Affiliation:
1. The Kennedy Institute of Rheumatology, University of Oxford , Old Road Campus Research Build, Roosevelt Dr, Headington, Oxford OX3 7DQ , United Kingdom
Abstract
Abstract
Neutrophils are innate immune cells that are key to protecting the host against infection and maintaining body homeostasis. However, if dysregulated, they can contribute to disease, such as in cancer or chronic autoinflammatory disorders. Recent studies have highlighted the heterogeneity in the neutrophil compartment and identified the presence of immature neutrophils and their precursors in these pathologies. Therefore, understanding neutrophil maturity and the mechanisms through which they contribute to disease is critical. Neutrophils were first characterized morphologically by Ehrlich in 1879 using microscopy, and since then, different technologies have been used to assess neutrophil maturity. The advances in the imaging field, including state-of-the-art microscopy and machine learning algorithms for image analysis, reinforce the use of neutrophil nuclear morphology as a fundamental marker of maturity, applicable for objective classification in clinical diagnostics. New emerging approaches, such as the capture of changes in chromatin topology, will provide mechanistic links between the nuclear shape, chromatin organization, and transcriptional regulation during neutrophil maturation.
Funder
Research into Inflammatory Arthritis Centre Versus Arthritis UK
Universities of Oxford, Glasgow, Birmingham, and Newcastle
Kennedy Trust Prize
EPA Cephalosporin Fund and the Kennedy Trust
Rosalind Franklin Institute
Kennedy Trust
Wellcome Trust
Engineering and Physical Sciences Research Council
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Immunology,Immunology and Allergy
Cited by
1 articles.
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