Evidence map›Paper›PMID 20699218›Full record

ArticleThe Journal of biological chemistry2010

Ctr1 is an apical copper transporter in mammalian intestinal epithelial cells in vivo that is controlled at the level of protein stability.

Yasuhiro Nose, L Kent Wood, Byung-Eun Kim, Joseph R Prohaska, Robert S Fry, Jerry W Spears, Dennis J Thiele

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 1 pooled it
7.6field-weighted citation impact, top 2% 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

85 citing papers in PubMed, 1 synthesis or guideline pooled it, 152 citations in OpenAlex.

  1. Pooled it
  2. Balancing cellular copper levels via the post-translational regulation of copper transport.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Copper Import via CTR1 Supports the β3-Adrenergic Thermogenic Program.bioRxiv : the preprint server for biology · 2026
    Article
  8. Review
  9. Copper Homeostasis and Cuproptosis in Neurological Disorders.Drug design, development and therapy · 2026
    Review
  10. Review
  11. Excess copper exposure and male reproductive toxicity: molecular mechanisms and potential interventions.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2025
    Review
  12. Article
  13. Review
  14. Effect of primary copper metabolism disturbance on elemental, protein, and lipid composition of the organs in Jackson toxic milk mouse.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2025
    Article
  15. Review
  16. Review
  17. Cuproptosis: Mechanism and Application in Lymphoma.Current cancer drug targets · 2025
    Review
  18. Article
  19. Review
  20. Review

25 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 1 country.

Yasuhiro NoseDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.
L Kent Wood
Byung-Eun Kim
Joseph R Prohaska
Robert S Fry
Jerry W Spears
Dennis J Thiele
Duke Medical Center · USDuke University Hospital · USNorth Carolina State University · USUniversity of Minnesota, Duluth · US

Funding

Copper Homeostasis in MammalsR01DK074192 · NIDDK · DUKE UNIVERSITY · PI MATSUNAMI, HIROAKI · 2006 to 2021
$5.2M
NUTRITIONAL COPPER STATUS AND THE NERVOUS SYSTEMR01HD039708 · NICHD · UNIVERSITY OF MINNESOTA DULUTH · PI PROHASKA, JOSEPH ROBERT · 2001 to 2010
$1.5M
NICHD NIH HHS HD039708-08NICHD NIH HHS R01 HD039708NIDDK NIH HHS DK074192-09NIDDK NIH HHS R01 DK074192
6 · The paper itself

Abstract

Copper is an essential trace element that functions in a diverse array of biochemical processes that include mitochondrial respiration, neurotransmitter biogenesis, connective tissue maturation, and reactive oxygen chemistry. The Ctr1 protein is a high-affinity Cu(+) importer that is structurally and functionally conserved in yeast, plants, fruit flies, and humans and that, in all of these organisms, is localized to the plasma membrane and intracellular vesicles. Although intestinal epithelial cell-specific deletion of Ctr1 in mice demonstrated a critical role for Ctr1 in dietary copper absorption, some controversy exists over the localization of Ctr1 in intestinal epithelial cells in vivo. In this work, we assess the localization of Ctr1 in intestinal epithelial cells through two independent mechanisms. Using immunohistochemistry, we demonstrate that Ctr1 localizes to the apical membrane in intestinal epithelial cells of the mouse, rat, and pig. Moreover, biotinylation of intestinal luminal proteins from mice fed a control or a copper-deficient diet showed elevated levels of both total and apical membrane Ctr1 protein in response to transient dietary copper limitation. Experiments in cultured HEK293T cells demonstrated that alterations in the levels of the glycosylated form of Ctr1 in response to copper availability were a time-dependent, copper-specific posttranslational response. Taken together, these results demonstrate apical localization of Ctr1 in intestinal epithelia across three mammalian species and suggest that increased Ctr1 apical localization in response to dietary copper limitation may represent an adaptive response to homeostatically modulate Ctr1 availability at the site of intestinal copper absorption.

Indexed as

Protein StabilityAmino Acid SequenceAnimalsCation Transport ProteinsCell PolarityCopperCopper Transporter 1DietEpithelial CellsHumansIntestinal MucosaMiceMice, Inbred C57BLMice, KnockoutMolecular Sequence DataRatsCation Transport ProteinsCopperCopper Transporter 1SLC31A1 protein, humanSlc31a1 protein, mouseSlc31a1 protein, rat

Identifiers

PMID20699218
PMCPMC2952240
OpenAlexW2024427829

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.