Berdyshev Evgeny V, Serban Karina A, Schweitzer Kelly S, Bronova Irina A, Mikosz Andrew, Petrache Irina
Department of Medicine, National Jewish Health, Denver, Colorado, USA.
Department of Medicine, University of Illinois Chicago, Chicago, Illinois, USA.
Thorax. 2021 Jan 29. doi: 10.1136/thoraxjnl-2020-215892.
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.
利用动物模型和患者血浆对慢性阻塞性肺疾病(COPD)进行的研究表明,鞘脂代谢存在失调,但COPD肺部的数据较少。对69例COPD患者、16例无COPD的吸烟者和13例间质性肺疾病患者的肺部进行质谱分析和免疫染色测量,发现COPD患者肺部神经酰胺和1-磷酸鞘氨醇(S1P)水平解偶联,鞘氨醇激酶-1(SphK1)活性降低。远端COPD肺部神经酰胺丰度与细胞凋亡的相关性以及SphK1活性与肺气肿存在之间的负相关性表明,神经酰胺向S1P代谢的破坏是COPD肺气肿表型的重要决定因素。