Evidence map›Paper›PMID 19179618›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2009

Interleukin-1beta contributes via nitric oxide to the upregulation and functional activity of the zinc transporter Zip14 (Slc39a14) in murine hepatocytes.

Louis A Lichten, Juan P Liuzzi, Robert J Cousins

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Role of zinc in health and disease.Clinical and experimental medicine · 2024
    Review
  3. Article
  4. Zinc homeostasis and redox alterations in obesity.Frontiers in endocrinology · 2023
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. The classic metal-sensing transcription factor MTF1 promotes myogenesis in response to copper.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  13. Zinc and Sepsis.Nutrients · 2018
    Review
  14. Review
  15. Article
  16. Metal TransporterThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Louis A LichtenFood Science and Human Nutrition Department, Center for Nutritional Sciences, University of Florida, Gainesville, FL 32611-0370, USA.
Juan P Liuzzi
Robert J Cousins
University of Florida · US

Funding

ZINC AND THE SYNTHESIS OF ZINC BINDING PROTEINSR01DK031127 · NIDDK · UNIVERSITY OF FLORIDA · PI COUSINS, ROBERT J · 1986 to 2009
$2.9M
Zinc and the Synthesis of Binding ProteinsR56DK031127 · NIDDK · UNIVERSITY OF FLORIDA · PI COUSINS, ROBERT J · 2010 to 2010
$325k
ZINC AND THE SYTHESIS OF ZINC BINDING PROTEINSR37DK031127 · NIDDK · UNIVERSITY OF FLORIDA · PI COUSINS, ROBERT J · 1992 to 1999
–
NIDDK NIH HHS DK 31127
6 · The paper itself

Abstract

Zinc metabolism during chronic disease is dysregulated by inflammatory cytokines. Experiments with IL-6 knockout mice show that LPS regulates expression of the zinc transporter, Zip14, by a mechanism that is partially independent of IL-6. The LPS-induced model of sepsis may occur by a mechanism signaled by nitric oxide (NO) as a secondary messenger. To address the hypothesis that NO can modulate Zip14 expression, we treated primary hepatocytes from wild-type mice with the NO donor S-nitroso N-acetyl penicillamine (SNAP). After treatment with SNAP, steady-state Zip14 mRNA levels displayed a maximal increase after 8 h and a concomitant increase in the transcriptional activity of the gene. Chromatin immunoprecipitation documented the kinetics of activator protein (AP)-1 and RNA polymerase II association with the Zip14 promoter after NO exposure, indicating a role of AP-1 in transcription of Zip14. We then stimulated the primary murine hepatocytes with IL-1beta, an LPS-induced proinflammatory cytokine and a potent activator of inducible NO synthase (iNOS) and NO production. In support of our hypothesis, IL-1beta treatment led to a threefold increase in Zip14 mRNA and enhanced zinc transport, as measured with a zinc fluorophore, in wild-type but not iNOS-/- hepatocytes. These data suggest that signaling pathways activated by NO are factors in the upregulation of Zip14, which in turn mediates hepatic zinc accumulation and hypozincemia during inflammation and sepsis.

Indexed as

AnimalsCation Transport ProteinsGene Expression RegulationHepatocytesInterleukin-1betaLipopolysaccharidesMiceMice, Inbred C57BLMice, KnockoutNitric OxideNitric Oxide Synthase Type IIUp-RegulationCation Transport ProteinsInterleukin-1betaLipopolysaccharidesNitric OxideNitric Oxide Synthase Type IISLC39A14 protein, mouse

Identifiers

PMID19179618
PMCPMC2670674
OpenAlexW2096803925

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.