Evidence map›Paper›PMID 28062486›Full record

ReviewAmerican journal of physiology. Lung cellular and molecular physiology2017

Plasma membrane wounding and repair in pulmonary diseases.

Xiaofei Cong, Rolf D Hubmayr, Changgong Li, Xiaoli Zhao

Open access · bronzeAbstract readReview
In one paragraph

Review in American journal of physiology. Lung cellular and molecular physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 48 citations in OpenAlex.

  1. The importance of mechanical forces in chronic respiratory diseases.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  2. Article
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  5. Review
  6. Article
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  8. Article
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  10. Lung-on-a-Chip Models of the Lung Parenchyma.Advances in experimental medicine and biology · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Acute respiratory distress syndrome.Nature reviews. Disease primers · 2019
    Review
  19. Review
  20. Review
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

4 authors at 3 institutions in 1 country.

Xiaofei CongDepartment of Physiological Sciences, Eastern Virginia Medical School, Norfolk, Virginia.
Rolf D HubmayrEmerius, Thoracic Diseases Research Unit, Mayo Clinic, Rochester, Minnesota; and.
Changgong LiDepartment of Pediatrics, University of Southern California, Los Angeles, California.
Xiaoli ZhaoDepartment of Physiological Sciences, Eastern Virginia Medical School, Norfolk, Virginia; zhaox@evms.edu.
Eastern Virginia Medical School · USMayo Clinic in Florida · USUniversity of Southern California · US

Funding

Targeting Membrane Repair in Deformation-Induced Lung InjuryR01HL116826 · NHLBI · OHIO STATE UNIVERSITY · PI ZHAO, XIAOLI · 2013 to 2017
$1.9M
Tuning of innate immunity in local lungR21AI133465 · NIAID · EASTERN VIRGINIA MEDICAL SCHOOL · PI ZHAO, XIAOLI · 2017 to 2018
$427k
NHLBI NIH HHS R01 HL116826NIAID NIH HHS R21 AI133465
6 · The paper itself

Abstract

Various pathophysiological conditions such as surfactant dysfunction, mechanical ventilation, inflammation, pathogen products, environmental exposures, and gastric acid aspiration stress lung cells, and the compromise of plasma membranes occurs as a result. The mechanisms necessary for cells to repair plasma membrane defects have been extensively investigated in the last two decades, and some of these key repair mechanisms are also shown to occur following lung cell injury. Because it was theorized that lung wounding and repair are involved in the pathogenesis of acute respiratory distress syndrome (ARDS) and idiopathic pulmonary fibrosis (IPF), in this review, we summarized the experimental evidence of lung cell injury in these two devastating syndromes and discuss relevant genetic, physical, and biological injury mechanisms, as well as mechanisms used by lung cells for cell survival and membrane repair. Finally, we discuss relevant signaling pathways that may be activated by chronic or repeated lung cell injury as an extension of our cell injury and repair focus in this review. We hope that a holistic view of injurious stimuli relevant for ARDS and IPF could lead to updated experimental models. In addition, parallel discussion of membrane repair mechanisms in lung cells and injury-activated signaling pathways would encourage research to bridge gaps in current knowledge. Indeed, deep understanding of lung cell wounding and repair, and discovery of relevant repair moieties for lung cells, should inspire the development of new therapies that are likely preventive and broadly effective for targeting injurious pulmonary diseases.

Indexed as

Wound HealingAnimalsCell MembraneHumansLung DiseasesLung InjuryModels, BiologicalSignal Transductionacute respiratory distress syndromeepithelium mesenchymal cross talklung cellspulmonary fibrosis

Identifiers

PMID28062486
PMCPMC5374305
OpenAlexW2569159701

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.