Evidence map›Paper›PMID 21254280›Full record

ArticleMolecular reproduction and development2011

Binding of nickel to testicular glutamate-ammonia ligase inhibits its enzymatic activity.

Yingbiao Sun, Young Ou, Min Cheng, Yibing Ruan, Frans A van der Hoorn

Open access · greenAbstract read
In one paragraph

Article in Molecular reproduction and development, 2011. 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
0.5field-weighted citation impact, top 30% 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, 11 citations in OpenAlex.

  1. Co-exposure to arsenic and nickel induces oxidative stress and mineral imbalance, impairing male reproductive parameters in Wistar rats.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Article
  2. Iranian journal of pharmaceutical research : IJPR · 2020
    Article
  3. Hormonal Perturbations in Occupationally Exposed Nickel Workers.Open access Macedonian journal of medical sciences · 2016
    Article
  4. Article
  5. 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 2 institutions in 2 countries.

Yingbiao SunSchool of Public Health, Lanzhou University, Lanzhou, China.
Young Ou
Min Cheng
Yibing Ruan
Frans A van der Hoorn
University of Calgary · CALanzhou University · CN

Funding

CIHR 11361CIHR 82709
6 · The paper itself

Abstract

Exposure to nickel has been shown to cause damage to the testis in several animal models. It is not known if the testis expresses protein(s) that can bind nickel. To test this, we used a nickel-binding assay to isolate testicular nickel-binding proteins. We identified glutamate-ammonia ligase (GLUL) as a prominent nickel-binding protein by mass spectrometry. Protein analysis and reverse transcriptase polymerase chain reaction showed that GLUL is expressed in the testis, predominantly in interstitial cells. We determined that GLUL has a higher affinity for nickel than for its regular co-factor manganese. We produced an enzymatically active, recombinant GLUL protein. Upon binding, nickel interferes with the manganese-catalyzed enzymatic activity of recombinant GLUL protein. We also determined that GLUL activity in testes of animals exposed to nickel sulfate is reduced. Our results identify testicular GLUL as the first testicular protein shown to be affected by nickel exposure.

Indexed as

AnimalsGlutamate-Ammonia LigaseMaleManganeseMass SpectrometryNickelProtein BindingRatsRats, WistarTestisGlutamate-Ammonia LigaseManganeseNickelnickel sulfate

Identifiers

PMID21254280
PMCPMC5059155
OpenAlexW2163501721

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.