Evidence map›Paper›PMID 37365564›Full record

ArticleBMC biology2023

Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona.

William R Jeffery, Bo Li, Mandy Ng, Lianwei Li, Špela Gorički, Li Ma

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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 4 institutions in 4 countries.

William R JefferyDepartment of Biology, University of Maryland, College Park, MD, 20742, USA. jeffery@umd.edu.ORCID 0000-0002-6997-2946
Bo LiKunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650223, China.
Mandy NgDepartment of Biology, University of Maryland, College Park, MD, 20742, USA.
Lianwei LiKunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650223, China.
Špela GoričkiStation Biologique, 29680, Roscoff, France.
Li MaDepartment of Biology, University of Maryland, College Park, MD, 20742, USA. mali@mail.kiz.ac.cn.
Kunming Institute of Zoology · CNMarine Biological Laboratory · USStation Biologique de Roscoff · FRUniversity of Maryland, College Park · US

Funding

The Tunicate Ciona: A New Model for the Effects of Aging on Tissue RegenerationR01AG055411 · NIA · UNIV OF MARYLAND, COLLEGE PARK · PI JEFFERY, WILLIAM R · 2018 to 2022
$1.7M
NIA NIH HHS R01 AG055411
6 · The paper itself

Abstract

backgroundUnidirectional regeneration in the basal chordate Ciona intestinalis involves the proliferation of adult stem cells residing in the branchial sac vasculature and the migration of progenitor cells to the site of distal injury. However, after the Ciona body is bisected, regeneration occurs in the proximal but not in the distal fragments, even if the latter include a part of the branchial sac with stem cells. A transcriptome was sequenced and assembled from the isolated branchial sacs of regenerating animals, and the information was used to provide insights into the absence of regeneration in distal body fragments.

resultsWe identified 1149 differentially expressed genes, which were separated into two major modules by weighted gene correlation network analysis, one consisting of mostly upregulated genes correlated with regeneration and the other consisting of only downregulated genes associated with metabolism and homeostatic processes. The hsp70, dnaJb4, and bag3 genes were among the highest upregulated genes and were predicted to interact in an HSP70 chaperone system. The upregulation of HSP70 chaperone genes was verified and their expression confirmed in BS vasculature cells previously identified as stem and progenitor cells. siRNA-mediated gene knockdown showed that hsp70 and dnaJb4, but not bag3, are required for progenitor cell targeting and distal regeneration. However, neither hsp70 nor dnaJb4 were strongly expressed in the branchial sac vasculature of distal fragments, implying the absence of a stress response. Heat shock treatment of distal body fragments activated hsp70 and dnaJb4 expression indicative of a stress response, induced cell proliferation in branchial sac vasculature cells, and promoted distal regeneration.

conclusionsThe chaperone system genes hsp70, dnaJb4, and bag3 are significantly upregulated in the branchial sac vasculature following distal injury, defining a stress response that is essential for regeneration. The stress response is absent from distal fragments, but can be induced by a heat shock, which activates cell division in the branchial sac vasculature and promotes distal regeneration. This study demonstrates the importance of a stress response for stem cell activation and regeneration in a basal chordate, which may have implications for understanding the limited regenerative activities in other animals, including vertebrates.

Indexed as

CionaCiona intestinalisAnimalsChromosome MappingHSP70 Heat-Shock ProteinsMolecular ChaperonesStem CellsHSP70 Heat-Shock ProteinsMolecular ChaperonesBasal chordateBranchial sac transcriptomeCiona intestinalisHSP70 chaperone systemRegenerationStress response

Identifiers

PMID37365564
PMCPMC10294541
OpenAlexW4382020937

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.