Evidence map›Paper›PMID 24040256›Full record

ArticlePloS one2013

A new approach for the study of lung smooth muscle phenotypes and its application in a murine model of allergic airway inflammation.

Jesus Paez-Cortez, Ramaswamy Krishnan, Anneliese Arno, Linh Aven, Sumati Ram-Mohan, Kruti R Patel, Jining Lu, Oliver D King, Xingbin Ai, Alan Fine

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Lung CD4Cell reports · 2025
    Article
  2. Article
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  8. Mode Switch of CaFrontiers in physiology · 2021
    Article
  9. Article
  10. Article
  11. Smooth muscle: a stiff sculptor of epithelial shapes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. An NT4/TrkB-dependent increase in innervation links early-life allergen exposure to persistent airway hyperreactivity.FASEB journal : official publication of the Federation of American Societies for Experimental 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

10 authors at 4 institutions in 1 country.

Jesus Paez-CortezThe Pulmonary Center, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Ramaswamy Krishnan
Anneliese Arno
Linh Aven
Sumati Ram-Mohan
Kruti R Patel
Jining Lu
Oliver D King
Xingbin Ai
Alan Fine
Boston University · USBeth Israel Deaconess Medical Center · USCenter for Vascular Biology Research · USUniversity of Massachusetts Chan Medical School · US

Funding

BIOLOGY OF THE LUNG--MULTIDISCIPLINARY PROGRAMT32HL007035 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Darrell N. Kotton, JOSEPH P MIZGERD · 1985 to 2026
$24.3M
Boston University Clinical and Translational Science Award (CTSA) Program UL1UL1TR000157 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2012 to 2013
$7.9M
Identifying Molecular Phenotype of Normal and Asthmatic Bronchial Smooth MuscleR21HL112619 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI AI, XINGBIN, FINE, ALAN FINE · 2012 to 2013
$440k
NCATS NIH HHS UL1 TR000157NCATS NIH HHS UL1-TR000157NHLBI NIH HHS R21 HL112619NHLBI NIH HHS R21HL112619NHLBI NIH HHS T32 HL007035NHLBI NIH HHS T32HL007035
6 · The paper itself

Abstract

Phenotypes of lung smooth muscle cells in health and disease are poorly characterized. This is due, in part, to a lack of methodologies that allow for the independent and direct isolation of bronchial smooth muscle cells (BSMCs) and vascular smooth muscle cells (VSMCs) from the lung. In this paper, we describe the development of a bi-fluorescent mouse that permits purification of these two cell populations by cell sorting. By subjecting this mouse to an acute allergen based-model of airway inflammation that exhibits many features of asthma, we utilized this tool to characterize the phenotype of so-called asthmatic BSMCs. First, we examined the biophysical properties of single BSMCs from allergen sensitized mice and found increases in basal tone and cell size that were sustained ex vivo. We then generated for the first time, a comprehensive characterization of the global gene expression changes in BSMCs isolated from the bi-fluorescent mice with allergic airway inflammation. Using statistical methods and pathway analysis, we identified a number of differentially expressed mRNAs in BSMCs from allergen sensitized mice that code for key candidate proteins underlying changes in matrix formation, contractility, and immune responses. Ultimately, this tool will provide direction and guidance for the logical development of new markers and approaches for studying human lung smooth muscle.

Indexed as

PhenotypeAllergensAnimalsAsthmaBronchiBronchial HyperreactivityCell SizeDisease Models, AnimalFluorescenceGene ExpressionGene Expression ProfilingHumansImmunizationInflammationMiceMice, TransgenicAllergensOvalbuminProteomeRNA, Messenger

Identifiers

PMID24040256
PMCPMC3767675
OpenAlexW2042068972

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.