Evidence map›Paper›PMID 29526794›Full record

ArticleExperimental eye research2018

Role of SARM1 and DR6 in retinal ganglion cell axonal and somal degeneration following axonal injury.

Kimberly A Fernandes, Katherine L Mitchell, Amit Patel, Olivia J Marola, Peter Shrager, Donald J Zack, Richard T Libby, Derek S Welsbie

Abstract read
In one paragraph

Article in Experimental eye research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.1field-weighted citation impact, top 8% 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, 82 citations in OpenAlex.

  1. Article
  2. IL1A enhances TNF-induced retinal ganglion cell death.Frontiers in aging neuroscience · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

8 authors at 3 institutions in 1 country.

Kimberly A FernandesDepartment of Ophthalmology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Katherine L MitchellDepartment of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Amit PatelDepartment of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA; Shiley Eye Institute, University of California, La Jolla, San Diego, CA 92037, USA.
Olivia J MarolaDepartment of Ophthalmology, University of Rochester Medical Center, Rochester, NY 14642, USA; Department of Pathology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Peter ShragerDepartment of Neuroscience and Del Monte Institute for Neuroscience, University of Rochester Medical Center, Rochester, NY 14642, USA.
Donald J ZackDepartment of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA; Department of Neuroscience, Department of Molecular Biology and Genetics, Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Richard T LibbyDepartment of Ophthalmology, University of Rochester Medical Center, Rochester, NY 14642, USA; Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA; The Center for Visual Sciences, University of Rochester Medical Center, Rochester, NY 14642, USA. Electronic address: richard_libby@urmc.rochester.edu.
Derek S WelsbieShiley Eye Institute, University of California, La Jolla, San Diego, CA 92037, USA. Electronic address: dwelsbie@ucsd.edu.
University of Rochester Medical Center · USJohns Hopkins University · USUniversity of California San Diego · US

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Jiang Qian · 1985 to 2026
$22.1M
VISUAL SCIENCET32EY007125 · NEI · UNIVERSITY OF ROCHESTER · PI Krystel R Huxlin, Duje Tadin · 1990 to 2026
$7.1M
Cell Death Pathways in Glaucomatous NeurodegenerationR01EY018606 · NEI · UNIVERSITY OF ROCHESTER · PI JOHN, SIMON W, LIBBY, RICHARD T · 2008 to 2023
$5.8M
Dual Leucine Zipper Kinase (DLK) as a Mediator of Retinal Ganglion Cell InjuryR01EY023754 · NEI · JOHNS HOPKINS UNIVERSITY · PI ZACK, DONALD J. · 2013 to 2016
$1.6M
NEI NIH HHS P30 EY001765NEI NIH HHS R01 EY018606NEI NIH HHS R01 EY023754NEI NIH HHS T32 EY007125
6 · The paper itself

Abstract

Optic neuropathies such as glaucoma are characterized by the degeneration of retinal ganglion cells (RGCs) and the irreversible loss of vision. In these diseases, focal axon injury triggers a propagating axon degeneration and, eventually, cell death. Previous work by us and others identified dual leucine zipper kinase (DLK) and JUN N-terminal kinase (JNK) as key mediators of somal cell death signaling in RGCs following axonal injury. Moreover, others have shown that activation of the DLK/JNK pathway contributes to distal axonal degeneration in some neuronal subtypes and that this activation is dependent on the adaptor protein, sterile alpha and TIR motif containing 1 (SARM1). Given that SARM1 acts upstream of DLK/JNK signaling in axon degeneration, we tested whether SARM1 plays a similar role in RGC somal apoptosis in response to optic nerve injury. Using the mouse optic nerve crush (ONC) model, our results show that SARM1 is critical for RGC axonal degeneration and that axons rescued by SARM1 deficiency are electrophysiologically active. Genetic deletion of SARM1 did not, however, prevent DLK/JNK pathway activation in RGC somas nor did it prevent or delay RGC cell death. These results highlight the importance of SARM1 in RGC axon degeneration and suggest that somal activation of the DLK/JNK pathway is activated by an as-yet-unidentified SARM1-independent signal.

Indexed as

Disease Models, AnimalAnimalsApoptosisArmadillo Domain ProteinsAxonsCell CountCell SurvivalCytoskeletal ProteinsElectrophysiologyImmunohistochemistryMiceMice, Inbred C57BLMice, KnockoutNerve CrushOptic Nerve InjuriesReceptors, Tumor Necrosis FactorArmadillo Domain ProteinsCytoskeletal ProteinsReceptors, Tumor Necrosis FactorSARM1 protein, mouseTnfrsf21 protein, mouseAxon degenerationDual leucine zipper kinase (DLK)Neurodegenerative diseaseRetinal ganglion cell (RGC)Sterile alpha and TIR motif containing 1 (SARM1)

Identifiers

PMID29526794
PMCPMC5964014
OpenAlexW2793093998

What OpenQuestion 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 OpenQuestion graph.