Alveolar macrophage transcriptomic profiling in COPD shows major lipid metabolism changes

Wataru Fujii(University of Bonn), Theodore S. Kapellos(University of Bonn), Kevin Baßler(University of Bonn), Kristian Händler(University of Bonn), Lisa Holsten(University of Bonn), Rainer Knoll(University of Bonn), Stefanie Warnat‐Herresthal(University of Bonn), Marie Oestreich(University of Bonn), Emily Hinkley(University of Bonn), Jan Hasenauer(University of Bonn), Carmen Pizarro(University Hospital Bonn), Christoph Thiele(University of Bonn), Anna C. Aschenbrenner(University of Bonn), Thomas Ulas(University of Bonn), Dirk Skowasch(University Hospital Bonn), Joachim L. Schultze(University of Bonn)
ERJ Open Research
May 13, 2021
Cited by 57Open Access
Full Text

Abstract

Background Immune cells play a major role in the pathogenesis of COPD. Changes in the distribution and cellular functions of major immune cells, such as alveolar macrophages (AMs) and neutrophils are well known; however, their transcriptional reprogramming and contribution to the pathophysiology of COPD are still not fully understood. Method To determine changes in transcriptional reprogramming and lipid metabolism in the major immune cell type within bronchoalveolar lavage fluid, we analysed whole transcriptomes and lipidomes of sorted CD45 + Lin − HLA-DR + CD66b − Autofluorescence hi AMs from controls and COPD patients. Results We observed global transcriptional reprogramming featuring a spectrum of activation states, including pro- and anti-inflammatory signatures. We further detected significant changes between COPD patients and controls in genes involved in lipid metabolism, such as fatty acid biosynthesis in GOLD2 patients. Based on these findings, assessment of a total of 202 lipid species in sorted AMs revealed changes of cholesteryl esters, monoacylglycerols and phospholipids in a disease grade-dependent manner. Conclusions Transcriptome and lipidome profiling of COPD AMs revealed GOLD grade-dependent changes, such as in cholesterol metabolism and interferon-α and γ responses.


Related Papers

No related papers found

Powered by citation graph analysis