Evidence map›Paper›PMID 24280772›Full record

ArticleNature communications2013

The TSC-mTOR pathway regulates macrophage polarization.

Vanessa Byles, Anthony J Covarrubias, Issam Ben-Sahra, Dudley W Lamming, David M Sabatini, Brendan D Manning, Tiffany Horng

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 354 papers.

0numbers the graph read from it
0cells of the map it votes in
354citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

354 citing papers in PubMed, 611 citations in OpenAlex.

  1. Review
  2. The role of mTORC2/RICTOR in immune cells and inflammatory diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
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  17. Neuroinflammation and autism: what have we learned so far?International journal of developmental disabilities · 2026
    Article
  18. Article
  19. Review
  20. Article

294 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

Vanessa Byles1] Department of Genetics & Complex Diseases, Harvard School of Public Health, Boston, Massachusetts 02115, USA [2].
Anthony J Covarrubias
Issam Ben-Sahra
Dudley W Lamming
David M Sabatini
Brendan D Manning
Tiffany Horng
Harvard University · USAllen Institute · USKoch Institute for Integrative Cancer Research At MIT

Funding

Regulation of the mTOR Pathway By NutrientsR01CA103866 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI WEISSMAN, JONATHAN S. · 2004 to 2021
$7.0M
Cell Growth Signaling in Cancer DevelopmentR01CA129105 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI WEISSMAN, JONATHAN S. · 2008 to 2021
$5.9M
TRANSLATIONAL CONTROL BY RAPAMYCIN-SENSITIVE SIGNALINGR01AI047389 · NIAID · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI WEISSMAN, JONATHAN S. · 2000 to 2021
$4.9M
Novel Components of the mTORC1 and mTORC2 PathwaysR37AI047389 · NIAID · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI SABATINI, DAVID M. · 2010 to 2019
$4.8M
Regulatory mechanisms and role of the PI3K-TSC-mTOR signaling network in tumorsR01CA122617 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI MANNING, BRENDAN D. · 2006 to 2015
$2.7M
Elucidating a role for Calcium signaling in activation of the Nlrp3 inflammasomeR01AI102964 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI HORNG, TIFFANY · 2013 to 2017
$2.0M
The in vivo regulation of glucose homeostasis and lifespan by mTORC2K99AG041765 · NIA · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI LAMMING, DUDLEY WILLIAM · 2012 to 2013
$141k
Howard Hughes Medical InstituteNCI NIH HHS R01 CA103866NCI NIH HHS R01 CA122617NCI NIH HHS R01-CA122617NCI NIH HHS R01 CA129105NIAID NIH HHS R01 AI047389NIAID NIH HHS R01 AI102964NIAID NIH HHS R01AI102964NIAID NIH HHS R37 AI047389NIA NIH HHS 1K99AG041765-01A1NIA NIH HHS K99 AG041765
6 · The paper itself

Abstract

Macrophages are able to polarize to proinflammatory M1 or alternative M2 states with distinct phenotypes and physiological functions. How metabolic status regulates macrophage polarization remains not well understood, and here we examine the role of mTOR (mechanistic target of rapamycin), a central metabolic pathway that couples nutrient sensing to regulation of metabolic processes. Using a mouse model in which myeloid lineage-specific deletion of Tsc1 (Tsc1(Δ/Δ)) leads to constitutive mTOR complex 1 (mTORC1) activation, we find that Tsc1(Δ/Δ) macrophages are refractory to IL-4-induced M2 polarization, but produce increased inflammatory responses to proinflammatory stimuli. Moreover, mTORC1-mediated downregulation of Akt signalling critically contributes to defective polarization. These findings highlight a key role for the mTOR pathway in regulating macrophage polarization, and suggest how nutrient sensing and metabolic status could be 'hard-wired' to control of macrophage function, with broad implications for regulation of type 2 immunity, inflammation and allergy.

Indexed as

AnimalsCell PolarityChitinInflammation MediatorsInterleukin-4LipopolysaccharidesMacrophagesMaleMicePPAR gammaProto-Oncogene Proteins c-aktSTAT6 Transcription FactorTOR Serine-Threonine KinasesTuberous Sclerosis Complex 1 ProteinTumor Suppressor ProteinsChitinInflammation MediatorsInterleukin-4LipopolysaccharidesmTOR protein, mousePPAR gammaProto-Oncogene Proteins c-aktStat6 protein, mouseSTAT6 Transcription FactorTOR Serine-Threonine KinasesTsc1 protein, mouseTuberous Sclerosis Complex 1 ProteinTumor Suppressor Proteins

Identifiers

PMID24280772
PMCPMC3876736
OpenAlexW2152701478

What OpenQuestion holds

Textmetadata
LicenceTDM
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.