Neutrophil extracellular traps induce endothelial dysfunction in systemic lupus erythematosus through the activation of matrix metalloproteinase-2
- 1Systemic Autoimmunity Branch, Intramural Research Program, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland, USA
- 2Division of Rheumatology, University of Michigan, Ann Arbor, Michigan, USA
- Correspondence to Dr Mariana J Kaplan, Systemic Autoimmunity Branch, Intramural Research Program, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, 10 Center Drive, Building 10; Room 6D-47C, Bethesda, MD 20892, USA;
- Received 29 October 2013
- Revised 30 January 2014
- Accepted 2 February 2014
- Published Online First 25 February 2014
Rationale The structural and functional integrity of the endothelium is crucial in maintaining vascular homeostasis and preventing atherosclerosis. Patients with systemic lupus erythematosus (SLE) have an increased risk of developing endothelial dysfunction and premature cardiovascular disease. Neutrophil extracellular trap (NET) formation is increased in SLE and has been proposed to contribute to endothelial damage, but the mechanism remains unclear.
Objective To determine the mechanism by which enhanced NET formation by low-density granulocytes (LDGs) in SLE contributes to endothelial damage and disrupts the endothelium.
Results The putative role of NET-externalised matrix metalloproteinases (MMPs) in altering the functional integrity of the endothelium was examined. MMP-9 externalised by lupus LDGs during NET formation specifically impaired murine aortic endothelium-dependent vasorelaxation and induced endothelial cell apoptosis. Endothelial dysfunction correlated with the activation of endothelial MMP-2 by MMP-9 present in NETs, while inhibition of MMP-2 activation restored endothelium-dependent function and decreased NET-induced vascular cytotoxicity. Moreover, immunogenic complexes composed of MMP-9 and anti-MMP-9 were identified in SLE sera. These complexes, as well as anti-MMP-9 autoantibodies, induced NETosis and enhanced MMP-9 activity.
Conclusions These observations implicate activation of endothelial MMP-2 by MMP-9 contained in NETs as an important player in endothelial dysfunction, and MMP-9 as a novel self-antigen in SLE. These results further support that aberrant NET formation plays pathogenic roles in SLE.
Neutrophil extracellular traps (NETs) are networks of extracellular decondensed chromatin fibres decorated with histones, granule-derived enzymes and several cytoplasmic proteins.1 Besides their physiological antimicrobial functions, NETs may play pathogenic roles in several conditions, including atherosclerosis,2 rheumatoid arthritis (RA),3 systemic vasculitides4 and systemic lupus erythematosus (SLE).5 ,6
Recently, a central role for neutrophils in lupus pathogenesis has been proposed. Human and mouse lupus neutrophils are primed to make NETs, and this is particularly the case for low-density granulocytes (LDGs),5–8 a proinflammatory neutrophil subset isolated from human lupus peripheral blood mononuclear cell (PBMC) fractions.6 ,9 Further, sera from a subset of lupus patients shows impairment in the capacity to degrade NETs.10 While the mechanisms associated to enhanced NETosis in SLE remain to be fully characterised, cytokines, immune complexes (ICs) and autoantibodies are putative inducers.5–7 ,11 Importantly, LDG-NETs are deleterious to the endothelium, with potential implications in the development of premature atherosclerosis in SLE.6 ,9 Indeed, impaired endothelium-dependent vasorelaxation, a phenomenon that predicts atherogenesis, is highly prevalent in SLE.12 ,13 However, the mechanisms by which NETs damage the endothelium remain to be fully characterised.
Due to their capacity to degrade the extracellular matrix, regulate tissue architecture and induce proteolysis, matrix metalloproteinases (MMPs) are implicated in atherogenesis and vascular damage.14 ,15 In SLE, elevated serum levels of MMPs, in particular MMP-9, have been reported.16 As MMPs are present in neutrophil granules and may be externalised during NET formation,1 we further examined how they may alter the functional integrity of the endothelium.
