Evidence map›Paper›PMID 32718989›Full record

ArticleScience translational medicine2020

Apoptosis of hematopoietic progenitor-derived adipose tissue-resident macrophages contributes to insulin resistance after myocardial infarction.

Sathish Babu Vasamsetti, Emilie Coppin, Xinyi Zhang, Jonathan Florentin, Sasha Koul, Matthias Götberg, Andrew S Clugston, Floyd Thoma, John Sembrat, Grant C Bullock and 6 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 4 countries.

Sathish Babu VasamsettiPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0002-9682-7437
Emilie CoppinPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0001-8987-0050
Xinyi ZhangPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0002-5846-337X
Jonathan FlorentinPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Sasha KoulDepartment of Cardiology, Lund University, Skane University Hospital, Lund, 22184, Sweden.
Matthias GötbergDepartment of Cardiology, Lund University, Skane University Hospital, Lund, 22184, Sweden.ORCID 0000-0002-0912-7927
Andrew S ClugstonDepartment of Developmental Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0002-8521-9452
Floyd ThomaDivision of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
John SembratPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0003-4108-803X
Grant C BullockPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0002-8225-0497
Dennis KostkaDepartment of Developmental Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0002-1460-5487
Claudette M St CroixDepartment of Cell Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Ansuman ChattopadhyayHealth Sciences Library System, University of Pittsburgh, PA 15213, USA.ORCID 0000-0002-5412-3749
Mauricio RojasPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0001-7340-4784
Suresh R MulukutlaDivision of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Partha DuttaPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA. duttapa@pitt.edu.ORCID 0000-0001-7456-1757
University of Pittsburgh · USSkåne University Hospital · SECentral South University · CNVA Pittsburgh Healthcare System · US

Funding

Renal and Epithelial Biology Training ProgramT32DK061296 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLEYMAN, THOMAS R · 2002 to 2022
$3.1M
Mechanisms of Myocardial Infarction-induced insulin resistanceR01HL143967 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DUTTA, PARTHA · 2018 to 2022
$2.6M
The role of microglia Nek6 in myocardial infarction-induced cognitive impairmentR01HL142629 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DUTTA, PARTHA · 2020 to 2023
$2.3M
Effect of diabetes on myelopoiesis and atherosclerosisR00HL121076 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DUTTA, PARTHA · 2016 to 2018
$732k
Request for a Nikon A1 confocal microscopeS10OD019973 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WATKINS, SIMON C · 2015 to 2015
$358k
NHLBI NIH HHS R00 HL121076NHLBI NIH HHS R01 HL142629NHLBI NIH HHS R01 HL143967NIDDK NIH HHS T32 DK061296NIH HHS S10 OD019973
6 · The paper itself

Abstract

Patients with insulin resistance have high risk of cardiovascular disease such as myocardial infarction (MI). However, it is not known whether MI can initiate or aggravate insulin resistance. We observed that patients with ST-elevation MI and mice with MI had de novo hyperglycemia and features of insulin resistance, respectively. In mouse models of both myocardial and skeletal muscle injury, we observed that the number of visceral adipose tissue (VAT)-resident macrophages decreased because of apoptosis after these distant organ injuries. Patients displayed a similar decrease in VAT-resident macrophage numbers and developed systemic insulin resistance after ST-elevation MI. Loss of VAT-resident macrophages after MI injury led to systemic insulin resistance in non-diabetic mice. Danger signaling-associated protein high mobility group box 1 was released by the dead myocardium after MI in rodents and triggered macrophage apoptosis via Toll-like receptor 4. The VAT-resident macrophage population in the steady state in mice was transcriptomically distinct from macrophages in the brain, skin, kidney, bone marrow, lungs, and liver and was derived from hematopoietic progenitor cells just after birth. Mechanistically, VAT-resident macrophage apoptosis and de novo insulin resistance in mouse models of MI were linked to diminished concentrations of macrophage colony-stimulating factor and adiponectin. Collectively, these findings demonstrate a previously unappreciated role of adipose tissue-resident macrophages in sensing remote organ injury and promoting MI pathogenesis.

Indexed as

Hematopoietic Stem Cell TransplantationInsulin ResistanceMyocardial InfarctionAdipose TissueAnimalsApoptosisHumansMacrophagesMiceMice, Inbred C57BL

Identifiers

PMID32718989
PMCPMC7813555
OpenAlexW3043848689

What OpenQuestion holds

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Registered trials

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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.