Evidence map›Paper›PMID 30626754›Full record

ArticleJCI insight2019

Registration of the extracellular matrix components constituting the fibroblastic focus in idiopathic pulmonary fibrosis.

Jeremy Herrera, Colleen Forster, Thomas Pengo, Angeles Montero, Joe Swift, Martin A Schwartz, Craig A Henke, Peter B Bitterman

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.7field-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

51 citing papers in PubMed, 90 citations in OpenAlex.

  1. ADAMTS14 is a novel modulator of fibroblast mechanoactivation in pulmonary fibrosis.American journal of respiratory and critical care medicine · 2026
    Article
  2. Review
  3. Article
  4. Mechanobiology and Resolution of Lung Fibrosis.Annual review of physiology · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Pulmonary Fibrosis-Focusing on the Future: Aspen Lung Conference 2024 Summary.American journal of respiratory cell and molecular biology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
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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

8 authors at 3 institutions in 2 countries.

Jeremy HerreraWellcome Centre for Cell-Matrix Research, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Colleen ForsterUniversity of Minnesota, Clinical and Translational Science Institute, Minneapolis, Minnesota, USA.
Thomas PengoUniversity of Minnesota Informatics Institute, University of Minnesota Twin Cities, Minneapolis, Minnesota, USA.
Angeles MonteroManchester University Foundation Trust, Department of Histopathology, Manchester, United Kingdom.
Joe SwiftWellcome Centre for Cell-Matrix Research, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Martin A SchwartzWellcome Centre for Cell-Matrix Research, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Craig A HenkeUniversity of Minnesota, Department of Medicine, Minneapolis, Minnesota, USA.
Peter B BittermanUniversity of Minnesota, Department of Medicine, Minneapolis, Minnesota, USA.
University of Minnesota · USWellcome Centre for Cell-Matrix Research · GBManchester University NHS Foundation Trust · GB

Funding

TRAINING-PULMONARY CELL &MOLECULAR BIOLOGY &PHYSIOLOGYT32HL007741 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI DUDLEY, R. ADAMS, INGBAR, DAVID H · 1994 to 2023
$13.9M
Translational control of the fibroblast phenotype in IPFP01HL091775 · NHLBI · UNIVERSITY OF MINNESOTA · PI HENKE, CRAIG A · 2009 to 2013
$8.3M
S100A4 Regulation of IPF Mesenchymal Progenitor Cell FibrogenicityR01HL146501 · NHLBI · UNIVERSITY OF MINNESOTA · PI HENKE, CRAIG A · 2019 to 2022
$2.3M
Role of fibrotic extracellular matrix in generating the IPF FibroblastR01HL125236 · NHLBI · UNIVERSITY OF MINNESOTA · PI BITTERMAN, PETER B · 2015 to 2018
$1.9M
Integrin-Matrix Regulation of IPF Fibroblast PhenotypeR01HL125227 · NHLBI · UNIVERSITY OF MINNESOTA · PI HENKE, CRAIG A · 2015 to 2018
$1.8M
NHLBI NIH HHS P01 HL091775NHLBI NIH HHS R01 HL125227NHLBI NIH HHS R01 HL125236NHLBI NIH HHS R01 HL146501NHLBI NIH HHS T32 HL007741Wellcome Trust
6 · The paper itself

Abstract

The extracellular matrix (ECM) in idiopathic pulmonary fibrosis (IPF) drives fibrosis progression; however, the ECM composition of the fibroblastic focus (the hallmark lesion in IPF) and adjacent regions remains incompletely defined. Herein, we serially sectioned IPF lung specimens constructed into tissue microarrays and immunostained for ECM components reported to be deregulated in IPF. Immunostained sections were imaged, anatomically aligned, and 3D reconstructed. The myofibroblast core of the fibroblastic focus (defined by collagen I, α-smooth muscle actin, and procollagen I immunoreactivity) was associated with collagens III, IV, V, and VI; fibronectin; hyaluronan; and versican immunoreactivity. Hyaluronan immunoreactivity was also present at the fibroblastic focus perimeter and at sites where early lesions appear to be forming. Fibrinogen immunoreactivity was often observed at regions of damaged epithelium lining the airspace and the perimeter of the myofibroblast core but was absent from the myofibroblast core itself. The ECM components of the fibroblastic focus were distributed in a characteristic and reproducible manner in multiple patients. This information can inform the development of high-fidelity model systems to dissect mechanisms by which the IPF ECM drives fibrosis progression.

Indexed as

FibrosisPulmonology

Identifiers

PMID30626754
PMCPMC6485370
OpenAlexW2908667401

What OpenQuestion holds

Textmetadata
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.