MMP-9 is upregulated in lupus LDG-NETs
The source of elevated MMP-9 in SLE sera remains unclear. Since MMP-9 is present in neutrophil granules, we investigated whether this molecule is externalised in NETs. Proteins from digested NETs obtained from control neutrophils (through lipopolysaccharide (LPS) stimulation) or spontaneously formed in SLE normal density neutrophils and in SLE LDGs were separated in a SDS-gradient gel. Western blot analysis showed that MMP-9 is present in NETs from control and lupus neutrophils (figure 1A). Densitometry analysis demonstrated that MMP-9 is externalised at significantly higher levels in LDG-NETs compared with healthy control or with normal density SLE neutrophils (figure 1B). Zymography analysis of NETs demonstrated the presence of another neutrophil metalloproteinase, MMP-25 (figure 1C), an endopeptidase specifically expressed in leucocytes.17 ,18 Immunofluorescence microscopy confirmed the presence of MMP-9 and MMP-25 in NETs (figure 1D). These results indicate that specific MMPs decorate the NETs and that this phenomenon is enhanced in lupus LDGs. As lupus LDGs distinctly upregulate MMPs in NETs and are primed for enhanced NETosis, subsequent experiments compared solely control neutrophils with lupus LDGs and did not examine normal density lupus neutrophils.
MMPs contained in NETs damage the endothelium and activate MMP-2
To gain further insight into the role of LDGs NETs in endothelial cell (EC) damage, human umbilical vein endothelial cells (HUVECs) were incubated with LPS-induced digested or intact NETs from control neutrophils, degranulated supernatant from LPS-induced neutrophils or with spontaneously generated (unstimulated) NETs from lupus LDGs. Distinct morphological changes were evident after 3 h incubation with digested or intact NETs compared with untreated HUVECs or with cells exposed to supernatants from degranulated neutrophils (figure 2A and online supplementary figure S1A). A significant proportion of HUVECs exposed to NETs lost their ‘cobblestone’ appearance and acquired round-like shape. NETs modified contour, area and perimeter of ECs, indicating NET-induced endothelial cytotoxicity. Accumulation of NET-derived MMP-9 in HUVECs’ membrane was evident after incubation with control neutrophil and lupus LDG-NETs, although it was more prominent in the latter (figure 2B). These observations further support that LDG-derived NETs externalise higher amounts of MMP-9 than control NETs. That MMP-9 was bound to NETs was further confirmed by assessing co-localisation of this molecule with LL-37 (figure 2C and online supplementary figure S2), an antimicrobial peptide previously reported to be externalised in NETs.5 ,11 NET-derived MMP-9 was in direct contact with HUVECs’ membranes and clustered in HUVEC plasma membrane after 3 h of co-incubation. Vesicle-like structures containing MMP-9 and LL-37 present in distinct areas of the cell plasma membrane were visualised in the HUVECs (figure 2B,C and online supplementary figure S2).
Latent MMP-2 is secreted by ECs and undergoes activation through interaction with others MMPs.19 Analysis of supernatants from HUVECs alone or incubated with NETs demonstrated activation of endothelial pro-MMP-2 when NETs were present, but not by exposure to supernatants from degranulated neutrophils (figure 2D,E and online supplementary figure S1C). To further examine the role of NETs on endothelial function, thoracic aorta rings from C57BL/6 female mice were incubated with NETs purified from LPS-stimulated control neutrophils, from spontaneously formed LDG-NETs obtained from equal amounts of cells or from heat-inactivated NETs, followed by assessment of endothelium-dependent vasorelaxation in response to acetylcholine (figure 2F and online supplementary figure S1B). Significant impairment in endothelium-dependent vasorelaxation was observed in the presence of LDG-NETs compared with control NETs (figure 2F). To determine whether differences in vasorelaxation between lupus and controls NETs were related to different amounts generated/cell number, we adjusted the concentration of NETs generated by the control neutrophils to NETs generated by lupus LDGs. Under these conditions, control NETs induced significant impairment in vasorelaxation similar to LDG-NETs (figure 2F). These results indicate that lupus LDG-NETs more potently induce impaired vasorelaxation, likely due to their enhanced capacity to form these structures and to externalisation of higher concentrations of molecules displaying negative effects on endothelial function.
