Evidence map›Paper›PMID 36028574›Full record

ArticleCommunications biology2022

mTOR regulation of metabolism limits LPS-induced monocyte inflammatory and procoagulant responses.

Nina C Lund, Yetunde Kayode, Melanie R McReynolds, Deanna C Clemmer, Hannah Hudson, Isabelle Clerc, Hee-Kyung Hong, Jason M Brenchley, Joseph Bass, Richard T D'Aquila and 1 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  9. COVID-19 and Diarylamidines: The Parasitic Connection.International journal of molecular sciences · 2023
    Review
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.

Nina C LundDivision of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.ORCID http://orcid.org/0000-0001-7491-7071
Yetunde KayodeDepartment of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.
Melanie R McReynoldsDepartment of Biochemistry and Molecular Biology, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
Deanna C ClemmerDepartment of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.
Hannah HudsonDivision of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Isabelle ClercDivision of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.ORCID http://orcid.org/0000-0002-7140-7049
Hee-Kyung HongDivision of Endocrinology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Jason M BrenchleyBarrier Immunity Section, Laboratory of Viral Disease, National Institute of Allergy and Infectious Diseases, Bethesda, MD, 20892, USA.
Joseph BassDivision of Endocrinology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.ORCID http://orcid.org/0000-0002-1602-8601
Richard T D'AquilaDivision of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA. richard.daquila@northwestern.edu.ORCID http://orcid.org/0000-0002-9653-5987
Harry E TaylorDepartment of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA. taylorha@upstate.edu.ORCID http://orcid.org/0000-0002-5045-2748
Northwestern University · USSUNY Upstate Medical University · USNational Institute of Allergy and Infectious Diseases · USPennsylvania State University · US

Funding

Virology and Immunology Technology CoreP30AI117943 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Richard D'Aquila, Brian Mustanski · 2015 to 2026
$38.4M
SLOW WAVE SLEEP AND TYPE 2 DIABETES RISK IN AGINGP01AG011412 · NIA · UNIVERSITY OF CHICAGO · PI ZEE, PHYLLIS C. · 1994 to 2021
$31.5M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008152 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARDEHALI, HOSSEIN · 1987 to 2021
$24.0M
Pathogenesis of Rebound SIV/HIV Viremia after Antiretrovral TherapyP01AI131346 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2017 to 2021
$8.0M
Integration of Feeding Time and Glucose Metabolism by the Circadian Gene NetworkR01DK090625 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BASS, JOSEPH, LERNER, TALIA NEWCOMBE · 2011 to 2025
$6.9M
PDX-1,A TRANSCRIPTIONAL ACTIVATOR OF THE INSULIN GENER01DK050203 · NIDDK · VANDERBILT UNIVERSITY · PI BASS, JOSEPH, STEIN, ROLAND W · 1995 to 2020
$6.8M
Cross-regulation of Immunometabolism and Circadian Pathways in Obesity PathophysiologyR01DK127800 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BASS, JOSEPH · 2021 to 2025
$2.3M
Bioenergetic Mechanisms Underlying Circadian Dietary InterventionR01AG065988 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BASS, JOSEPH · 2019 to 2023
$2.0M
The Circadian System as a Neuronal Regulator of Feeding Time and Body Weight SetpointR01DK113011 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BASS, JOSEPH · 2018 to 2021
$1.7M
Role of mTOR in inflammatory monocytes in HIV infectionF30AI131937 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CALANTONE, NINA · 2017 to 2020
$189k
Howard Hughes Medical InstituteNIAID NIH HHS F30 AI131937NIAID NIH HHS P01 AI131346NIAID NIH HHS P30 AI117943NIA NIH HHS P01 AG011412NIA NIH HHS R01 AG065988NIDDK NIH HHS R01 DK050203NIDDK NIH HHS R01 DK090625NIDDK NIH HHS R01 DK113011NIDDK NIH HHS R01 DK127800NIGMS NIH HHS T32 GM008152
6 · The paper itself

Abstract

Translocated lipopolysaccharide (LPS) activates monocytes via TLR4 and is hypothesized to increase cardiovascular disease risk in persons living with HIV. We tested whether mTOR activity supports LPS-stimulated monocyte production of pro-inflammatory cytokines and tissue factor (TF), as it propels the inflammatory response in several immune cell types besides monocytes. However, multi-omics analyses here demonstrate that mTOR activates a metabolic pathway that limits abundance of these gene products in monocytes. Treatment of primary human monocytes with catalytic mTOR inhibitors (mTORi) increased LPS-induced polyfunctional responses, including production of IL-1β, IL-6, and the pro-coagulant, TF. NF-κB-driven transcriptional activity is enhanced with LPS stimulation after mTORi treatment to increase expression of F3 (TF). Moreover, intracellular NAD

Indexed as

LipopolysaccharidesMonocytesTOR Serine-Threonine KinasesCytokinesHumansThromboplastinCytokinesLipopolysaccharidesMTOR protein, humanThromboplastinTOR Serine-Threonine Kinases

Identifiers

PMID36028574
PMCPMC9412771
OpenAlexW4293116413

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.