Evidence map›Paper›PMID 38289348›Full record

ArticleThe Journal of experimental medicine2024

Microglia at sites of atrophy restrict the progression of retinal degeneration via galectin-3 and Trem2.

Chen Yu, Eleonora M Lad, Rose Mathew, Nobuhiko Shiraki, Sejiro Littleton, Yun Chen, Jinchao Hou, Kai Schlepckow, Simone Degan, Lindsey Chew and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
12.4field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Neuroinflammation in glaucoma: a myriad of cellular pathways and players.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  6. Article
  7. Article
  8. Microglial polarization in retinal neovascularization: Friend or foe?Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Selective deletion ofiScience · 2026
    Article
  15. Review
  16. A mutation inMolecular vision · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Chen YuDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-9651-9875
Eleonora M LadDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-8435-521X
Rose MathewDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-7376-1837
Nobuhiko ShirakiDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-9420-8440
Sejiro LittletonDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-4845-4170
Yun ChenDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-0547-9463
Jinchao HouDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-3829-7551
Kai SchlepckowGerman Center for Neurodegenerative Diseases Munich , Munich, Germany.ORCID 0000-0002-1119-2293
Simone DeganDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-5417-1196
Lindsey ChewDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-2040-1579
Joshua AmasonDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-8459-7243
Joan KalnitskyDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0009-0008-7025-0749
Catherine Bowes RickmanDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-8555-9596
Alan D ProiaDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-6646-2695
Marco ColonnaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0001-5222-4987
Christian HaassGerman Center for Neurodegenerative Diseases Munich , Munich, Germany.ORCID 0000-0002-4869-1627
Daniel R SabanDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0003-4177-8065
Duke University · USWashington University in St. Louis · USGerman Center for Neurodegenerative Diseases · DECampbell University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
Defining the Immune Cell Roles in Meibomian Gland Dysfunction in the Context of Ocular Surface Immune DiseasesR01EY021798 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI SABAN, DANIEL RAPHAEL · 2012 to 2025
$5.3M
Cellular and Molecular Dynamics of Retinal Microglial in the Context of Photoreceptor DegenerationR01EY030906 · NEI · DUKE UNIVERSITY · PI Daniel Raphael Saban · 2020 to 2026
$3.5M
Complement factor H modulates lipoprotein clearance in AMDR01EY031748 · NEI · DUKE UNIVERSITY · PI BOWES RICKMAN, CATHERINE · 2020 to 2024
$2.8M
Monocytes in Dry Age-Related Macular DegenerationK23EY026988 · NEI · DUKE UNIVERSITY · PI LAD, ELEONORA GEORGETA · 2016 to 2018
$420k
NEI NIH HHS K23 EY026988NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY021798NEI NIH HHS R01 EY030906NEI NIH HHS R01 EY031748NIGMS NIH HHS T32 GM007171NIH HHS R01EY030906
6 · The paper itself

Abstract

Outer retinal degenerations, including age-related macular degeneration (AMD), are characterized by photoreceptor and retinal pigment epithelium (RPE) atrophy. In these blinding diseases, macrophages accumulate at atrophic sites, but their ontogeny and niche specialization remain poorly understood, especially in humans. We uncovered a unique profile of microglia, marked by galectin-3 upregulation, at atrophic sites in mouse models of retinal degeneration and human AMD. In disease models, conditional deletion of galectin-3 in microglia led to phagocytosis defects and consequent augmented photoreceptor death, RPE damage, and vision loss, indicating protective roles. Mechanistically, Trem2 signaling orchestrated microglial migration to atrophic sites and induced galectin-3 expression. Moreover, pharmacologic Trem2 agonization led to heightened protection but in a galectin-3-dependent manner. In elderly human subjects, we identified this highly conserved microglial population that expressed galectin-3 and Trem2. This population was significantly enriched in the macular RPE-choroid of AMD subjects. Collectively, our findings reveal a neuroprotective population of microglia and a potential therapeutic target for mitigating retinal degeneration.

Indexed as

Galectin 3Membrane GlycoproteinsReceptors, ImmunologicRetinal DegenerationAgedAnimalsAtrophyHumansMacrophagesMiceMicrogliaGalectin 3Lgals3 protein, mouseMembrane GlycoproteinsReceptors, ImmunologicTrem2 protein, mouse

Identifiers

PMID38289348
PMCPMC10826045
OpenAlexW4391348413

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.