Evidence map›Paper›PMID 27704212›Full record

ArticleHistochemistry and cell biology2017

High mobility group box 1 (HMGB1): dual functions in the cochlear auditory neurons in response to stress?

Sabine Ladrech, Jing Wang, Marc Mathieu, Jean-Luc Puel, Marc Lenoir

Abstract read
PubMed Publisher
In one paragraph

Article in Histochemistry and cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Molecular Behavior of HMGB1 in the Cochlea Following Noise Exposure andFrontiers in cell and developmental biology · 2021
    Article
  6. In focus in HCB.Histochemistry and cell biology · 2017
    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

5 authors at 3 institutions in 1 country.

Sabine LadrechINSERM, U1051, Institute for Neurosciences (INM), Hôpital Saint Eloi, 80 rue Augustin Fliche, 34091, Montpellier Cedex 5, France.
Jing WangINSERM, U1051, Institute for Neurosciences (INM), Hôpital Saint Eloi, 80 rue Augustin Fliche, 34091, Montpellier Cedex 5, France.
Marc MathieuINSERM, U1183, Institute of Regenerative Medicine and Biotherapy (IRMB), Montpellier, France.
Jean-Luc PuelINSERM, U1051, Institute for Neurosciences (INM), Hôpital Saint Eloi, 80 rue Augustin Fliche, 34091, Montpellier Cedex 5, France.
Marc LenoirINSERM, U1051, Institute for Neurosciences (INM), Hôpital Saint Eloi, 80 rue Augustin Fliche, 34091, Montpellier Cedex 5, France. marc.lenoir@inserm.fr.
Hôpital Saint Eloi · FRUniversité de Montpellier · FRInstitute for Neurosciences of Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High mobility group box 1 (HMGB1) is a DNA-binding protein that facilitates gene transcription and may act extracellularly as a late mediator of inflammation. The roles of HMGB1 in the pathogenesis of the spiral ganglion neurons (SGNs) of the cochlea are currently unknown. In the present study, we tested the hypothesis that early phenotypical changes in the SGNs of the amikacin-poisoned rat cochlea are mediated by HMGB1. Our results showed that a marked downregulation of HMGB1 had occurred by completion of amikacin treatment, coinciding with acute damage at the dendrite extremities of the SGNs. A few days later, during the recovery of the SGN dendrites, the protein was re-expressed and transiently accumulated within the nuclei of the SGNs. The phosphorylated form of the transcription factor c-Jun (p-c-Jun) was concomitantly detected in the nuclei of the SGNs where it often co-localized with HMGB1, while the anti-apoptotic protein BCL2 was over-expressed in the cytoplasm. In animals co-treated with amikacin and the histone deacetylase inhibitor trichostatin A, both HMGB1 and p-c-Jun were exclusively found within the cytoplasm. The initial disappearance of HMGB1 from the affected SGNs may be due to its release into the external medium, where it may have a cytokine-like function. Once re-expressed and translocated into the nucleus, HMGB1 may facilitate the transcriptional activity of p-c-Jun, which in turn may promote repair mechanisms. Our study therefore suggests that HMGB1 can positively influence the survival of SGNs following ototoxic exposure via both its extracellular and intranuclear functions.

Indexed as

Stress, PhysiologicalAmikacinAnimalsDose-Response Relationship, DrugDown-RegulationHMGB1 ProteinHydroxamic AcidsNeuronsRatsRats, WistarSpiral GanglionStructure-Activity RelationshipAmikacinHbp1 protein, ratHMGB1 ProteinHydroxamic Acidstrichostatin ABCL2c-JunExcitotoxicityGamma-H2axOtotoxicityTSA

Identifiers

PMID27704212
OpenAlexW2529133091

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.