Evidence map›Paper›PMID 16164753›Full record

ArticleBMC immunology2005

Metallothionein mediates leukocyte chemotaxis.

Xiuyun Yin, David A Knecht, Michael A Lynes

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Microorganisms · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Observational
  10. The impact of metal availability on immune function during infection.Trends in endocrinology and metabolism: TEM · 2021
    Review
  11. Review
  12. Review
  13. Article
  14. Evaluation of metallothionein and Ki-67 expression in chronic cholangiohepatitis in cats.Canadian journal of veterinary research = Revue canadienne de recherche veterinaire · 2021
    Article
  15. Emerging Biomarkers in Cutaneous Melanoma.Molecular diagnosis & therapy · 2018
    Review
  16. Metallothioneins: Emerging Modulators in Immunity and Infection.International journal of molecular sciences · 2017
    Review
  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.

Xiuyun YinDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269-3125, USA. xiuyun.yin@uconn.edu
David A Knecht
Michael A Lynes
University of Connecticut · US

Funding

Molecular Genetics of the CytoskeletonR01GM040599 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI KNECHT, DAVID A · 1988 to 2009
$1.8M
MECHANISM OF METAL MEDIATED IMMUNOSUPPRESSIONR01ES007408 · NIEHS · UNIVERSITY OF CONNECTICUT STORRS · PI LYNES, MICHAEL A · 1997 to 2007
$1.6M
Automated Monitoring of Chemotactic Cell MovementR42EB000208 · NIBIB · APPLIED BIOPHYSICS, INC. · PI LYNES, MICHAEL A · 2002 to 2002
$247k
NIBIB NIH HHS EB000208NIEHS NIH HHS ES007408NIEHS NIH HHS R01 ES007408NIGMS NIH HHS GM40599NIGMS NIH HHS R01 GM040599
6 · The paper itself

Abstract

backgroundMetallothionein (MT) is a cysteine-rich, metal-binding protein that can be induced by a variety of agents. Modulation of MT levels has also been shown to alter specific immune functions. We have noticed that the MT genes map close to the chemokines Ccl17 and Cx3cl1. Cysteine motifs that characterize these chemokines are also found in the MT sequence suggesting that MT might also act as a chemotactic factor.

resultsIn the experiments reported here, we show that immune cells migrate chemotactically in the presence of a gradient of MT. This response can be specifically blocked by two different monoclonal anti-MT antibodies. Exposure of cells to MT also leads to a rapid increase in F-actin content. Incubation of Jurkat T cells with cholera toxin or pertussis toxin completely abrogates the chemotactic response to MT. Thus MT may act via G-protein coupled receptors and through the cyclic AMP signaling pathway to initiate chemotaxis.

conclusionThese results suggest that, under inflammatory conditions, metallothionein in the extracellular environment may support the beneficial movement of leukocytes to the site of inflammation. MT may therefore represent a "danger signal"; modifying the character of the immune response when cells sense cellular stress. Elevated metallothionein produced in the context of exposure to environmental toxicants, or as a result of chronic inflammatory disease, may alter the normal chemotactic responses that regulate leukocyte trafficking. Thus, MT synthesis may represent an important factor in immunomodulation that is associated with autoimmune disease and toxicant exposure.

Indexed as

ActinsAmino Acid SequenceAnimalsAntibodies, MonoclonalChemokine CCL17Chemokine CXCL12Chemokines, CCChemokines, CXCChemotaxis, LeukocyteCysteineDose-Response Relationship, DrugHumansJurkat CellsMetallothioneinMicroscopy, VideoMolecular Sequence DataActinsAntibodies, MonoclonalCCL17 protein, humanCcl17 protein, mouseChemokine CCL17Chemokine CXCL12Chemokines, CCChemokines, CXCCXCL12 protein, humanCxcl12 protein, mouseCysteineMetallothionein

Identifiers

PMID16164753
PMCPMC1262721
OpenAlexW1758183764

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.