Evidence map›Paper›PMID 28128208›Full record

ArticleNature communications2017

mTORC2 signalling regulates M2 macrophage differentiation in response to helminth infection and adaptive thermogenesis.

R W Hallowell, S L Collins, J M Craig, Y Zhang, M Oh, P B Illei, Y Chan-Li, C L Vigeland, W Mitzner, A L Scott and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

71 citing papers in PubMed, 128 citations in OpenAlex.

  1. Article
  2. Review
  3. Infection and immunity · 2026
    Article
  4. bioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. mTOR Signaling in Macrophages: All Depends on the Context.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review

11 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

12 authors at 4 institutions in 2 countries.

R W HallowellDepartment of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brooklyn Avenue, Boston, Massachusetts 02215, USA.
S L CollinsDepartment of Medicine, Johns Hopkins University School of Medicine, 735 North Broadway, Baltimore, Maryland 21205, USA.
J M CraigDepartment of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, 650 North Wolfe Street, Baltimore, Maryland 21205, USA.
Y ZhangDepartment of Respiratory Diseases, Shanghai Pulmonary Hospital, Tongji University School of Medicine, 1239 Siping Road, Shanghai 200433, China.
M OhDepartment of Oncology, Johns Hopkins University School of Medicine, 735 North Broadway, Baltimore, Maryland 21205, USA.
P B IlleiDepartment of Pathology, Johns Hopkins University School of Medicine, 735 North Broadway, Baltimore, Maryland 21205, USA.
Y Chan-LiDepartment of Medicine, Johns Hopkins University School of Medicine, 735 North Broadway, Baltimore, Maryland 21205, USA.
C L VigelandDepartment of Medicine, Johns Hopkins University School of Medicine, 735 North Broadway, Baltimore, Maryland 21205, USA.
W MitznerW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, 650 North Wolfe Street, Baltimore, Maryland 21205, USA.
A L ScottW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, 650 North Wolfe Street, Baltimore, Maryland 21205, USA.
J D PowellDepartment of Oncology, Johns Hopkins University School of Medicine, 735 North Broadway, Baltimore, Maryland 21205, USA.
M R HortonDepartment of Medicine, Johns Hopkins University School of Medicine, 735 North Broadway, Baltimore, Maryland 21205, USA.
Johns Hopkins University · USJohns Hopkins Medicine · USHarvard University · USShanghai Pulmonary Hospital · CN

Funding

THE INTEGRATED FUNCTION OF RESPIRATION &CIRCULATIONP01HL010342 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MITZNER, WAYNE · 1985 to 2015
$24.4M
CELLULAR &MOLECULAR MECH OF INFLAMMATORY REACTIONST32AI007247 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Joel L Pomerantz · 1985 to 2026
$10.2M
mTORC1 and mTORC2 selectively regulate macrophage differentiationR21HL111783 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI HORTON, MAUREEN RENEE · 2012 to 2013
$436k
Role of the IL-33/ST2 Axis in the Development of EmphysemaF32HL124823 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CRAIG, JOHN MATTHEW · 2014 to 2015
$106k
NHLBI NIH HHS F32 HL124823NHLBI NIH HHS P01 HL010342NHLBI NIH HHS R21 HL111783
6 · The paper itself

Abstract

Alternatively activated macrophages (M2) have an important function in innate immune responses to parasitic helminths, and emerging evidence also indicates these cells are regulators of systemic metabolism. Here we show a critical role for mTORC2 signalling in the generation of M2 macrophages. Abrogation of mTORC2 signalling in macrophages by selective conditional deletion of the adaptor molecule Rictor inhibits the generation of M2 macrophages while leaving the generation of classically activated macrophages (M1) intact. Selective deletion of Rictor in macrophages prevents M2 differentiation and clearance of a parasitic helminth infection in mice, and also abrogates the ability of mice to regulate brown fat and maintain core body temperature. Our findings define a role for mTORC2 in macrophages in integrating signals from the immune microenvironment to promote innate type 2 immunity, and also to integrate systemic metabolic and thermogenic responses.

Indexed as

AnimalsCell DifferentiationCells, CulturedDisease Models, AnimalFemaleGene Knockout TechniquesHelminthiasis, AnimalHumansImmunity, InnateMacrophagesMaleMechanistic Target of Rapamycin Complex 2MiceMice, Inbred C57BLNippostrongylusRapamycin-Insensitive Companion of mTOR ProteinMechanistic Target of Rapamycin Complex 2Rapamycin-Insensitive Companion of mTOR Proteinrictor protein, mouse

Identifiers

PMID28128208
PMCPMC5290163
OpenAlexW2581321289

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.