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Multiple Roles for Chemokines in Neutrophil Biology. | LitMetric

Multiple Roles for Chemokines in Neutrophil Biology.

Front Immunol

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.

Published: April 2021

AI Article Synopsis

  • Chemokines play a crucial role in controlling how neutrophils are recruited during inflammation, as well as regulating their movement from the bone marrow to the bloodstream and back for cleanup.
  • Beyond recruitment, chemokines also influence neutrophil functions like oxidative burst, degranulation, and the formation of neutrophil extracellular traps (NETosis).
  • Recent studies have revealed that neutrophils are not a uniform population; instead, there are various stages and subsets with distinct roles, particularly in disease contexts like infections, autoimmune disorders, and cancer.

Article Abstract

Chemokines are recognized as the most critical mediators for selective neutrophil recruitment during inflammatory conditions. Furthermore, they are considered fundamental regulators of neutrophil mobilization from the bone marrow (BM) to the bloodstream and for their homing back at the end of their life for apoptosis and clearance. However, chemokines are also important mediators of neutrophil effector functions including oxidative burst, degranulation, neutrophil extracellular trap (NET)osis, and production of inflammatory mediators. Neutrophils have been historically considered as a homogeneous population. In recent years, several maturation stages and subsets with different phenotypic profiles and effector functions were described both in physiological and pathological conditions such as infections, autoimmunity, and cancer. The aim of this review is to give an overview of the current evidence regarding the role of chemokines and chemokine receptors in neutrophil biology, including their possible role in neutrophil maturation, differentiation, and in defining emerging neutrophil subsets.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363767PMC
http://dx.doi.org/10.3389/fimmu.2020.01259DOI Listing

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