Evidence map›Paper›PMID 33622104›Full record

ArticleOpen biology2021

Injury-induced Cavl-expressing cells at lesion rostral side play major roles in spinal cord regeneration.

Chih-Wei Zeng, Yasuhiro Kamei, Shuji Shigenobu, Jin-Chuan Sheu, Huai-Jen Tsai

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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, 22 citations in OpenAlex.

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  13. Functional trajectories during innate spinal cord repair.Frontiers in molecular neuroscience · 2023
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  15. International journal of molecular sciences · 2022
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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

5 authors at 4 institutions in 2 countries.

Chih-Wei ZengInstitute of Molecular and Cellular Biology, College of Life Science, National Taiwan University, Taipei 10617, Taiwan.
Yasuhiro KameiSpectrography and Bioimaging Facility, National Institute for Basic Biology (NIBB), National Institutes of Natural Sciences (NINS), Okazaki 444-8585, Japan.
Shuji ShigenobuDepartment of Basic Biology, The Graduate University for Advanced Studies (SOKENDAI), Okazaki 444-8585, Japan.
Jin-Chuan SheuLiver Disease Prevention and Treatment Research Foundation, Taipei 10008, Taiwan.
Huai-Jen TsaiInstitute of Biomedical Sciences, Mackay Medical College, New Taipei City 25245, Taiwan.
Fu Jen Catholic University · TWNational Institute for Basic Biology · JPNational Taiwan University · TWThe Graduate University for Advanced Studies, SOKENDAI · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extent of cellular heterogeneity involved in neuronal regeneration after spinal cord injury (SCI) remains unclear. Therefore, we established stress-responsive transgenic zebrafish embryos with SCI. As a result, we found an SCI-induced cell population, termed SCI stress-responsive regenerating cells (SrRCs), essential for neuronal regeneration post-SCI. SrRCs were mostly composed of subtypes of radial glia (RGs-SrRCs) and neuron stem/progenitor cells (NSPCs-SrRCs) that are able to differentiate into neurons, and they formed a bridge across the lesion and connected with neighbouring undamaged motor neurons post-SCI. Compared to SrRCs at the caudal side of the SCI site (caudal-SrRCs), rostral-SrRCs participated more actively in neuronal regeneration. After RNA-seq analysis, we discovered that

Indexed as

Spinal Cord RegenerationAnimalsCaveolin 1Cells, CulturedMotor NeuronsNeural Stem CellsNeuronal OutgrowthSpinal Cord InjuriesUp-RegulationZebrafishZebrafish ProteinsCaveolin 1Zebrafish Proteinsaxoncaveolin-1motoneuronneuronal regenerationspinal cord injurytransgenic zebrafish

Identifiers

PMID33622104
PMCPMC8061693
OpenAlexW3131175737

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.