all chronic CNS pathologies is thus paralleled by local microgliosis and microglia activation, which begin at early stages of the disease. However, the possibility of using live monitoring of microglia during early disease progression to predict the severity of neurodegeneration has not been explored. Because the retina allows live tracking of fluorescent microglia in their intact niche, here we investigated their early changes in relation to later optic nerve neurodegeneration. To achieve this, we used the DBA/2J mouse model of inherited glaucoma, which develops progressive retinal ganglion cell degeneration of variable severity during aging, and represents a useful model to study pathogenic mechanisms of retinal ganglion cell decline that are similar to those in human glaucoma. We imaged CX3CR1(+/GFP) microglial cells in vivo at ages ranging from 1 to 5 months by confocal scanning laser ophthalmoscopy (cSLO) and quantified cell density and morphological activation. We detected early microgliosis at the optic nerve head (ONH), where axonopathy first manifests, and could track attenuation of this microgliosis induced by minocycline. We also observed heterogeneous and dynamic patterns of early microglia activation in the retina. When the same animals were aged and analyzed for the severity of optic nerve pathology at 10 months of age, we found a strong correlation with the levels of ONH microgliosis at 3 to 4 months. Our findings indicate that live imaging and monitoring the time course and levels of early retinal microgliosis and microglia activation in glaucoma could serve as indicators of future neurodegeneration severity.

Indexed as

AnimalsCX3C Chemokine Receptor 1Disease Models, AnimalFemaleGlaucomaGliosisLasersMaleMice, Inbred C57BLMice, Inbred DBAMicrogliaNerve DegenerationOphthalmoscopyOptic DiskReceptors, ChemokineRetinaCX3C Chemokine Receptor 1Cx3cr1 protein, mouseReceptors, ChemokineConfocal ophthalmoscopyCx3cr1GFP/+ DBA/2JLive image analysisMicroglia activationMicrogliosisRetinal ganglion cells

Identifiers

PMID25755083
PMCPMC4415894
OpenAlexW2108824480

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.