Abstract

The formation of neutrophil extracellular traps (NETs) is an immune defense mechanism of neutrophilic granulocytes. Moreover, it is also involved in the pathogenesis of autoimmune, inflammatory, and neoplastic diseases. For that reason, the process of NET formation (NETosis) is subject of intense ongoing research. In vitro approaches to quantify NET formation are commonly used and involve neutrophil stimulation with various activators such as phorbol 12-myristate 13-acetate (PMA), lipopolysaccharides (LPS), or calcium ionophores (CaI). However, the experimental conditions of these experiments, particularly the media and media supplements employed by different research groups, vary considerably, rendering comparisons of results difficult. Here, we present the first standardized investigation of the influence of different media supplements on NET formation in vitro. The addition of heat-inactivated (hi) fetal calf serum (FCS), 0.5% human serum albumin (HSA), or 0.5% bovine serum albumin (BSA) efficiently prevented NET formation of human neutrophils following stimulation with LPS and CaI, but not after stimulation with PMA. Thus, serum components such as HSA, BSA and hiFCS (at concentrations typically found in the literature) inhibit NET formation to different degrees, depending on the NETosis inducer used. In contrast, in murine neutrophils, NETosis was inhibited by FCS and BSA, regardless of the inducer employed. This shows that mouse and human neutrophils have different susceptibilities toward the inhibition of NETosis by albumin or serum components. Furthermore, we provide experimental evidence that albumin inhibits NETosis by scavenging activators such as LPS. We also put our results into the context of media supplements most commonly used in NET research. In experiments with human neutrophils, either FCS (0.5–10%), heat-inactivated (hiFCS, 0.1–10%) or human serum albumin (HSA, 0.05–2%) was commonly added to the medium. For murine neutrophils, serum-free medium was used in most cases for stimulation with LPS and CaI, reflecting the different sensitivities of human and murine neutrophils to media supplements. Thus, the choice of media supplements greatly determines the outcome of experiments on NET-formation, which must be taken into account in NETosis research.

Highlights

  • The discovery of neutrophil extracellular traps (NETs) in 2004 [1] marked the beginning of an impressive scientific career of these extracellular DNA meshworks

  • We did not observe any difference in NETosis studied in 70◦C hiFCS compared to 56◦C hiFCS on the results in our setup and decided for the more frequently used 56◦C hiFCS for this study

  • We stimulated freshly isolated human neutrophils with calcium ionophores (CaI) at 4 μM, phorbol 12-myristate 13-acetate (PMA) at 100 nM and LPS at 10 μg/ml, 25 μg/ml and 100 μg/ml to assess whether neutrophils stimulated by different inducers of NETosis would react differently to the media supplements (Figure 1)

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Summary

Introduction

The discovery of neutrophil extracellular traps (NETs) in 2004 [1] marked the beginning of an impressive scientific career of these extracellular DNA meshworks. The cells release the NET consisting of decondensed chromatin, decorated with antimicrobial peptides and, most likely, a plethora of cytokines and other proteins This release occurs after the rupture of the cell membrane into the extracellular space, leaving the neutrophil to die. Some publications have described a faster, different form of NET formation mainly in response to bacteria which leaves the neutrophil alive and functional (“vital NETosis” or “vital NET formation”) [5]. It remains a matter of debate whether these phenotypes are truly distinct biological processes

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