Evidence map›Paper›PMID 28898265›Full record

ArticlePloS one2017

Sigma 1 receptor regulates ERK activation and promotes survival of optic nerve head astrocytes.

Jing Zhao, Barbara A Mysona, Jing Wang, Graydon B Gonsalvez, Sylvia B Smith, Kathryn E Bollinger

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Sigma 1 Receptor Modulates Optic Nerve Head Astrocyte Reactivity.Investigative ophthalmology & visual science · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Sigma 1 receptor: A novel therapeutic target in retinal disease.Progress in retinal and eye research · 2018
    Review
  18. 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

6 authors at 2 institutions in 1 country.

Jing ZhaoJames and Jean Culver Vision Discovery Institute, Augusta, Georgia, United States of America.
Barbara A MysonaJames and Jean Culver Vision Discovery Institute, Augusta, Georgia, United States of America.
Jing WangJames and Jean Culver Vision Discovery Institute, Augusta, Georgia, United States of America.
Graydon B GonsalvezDepartment of Cellular Biology and Anatomy, Medical College of Georgia, Augusta University, Augusta, Georgia, United States of America.
Sylvia B SmithJames and Jean Culver Vision Discovery Institute, Augusta, Georgia, United States of America.
Kathryn E BollingerJames and Jean Culver Vision Discovery Institute, Augusta, Georgia, United States of America.
Augusta University · USDiscovery Institute · US

Funding

Diabetic retinopathy: sigma receptor 1 (??R1) as a novel therapeutic target.R01EY014560 · NEI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI SMITH, SYLVIA B. · 2004 to 2013
$2.7M
Sigma 1 Receptor: a novel therapeutic target for retinal degenerationR01EY028103 · NEI · AUGUSTA UNIVERSITY · PI SMITH, SYLVIA B. · 2017 to 2019
$1.2M
Molecular Mechanisms of Sigma Receptor 1-Mediated NeuroprotectionK08EY021758 · NEI · AUGUSTA UNIVERSITY · PI BOLLINGER, KATHRYN · 2011 to 2015
$1.1M
NEI NIH HHS K08 EY021758NEI NIH HHS R01 EY014560NEI NIH HHS R01 EY028103
6 · The paper itself

Abstract

The sigma 1 receptor (S1R) is a unique transmembrane protein that has been shown to regulate neuronal differentiation and cellular survival. It is expressed within several cell types throughout the nervous system and visceral organs, including neurons and glia within the eye. S1R ligands are therapeutic targets for diseases ranging from neurodegenerative conditions to neoplastic disorders. However, effects of S1R activation and inhibition within glia cells are not well characterized. Within the eye, the astrocytes at the optic nerve head are crucial to the health and survival of the neurons that send visual information to the brain. In this study, we used the S1R-specific agonist, (+)-pentazocine, to evaluate S1R activation within optic nerve head-derived astrocytes (ONHAs). Treatment of ONHAs with (+)-pentazocine attenuated the level and duration of stress-induced ERK phosphorylation following oxidative stress exposure and promoted survival of ONHAs. These effects were specific to S1R activation because they were not observed in ONHAs that were depleted of S1R using siRNA-mediated knockdown. Collectively, our results suggest that S1R activation suppresses ERK1/2 phosphorylation and protects ONHAs from oxidative stress-induced death.

Indexed as

Analgesics, OpioidAnimalsAstrocytesCells, CulturedHeLa CellsHumansMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Optic NerveOxidative StressPentazocineRatsRats, Sprague-DawleyReceptors, sigmaSigma-1 ReceptorAnalgesics, OpioidMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3PentazocineReceptors, sigmaSigma-1 Receptor

Identifiers

PMID28898265
PMCPMC5595338
OpenAlexW2755726786

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.