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Blood neutrophils in COPD derive from activated progenitors in the bone marrow

Chronic obstructive pulmonary disease (COPD) is a major respiratory disease characterized by small airway inflammation, emphysema and severe breathing difficulties. Low-grade systemic inflammation is an established hallmark of severe disease, however, the molecular changes in peripheral immune cells remain far from understood. We combined multi-color flow cytometry with single-cell RNA sequencing and showed that blood neutrophil numbers are significantly increased in COPD and they are a heterogeneous population. A transcriptomic state that expressed interferon response genes correlated with alveolar damage and acute exacerbations. Furthermore, bronchoalveolar neutrophils expressed gene signatures corresponding to certain blood neutrophil states. Last, our data in a murine model of cigarette smoke exposure demonstrated that bone marrow neutrophil progenitors are expanded in smoke-treated animals and display signs of immune activation. Our study provides evidence that COPD systemic inflammation may derive from an activated haematopoietic precursor compartment.

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Chronic obstructive pulmonary disease (COPD) is a major respiratory disease characterized by small airway inflammation, emphysema and severe breathing difficulties. Low-grade systemic inflammation is an established hallmark of severe disease, however, the molecular changes in peripheral immune cells remain far from understood. We combined multi-color flow cytometry with single-cell RNA sequencing and showed that blood neutrophil numbers are significantly increased in COPD and they are a heterogeneous population. A transcriptomic state that expressed interferon response genes correlated with alveolar damage and acute exacerbations. Furthermore, bronchoalveolar neutrophils expressed gene signatures corresponding to certain blood neutrophil states. Last, our data in a murine model of cigarette smoke exposure demonstrated that bone marrow neutrophil progenitors are expanded in smoke-treated animals and display signs of immune activation. Our study provides evidence that COPD systemic inflammation may derive from an activated haematopoietic precursor compartment.

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Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS00001006281 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00006173277 fastq.gz 2.0 GB
EGAF00006173278 fastq.gz 851.9 MB
EGAF00006173279 fastq.gz 1.8 GB
EGAF00006173280 fastq.gz 714.8 MB
EGAF00006173281 fastq.gz 706.4 MB
EGAF00006173282 fastq.gz 1.3 GB
EGAF00006173283 fastq.gz 545.1 MB
EGAF00006173284 fastq.gz 740.6 MB
EGAF00006173285 fastq.gz 1.1 GB
EGAF00006173286 fastq.gz 533.4 MB
EGAF00006173287 fastq.gz 1.3 GB
EGAF00006173288 fastq.gz 481.7 MB
EGAF00006173289 fastq.gz 810.7 MB
EGAF00006173290 fastq.gz 435.7 MB
EGAF00006173291 fastq.gz 533.3 MB
EGAF00006173292 fastq.gz 1.2 GB
EGAF00006173293 fastq.gz 391.2 MB
EGAF00006173294 fastq.gz 933.2 MB
EGAF00006173295 fastq.gz 705.8 MB
EGAF00006173296 fastq.gz 1.1 GB
EGAF00006173297 fastq.gz 1.4 GB
EGAF00006173298 fastq.gz 1.1 GB
EGAF00006173299 fastq.gz 1.3 GB
EGAF00006173300 fastq.gz 782.4 MB
EGAF00006173301 fastq.gz 542.9 MB
25 Files (23.3 GB)