Evidence map›Paper›PMID 28834283›Full record

ArticleCNS neuroscience & therapeutics2017

RNAi-mediated ephrin-B2 silencing attenuates astroglial-fibrotic scar formation and improves spinal cord axon growth.

Yi Li, Ying Chen, Ling Tan, Jing-Ying Pan, Wei-Wei Lin, Jian Wu, Wen Hu, Xue Chen, Xiao-Dong Wang

Open access · bronzeAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 35% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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  15. Unraveling Axon Guidance during Axotomy and Regeneration.International journal of molecular sciences · 2021
    Review
  16. EphrinB2-EphB2 signaling for dendrite protection after neuronal ischemiaJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
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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

9 authors at 2 institutions in 1 country.

Yi LiDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.
Ying ChenDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.
Ling TanDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.
Jing-Ying PanDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.
Wei-Wei LinDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.
Jian WuDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.
Wen HuKey Laboratory for Neuroregeneration of Ministry of Education and Co-innovation Center for Neuroregeneration of Jiangsu Province, Nantong University, Nantong, China.
Xue ChenDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.
Xiao-Dong WangDepartment of Histology and Embryology, Medical College, Nantong University, Nantong, China.ORCID http://orcid.org/0000-0003-4813-6858
Nantong University · CNJiangnan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsAstroglial-fibrotic scar formation following central nervous system injury can help repair blood-brain barrier and seal the lesion, whereas it also represents a strong barrier for axonal regeneration. Intensive preclinical efforts have been made to eliminate/reduce the inhibitory part and, in the meantime, preserve the beneficial role of astroglial-fibrotic scar.

methodsIn this study, we established an in vitro system, in which coculture of astrocytes and meningeal fibroblasts was treated with exogenous transforming growth factor-β1 (TGF-β1) to form astroglial-fibrotic scar-like cell clusters, and thereby evaluated the efficacy of RNAi targeting ephrin-B2 in preventing scar formation from the very beginning. We further tested the effect of RNAi-based mitigation of astroglial-fibrotic scar on spinal axon outgrowth on a custom-made microfluidic platform.

resultsWe found that siRNA targeting ephrin-B2 significantly reduced both the number and the diameter of cell clusters induced by TGF-β1 and diminished the expression of aggrecan and versican in the coculture, and allowed for significantly longer extension of outgrowing spinal cord axons into astroglial-fibrotic scar as assessed on the microfluidic platform.

conclusionsThese results suggest that astroglial-fibrotic scar formation and particularly the expression of aggrecan and versican could be mitigated by ephrin-B2 specific siRNA, thus improving the microenvironment for spinal axon regeneration.

Indexed as

AggrecansAnimalsAstrocytesAxonsCicatrixCoculture TechniquesEphrin-B2FibroblastsMeningesMotor NeuronsNeuronal OutgrowthRats, Sprague-DawleyReceptor, EphB2RNA InterferenceRNAi TherapeuticsSpinal CordAggrecansEphrin-B2Receptor, EphB2Transforming Growth Factor beta1Vcan protein, ratVersicansastroglial-fibrotic scaraxonal regenerationephrin-B2microfluidic platformsiRNAspinal cord injury

Identifiers

PMID28834283
PMCPMC6492699
OpenAlexW2748502325

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.