Evidence map›Paper›PMID 36516756›Full record

ArticleCell reports2022

Macrophage NFATC2 mediates angiogenic signaling during mycobacterial infection.

W Jared Brewer, Ana María Xet-Mull, Anne Yu, Mollie I Sweeney, Eric M Walton, David M Tobin

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  8. Journal of bacteriology · 2025
    Review
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  12. Impact of MSMEG5257 Deletion onMicroorganisms · 2024
    Article
  13. Article
  14. Targeting EB3-IPAmerican journal of respiratory cell and molecular biology · 2023
    Article
  15. Adult zebrafish as advanced models of human disease.Disease models & mechanisms · 2023
    Article
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

6 authors at 1 institution in 1 country.

W Jared BrewerDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.
Ana María Xet-MullDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.
Anne YuDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.
Mollie I SweeneyDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.
Eric M WaltonDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.
David M TobinDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA; Department of Immunology, Duke University School of Medicine, Durham, NC 27710, USA. Electronic address: david.tobin@duke.edu.
Duke University · US

Funding

Macrophage Reprogramming During Granuloma Formation in the ZebrafishR01AI130236 · NIAID · DUKE UNIVERSITY · PI David M. Tobin · 2017 to 2026
$4.5M
Genetic dissection of angiogenesis in the tuberculous granulomaR01AI125517 · NIAID · DUKE UNIVERSITY · PI David M. Tobin · 2017 to 2026
$4.4M
Linking Human TB Genetic Susceptibility Loci to Granuloma BiologyR01AI166304 · NIAID · DUKE UNIVERSITY · PI David M. Tobin · 2022 to 2026
$3.4M
The Genetic Basis of Bone Disease in Mycobacterial InfectionR01AI127715 · NIAID · DUKE UNIVERSITY · PI Clare Margaret Smith, David M. Tobin · 2017 to 2026
$3.3M
NIAID NIH HHS R01 AI125517NIAID NIH HHS R01 AI127715NIAID NIH HHS R01 AI130236NIAID NIH HHS R01 AI166304
6 · The paper itself

Abstract

During mycobacterial infections, pathogenic mycobacteria manipulate both host immune and stromal cells to establish and maintain a productive infection. In humans, non-human primates, and zebrafish models of infection, pathogenic mycobacteria produce and modify the specialized lipid trehalose 6,6'-dimycolate (TDM) in the bacterial cell envelope to drive host angiogenesis toward the site of forming granulomas, leading to enhanced bacterial growth. Here, we use the zebrafish-Mycobacterium marinum infection model to define the signaling basis of the host angiogenic response. Through intravital imaging and cell-restricted peptide-mediated inhibition, we identify macrophage-specific activation of NFAT signaling as essential to TDM-mediated angiogenesis in vivo. Exposure of cultured human cells to Mycobacterium tuberculosis results in robust induction of VEGFA, which is dependent on a signaling pathway downstream of host TDM detection and culminates in NFATC2 activation. As granuloma-associated angiogenesis is known to serve bacterial-beneficial roles, these findings identify potential host targets to improve tuberculosis disease outcomes.

Indexed as

Mycobacterium marinumMycobacterium tuberculosisTuberculosisAnimalsGranulomaHumansMacrophagesNFATC Transcription FactorsSignal TransductionZebrafishNFATC2 protein, humanNFATC Transcription FactorsangiogenesisCP: ImmunologyCP: MicrobiologymacrophageMycobacterium marinumMycobacterium tuberculosisNFATpathogenic mycobacteriatrehalose dimycolateVegfazebrafish

Identifiers

PMID36516756
PMCPMC9880963
OpenAlexW4311672109

What OpenQuestion holds

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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.