Modulation of neutrophil activity by soluble complement cleavage products

• Verfasst von: Wohlgemuth, Lisa [VerfasserIn]
• Verfasst von: Stratmann, Alexander Elias Paul [VerfasserIn]
• Verfasst von: Münnich, Frederik [VerfasserIn]
• Verfasst von: Bernhard, Stefan [VerfasserIn]
• Verfasst von: Thomaß, Bertram Dietrich [VerfasserIn]
• Verfasst von: Münnich, Finn [VerfasserIn]
• Verfasst von: Mohamed, Adam Omar Khalaf [VerfasserIn]
• Verfasst von: Mannes, Marco [VerfasserIn]
• Verfasst von: Schmidt, Christoph Quirin [VerfasserIn]
• Verfasst von: Nilsson Ekdahl, Kristina [VerfasserIn]
• Verfasst von: Nilsson, Bo [VerfasserIn]
• Verfasst von: Fauler, Michael [VerfasserIn]
• Verfasst von: Föhr, Karl Josef [VerfasserIn]
• Verfasst von: Huber-Lang, Markus [VerfasserIn]
• Verfasst von: Messerer, David Alexander Christian [VerfasserIn]
• Titel: Modulation of neutrophil activity by soluble complement cleavage products
• Titelzusatz: an in-depth analysis
• Verf.angabe: Lisa Wohlgemuth, Alexander Elias Paul Stratmann, Frederik Münnich, Stefan Bernhard, Bertram Dietrich Thomaß, Finn Münnich, Adam Omar Khalaf Mohamed, Marco Mannes, Christoph Quirin Schmidt, Kristina Nilsson Ekdahl, Bo Nilsson, Michael Fauler, Karl Josef Föhr, Markus Huber-Lang, David Alexander and Christian Messerer
• E-Jahr: 2022
• Jahr: 20 October 2022
• Umfang: 17 S.
• Fussnoten: Gesehen am 11.01.2023
• Titel Quelle: Enthalten in: Cells
• Ort Quelle: Basel : MDPI, 2012
• Jahr Quelle: 2022
• Band/Heft Quelle: 11(2022), 20, Artikel-ID 3297, Seite 1-17
• ISSN Quelle: 2073-4409
• DOI: doi:10.3390/cells11203297
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: anaphylatoxins
• Sach-SW: complement system
• Sach-SW: inflammation
• Sach-SW: innate immunity
• Sach-SW: neutrophils
• K10plus-PPN: 1830818392

Abstract

The cellular and fluid phase-innate immune responses of many diseases predominantly involve activated neutrophil granulocytes and complement factors. However, a comparative systematic analysis of the early impact of key soluble complement cleavage products, including anaphylatoxins, on neutrophil granulocyte function is lacking. Neutrophil activity was monitored by flow cytometry regarding cellular (electro-)physiology, cellular activity, and changes in the surface expression of activation markers. The study revealed no major effects induced by C3a or C4a on neutrophil functions. By contrast, exposure to C5a or C5a des-Arg stimulated neutrophil activity as reflected in changes in membrane potential, intracellular pH, glucose uptake, and cellular size. Similarly, C5a and C5a des-Arg but no other monitored complement cleavage product enhanced phagocytosis and reactive oxygen species generation. C5a and C5a des-Arg also altered the neutrophil surface expression of several complement receptors and neutrophil activation markers, including C5aR1, CD62L, CD10, and CD11b, among others. In addition, a detailed characterization of the C5a-induced effects was performed with a time resolution of seconds. The multiparametric response of neutrophils was further analyzed by a principal component analysis, revealing CD11b, CD10, and CD16 to be key surrogates of the C5a-induced effects. Overall, we provide a comprehensive insight into the very early interactions of neutrophil granulocytes with activated complement split products and the resulting neutrophil activity. The results provide a basis for a better and, importantly, time-resolved and multiparametric understanding of neutrophil-related (patho-)physiologies.