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Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice

[Image: see text] To capture interplay between biological pathways, we analyzed the proteome from matched lung tissues and bronchoalveolar lavage fluid (BALF) of individual allergen-naïve and house dust mite (HDM)-challenged BALB/c mice, a model of allergic asthma. Unbiased label-free liquid chromat...

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Autores principales: Mahood, Thomas H., Pascoe, Christopher D., Karakach, Tobias K., Jha, Aruni, Basu, Sujata, Ezzati, Peyman, Spicer, Victor, Mookherjee, Neeloffer, Halayko, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818314/
https://www.ncbi.nlm.nih.gov/pubmed/33490776
http://dx.doi.org/10.1021/acsomega.0c04269
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author Mahood, Thomas H.
Pascoe, Christopher D.
Karakach, Tobias K.
Jha, Aruni
Basu, Sujata
Ezzati, Peyman
Spicer, Victor
Mookherjee, Neeloffer
Halayko, Andrew J.
author_facet Mahood, Thomas H.
Pascoe, Christopher D.
Karakach, Tobias K.
Jha, Aruni
Basu, Sujata
Ezzati, Peyman
Spicer, Victor
Mookherjee, Neeloffer
Halayko, Andrew J.
author_sort Mahood, Thomas H.
collection PubMed
description [Image: see text] To capture interplay between biological pathways, we analyzed the proteome from matched lung tissues and bronchoalveolar lavage fluid (BALF) of individual allergen-naïve and house dust mite (HDM)-challenged BALB/c mice, a model of allergic asthma. Unbiased label-free liquid chromatography with tandem mass spectrometry (LC-MS/MS) analysis quantified 2675 proteins from tissues and BALF of allergen-naïve and HDM-exposed mice. In comparing the four datasets, we found significantly greater diversity in proteins between lung tissues and BALF than in the changes induced by HDM challenge. The biological pathways enriched after allergen exposure were compartment-dependent. Lung tissues featured innate immune responses and oxidative stress, while BALF most strongly revealed changes in metabolism. We combined lung tissues and BALF proteomes, which principally highlighted oxidation reduction (redox) pathways, a finding influenced chiefly by the lung tissue dataset. Integrating lung and BALF proteomes also uncovered new proteins and biological pathways that may mediate lung tissue and BALF interactions after allergen challenge, for example, B-cell receptor signaling. We demonstrate that enhanced insight is fostered when different biological compartments from the lung are investigated in parallel. Integration of proteomes from lung tissues and BALF compartments reveals new information about protein networks in response to environmental challenge and interaction between intracellular and extracellular processes.
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spelling pubmed-78183142021-01-22 Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice Mahood, Thomas H. Pascoe, Christopher D. Karakach, Tobias K. Jha, Aruni Basu, Sujata Ezzati, Peyman Spicer, Victor Mookherjee, Neeloffer Halayko, Andrew J. ACS Omega [Image: see text] To capture interplay between biological pathways, we analyzed the proteome from matched lung tissues and bronchoalveolar lavage fluid (BALF) of individual allergen-naïve and house dust mite (HDM)-challenged BALB/c mice, a model of allergic asthma. Unbiased label-free liquid chromatography with tandem mass spectrometry (LC-MS/MS) analysis quantified 2675 proteins from tissues and BALF of allergen-naïve and HDM-exposed mice. In comparing the four datasets, we found significantly greater diversity in proteins between lung tissues and BALF than in the changes induced by HDM challenge. The biological pathways enriched after allergen exposure were compartment-dependent. Lung tissues featured innate immune responses and oxidative stress, while BALF most strongly revealed changes in metabolism. We combined lung tissues and BALF proteomes, which principally highlighted oxidation reduction (redox) pathways, a finding influenced chiefly by the lung tissue dataset. Integrating lung and BALF proteomes also uncovered new proteins and biological pathways that may mediate lung tissue and BALF interactions after allergen challenge, for example, B-cell receptor signaling. We demonstrate that enhanced insight is fostered when different biological compartments from the lung are investigated in parallel. Integration of proteomes from lung tissues and BALF compartments reveals new information about protein networks in response to environmental challenge and interaction between intracellular and extracellular processes. American Chemical Society 2021-01-05 /pmc/articles/PMC7818314/ /pubmed/33490776 http://dx.doi.org/10.1021/acsomega.0c04269 Text en © 2021 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Mahood, Thomas H.
Pascoe, Christopher D.
Karakach, Tobias K.
Jha, Aruni
Basu, Sujata
Ezzati, Peyman
Spicer, Victor
Mookherjee, Neeloffer
Halayko, Andrew J.
Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice
title Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice
title_full Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice
title_fullStr Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice
title_full_unstemmed Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice
title_short Integrating Proteomes for Lung Tissues and Lavage Reveals Pathways That Link Responses in Allergen-Challenged Mice
title_sort integrating proteomes for lung tissues and lavage reveals pathways that link responses in allergen-challenged mice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818314/
https://www.ncbi.nlm.nih.gov/pubmed/33490776
http://dx.doi.org/10.1021/acsomega.0c04269
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