Neutrophil Extracellular Traps: Double-Edged Swords of Innate Immunity Free

Neutrophils are the most abundant leukocytes in mammals and, as a first line of defense against microbes, they play crucial roles in innate immune responses. The homeostasis of neutrophils is maintained by balancing their short lifespan in the circulation with their regulated release from the bone marrow. Neutrophils have various types of granules, containing hundreds of proteins. These include bactericidal proteins, some of them with important effects on innate and adaptive immune responses, such as α-defensins, the cathelicidin human cationic antimicrobial protein of 18 kDa, and lactoferrin, among others. LL-37, a proteolytic product of human cationic antimicrobial protein of 18 kDa, has important chemotactic and immunostimulatory effects, as discussed below (1).

The mechanisms used by neutrophils to eliminate microbes include phagocytosis, generation of reactive oxygen species (ROS), and the release of microbicidal molecules from granules (degranulation). In 2004, another distinct antimicrobial activity was described: neutrophils extrude a meshwork of chromatin fibers that are decorated with granule-derived antimicrobial peptides and enzymes such as neutrophil elastase (Fig. 1), cathepsin G, and myeloperoxidase (MPO) (2). These structures, called neutrophil extracellular traps (NETs), represent an important strategy to immobilize and kill invading microorganisms. The NET scaffold consists of chromatin fibers with a diameter of 15–17 nm; DNA and histones represent the major NET constituents (2). Mass spectrometry has identified various additional proteins associated with NETs, including components from various types of granules. Although conserved proteins are found in extracellular trap fractions, it is still unclear whether the peptide composition of these structures may vary depending on the specific stimulus that promotes NET formation (3, 4).

The putative role of extracellular traps in host defense is exemplified by their conserved nature in various vertebrates (5–8), insects (9) and even plants (10). Whereas the initial observation of NET formation placed the process within the context of innate immune responses to infections, recent evidence suggests that these structures also figure prominently at the center of various pathologic states. As such, NETs may function as double-edged swords, serving as effective antimicrobial defenses, but also as putative sources of molecules with immune effector and proinflammatory roles that, in susceptible individuals, may promote tissue damage and autoimmunity. Furthermore, other granulocytes (mast cells and eosinophils) can form extracellular traps upon stimulation, a process thus renamed as ETosis (11, 12). In the case of eosinophils, NET-like structures containing mitochondrial DNA and granular proteins have been proposed to contribute to host defense and to allergic responses (12, 13).

Two models for NET release have been proposed. In the first model, NETosis, a distinct form of active cell death, is characterized by release of decondensed chromatin and granular contents to the extracellular space. During NETosis, nuclear and granular membranes dissolve, and nuclear contents decondense into the cytoplasm. This is followed by plasma membrane rupture and release of chromatin decorated with granular proteins into the extracellular space (2, 14, 15). In contrast to apoptotic cells, netting neutrophils do not appear to display “eat me” signals, and this may prevent their clearance by phagocytes. Indeed, NETs are disassembled primarily by nucleases (15). The second model involves a DNA/serine protease extrusion mechanism from intact neutrophils, where mitochondrial DNA release is apparently not associated to cell death (16). Furthermore, autophagy may contribute to NETosis (17).

Intact chromatin lattices appear to be required for the antimicrobial function of NETs (2). In addition to microorganisms, NETosis is triggered by other various stimuli, including proinflammatory cytokines (TNF-α, IL-8), platelets, activated endothelial cells (ECs), NO, monosodium urate crystals, and various autoantibodies (18–26). NETs are identified by various techniques. Fluorescence microscopy and immunohistochemical analysis of transmission electron microscopy data may be preferred approaches to characterize NETosis. Importantly, fibrin may mimic NETs in scanning electron microscopy (27).

Kinetic studies in both human and mouse neutrophils have been published. Whereas phagocytosis and degranulation usually take minutes to occur after microbe exposure, NETosis is a more protracted event (5, 14). It is unclear which factors determine the selection between these alternative antimicrobial activities and whether these processes can coexist in the same cell. About 20–60% of isolated human neutrophils typically release NETs 2–4 h after stimulation with microbes or protein kinase C (PKC) activators; however, they respond within minutes when activated by LPS-stimulated platelets under conditions of flow (22). The differences in predisposition to form NETs and the characteristics of these structures made by immature and mature neutrophils remain to be determined. Priming with type I or type II IFNs and subsequent stimulation with C5a leads to NETosis in mature, but not immature, neutrophils (28).

