» Articles » PMID: 35916035

Neutrophil Functional Heterogeneity is a Fixed Phenotype and is Associated with Distinct Gene Expression Profiles

Abstract

Differences in the ability of neutrophils to perform relevant effector functions has been identified in a variety of disease states. Although neutrophil functional heterogeneity is increasingly recognized during disease, few studies have examined neutrophil functional heterogeneity during periods of health. In this study, we systematically characterize neutrophil functional heterogeneity in a cohort of healthy human subjects using a range of biologically relevant agonists including immune complexes, bacterial ligands, and pathogens. With repeated testing over several years, we show that neutrophil functional capability represents a fixed phenotype for each individual. This neutrophil phenotype is preserved across a range of agonists and extends to a variety of effector functions including degranulation, neutrophil extracellular trap release, reactive oxygen species generation, phagocytosis, and bacterial killing. Using well-phenotyped healthy human subjects, we demonstrate that neutrophil functional heterogeneity is characterized by differences in neutrophil gene expression patterns. Altogether, our findings demonstrate that while neutrophil function is highly heterogeneous among healthy subjects, each individual's functional capability represents a fixed phenotype defined by a distinct neutrophil gene expression profile. These findings may be relevant during disease states where the ability to perform relevant neutrophil effector functions may impact disease course and/or clinical outcome.

Citing Articles

Decoding the biology and clinical implication of neutrophils in intracranial aneurysm.

Ji H, Han Y, Jie D, Li Y, Yang H, Sun H Ann Clin Transl Neurol. 2024; 11(4):958-972.

PMID: 38317016 PMC: 11021671. DOI: 10.1002/acn3.52014.


Molecular regulation of neutrophil swarming in health and disease: Lessons from the phagocyte oxidase.

Song Z, Bhattacharya S, Clemens R, Dinauer M iScience. 2023; 26(10):108034.

PMID: 37854699 PMC: 10579437. DOI: 10.1016/j.isci.2023.108034.

References
1.
Anders S, Pyl P, Huber W . HTSeq--a Python framework to work with high-throughput sequencing data. Bioinformatics. 2014; 31(2):166-9. PMC: 4287950. DOI: 10.1093/bioinformatics/btu638. View

2.
Middleton E, He X, Denorme F, Campbell R, Ng D, Salvatore S . Neutrophil extracellular traps contribute to immunothrombosis in COVID-19 acute respiratory distress syndrome. Blood. 2020; 136(10):1169-1179. PMC: 7472714. DOI: 10.1182/blood.2020007008. View

3.
Love M, Huber W, Anders S . Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014; 15(12):550. PMC: 4302049. DOI: 10.1186/s13059-014-0550-8. View

4.
Pozzan T, Lew D, Wollheim C, Tsien R . Is cytosolic ionized calcium regulating neutrophil activation?. Science. 1983; 221(4618):1413-5. DOI: 10.1126/science.6310757. View

5.
Perdomo J, Leung H, Ahmadi Z, Yan F, Chong J, Passam F . Neutrophil activation and NETosis are the major drivers of thrombosis in heparin-induced thrombocytopenia. Nat Commun. 2019; 10(1):1322. PMC: 6428879. DOI: 10.1038/s41467-019-09160-7. View