Identification of the Centrifugation-Caused Paralytic Impact on Neutrophils

To investigate granulocytes under laboratory conditions, centrifugation steps are typically required for the isolation of neutrophil granulocytes from whole blood. However, only a few studies to date have addressed the direct effects of centrifugation itself on the functional state of neutrophils. This study aims to elucidate the mechanisms that contribute to the modification of granulocytes during centrifugation. We hypothesize that granules sustain morphological alterations during centrifugation, leading to the release of highly potent antimicrobial enzymes into the cytosol of the cells. Neutrophils were isolated from whole blood using different methods with and without centrifugation and analyzed by flow cytometry, ELISA, and mass spectrometry. Our findings demonstrate that intracellular granules incur damage during centrifugation, resulting in the presence of intragranular enzymes within the cytosol. Furthermore, the formation of the highly reactive hypochlorous acid (HOCl) as a consequence of centrifugation could be verified. The generation of intracellular HOCl may explain many of the alterations observed in neutrophils following centrifugation-based isolation, including modified surface antigen expression and altered responses to stimulation. In future studies, centrifugation steps during cell isolation should be avoided. The more time-consuming but gentler method of sedimentation is preferable and can be used as long as it is not necessary to obtain a highly purified neutrophil fraction.

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Publication Details

Journal
Cells
Published
2025-08-30
DOI
https://doi.org/10.3390/cells14171350
Citations
1
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
0.80
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article

Identification of the Centrifugation-Caused Paralytic Impact on Neutrophils

Richard F. Kraus, Fabian Kellermeier, Simon Heckscher, Tobias Hundhammer et al.
1 citations
Cells
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
0.80
article

Identification of the Centrifugation-Caused Paralytic Impact on Neutrophils

Richard F. Kraus, Fabian Kellermeier, Simon Heckscher, Tobias Hundhammer, Michael Gruber, Julia Rimboeck, Sigrid Wittmann, Sophie Pehl
article en
1 citations

Abstract

To investigate granulocytes under laboratory conditions, centrifugation steps are typically required for the isolation of neutrophil granulocytes from whole blood. However, only a few studies to date have addressed the direct effects of centrifugation itself on the functional state of neutrophils. This study aims to elucidate the mechanisms that contribute to the modification of granulocytes during centrifugation. We hypothesize that granules sustain morphological alterations during centrifugation, leading to the release of highly potent antimicrobial enzymes into the cytosol of the cells. Neutrophils were isolated from whole blood using different methods with and without centrifugation and analyzed by flow cytometry, ELISA, and mass spectrometry. Our findings demonstrate that intracellular granules incur damage during centrifugation, resulting in the presence of intragranular enzymes within the cytosol. Furthermore, the formation of the highly reactive hypochlorous acid (HOCl) as a consequence of centrifugation could be verified. The generation of intracellular HOCl may explain many of the alterations observed in neutrophils following centrifugation-based isolation, including modified surface antigen expression and altered responses to stimulation. In future studies, centrifugation steps during cell isolation should be avoided. The more time-consuming but gentler method of sedimentation is preferable and can be used as long as it is not necessary to obtain a highly purified neutrophil fraction.

CellsVol. 14(17)
University Hospital Regensburg (DE), University of Regensburg (DE)
Openalex Percentile: Top 24%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
0.80
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Identification of the Centrifugation-Caused Paralytic Impact on Neutrophils — Richard F. Kraus, Fabian Kellermeier, et al. · Cells (2025) | TGRS Research Map | TGRS