Evidence map›Paper›PMID 29792530›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2018

Manganese transport and toxicity in polarized WIF-B hepatocytes.

Khristy J Thompson, Jennifer Hein, Andrew Baez, Jose Carlo Sosa, Marianne Wessling-Resnick

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Characterization of in vitro models of SLC30A10 deficiency.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2021
    Article
  6. Article
  7. Iron and manganese transport in mammalian systems.Biochimica et biophysica acta. Molecular cell research · 2021
    Review
  8. Article
  9. Article
  10. ZIP14 is degraded in response to manganese exposure.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2019
    Article
  11. Article
  12. Genetic Disorders of Manganese Metabolism.Current neurology and neuroscience reports · 2019
    Review
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 1 institution in 1 country.

Khristy J ThompsonDepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Harvard University , Boston, Massachusetts.
Jennifer HeinDepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Harvard University , Boston, Massachusetts.
Andrew BaezDepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Harvard University , Boston, Massachusetts.
Jose Carlo SosaDepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Harvard University , Boston, Massachusetts.
Marianne Wessling-ResnickDepartment of Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Harvard University , Boston, Massachusetts.
Harvard University · US

Funding

Manganese Transport and ToxicityR01ES014638 · NIEHS · HARVARD SCHOOL OF PUBLIC HEALTH · PI WESSLING-RESNICK, MARIANNE · 2006 to 2017
$4.4M
NIEHS NIH HHS R01 ES014638
6 · The paper itself

Abstract

Manganese (Mn) toxicity arises from nutritional problems, community and occupational exposures, and genetic risks. Mn blood levels are controlled by hepatobiliary clearance. The goals of this study were to determine the cellular distribution of Mn transporters in polarized hepatocytes, to establish an in vitro assay for hepatocyte Mn efflux, and to examine possible roles the Mn transporters would play in metal import and export. For these experiments, hepatocytoma WIF-B cells were grown for 12-14 days to achieve maximal polarity. Immunoblots showed that Mn transporters ZIP8, ZnT10, ferroportin (Fpn), and ZIP14 were present. Indirect immunofluorescence microscopy localized Fpn and ZIP14 to WIF-B cell basolateral domains whereas ZnT10 and ZIP8 associated with intracellular vesicular compartments. ZIP8-positive structures were distributed uniformly throughout the cytoplasm, but ZnT10-positive vesicles were adjacent to apical bile compartments. WIF-B cells were sensitive to Mn toxicity, showing decreased viability after 16 h exposure to >250 μM MnCl

Indexed as

Brefeldin AHepatocytesHepcidinsManganeseAnimalsBiological TransportCation Transport ProteinsCell LineCell MembraneCell PolarityCytoplasmic VesiclesFerroportinHumansProtein Synthesis InhibitorsBrefeldin ACation Transport ProteinsFerroportinHepcidinsManganeseProtein Synthesis InhibitorshepatotoxicitymanganeseMn transportersWIF-B cells

Identifiers

PMID29792530
PMCPMC6335010
OpenAlexW2806478393

What Socratic 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 Socratic graph.