Evidence map›Paper›PMID 40442071›Full record

ArticleCell death & disease2025

Reln-Dab1 pathway mitigates retinal ganglion cell apoptosis in retinal ischemia-reperfusion injury.

Ning Xu, Zongyuan Li, Xiangwen Zeng, Yilin Jiang, Tunan Sun, Shuyu Liu, Na Li, Zhao Li, Yifei Huang, Liqiang Wang

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

10 authors.

Ning Xu *Medical School of Chinese People's Liberation Army, Beijing, China.
Zongyuan Li *Medical School of Chinese People's Liberation Army, Beijing, China.
Xiangwen Zeng *Medical School of Chinese People's Liberation Army, Beijing, China.
Yilin JiangMedical School of Chinese People's Liberation Army, Beijing, China.
Tunan SunMedical School of Chinese People's Liberation Army, Beijing, China.
Shuyu LiuMedical School of Chinese People's Liberation Army, Beijing, China.
Na LiMedical School of Chinese People's Liberation Army, Beijing, China.
Zhao LiMedical School of Chinese People's Liberation Army, Beijing, China.
Yifei HuangMedical School of Chinese People's Liberation Army, Beijing, China. 301yk@sina.com.
Liqiang WangMedical School of Chinese People's Liberation Army, Beijing, China. liqiangw301@163.com.ORCID http://orcid.org/0000-0002-1718-0453

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemia-reperfusion (I/R) injury is associated with a variety of retinal diseases, resulting in loss of the number of ganglion cells (RGCs), retinal structural disorders, and retinal dysfunction. The Reelin protein is an important regulator of neuronal migration and synaptogenesis, and the Reln signaling pathway plays an essential role in regulating the targeted projection of RGC dendrites and neuronal survival, which has not been reported in retinal I/R injury. The aim of this study was to investigate the expression, role and mechanism of Reln in retinal I/R injury. By establishing Reln-CreERT2 mTmG transgenic mice, it was observed that the expression of Reln initially decreased and then increased after retinal I/R injury. After supplementing exogenous Reelin protein and adeno-associated virus (AAV)-targeted regulation of Reln in vivo, morphological and functional experiments demonstrated its effectiveness in protecting RGCs survival, maintaining morphological integrity of the retina, and inhibiting post-injury retinal dysfunction. Furthermore, integrin β1 (Itgb1) was identified as the main receptor through which Reelin exerts neuroprotective effects while regulating retinal I/R injury repair through the Dab1-PI3K-Akt pathway. These findings provide evidence supporting Reln pathway's role in maintaining retinal homeostasis and facilitating injury repair. Moreover, these findings have significant implications for identifying new targets for preventing and treating various retinal diseases.

Indexed as

Adaptor Proteins, Signal TransducingApoptosisCell Adhesion Molecules, NeuronalExtracellular Matrix ProteinsNerve Tissue ProteinsReperfusion InjuryRetinal Ganglion CellsSerine EndopeptidasesAnimalsIntegrin beta1MaleMiceMice, Inbred C57BLMice, TransgenicReelin ProteinSignal TransductionAdaptor Proteins, Signal TransducingCell Adhesion Molecules, NeuronalDab1 protein, mouseExtracellular Matrix ProteinsIntegrin beta1Nerve Tissue ProteinsReelin ProteinReln protein, mouseSerine Endopeptidases

Identifiers

PMID40442071
PMCPMC12122947

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.