MMP-9 promotes endothelial dysfunction
Histones are the most abundant proteins in NETs20 and have been implicated in endothelial damage, in particular histone H2A.21 To assess the putative role of MMP-9 in the activation of pro-MMP-2 and its possible implications in endothelial damage, compared with other NET components, HUVECs and human aortic ECs (HAECs) were incubated with anti-H2A, anti-MMP-9, NETs, NETs depleted of MMP-9, NETs depleted of histone H2A, NETs plus neutralising anti-MMP-9, or NETs plus MMP inhibitors. Upon depletion or neutralisation of MMP-9 or broad inhibition of MMPs, ECs displayed improvements in morphology and cell–cell contact (figure 3A and online supplementary figure S3A) and decreases in apoptosis (figure 3B and online supplementary figure S3B). Furthermore, activation of endothelial MMP-2, following addition of NETs, was significantly decreased when MMP-9 was depleted or neutralised in the NETs compared with untouched NETs or NETs depleted of histone H2A (figure 3C,D). These results suggest that MMP-9 externalised in the NETs plays a prominent role in the activation of endothelial MMP-2 and contributes to the development of NET-induced vascular cytotoxicity. Indeed, aortic endothelium-dependent vasorelaxation was significantly improved when MMP-9 was neutralised or inhibited following exposure to LDG-NETs (figure 3D). These observations support the hypothesis that MMP-9 externalised in NETs plays a prominent role in inducing EC death and vascular dysfunction.
Active MMP-9 activates MMP-2 and triggers endothelial cytotoxicity
To corroborate that activation of endothelial MMP-2 by MMP-9 induces endothelial dysfunction, ECs were incubated with pro-MMP-9 or active-MMP-9 for 3 h in serum-free media. Pro-MMP-9 addition induced no changes in morphology or cell–cell contact (figure 4A). In contrast, ECs incubated with active MMP-9 displayed enhanced apoptosis (figure 4B) and activation of MMP-2 (figure 4C). These results support the hypothesis that activation of endothelial MMP-2 by active MMP-9 triggers endothelial dysfunction.
ICs containing MMP-9 and anti-MMP-9 Abs are present in SLE and stimulate NET formation
While detectable levels of MMP-9 were identified in all serum samples from healthy controls and patients with SLE, significantly higher concentrations were detected in lupus samples (figure 5A). As ICs play prominent pathogenic roles in SLE, we investigated whether MMP-9 is detected in these complexes in lupus patients. Total IgG was purified from sera obtained from patients with SLE with high levels of anti-dsDNA (74–83 IU/mL). Zymography analysis showed that MMP-9 is present in purified IgG fractions isolated from patients with SLE, but not from healthy donors (figure 5B). ICs containing MMP-9, but not irrelevant ICs, significantly enhanced NET formation (figure 5C,F). To characterise the signalling pathways involved in NET formation induced by lupus MMP-9-containing ICs, we used pharmacological inhibition of reactive oxygen species (ROS) generation. Both diphenyleneiodonium (DPI, NOX inhibitor) and N-acetylcysteine (NAC, ROS scavenger) significantly decreased NET formation following stimulation with MMP-9-containing ICs (figure 5C). These results indicate that NETosis induced by SLE-ICs containing MMP-9 requires intact ROS/NOX pathways.
Autoantibodies to MMP-9 are present in SLE and stimulate NETosis
Considering the presence of MMP-9 in ICs, we hypothesised that SLE patients develop autoantibodies against MMP-9. Elevated levels of anti-MMP-9 IgG were detected in SLE and RA (another condition characterised by increased NET formation and enhanced cardiovascular disease (CVD) risk) sera compared with control sera (figure 5D). To corroborate this finding, immunoblot was employed using both recombinant MMP-9 and LL-37. Although none of the SLE sera tested demonstrated anti-LL-37 Abs, three out of five showed positivity for anti-MMP-9 (figure 5E). Further, enhanced NET formation in control neutrophils was observed after 1 h incubation with lupus anti-MMP-9 Abs and with MMP-9 ICs but not with irrelevant ICs (figure 5F), while anti-MMP-9 Abs bound to MMP-9 externalised in the NETs (figure 5G). Anti-MMP-9 Abs enhanced MMP-9 activity in LDG-NETs (figure 5H). These results suggest that autoantibodies against MMP-9 are generated and can induce NETosis in SLE, enhancing NET-MMP-9 activity.
The cardiovascular risk described in SLE is not fully explained by the Framingham risk equation.22 ,23 While accelerated EC apoptosis associated to vascular dysfunction has been reported in SLE,12 ,24 the mechanisms leading to this phenomenon remain unclear. Recent evidence implicates accelerated NETosis in endothelial damage in lupus and other conditions. While histones contained in the NETs have been implicated in vessel dysfunction,21 other molecules present in these structures may also contribute to endothelial damage.