Bone marrow-derived neutrophils from common murine strains used in immunology research appear equally capable of forming NETs upon stimulation. When comparing mouse and human neutrophils, murine cells make NETs more slowly and less efficiently and these structures have more compact appearance than do human cells (5). Most studies of NETs in mice use bone marrow neutrophils, whereas the preferred source in humans is peripheral blood. This may account for some differences identified between these species.

An astounding variety of microbes induce NET formation (2, 29–35). NET-inducing stimuli include whole bacteria as well as cell surface components of Gram-positive and Gram-negative bacterial lipoteichoic acid and LPS, as well as breakdown products of prokaryotic proteins, such as fMLP (18). Notable examples of bacteria that potently induce NETs include Staphylococcus aureus (36, 37), Streptococcus sp. (29, 38), Haemophilus influenzae (30), Klebsiella pneumoniae (39), Listeria monocytogenes (40), Mycobacterium tuberculosis (31), and Shigella flexneri (2). Other examples include pathogens such as Yersinia (41) and members of the oral microbiome, including Porphyromonas gingivalis (33).

Neutrophils from neonates, compared with adult neutrophils, are less capable of forming NETs in response to various microbial stimuli, a phenomenon that may contribute to the enhanced susceptibility to infections observed in this age group (42). Containment of microbial pathogens to sites of initial infection may be an important function of NETs. Indeed, staphylococci and streptococci express virulence factors that degrade extracellular traps and may free the bacterium from NET chromatin (29). In cystic fibrosis, pathogens such as Pseudomonas aeruginosa thrive in the lungs of affected patients and NETs accumulate, promoting chronic lung obstruction. Clinical lung isolates from cystic fibrosis patients acquire a mucoid phenotype that makes P. aeruginosa less sensitive to NET inhibition (35). This suggests that microbes may develop adaptations to resist NET-mediated growth suppression.

Fungi known to elicit NETs include Aspergillus nidulans, Aspergillus fumigatus, and Candida albicans (43–45). Patients with chronic granulomatous disease (CGD), who are deficient in the expression of a fully functional NADPH oxidase, are unable to form NETs and often die of infection with A. nidulans. Gene therapy to reconstitute NADPH oxidase function in CGD patients was associated with decreased fungal load and a gain in capacity to form NETs (45). The NET component implicated in immune defense against A. nidulans and C. albicans is calprotectin, a Zn²⁺ chelator and heterodimer of the cytosolic S100A8 and S100A9 proteins present in the NETs. Thus, NETs contain neutrophil proteins that serve specialized functions in fungal immunity and provide high local inhibitor concentrations in close proximity to pathogens (3, 45).

Various protozoan parasites induce NETs (46–48). In vitro, Leishmania amazonensis or its surface lipophosphoglycan induces NETs, whereas their disruption with DNase I improves survival of the pathogen (46). In the Toxoplasma gondii infection model, the tachyzoite induces neutrophil influx into the infected tissues and release of NETs that may limit pathogen viability. In children with malaria, NETs have been observed in fresh blood smears and correlate with specific cytokine profiles and with the development of anti-DNA autoantibodies (48).

Given the diversity of microbes that elicit NETs, it is not surprising that, depending on the microbial agent, these lattices may have different effects on the spread and severity of an infection. Just how NETs contribute to immune defense is open to argument. It is important to distinguish microbial death mediated by NETs from failure to recover viable organisms as a result of their entrapment. Histones, the most abundant proteins in NETs, have bactericidal properties. Proteolytic fragments of histones function as defensins in the innate immune system (49). However, some bacteria may survive association with NETs without a loss of viability (50). For these, NETs may represent an important mechanism that limits their spread in the host.

Whereas some pathogens are susceptible to containment or damage by NETs, others may have found ways to counteract these lattices or even to incorporate NET chromatin into their support structures (51). In a surprising twist of evolutionary adaptation, certain bacteria may even benefit from NETs. Colonizing H. influenzae often resists treatment owing to their ability to form biofilms that contain structural elements of NETs. Thus, although stimuli produced by H. influenzae can induce NETs, the bacterium avoids damage by these structures. Instead, its lipooligosaccharide coat tightly associates with NETs and, as result, these bacteria escape phagocytic uptake and clearance (30).

