Evidence map›Paper›PMID 23845766›Full record

ArticleNeurotoxicology2013

Low level methylmercury enhances CNTF-evoked STAT3 signaling and glial differentiation in cultured cortical progenitor cells.

Nathan J Jebbett, Joshua W Hamilton, Matthew D Rand, Felix Eckenstein

Abstract read
In one paragraph

Article in Neurotoxicology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.8field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Single cell RNA sequencing detects persistent cell type- and methylmercury exposure paradigm-specific effects in a human cortical neurodevelopmental model.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2021
    Article
  7. Mercury Toxicity and Neurogenesis in the Mammalian Brain.International journal of molecular sciences · 2021
    Review
  8. Review
  9. Environmentally relevant developmental methylmercury exposures alter neuronal differentiation in a human-induced pluripotent stem cell model.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2021
    Article
  10. Review
  11. Article
  12. Chronic exposure to methylmercury enhances the anorexigenic effects of leptin in C57BL/6J male mice.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Biomarkers of mercury toxicity: Past, present, and future trends.Journal of toxicology and environmental health. Part B, Critical reviews · 2017
    Review
  18. Article
  19. Recent Advances in Mercury Research.Current environmental health reports · 2014
    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

4 authors at 2 institutions in 1 country.

Nathan J JebbettUniversity of Vermont, Department of Neurological Sciences, Burlington, VT, United States.
Joshua W Hamilton
Matthew D Rand
Felix Eckenstein
University of Vermont · USMarine Biological Laboratory · US

Funding

Proteomics Core for Neuroscience P20 RR16435P20RR016435 · NCRR · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI SPEES, JEFFREY L · 2001 to 2010
$23.5M
Mechanisms of methylmercury toxicity in neural developmentR01ES015550 · NIEHS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI RAND, MATTHEW D · 2007 to 2011
$1.4M
NCRR NIH HHS 5P20RR016435NCRR NIH HHS P20 RR016435NIEHS NIH HHS R01 ES 015550NIEHS NIH HHS R01 ES015550
6 · The paper itself

Abstract

Although many previous investigations have studied how mercury compounds cause cell death, sub-cytotoxic levels may affect mechanisms essential for the proper development of the nervous system. The present study investigates whether low doses of methylmercury (MeHg) and mercury chloride (HgCl2) can modulate the activity of JAK/STAT signaling, a pathway that promotes gliogenesis. We report that sub-cytotoxic doses of MeHg enhance ciliary neurotrophic factor (CNTF) evoked STAT3 phosphorylation in human SH-SY5Y neuroblastoma and mouse cortical neural progenitor cells (NPCs). This effect is specific for MeHg, since HgCl2 fails to enhance JAK/STAT signaling. Exposing NPCs to these low doses of MeHg (30-300nM) enhances CNTF-induced expression of STAT3-target genes such as glial fibrillary acidic protein (GFAP) and suppressors of cytokine signaling 3 (SOCS3), and increases the proportion of cells expressing GFAP following 2 days of differentiation. Higher, near-cytotoxic concentrations of MeHg and HgCl2 inhibit STAT3 phosphorylation and lead to increased production of superoxide. Lower concentrations of MeHg effective in enhancing JAK/STAT signaling (30nM) do not result in a detectable increase in superoxide nor increased expression of the oxidant-responsive genes, heme oxygenase 1, heat shock protein A5 and sirtuin 1. These findings suggest that low concentrations of MeHg inappropriately enhance STAT3 phosphorylation and glial differentiation, and that the mechanism causing this enhancement is distinct from the reactive oxygen species-associated cell death observed at higher concentrations of MeHg and HgCl2.

Indexed as

AnimalsCell DifferentiationCell SurvivalCiliary Neurotrophic FactorDose-Response Relationship, DrugGene ExpressionGlial Fibrillary Acidic ProteinHumansMercuric ChlorideMethylmercury CompoundsMicePhosphorylationSTAT3 Transcription FactorStem CellsSuperoxidesSuppressor of Cytokine Signaling ProteinsCiliary Neurotrophic FactorGlial Fibrillary Acidic ProteinMercuric Chloridemethylmercuric chlorideMethylmercury CompoundsSTAT3 Transcription FactorSuperoxidesSuppressor of Cytokine Signaling ProteinsDevelopmental neurotoxicityGFAPGliogenesisMethylmercuryNeural progenitor cellsSTAT3

Identifiers

PMID23845766
PMCPMC3802548
OpenAlexW2030059588

What OpenQuestion holds

Textmetadata
LicenceTDM
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.