Cargando…

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

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 pu...

Descripción completa

Detalles Bibliográficos
Autores principales: Pritchard, Kirkwood A., Jing, Xigang, Teng, Michelle, Wells, Clive, Jia, Shuang, Afolayan, Adeleye J., Jarzembowski, Jason, Day, Billy W., Naylor, Stephen, Hessner, Martin J., Konduri, G. Ganesh, Teng, Ru-Jeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417039/
https://www.ncbi.nlm.nih.gov/pubmed/36018859
http://dx.doi.org/10.1371/journal.pone.0269564
_version_ 1784776611927687168
author Pritchard, Kirkwood A.
Jing, Xigang
Teng, Michelle
Wells, Clive
Jia, Shuang
Afolayan, Adeleye J.
Jarzembowski, Jason
Day, Billy W.
Naylor, Stephen
Hessner, Martin J.
Konduri, G. Ganesh
Teng, Ru-Jeng
author_facet Pritchard, Kirkwood A.
Jing, Xigang
Teng, Michelle
Wells, Clive
Jia, Shuang
Afolayan, Adeleye J.
Jarzembowski, Jason
Day, Billy W.
Naylor, Stephen
Hessner, Martin J.
Konduri, G. Ganesh
Teng, Ru-Jeng
author_sort Pritchard, Kirkwood A.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-9417039
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-94170392022-08-27 Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia Pritchard, Kirkwood A. Jing, Xigang Teng, Michelle Wells, Clive Jia, Shuang Afolayan, Adeleye J. Jarzembowski, Jason Day, Billy W. Naylor, Stephen Hessner, Martin J. Konduri, G. Ganesh Teng, Ru-Jeng PLoS One Research Article 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. Public Library of Science 2022-08-26 /pmc/articles/PMC9417039/ /pubmed/36018859 http://dx.doi.org/10.1371/journal.pone.0269564 Text en © 2022 Pritchard et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pritchard, Kirkwood A.
Jing, Xigang
Teng, Michelle
Wells, Clive
Jia, Shuang
Afolayan, Adeleye J.
Jarzembowski, Jason
Day, Billy W.
Naylor, Stephen
Hessner, Martin J.
Konduri, G. Ganesh
Teng, Ru-Jeng
Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia
title Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia
title_full Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia
title_fullStr Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia
title_full_unstemmed Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia
title_short Role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia
title_sort role of endoplasmic reticulum stress in impaired neonatal lung growth and bronchopulmonary dysplasia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417039/
https://www.ncbi.nlm.nih.gov/pubmed/36018859
http://dx.doi.org/10.1371/journal.pone.0269564
work_keys_str_mv AT pritchardkirkwooda roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT jingxigang roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT tengmichelle roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT wellsclive roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT jiashuang roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT afolayanadeleyej roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT jarzembowskijason roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT daybillyw roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT naylorstephen roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT hessnermartinj roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT kondurigganesh roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia
AT tengrujeng roleofendoplasmicreticulumstressinimpairedneonatallunggrowthandbronchopulmonarydysplasia