Evidence map›Paper›PMID 37997694›Full record

ArticleDevelopment (Cambridge, England)2023

In toto imaging of glial JNK signaling during larval zebrafish spinal cord regeneration.

Clayton J Becker, Valentina Cigliola, Pierre Gillotay, Ashley Rich, Alessandro De Simone, Yanchao Han, Stefano Di Talia, Kenneth D Poss

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Journal of cardiovascular development and disease · 2024
    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

8 authors at 4 institutions in 4 countries.

Clayton J BeckerDuke Regeneration Center and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Valentina CigliolaDuke Regeneration Center and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Pierre GillotayDuke Regeneration Center and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Ashley RichDuke Regeneration Center and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Alessandro De SimoneDepartment of Genetics and Evolution, University of Geneva, 1211 Geneva, Switzerland.
Yanchao HanDepartment of Cardiovascular Surgery of the First Affiliated Hospital & Institute for Cardiovascular Science, Suzhou Medical College, Soochow University, Suzhou, 215006 Jiangsu, China.ORCID 0000-0002-1838-0836
Stefano Di TaliaDuke Regeneration Center and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0001-9758-7925
Kenneth D PossDuke Regeneration Center and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0002-6743-5709
Duke Medical Center · USCentre National de la Recherche Scientifique · FRSoochow University · CNUniversity of Geneva · CH

Funding

LIVE IMAGING OF BONE REGENERATION IN ZEBRAFISHR01AR076342 · NIAMS · DUKE UNIVERSITY · PI Stefano Di Talia, KENNETH D POSS · 2020 to 2026
$4.2M
Secreted Factors for Zebrafish Spinal Cord RegenerationR21NS124635 · NINDS · DUKE UNIVERSITY · PI POSS, KENNETH D · 2022 to 2023
$443k
NIAMS NIH HHS R01 AR076342NIH HHS R21 NS124635NINDS NIH HHS R21 NS124635
6 · The paper itself

Abstract

Identification of signaling events that contribute to innate spinal cord regeneration in zebrafish can uncover new targets for modulating injury responses of the mammalian central nervous system. Using a chemical screen, we identify JNK signaling as a necessary regulator of glial cell cycling and tissue bridging during spinal cord regeneration in larval zebrafish. With a kinase translocation reporter, we visualize and quantify JNK signaling dynamics at single-cell resolution in glial cell populations in developing larvae and during injury-induced regeneration. Glial JNK signaling is patterned in time and space during development and regeneration, decreasing globally as the tissue matures and increasing in the rostral cord stump upon transection injury. Thus, dynamic and regional regulation of JNK signaling help to direct glial cell behaviors during innate spinal cord regeneration.

Indexed as

Spinal Cord InjuriesSpinal Cord RegenerationAnimalsJNK Mitogen-Activated Protein KinasesLarvaMammalsNerve RegenerationNeurogliaSpinal CordZebrafishJNK Mitogen-Activated Protein KinasesJNK signalingKinase translocation reporterRegenerationSpinal cordZebrafish

Identifiers

PMID37997694
PMCPMC10753585
OpenAlexW4388974263

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.