An Overview of Neutrophil Markers

Introduction of Neutrophil

Neutrophils, constituting a pivotal element of the innate immune system, assume a paramount role in safeguarding the body against pathogens. These remarkable white blood cells exhibit remarkable migratory capabilities, promptly homing in on sites of infection or tissue injury to eliminate encroaching microorganisms. Moreover, the identification and characterization of neutrophils are facilitated by their possession of discernible surface markers. Notably, the activation of neutrophils is governed by a meticulously regulated process, wherein the upregulation of specific markers ensues, thereby endowing these cells with heightened antimicrobial functions. 

Neutrophil Markers

CD14
CD15
CD33
CD47
CD11b
CD63
CD16
CD24
CD86
CD177
CD66b
CXCR2
CXCR1
CXCR4
CD54
CCR7
CD217
ITGA4
Ly6g
CD43
CD10
CD45
CD62L
CD284
CD31
CD11C
TLR5
TLR7
TLR8
Others

Mouse Neutrophil Markers: The utilization of mouse models has been instrumental in advancing our understanding of diverse facets pertaining to neutrophil biology. In mouse studies, several markers have emerged as indispensable tools for the identification and analysis of neutrophils. Foremost among these markers is Ly6g, it is a glycosylphosphatidylinositol-anchored protein that expressed on the surface of mature neutrophils. Ly6g stands as a steadfast and dependable marker, facilitating the precise identification of these crucial cells. Another marker of considerable prominence is CXCR2, a chemokine receptor that orchestrates the recruitment and activation of neutrophils. Additionally, CD11b, a notable member of the integrin family, adorns the surface of neutrophils, further enhancing their characterization. The collective expression of Ly6g, CXCR2, and CD11b furnishes a formidable array of markers, empowering researchers to meticulously profile and investigate mouse neutrophils across a diverse range of experimental scenarios.

Human Neutrophil Markers: The translation of findings derived from mouse models to the realm of human physiology necessitates a comprehensive comprehension of markers specific to human neutrophils. Unlike their murine counterparts, the identification of human neutrophils presents a more intricate challenge, owing to the absence of a solitary, definitive marker. Nevertheless, a strategic amalgamation of markers can be employed to establish a reliable framework for discerning these cells. Among these markers, CD66b occupies a prominent position as a widely utilized surface marker for human neutrophils. Its robust expression serves as a steadfast cornerstone in the identification of these cells. Additionally, CD16, an Fcγ receptor, stands as a crucial component in the marker arsenal, contributing to the differentiation of neutrophils from other leukocytes. CD11b, which is conserved between mice and humans, this marker has significance in the characterization of human neutrophils. Moreover, the inclusion of auxiliary markers such as CD62L and CD63 can bestow added discriminative power, facilitating the distinction of various subsets within the realm of neutrophils. In the comprehensive understanding of human neutrophils, the judicious employment of this diverse repertoire of markers is imperative.

Markers for Neutrophil Activation

Neutrophil activation is a complex and dynamic process that occurs in response to infection or tissue injury. This activation leads to the enhancement of antimicrobial functions and the release of inflammatory mediators. One of the most informative markers of neutrophil activation is CD11b/CD18, also known as Mac-1 or complement receptor 3 (CR3). This marker is upregulated upon activation and plays a crucial role in adhesion to endothelial cells, allowing for subsequent migration to the site of inflammation. The intricate interplay between CD11b/CD18 and other adhesion molecules is essential for the recruitment and activation of neutrophils, ultimately leading to the elimination of pathogens. Another marker associated with neutrophil activation is CD63, a tetraspanin protein involved in granule secretion. CD63 is upregulated upon neutrophil stimulation and is associated with the release of antimicrobial proteins.

In addition to surface markers, intracellular markers are also informative indicators of neutrophil activation. Myeloperoxidase (MPO), an enzyme found within neutrophil granules, is released upon activation. MPO generates reactive oxygen species (ROS) and contributes to the oxidative burst, a critical mechanism of neutrophil-mediated pathogen killing. The release of elastase, another granule protein, during neutrophil activation aids in the degradation of extracellular matrix components, facilitating the migration of neutrophils to the site of infection or injury.

In summary, the markers associated with neutrophil activation provide important insights into the intricate mechanisms involved in host defense against pathogens. The upregulation of surface markers such as CD11b/CD18 and CD63, along with the release of intracellular markers such as MPO and elastase, highlights the dynamic and multifaceted nature of neutrophil activation. Further research into the roles of these markers could provide valuable targets for therapeutic interventions in the treatment of infectious and inflammatory diseases.

Note: If you don't receive our verification email, do the following:

Copyright © Amerigo Scientific. All rights reserved.