| Literature DB >> 33514670 |
Evgeny V Berdyshev1,2, Karina A Serban1,3,4, Kelly S Schweitzer1,3, Irina A Bronova1,2, Andrew Mikosz1, Irina Petrache5,3,4.
Abstract
Studies of chronic obstructive pulmonary disease (COPD) using animal models and patient plasma indicate dysregulation of sphingolipid metabolism, but data in COPD lungs are sparse. Mass spectrometric and immunostaining measurements of lungs from 69 COPD, 16 smokers without COPD and 13 subjects with interstitial lung disease identified decoupling of lung ceramide and sphingosine-1 phosphate (S1P) levels and decreased sphingosine kinase-1 (SphK1) activity in COPD. The correlation of ceramide abundance in distal COPD lungs with apoptosis and the inverse correlation between SphK1 activity and presence of emphysema suggest that disruption of ceramide-to-S1P metabolism is an important determinant of emphysema phenotype in COPD. © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: COPD exacerbations mechanisms; COPD pathology; emphysema; interstitial fibrosis; tobacco and the lung
Year: 2021 PMID: 33514670 PMCID: PMC9004347 DOI: 10.1136/thoraxjnl-2020-215892
Source DB: PubMed Journal: Thorax ISSN: 0040-6376 Impact factor: 9.102