Dysregulation of MMPs has been implicated in atherosclerosis development,15 but their role in SLE vascular damage had not been systematically addressed. In this study, we found that MMP-9 was externalised at higher levels in LDG-NETs and induced EC death and vascular dysfunction through the activation of endothelial MMP-2. Furthermore, MMP-9 autoantibodies and MMP-containing ICs are generated in SLE and contribute to NETosis. In turn, NETs externalise MMP-9 and this phenomenon may perpetuate a vicious cycle, leading to endothelial dysfunction (figure 6).
Previous work reported that, compared with controls, PBMCs from patients with SLE synthesise and release more MMP-925; since LDGs are purified from mononuclear cell fractions,9 ,26 it is possible that they represent the main source of this molecule in peripheral blood. Antimalarials inhibit MMP-9 secretion and restore MMP-9/TIMP-1 balance in patients with SLE.27 As such, the findings in this manuscript suggest an additional mechanism by which these drugs may be immunomodulatory and vasculoprotective in lupus.
This study further supports the concept that lupus autoantibodies contribute to increased NETosis in this disease. Anti-MMP-9 Abs were detected in lupus sera and directly bound to NETs. Further, both ICs containing MMP-9 and anti-MMP-9 Abs triggered NET release and enhance NET-MMP-9 activity; this provides a putative mechanism of enhanced NETosis, similar to what was described for autoAbs to other neutrophil proteins such as LL-37.3 ,5 While not fully specific for SLE, as we also detected them in a subset of RA patients, anti-MMP-9 antibodies may represent a marker of vascular risk in autoimmunity that deserves further exploration.
Increased MMP activity in NETs could also contribute to kidney damage in SLE. Deposition of ICs containing MMP-9 disturbs glomerular basement membrane integrity,28 ICs can induce MMP expression29 ,30 and MMP-9 upregulates gelatinolytic activity within the glomeruli28 and correlates with chromatin-IgG complex deposition28 in lupus-prone mice. Therefore, increased MMP activity could alter membrane composition/integrity and promote IC deposition. All these results point at a potentially crucial interaction between MMPs and endothelial health in various compartments in SLE.
MMP-2 activation by MMP-9 can damage endothelial integrity and function.31 Recent work has demonstrated that MMP-25 can also activate MMP-2.32 While it is known that neutrophils synthesise and store MMP-9 and MMP-25,17 ,18 ,33 we now demonstrate that they are externalised during NETosis and activate endothelial pro-MMP-2. While we focused on MMP-9, we cannot exclude that MMP-25 also plays a role in endothelial MMP-2 activation since a broad MMP inhibitor induced better vasorelaxation than anti-MMP-9. While previous evidence indicates that endothelial dysfunction is triggered by histones present in NETs,21 no significant reduction in cytotoxicity after histone depletion was observed in our system. During NETosis, histones are citrullinated,34 a phenomenon with potential immunoregulatory properties.35 Previous studies evaluated EC damage by histones using unmodified histones; therefore, it is possible that post-translational modifications during NETosis render histones less cytotoxic to the endothelium. This hypothesis should be tested in future studies.
When equal numbers of control neutrophils and lupus LDGs were compared, control NETs did not induce endothelial dysfunction, supporting the notion that the amount of MMP-9 released during NETosis could determine endothelial integrity. ECs exposed to NETs displayed MMP-9 clusters in the plasma membrane that led to generation of vesicle-like structures. This observation is in agreement with evidence that shed vesicles act as protease carriers36–38 that may be involved in autocrine regulation. It is possible that vesicles containing MMP-9 could account for increased levels of this metalloproteinase in SLE.
MMP inhibitors have been explored as potential therapeutic approaches in cardiovascular disease and also show promise in animal models.39 While broad-spectrum MMP inhibitors have given disappointing outcomes in some clinical studies, further research is needed to identify more selective MMP inhibitors and targets to better define therapeutic potential of these molecules. Defining molecular mechanism by which NETs modulate endothelial damage in SLE could provide new potential therapeutic targets in this disease and its associated vascular complications.
Handling editor Tore K Kvien
Contributors CC-R designed and performed experiments and drafted the manuscript. WZ and SY performed experiments and contributed to statistical analysis. MJK conceived and designed study and drafted the manuscript.
Funding This work was supported by the National Institutes of Health through the Intramural Research Program at NIAMS and by PHS grants HL088419 and T32AR007080.
Competing interests None.
Ethics approval University of Michigan IRB and National Institutes of Health IRB.
Provenance and peer review Not commissioned; externally peer reviewed.