Evidence map›Paper›PMID 32607759›Full record

ArticleJournal of molecular neuroscience : MN2021

Nrn1 Overexpression Attenuates Retinal Ganglion Cell Apoptosis, Promotes Axonal Regeneration, and Improves Visual Function Following Optic Nerve Crush in Rats.

Tingting Huang, He Li, Shoumei Zhang, Fang Liu, Dong Wang, Jiajun Xu

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-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

11 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Neuritin 1 Drives Therapeutic Preservation of Retinal Ganglion Cells in anJournal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2024
    Article
  6. Article
  7. Article
  8. Zfp503/Nlz2 Is Required for RPE Differentiation and Optic Fissure Closure.Investigative ophthalmology & visual science · 2022
    Article
  9. Article
  10. Article
  11. 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 1 institution in 1 country.

Tingting HuangDepartment of Anatomy, Second Military Medical University, Shanghai, 200433, People's Republic of China.
He LiDepartment of Anatomy, Second Military Medical University, Shanghai, 200433, People's Republic of China.
Shoumei ZhangDepartment of Anatomy, Second Military Medical University, Shanghai, 200433, People's Republic of China.
Fang LiuDepartment of Anatomy, Second Military Medical University, Shanghai, 200433, People's Republic of China.
Dong WangDepartment of Anatomy, Second Military Medical University, Shanghai, 200433, People's Republic of China.
Jiajun XuDepartment of Anatomy, Second Military Medical University, Shanghai, 200433, People's Republic of China. xujiajunsmmu@163.com.
Second Military Medical University · CN

Funding

National Natural Science Foundation of China 31271282
6 · The paper itself

Abstract

Neuritin (Nrn1) is a small highly conserved extracellular membrane protein involved in the process of neural cell survival and differentiation, axonal and dendritic growth, and synapse formation and maturation. Previous studies have demonstrated that intravitreal injection of recombinant Nrn1 as a gene therapy could alleviate retinal ganglion cell (RGC) apoptosis and promote optic nerve axon regeneration after optic nerve crush (ONC). However, the mechanism underlying the repairing effect of Nrn1 against optic never injury remains elusive. In this study, a rAAV2-mediated Nrn1 overexpression vector (AAV2-Nrn1) was applied to treat ONC through intravitreal injection for the purpose of further exploring the effect and mechanism of Nrn1 in repairing the injured optic nerve. The results showed that AAV2-Nrn1 was mainly transfected into RGCs without affecting astrocytes. Nrn1 overexpression effectively reduced RGC apoptosis and promoted optic nerve regeneration and visual function restoration as demonstrated by retinal imaging, histopathological analysis, and physiological function detection in vivo following ONC. Immunoblot assay revealed that functional molecules of Nrn1 activated the Akt1 and Stat3 pathways and inhibited the mitochondrial apoptotic pathway. The results of the present study may provide experimental evidence for further application of Nrn1 to the clinical treatment of optic nerve injury.

Indexed as

AnimalsApoptosisAxonsDependovirusEvoked Potentials, VisualGene Expression RegulationGenetic VectorsGPI-Linked ProteinsHEK293 CellsHumansMaleNerve CrushNerve RegenerationNeuropeptidesOptic NerveOptic Nerve InjuriesGPI-Linked ProteinsNeuropeptidesNrn1 protein, ratRecombinant Fusion ProteinsAAV2-Nrn1ApoptosisOptic nerve crushOverexpressionRegenerationSignaling pathway

Identifiers

PMID32607759
OpenAlexW3039323277

What OpenQuestion holds

Textmetadata
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.