Evidence map›Paper›PMID 24526697›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2014

Vascular smooth muscle cell-derived transforming growth factor-β promotes maturation of activated, neointima lesion-like macrophages.

Allison Ostriker, Henrick N Horita, Joanna Poczobutt, Mary C M Weiser-Evans, Raphael A Nemenoff

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
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  5. Article
  6. Mechanistic regulation of SPHK1 expression and translocation by EMAP II in pulmonary smooth muscle cells.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    Article
  7. Article
  8. Review
  9. A computational bio-chemo-mechanical model of in vivo tissue-engineered vascular graft development.Integrative biology : quantitative biosciences from nano to macro · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Transforming Growth Factor-International journal of nephrology · 2018
    Article
  15. LC3-Associated Phagocytosis and Inflammation.Journal of molecular biology · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Arterial smooth muscle.Arteriosclerosis, thrombosis, and vascular biology · 2014
    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

5 authors at 1 institution in 1 country.

Allison OstrikerFrom the Department of Medicine, Division of Renal Diseases and Hypertension (H.N.H., J.P., M.C.M.W.-E., R.A.N.), Department of Pharmacology (A.O., M.C.M.W.-E., R.A.N.), and Cardiovascular and Pulmonary Research Laboratory (M.C.M.W.-E., R.A.N.), University of Colorado Denver, Aurora.
Henrick N Horita
Joanna Poczobutt
Mary C M Weiser-Evans
Raphael A Nemenoff
Anna Needs Neuroblastoma Answers · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
VRAC and Rho in pulmonary EC proliferationP01HL014985 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STENMARK, KURT R. · 1985 to 2019
$35.1M
Translational Pulmonary Vascular Biology ProgramT32HL007171 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Sonia Castro Flores, Tim Lahm · 1985 to 2026
$9.4M
Preroxisome Proliferator-Activated Receptors in lung CancerR01CA108610 · NCI · UNIVERSITY OF COLORADO DENVER · PI NEMENOFF, RAPHAEL A. · 2004 to 2015
$2.9M
Role of cPLA2 in Lung Cancer: Microenvironment vs Tumor CellsR01CA103618 · NCI · UNIVERSITY OF COLORADO DENVER · PI NEMENOFF, RAPHAEL A. · 2003 to 2010
$1.9M
Role of PTEN in Vascular Lesion FormationR01HL088643 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI WEISER-EVANS, MARY CM. · 2009 to 2012
$1.5M
Microenvironmental Endogenous Reprogramming of Differentiated Smooth Muscle CellsR21HL114126 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI WEISER-EVANS, MARY CM. · 2013 to 2014
$410k
NCATS NIH HHS UL1 TR001082NCI NIH HHS R01 CA103618NCI NIH HHS R01 CA108610NHLBI NIH HHS P01 HL014985NHLBI NIH HHS R01 HL088643NHLBI NIH HHS R21 HL114126NHLBI NIH HHS T32 HL007171
6 · The paper itself

Abstract

objectiveTo define the contribution of vascular smooth muscle cell (SMC)-derived factors to macrophage phenotypic modulation in the setting of vascular injury. APPROACH AND

resultsBy flow cytometry, macrophages (M4) were the predominant myeloid cell type recruited to wire-injured femoral arteries, in mouse, compared with neutrophils or eosinophils. Recruited macrophages from injured vessels exhibited a distinct expression profile relative to circulating mononuclear cells (peripheral blood monocytes; increased: interleukin-6, interleukin-10, interleukin-12b, CC chemokine receptor [CCR]3, CCR7, tumor necrosis factor-α, inducible nitric oxide synthase, arginase 1; decreased: interleukin-12a, matrix metalloproteinase [MMP]9). This phenotype was recapitulated in vitro by maturing rat bone marrow cells in the presence of macrophage-colony stimulating factor and 20% conditioned media from cultured rat SMC (sMϕ) compared with maturation in macrophage-colony stimulating factor alone (M0). Recombinant transforming growth factor (TGF)-β1 recapitulated the effect of SMC conditioned media. Macrophage maturation studies performed in the presence of a pan-TGF-β neutralizing antibody, a TGF-β receptor inhibitor, or conditioned media from TGF-β-depleted SMCs confirmed that the SMC-derived factor responsible for macrophage activation was TGF-β. Finally, the effect of SMC-mediated macrophage activation on SMC biology was assessed. SMCs cocultured with sMϕ exhibited increased rates of proliferation relative to SMCs cultured alone or with M0 macrophages.

conclusionsSMC-derived TGF-β modulates the phenotype of maturing macrophages in vitro, recapitulating the phenotype found in vascular lesions in vivo. SMC-modulated macrophages induce SMC activation to a greater extent than control macrophages.

Indexed as

Macrophage ActivationNeointimaParacrine CommunicationAnimalsBiomarkersCell ProliferationCells, CulturedCoculture TechniquesCulture Media, ConditionedCytokinesDisease Models, AnimalFemoral ArteryHumansMacrophage Colony-Stimulating FactorMacrophagesMiceBiomarkersCulture Media, ConditionedCytokinesMacrophage Colony-Stimulating Factorp38 Mitogen-Activated Protein KinasesTGFB1 protein, humanTransforming Growth Factor betaTransforming Growth Factor beta1macrophagesmuscle, smooth, vascularneointimatransforming growth factor betavascular system injuries

Identifiers

PMID24526697
PMCPMC3966963
OpenAlexW2130141518

What OpenQuestion holds

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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.