Evidence map›Paper›PMID 34338042›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2021

Myeloid-specific deletion of ferroportin impairs macrophage bioenergetics but is disconnected from systemic insulin action in adult mice.

Nathan C Winn, Elysa M Wolf, Matthew A Cottam, Monica Bhanot, Alyssa H Hasty

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2021. 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
2.6field-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

12 citing papers in PubMed, 21 citations in OpenAlex.

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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 2 institutions in 1 country.

Nathan C WinnDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee.ORCID 0000-0002-5276-0592
Elysa M WolfDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Matthew A CottamDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee.ORCID 0000-0003-0619-1605
Monica BhanotDivision of Diabetes, Endocrinology and Metabolism, Vanderbilt Medical Center, Nashville, Tennessee.
Alyssa H HastyDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee.ORCID 0000-0001-7302-8045
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
MULTIDISCIPLINARY TRAINING IN MOLECULAR ENDOCRINOLOGYT32DK007563 · NIDDK · VANDERBILT UNIVERSITY · PI Richard M O'Brien · 1988 to 2026
$15.9M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
TRAINING IN GASTROENTEROLOGYT32DK007673 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 1992 to 2026
$8.4M
Adipose Macrophage Iron HandlingR01DK121520 · NIDDK · VANDERBILT UNIVERSITY · PI WINN, NATHAN C · 2019 to 2023
$2.8M
Immunological Mechanisms of Disease Training ProgramT32AI138932 · NIAID · VANDERBILT UNIVERSITY · PI MAJOR, AMY S, RATHMELL, JEFFREY C. · 2019 to 2023
$1.4M
XFe96 AnalyzerS10OD018015 · OD · VANDERBILT UNIVERSITY · PI LANNIGAN, DEBORAH · 2014 to 2014
$200k
The role of T cells in adipose tissue inflammation and insulin resistance during weight cyclingF31DK123881 · NIDDK · VANDERBILT UNIVERSITY · PI COTTAM, MATTHEW ALEXANDER · 2020 to 2022
$73k
Turnover of Adipose Tissue MacrophagesI01BX002195 · VA · VETERANS HEALTH ADMINISTRATION · PI HASTY, ALYSSA H · 2014 to 2024
–
BLRD VA I01 BX002195HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK007673HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) R01DK121520HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) T32 DK007563-31HHS | NIH | NIAID | Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases (DMID) T32AI138932NCI NIH HHS P30 CA068485NIAID NIH HHS T32 AI138932NIDDK NIH HHS F31 DK123881NIDDK NIH HHS P30 DK020593NIDDK NIH HHS R01 DK121520NIDDK NIH HHS T32 DK007563NIDDK NIH HHS T32 DK007673NIDDK NIH HHS U24 DK059637NIH HHS S10 OD018015
6 · The paper itself

Abstract

Tissue iron overload is associated with insulin resistance and mitochondrial dysfunction in rodents and humans; however, the mechanisms or cell types that mediate this phenotype are not completely understood. Macrophages (Mɸs) are known to contribute to iron handling; thus, we hypothesized that perturbed iron handling by Mɸs impairs mitochondrial energetics and evokes systemic insulin resistance in mice. Male and female mice with myeloid-targeted (LysMCre) deletion of the canonical iron exporter, ferroportin (Fpn, encoded by

Indexed as

AnimalsCation Transport ProteinsEnergy MetabolismFemaleFerroportinGlucoseInsulinMacrophagesMembrane GlycoproteinsMiceMice, Inbred C57BLMitochondriaMyeloid CellsReceptors, Interleukin-1Cation Transport ProteinsFerroportinGlucoseInsulinMembrane GlycoproteinsReceptors, Interleukin-1TIRAP protein, humanadipose tissueinsulin resistanceiron handlingmacrophagesobesity

Identifiers

PMID34338042
PMCPMC8461794
OpenAlexW3192846737

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.