Conflicting reports of bacterial killing by NET chromatin have prompted examination of bactericidal properties of in vitro-generated NETs. Purified NET chromatin alone is not very efficient at killing S. aureus, and MPO present in NETs provides the bactericidal activity needed to kill this pathogen in the presence of hydrogen peroxide (52). Other NET components with antibacterial properties include LL-37, lactoferrin, neutrophil elastase, and proteinase-3.

One added level of complexity in studies of the bactericidal and bacteriostatic properties of NETs is that some of the components of these structures, such as MPO, assist in the production of NETs and also directly promote pathogen degradation (53). Additionally, proteases that damage captured microbes also may have important roles in shaping the structure of NET chromatin. Histones associated with NETs are “trimmed” by proteases, whereby they lose specific lengths of their amino termini. These histone “tails” have important roles in organizing the higher order structure of chromatin, and their cleavage may play a crucial role in producing the “beads on a string” structure of extended NET chromatin (2, 3).

The role of NETs in fighting viral infections remains to be fully characterized, although these web structures may promote lung injury following influenza infection (7, 54, 55). NETs capture HIV and promote its elimination through MPO and α-defensin. This virus can develop an anti-NET response mediated by IL-10 (56).

Studies of NETosis are difficult to design and interpret. The use of pharmacologic stimuli for NETosis only compounds the problem. Despite these caveats, important insights have been gained into the mechanisms of NETosis (Fig. 2). The stimuli that induce NETosis can be broadly classified into microbe-associated, inflammatory, or endogenous (“sterile”) triggers. Diverse neutrophil receptors can signal to induce NETosis, as binding via TLRs, Fc receptors, or complement receptors has been implicated in the induction of NETs (2, 24, 57). Cytokine receptors likely play roles in NETosis signaling, as IL-8, TNF, and IFN-γ can trigger this process (2, 18, 28). More studies are required to address the synergy or cross-talk between different classes of neutrophil receptors in the induction of NETosis.

The most frequently used compound to induce NETosis is PMA, a synthetic activator of the PKC family of enzymes. PKC is directly responsible for activation of NADPH oxidase and ROS production. Many of the natural NET inducers lead to PKC activation, as elevated cytoplasmic calcium and its release from endoplasmic reticulum stores are direct consequences of receptor activation. The requirement for ROS production is consistent with the inhibition of NETosis by ROS scavengers such as N-acetylcysteine, diphenylene iodinium, or Trolox (15, 58). How ROS contribute to NETosis is controversial. One possibility is that they directly promote the observed morphologic changes occurring in neutrophils during NETosis (39). A proposed alternative is that ROS serve to inactivate caspases, thereby inhibiting apoptosis and instead inducing autophagy, a process leading to dissolution of cellular membranes (17). These alternatives may not be mutually exclusive and they each may occur under different experimental conditions.

How NETosis signals are transduced is suggested by studies on Rac2. Phosphorylation of gp91^phox by PKC allows the cytosolic and membrane-bound subunits of NADPH oxidase to assemble into a functional complex that generates ROS and, in particular, superoxide ions (59). Whereas Rac1-deficient neutrophils release similar quantities of NET chromatin as wild-type neutrophils in response to PMA or LPS, Rac2-deficient cells cannot form a functional enzyme complex and are impaired in NET formation (58). Further steps in the conversion of superoxide to hydrogen peroxide and to perchloric acid are also essential for NET release. Superoxide itself is not essential, as rescue of the NETosis pathway in CGD neutrophils was observed with addition of exogenous peroxide. NETosis may also occur in certain conditions through ROS-independent pathways (42, 60), which suggests that specific stimuli and the surrounding inflammatory milieu may modulate how NETs are generated.

Histone deimination by peptidylarginine deiminase 4 (PAD4) is a prominent posttranslational modification in NETs that is induced by inflammatory or infectious stimuli (18, 61). The conversion of certain arginine residues to citrullines in core histones by PAD4 eliminates the positive charge from that residue and may thereby weaken the binding of histones to DNA. Because the PAD4 substrate arginines are part of histone tails that mediate interactions between nucleosomes, loss of positive charge may unravel the compact nature of nuclear chromatin and allow it to disperse in the form of NETs. Analysis of neutrophils from mice deficient in PAD4 revealed that they were impaired in their capacity to form NETs in vitro (54, 62). In vivo, PAD4-deficient mice had more severe bacterial infections, although the inability to form NETs did not affect viral titers and leukocyte infiltration rates during influenza infections (54).

