Evidence map›Paper›PMID 35806422›Full record

ArticleInternational journal of molecular sciences2022

An Iron Refractory Phenotype in Obese Adipose Tissue Macrophages Leads to Adipocyte Iron Overload.

Magdalene K Ameka, William N Beavers, Ciara M Shaver, Lorraine B Ware, Vern Eric Kerchberger, Kelly Q Schoenfelt, Lili Sun, Tatsuki Koyama, Eric P Skaar, Lev Becker and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  12. Metaflammation in obesity and its therapeutic targeting.Science translational medicine · 2023
    Review
  13. New Insights into Adipose Tissue Metabolic Function and Dysfunction.International journal of molecular sciences · 2023
    Article
  14. Peripheral and central macrophages in obesity.Frontiers in endocrinology · 2023
    Review
  15. 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

11 authors at 4 institutions in 1 country.

Magdalene K AmekaDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN 37212, USA.
William N BeaversDepartment of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.
Ciara M ShaverDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN 37212, USA.
Lorraine B WareDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN 37212, USA.ORCID 0000-0002-9429-4702
Vern Eric KerchbergerDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN 37212, USA.ORCID 0000-0002-0342-1965
Kelly Q SchoenfeltDepartment of Cancer Research, University of Chicago, Chicago, IL 60637, USA.
Lili SunDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN 37212, USA.
Tatsuki KoyamaDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN 37212, USA.ORCID 0000-0002-8908-9165
Eric P SkaarDepartment of Pathology, Microbiology, and Immunology, School of Medicine, Vanderbilt University Medical Center, Nashville, TN 37212, USA.
Lev BeckerDepartment of Cancer Research, University of Chicago, Chicago, IL 60637, USA.
Alyssa H HastyDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN 37212, USA.ORCID 0000-0001-7302-8045
Vanderbilt University Medical Center · USUniversity of Chicago · USVanderbilt University · USLouisiana State University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
'Metabolically Activated' Macrophages in Obesity and Insulin ResistanceR01DK102960 · NIDDK · UNIVERSITY OF CHICAGO · PI BECKER, LEV · 2015 to 2024
$4.4M
Adipose Macrophage Iron HandlingR01DK121520 · NIDDK · VANDERBILT UNIVERSITY · PI WINN, NATHAN C · 2019 to 2023
$2.8M
Mechanisms of airspace inflammation caused by cell-free hemoglobin during ARDSK08HL136888 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SHAVER, CIARA M · 2017 to 2021
$858k
Tissue-specific functional genomics in the acute respiratory distress syndromeK01HL157755 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KERCHBERGER, VERN ERIC · 2021 to 2025
$845k
XFe96 AnalyzerS10OD018015 · OD · VANDERBILT UNIVERSITY · PI LANNIGAN, DEBORAH · 2014 to 2014
$200k
American Heart Association 18POST34030426American Heart Association 20POST35180180National Heart Lung and Blood Institute HL136888NCI NIH HHS CA68485NCI NIH HHS P30 CA068485NHLBI NIH HHS K01 HL157755NHLBI NIH HHS K08 HL136888NIDDK NIH HHS DK058404NIDDK NIH HHS DK102960NIDDK NIH HHS DK121520NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK102960NIDDK NIH HHS R01 DK121520NIH HHS S10 OD018015
6 · The paper itself

Abstract

Adipocyte iron overload is a maladaptation associated with obesity and insulin resistance. The objective of the current study was to determine whether and how adipose tissue macrophages (ATMs) regulate adipocyte iron concentrations and whether this is impacted by obesity. Using bone marrow-derived macrophages (BMDMs) polarized to M0, M1, M2, or metabolically activated (MMe) phenotypes, we showed that MMe BMDMs and ATMs from obese mice have reduced expression of several iron-related proteins. Furthermore, the bioenergetic response to iron in obese ATMs was hampered. ATMs from iron-injected lean mice increased their glycolytic and respiratory capacities, thus maintaining metabolic flexibility, while ATMs from obese mice did not. Using an isotope-based system, we found that iron exchange between BMDMs and adipocytes was regulated by macrophage phenotype. At the end of the co-culture, MMe macrophages transferred and received more iron from adipocytes than M0, M1, and M2 macrophages. This culminated in a decrease in total iron in MMe macrophages and an increase in total iron in adipocytes compared with M2 macrophages. Taken together, in the MMe condition, the redistribution of iron is biased toward macrophage iron deficiency and simultaneous adipocyte iron overload. These data suggest that obesity changes the communication of iron between adipocytes and macrophages and that rectifying this iron communication channel may be a novel therapeutic target to alleviate insulin resistance.

Indexed as

Insulin ResistanceIron OverloadAdipocytesAdipose TissueAnimalsInflammationIronMacrophagesMiceMice, ObeseObesityPhenotypeIronadipose tissue macrophageimmunometabolismironobesitypolarization

Identifiers

PMID35806422
PMCPMC9267114
OpenAlexW4283799180

What OpenQuestion holds

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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.