Transcriptomic-Metabolomic Profiling in Mouse Lung Tissues Reveals Sex- and Strain-Based Differences

Bibliographic Details
Title: Transcriptomic-Metabolomic Profiling in Mouse Lung Tissues Reveals Sex- and Strain-Based Differences
Authors: Jolyn Fernandes, Katelyn Dunigan-Russell, Hua Zhong, Vivian Lin, Mary Silverberg, Stephanie B. Moore, ViLinh Tran, Dean P. Jones, Peter F. Vitiello, Lynette K. Rogers, Trent E. Tipple
Source: Metabolites, Vol 12, Iss 10, p 932 (2022)
Publisher Information: MDPI AG, 2022.
Publication Year: 2022
Collection: LCC:Microbiology
Subject Terms: metabolomics, transcriptomics, xMWAS, sex differences, strain differences, Microbiology, QR1-502
More Details: Omics analyses are commonly used for identifying pathways and genes responsible for physiologic and pathologic processes. Though sex is considered a biological variable in rigorous assessments of pulmonary responses to oxidant exposures, the contribution of the murine strain is largely ignored. This study utilized an unbiased integrated assessment of high-resolution metabolomic profiling and RNA-sequencing to explore sex- and strain-dependent pathways in adult mouse lungs. The results indicated that strain exhibited a greater influence than sex on pathways associated with inflammatory and oxidant/antioxidant responses and that interaction metabolites more closely resembled those identified as differentially expressed by strain. Metabolite analyses revealed that the components of the glutathione antioxidant pathway were different between strains, specifically in the formation of mixed disulfides. Additionally, selenium metabolites such as selenohomocystiene and selenocystathionine were similarly differentially expressed. Transcriptomic analysis revealed similar findings, as evidenced by differences in glutathione peroxidase, peroxiredoxin, and the inflammatory transcription factors RelA and Jun. In summary, an multi-omics integrated approach identified that murine strain disproportionately impacts baseline expression of antioxidant systems in lung tissues. We speculate that strain-dependent differences contribute to discrepant pulmonary responses in preclincal mouse models, with deleterious effects on clinical translation.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2218-1989
Relation: https://www.mdpi.com/2218-1989/12/10/932; https://doaj.org/toc/2218-1989
DOI: 10.3390/metabo12100932
Access URL: https://doaj.org/article/789997480be447328f99394fe0810e25
Accession Number: edsdoj.789997480be447328f99394fe0810e25
Database: Directory of Open Access Journals
More Details
ISSN:22181989
DOI:10.3390/metabo12100932
Published in:Metabolites
Language:English