Evidence map›Paper›PMID 26727658›Full record

ArticleJournal of pediatric gastroenterology and nutrition2016

Eosinophilic Esophagitis-Associated Chemical and Mechanical Microenvironment Shapes Esophageal Fibroblast Behavior.

Amanda B Muir, Kara Dods, Steven J Henry, Alain J Benitez, Dale Lee, Kelly A Whelan, Maureen DeMarshall, Daniel A Hammer, Gary Falk, Rebecca G Wells and 3 more

Abstract read
In one paragraph

Article in Journal of pediatric gastroenterology and nutrition, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Immune functions of the esophagus.The Journal of allergy and clinical immunology · 2026
    Review
  4. Prostaglandin EbioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. The oesophagus as an immune organ.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Development and dysfunction of structural cells in eosinophilic esophagitis.The Journal of allergy and clinical immunology · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Persistent Basal Cell Hyperplasia Is Associated With Clinical and Endoscopic Findings in Patients With Histologically Inactive Eosinophilic Esophagitis.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2020
    Article
  17. Article
  18. Article
  19. EoE disease monitoring: Where we are and where we are going.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2020
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Amanda B Muir*Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, PA †Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania ‡Department of Bioengineering, University of Pennsylvania §University of Pennsylvania School of Engineering and Applied Science, Philadelphia ||Division of Gastroenterology, Seattle Children's Hospital ¶Gastroenterology Division, Department of Medicine #Abramson Cancer Center, University of Pennsylvania, Philadelphia **Division of Allergy and Immunology, The Children's Hospital of Philadelphia, Philadelphia, PA.
Kara Dods
Steven J Henry
Alain J Benitez
Dale Lee
Kelly A Whelan
Maureen DeMarshall
Daniel A Hammer
Gary Falk
Rebecca G Wells
Jonathan Spergel
Hiroshi Nakagawa
Mei-Lun Wang
University Gastroenterology · USUniversity of Pennsylvania · USChildren's Hospital of Philadelphia · USSeattle Children's Hospital · US

Funding

TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI REBECCA G WELLS · 1997 to 2026
$32.5M
TRAINING (CAREER DEVELOPMENT) COMPONENTU54AI117804 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI Marc E. Rothenberg · 2014 to 2026
$18.5M
Toll-like Receptor Signaling in the Esophageal EpitheliumR01DK087789 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI SPERGEL, JONATHAN MICHEAL · 2010 to 2014
$1.8M
Using micropost arrays to measure traction forces during dendritic cell motilityR01GM104287 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI HAMMER, DANIEL A · 2013 to 2016
$1.4M
Lysyl oxidase mediated fibrosis in eosinophilic esophagitisK08DK106444 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI MUIR, AMANDA BROOKE · 2015 to 2019
$778k
The functional role of mitophagy in esophageal cell biologyK01DK103953 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI WHELAN, KELLY A · 2015 to 2019
$637k
Maturational Characterization of Human Esophageal Fibroblasts in EoEF32DK100088 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI MUIR, AMANDA BROOKE · 2013 to 2014
$120k
NIAID NIH HHS U54 AI117804NIDDK NIH HHS F32 DK100088NIDDK NIH HHS K01 DK103953NIDDK NIH HHS K08 DK106444NIDDK NIH HHS L30 DK103160NIDDK NIH HHS P30 DK050306NIDDK NIH HHS R01 DK087789NIGMS NIH HHS R01 GM104287
6 · The paper itself

Abstract

objectivesEosinophilic esophagitis (EoE) is an immune-mediated allergic disease characterized by progressive esophageal dysmotility and fibrotic stricture associated with chronic esophageal fibroblast activation. It remains unknown how esophageal fibroblasts respond to EoE-relevant matrix stiffness or inflammatory cytokines.

methodsImmunofluorescence was used to evaluate α-smooth muscle actin (α-SMA) expression in endoscopic esophageal biopsies. Primary esophageal fibroblasts from adult and pediatric patients with or without EoE were exposed to transforming growth factor (TGF)β to determine gene expression, collagen-matrix contractility, and cytoskeletal organization. The influence of matrix stiffness upon fibroblast behavior was assessed on the engineered surface of polyacrylamide gels with varying stiffness. Fibroblast traction forces were measured using microfabricated-post-array-detectors.

resultsEoE esophageal fibroblasts had enhanced α-SMA expression. TGFβ not only stimulated enhanced fibroblast-specific gene expression but also promoted fibroblast-mediated collagen-matrix contraction, despite disease state or age of patients as the origin of cells. Unlike conventional monolayer cell, culture conditions using plastic surface (1 GPa) that activates fibroblasts constitutively, our engineered platforms recapitulating physiologically relevant stiffness (1-20 kPa) revealed that matrix stiffness defines the extent of α-SMA expression, intracellular collagen fibril organization, SMAD3 phosphorylation, and fibroblast traction force.

conclusionsMatrix stiffness may critically influence TGFβ-mediated gene expression and functions of esophageal fibroblasts ex vivo independent of age and disease conditions. These findings provide a novel insight into the pathogenesis of fibrostenotic disease in EoE.

Indexed as

ActinsAdultBiomarkersBlotting, WesternCells, CulturedCellular MicroenvironmentChildCytokinesEosinophilic EsophagitisEsophagusExtracellular MatrixFemaleFibroblastsFluorescent Antibody TechniqueGene Expression RegulationHumansACTA2 protein, humanActinsBiomarkersCytokinesTransforming Growth Factor beta

Identifiers

PMID26727658
PMCPMC4929044
OpenAlexW2330692593

What OpenQuestion holds

Textmetadata
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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.