NETs may play crucial roles in the regulation of immune responses, protease-mediated effector functions, and intercellular signal transduction. Until recently, the predominant model explaining the externalization of putative modified nuclear autoantigens (such as DNA) and their access to the immune system has been that apoptotic debris represents the primary source (63, 64). However, recent evidence that extracellular DNA is a common, and even necessary, process in naturally occurring immune responses mediated by NETosis has opened new possibilities of better understanding the mechanisms that lead to breaking of tolerance and the promotion of autoimmunity.

Several of the molecules decorating the NETs (e.g., MPO, dsDNA, histones) are autoantigens in systemic autoimmune diseases such as anti-neutrophil cytoplasmic Ab (ANCA)-positive vasculitis and systemic lupus erythematosus (SLE). Thus, various groups have proposed that aberrant NET formation may be important in the generation of autoimmune responses in predisposed individuals (24–26, 65). This hypothesis is supported by the observation that initiation or exacerbation of autoimmune responses often occurs following microbial infections. Various autoantibodies can promote the release of NETs containing antimicrobial proteins, including LL37 (24–26). This combination of DNA and LL37 is a potent stimulus for plasmacytoid dendritic cells (pDCs) to synthesize type I IFNs. Type I IFNs have antimicrobial roles but also potent immunostimulatory effects in autoimmune diseases such as SLE and psoriasis (11, 24, 26, 65). Importantly, neutrophils from patients with various autoimmune diseases appear more prone to NETose. However, isolated in vivo exposure to NETs may be insufficient to break tolerance, and additional factors (e.g., genetic influences, inflammatory milieu) may need to be present to trigger full, sustained autoimmune responses, as recently suggested (66).

Recent evidence also indicates that NETs can shape adaptive immune responses, as these structures can prime T cells and reduce their activation threshold (67). The specific role of NETs in other components of adaptive immune responses remains to be fully characterized. Below, we summarize recent discoveries on the potential role of NETs in the pathogenesis of autoimmune diseases.

Small vessel vasculitis is a systemic autoimmune disease characterized by necrotizing inflammation of small blood vessels. Many patients with this disease develop ANCAs with specific reactivity against PR3 or MPO, which are considered diagnostic of this disease. ANCAs induce NETosis, whereas NET-derived material is detected in blood and in kidney biopsies from a large proportion of small vessel vasculitis patients (25). Importantly, autoantigens recognized by ANCAs have been found in the NET structure (25). The drug propylthiouracil can induce ANCA vasculitis; this may occur through an effect on the conformation of NETs, leading to their impaired degradation (68). These observations suggest new mechanisms of ANCA generation and induction of organ damage in this autoimmune condition.

Psoriasis is a common inflammatory disorder of the skin and other organs, where IL-17 may play prominent pathogenic roles. Neutrophils and mast cells were recently reported to represent the predominant cell types expressing IL-17 in human skin in psoriasis, and this cytokine is released during ETosis (11). As such, externalization of IL-17 in the extracellular traps of neutrophils and mast cells may be central to psoriasis pathogenesis.

SLE is an autoimmune syndrome that affects many organs and is characterized by autoantibodies against DNA, chromatin, and DNA-associated proteins, including NET components. Recent evidence points to an imbalance between NET formation and NET clearance in this disease (24, 26, 65, 69). As such, patients with aberrantly elevated NETosis, in conjunction with impaired degradation of these structures by nucleases, may be particularly prone to NET-associated tissue damage. Decreased NET degradation occurs in a subset of SLE patients, correlating with renal disease, and secondary to DNase1 inhibitors and anti-NET Abs (69). Self DNA in lupus immune complexes contains LL37, which triggers TLR9 in pDCs, and consequent IFN-α synthesis, and it protects nucleic acids from degradation by nucleases (26). These DNA/antimicrobial complexes are released during NETosis, a process enhanced in SLE, and mediated in part by autoantibodies present in serum from a subset of lupus patients (24, 26). NETs may also activate complement, thereby amplifying disease (70). A subset of aberrant low-density granulocytes present in SLE displays enhanced capacity to form NETs and kill ECs in a NET-dependent manner. Furthermore, netting lupus neutrophils are detected in blood and infiltrate affected organs, where they expose immunostimulatory molecules (65). There is also preliminary evidence that nuclear material that is externalized on NETs promotes autoantibody formation in SLE (26).

