Evidence map›Paper›PMID 36018859›Full record

ArticlePloS one2022

Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia.

Kirkwood A Pritchard, Xigang Jing, Michelle Teng, Clive Wells, Shuang Jia, Adeleye J Afolayan, Jason Jarzembowski, Billy W Day, Stephen Naylor, Martin J Hessner and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Oxidative Stress Is a Double-Edged Sword for the Neonate.Antioxidants (Basel, Switzerland) · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. (Chemical) Roles of HOCl in Rheumatic Diseases.Antioxidants (Basel, Switzerland) · 2024
    Review
  13. Review
  14. Article
  15. Cellular Senescence Contributes to the Progression of Hyperoxic Bronchopulmonary Dysplasia.American journal of respiratory cell and molecular biology · 2024
    Article
  16. Bronchopulmonary Dysplasia and Cell Senescence: A Case of Old Lungs in Young Infants?American journal of respiratory cell and molecular biology · 2024
    Article
  17. Article
  18. 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

12 authors at 2 institutions in 1 country.

Kirkwood A PritchardDivision of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
Xigang JingChildren's Research Institute, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
Michelle TengDepartment of Pediatrics, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
Clive WellsElectron Microscope Facility, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
Shuang JiaDepartment of Pediatrics, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
Adeleye J AfolayanChildren's Research Institute, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
Jason JarzembowskiChildren's Research Institute, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.ORCID 0000-0002-9027-5686
Billy W DayReNeuroGen L.L.C. Milwaukee, Elm Grove, Wisconsin, United States of America.
Stephen NaylorReNeuroGen L.L.C. Milwaukee, Elm Grove, Wisconsin, United States of America.
Martin J HessnerChildren's Research Institute, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
G Ganesh KonduriChildren's Research Institute, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.
Ru-Jeng TengChildren's Research Institute, Medical College of Wisconsin, Wauwatosa, Wisconsin, United States of America.ORCID 0000-0003-4321-2452
Children's Hospital of Wisconsin · USMedical College of Wisconsin · US

Funding

Mechanisms of Inflammation in Sickle Cell DiseaseR01HL128371 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI PRITCHARD, KIRKWOOD ARTHUR · 2016 to 2024
$4.2M
Reducing innate inflammation in new onset T1D with Lactobacillus plantarumR01DK125014 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI CABRERA, SUSANNE M, HESSNER, MARTIN J · 2020 to 2024
$2.8M
Plasma-induced signatures as a measure disease heterogeneity and immunomodulation in T1D clinical trialsR01DK121528 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI HESSNER, MARTIN J · 2020 to 2023
$1.9M
AMP Kinase regulation in persistent pulmonary hypertension of the newbornR01HL136597 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI KONDURI, GIRIJA G. · 2018 to 2021
$1.5M
NHLBI NIH HHS R01 HL128371NHLBI NIH HHS R01 HL136597NHLBI NIH HHS R01 HL144519NIDDK NIH HHS R01 DK121528NIDDK NIH HHS R01 DK125014
6 · The paper itself

Abstract

Myeloperoxidase (MPO), oxidative stress (OS), and endoplasmic reticulum (ER) stress are increased in the lungs of rat pups raised in hyperoxia, an established model of bronchopulmonary dysplasia (BPD). However, the relationship between OS, MPO, and ER stress has not been examined in hyperoxia rat pups. We treated Sprague-Dawley rat pups with tunicamycin or hyperoxia to determine this relationship. ER stress was detected using immunofluorescence, transcriptomic, proteomic, and electron microscopic analyses. Immunofluorescence observed increased ER stress in the lungs of hyperoxic rat BPD and human BPD. Proteomic and morphometric studies showed that tunicamycin directly increased ER stress of rat lungs and decreased lung complexity with a BPD phenotype. Previously, we showed that hyperoxia initiates a cycle of destruction that we hypothesized starts from increasing OS through MPO accumulation and then increases ER stress to cause BPD. To inhibit ER stress, we used tauroursodeoxycholic acid (TUDCA), a molecular chaperone. To break the cycle of destruction and reduce OS and MPO, we used N-acetyl-lysyltyrosylcysteine amide (KYC). The fact that TUDCA improved lung complexity in tunicamycin- and hyperoxia-treated rat pups supports the idea that ER stress plays a causal role in BPD. Additional support comes from data showing TUDCA decreased lung myeloid cells and MPO levels in the lungs of tunicamycin- and hyperoxia-treated rat pups. These data link OS and MPO to ER stress in the mechanisms mediating BPD. KYC's inhibition of ER stress in the tunicamycin-treated rat pup's lung provides additional support for the idea that MPO-induced ER stress plays a causal role in the BPD phenotype. ER stress appears to expand our proposed cycle of destruction. Our results suggest ER stress evolves from OS and MPO to increase neonatal lung injury and impair growth and development. The encouraging effect of TUDCA indicates that this compound has the potential for treating BPD.

Indexed as

Bronchopulmonary DysplasiaHyperoxiaPneumoniaAnimalsAnimals, NewbornDisease Models, AnimalEndoplasmic Reticulum StressHumansInfant, NewbornLungProteomicsRatsRats, Sprague-DawleyTunicamycinTunicamycin

Identifiers

PMID36018859
PMCPMC9417039
OpenAlexW4293677567

What OpenQuestion holds

Textmetadata
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.