Journal Article DZNE-2023-00634

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png
Systemic alterations in neutrophils and their precursors in early-stage chronic obstructive pulmonary disease.

 ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;

2023
Elsevier [New York, NY]

Cell reports 42(6), 112525 () [10.1016/j.celrep.2023.112525]

This record in other databases:    

Please use a persistent id in citations: doi:

Abstract: Systemic inflammation is established as part of late-stage severe lung disease, but molecular, functional, and phenotypic changes in peripheral immune cells in early disease stages remain ill defined. Chronic obstructive pulmonary disease (COPD) is a major respiratory disease characterized by small-airway inflammation, emphysema, and severe breathing difficulties. Using single-cell analyses we demonstrate that blood neutrophils are already increased in early-stage COPD, and changes in molecular and functional neutrophil states correlate with lung function decline. Assessing neutrophils and their bone marrow precursors in a murine cigarette smoke exposure model identified similar molecular changes in blood neutrophils and precursor populations that also occur in the blood and lung. Our study shows that systemic molecular alterations in neutrophils and their precursors are part of early-stage COPD, a finding to be further explored for potential therapeutic targets and biomarkers for early diagnosis and patient stratification.

Keyword(s): Humans (MeSH) ; Animals (MeSH) ; Mice (MeSH) ; Neutrophils (MeSH) ; Pulmonary Disease, Chronic Obstructive: drug therapy (MeSH) ; Lung (MeSH) ; Pulmonary Emphysema (MeSH) ; Inflammation (MeSH) ; CP: Immunology ; blood ; bone marrow ; chronic obstructive pulmonary disease ; granulopoiesis ; neutrophil ; single-cell transcriptomics

Classification:

Contributing Institute(s):
  1. Platform for Single Cell Genomics and Epigenomics (Schultze - PRECISE)
  2. Immune Regulation (AG Capasso)
  3. Immunogenomics and Neurodegeneration (AG Beyer)
  4. Modular High Performance Computing and Artificial Intelligence (AG Becker)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)
  2. 351 - Brain Function (POF4-351) (POF4-351)
  3. 354 - Disease Prevention and Healthy Aging (POF4-354) (POF4-354)
Experiment(s):
  1. Platform for Single Cell Genomics and Epigenomics at DZNE University of Bonn

Appears in the scientific report 2023
Database coverage:
Medline ; Creative Commons Attribution-NonCommercial-NoDerivs CC BY-NC-ND 4.0 ; DOAJ ; OpenAccess ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; DOAJ Seal ; Essential Science Indicators ; Fees ; IF >= 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
Click to display QR Code for this record

The record appears in these collections:
Document types > Articles > Journal Article
Institute Collections > BN DZNE > BN DZNE-AG Capasso
Institute Collections > BN DZNE > BN DZNE-AG Becker
Institute Collections > BN DZNE > BN DZNE-AG Beyer
Institute Collections > BN DZNE > BN DZNE-PRECISE
Full Text Collection
Public records
Publications Database

 Record created 2023-06-20, last modified 2024-06-12