Felty’s syndrome is characterized as rheumatoid arthritis, splenomegaly, and neutropenia. In Felty’s syndrome, autoantibodies were found to be directed against PAD4-deiminated histones and to induce NETosis (71). Netting neutrophils were found to be reactive with autoantibodies from Felty’s syndrome, SLE, and rheumatoid arthritis patients, suggesting a common cellular mechanism in these disorders. The role that NETs play more broadly in rheumatoid arthritis pathogenesis remains to be determined.

Gout is characterized by acute neutrophilic joint inflammation triggered by inflammatory responses to uric acid crystals. Activation of neutrophils in gout is associated with the formation of proinflammatory NETs, a phenomenon that was linked to both autophagy and IL-1β release (23).

Additional studies are required to assess the exact role of aberrant NETosis in induction and perpetuation of the diseases mentioned above and in other chronic inflammatory diseases.

EC activation can elicit NETosis, and, in turn, NETs induce vascular damage. Furthermore, netting neutrophils may play important roles in the promotion of atherosclerosis, thrombosis, and other vascular complications (21, 65).

NETs can provide a stimulus and scaffold for thrombus formation by promoting platelet and RBC adhesion and by concentrating effector proteins and coagulation factors involved in clotting (72–74). Thrombus-resident neutrophils are indispensable for deep venous thrombosis propagation by binding factor XII and supporting its activation through NETosis. Interestingly, the anticoagulant heparin can remove histones from NET chromatin fibers, leading to their destabilization, suggesting an additional mechanism by which this compound is antithrombotic (72–74). Ligation of TLR4 by LPS in narrow vessels induces platelet binding to adherent neutrophils, promoting NETosis. Human β-defensin1 is an antimicrobial component of platelets that can induce NETs. Platelet–neutrophil interactions leading to NETs may play important roles in ECs and tissue damage not only during sepsis, but also in chronic inflammatory disorders (22).

Neutrophil-derived CRAMP (the murine equivalent of LL37) is proatherogenic by recruiting inflammatory monocytes into arteries. CRAMP/DNA complexes stimulate pDCs in plaque lesions and contribute to generation of autoantibodies and aggravation of atherosclerosis in apolipoprotein E^−/− mice (75, 76). These observations suggest a putative role for NETs components in atheroma formation that requires further investigation.

In preeclampsia, a pregnancy-related inflammatory and vasculopathic disorder, massive numbers of NETs have been reported in vivo in the intervillious space, apparently triggered by trophoblast microdebris and IL-8. A pathogenic role for NETs in preeclampsia and pregnancy outcomes remains to be proven (19).

There is already some precedent in manipulating NETosis for therapeutic purposes, as mentioned above in the case of CGD (45). Various ROS scavengers are effective at reducing the release of NETs (15), and similar avenues may be available to repress NETosis in vivo in chronic inflammatory disorders. MPO inhibitors, such as 4-aminobenzoic acid hydrazide, and various PAD4 inhibitors may have similar effects (39, 77). The role of colchicine or other drugs that destabilize the cytoskeleton, a structure implicated in NETosis, should be explored (78, 79). Inhibition of the effects of histones contained in NETs may prove beneficial in various inflammatory conditions or in EC damage. Clearly, a better understanding of how NETs are generated and whether NETs that form upon microbial exposure are distinct from those that form under “sterile” conditions, as exist in autoimmune or vasculopathic disorders, may allow the development of compounds that selectively target the deleterious aspects triggered by these lattices.

The biological significance of NETs is just beginning to be explored. In addition to playing a central part in antimicrobial innate immunity, NETs are generated upon noninfectious stimuli in various clinical settings. In acute or chronic inflammatory disorders, aberrantly enhanced NET formation and/or decreased NET degradation may play key roles in initiation and perpetuation of autoimmune responses and organ damage. Various areas pertinent to NET biology need to be better defined, including the molecular mechanisms governing their generation and the downstream pathways leading to their formation. At this point, it is unclear whether all NETs are created equal and whether traps from different disease conditions or species will be phenotypically and functionally identical. Identification of endogenous stimuli leading to NETosis has been incomplete and needs to be better understood. For example, a more accurate distinction between the effects of NET trapping and NET killing on different types of microbes and a better understanding of the kinetics of NET release in different tissues or in the bloodstream are needed. Better characterizing formation of NETs and their role in biological processes in vivo remains a priority. Unraveling the NET properties unique to specific disease states or microbial infections will be important to further the understanding of the role of these matrices in health and disease. Present and future research holds promise to open avenues for the development of tools to modulate inflammation.

We thank Tim Higgins and Ritika Khandpur for support with figures.

The authors have no financial conflicts of interest.