Background Beyond their fundamental role in homeostasis and host defense, neutrophilic granulocytes (neutrophils) are increasingly recognized to contribute to the pathogenesis of malignant tumors. Recently, aging of mature neutrophils in the systemic circulation has been identified to be critical for these immune cells to properly unfold their homeostatic and anti-infectious functional properties. The role of neutrophil aging in cancer remains largely obscure.
Methods Employing advanced in vivo microscopy techniques in different animal models of cancer as well as utilizing pulse-labeling and cell transfer approaches, various ex vivo/in vitro assays, and human data, we sought to define the functional relevance of neutrophil aging in cancer.
Results Here, we show that signals released during early tumor growth accelerate biological aging of circulating neutrophils, hence uncoupling biological from chronological aging of these immune cells. This facilitates the accumulation of highly reactive neutrophils in malignant lesions and endows them with potent protumorigenic functions, thus promoting tumor progression. Counteracting uncoupled biological aging of circulating neutrophils by blocking the chemokine receptor CXCR2 effectively suppressed tumor growth.
Conclusions Our data uncover a self-sustaining mechanism of malignant neoplasms in fostering protumorigenic phenotypic and functional changes in circulating neutrophils. Interference with this aberrant process might therefore provide a novel, already pharmacologically targetable strategy for cancer immunotherapy.
- head and neck neoplasms
- neutrophil infiltration
Data availability statement
All data relevant to the study are included in the article or uploaded as supplementary information.
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See https://creativecommons.org/licenses/by/4.0/.
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Neutrophils represent the prevailing leukocyte subset in the blood of most mammals.1 Besides their prominent role in host defense, these immune cells have recently been implicated in the pathogenesis of malignant tumors. Whereas neutrophils have initially been reported to eliminate cancer cells,2 previously published data also point to a protumorigenic potential of these immune cells. In this regard, neutrophils release specific molecular factors that support initiation (eg, reactive oxygen species, proteases),3 4 proliferation (eg, neutrophil elastase (NE)),5 angiogenesis (eg, matrix metalloproteinase 9 (MMP-9), vascular endothelial growth factor (VEGF)), immune evasion (eg, arginase-1),6 and metastasis (eg, neutrophil extracellular traps)7 of tumors. With respect to these divergent findings, the existence of antitumorigenic (‘N1’) and protumorigenic (‘N2’) neutrophil phenotypes has been proposed and is defined by distinct cell surface protein signatures.8
Neutrophils are short-lived cells that exhibit an average lifespan in the circulation of 6–12 hours, notwithstanding that longer lifetimes of these immune cells (up to 5.4 days) are subject of controversial discussions.9 Under homeostatic conditions, mature neutrophils undergo dramatic age-related changes in their molecular repertoire when chronologically (referring to the progressive passing of the actual amount of time after their release from the bone marrow) aging in the circulation. The resulting phenotypic and functional alterations in these immune cells have been termed ‘biological aging’ of neutrophils. This includes the upregulation of the cell surface chemokine receptor CXCR4 that allows ‘aged’ neutrophils to home back to bone marrow, liver, and spleen via the chemokine CXCL12/SDF-1α.10 Subsequently, these aged immune cells are cleared by resident macrophages, in turn releasing signals that adjust size and function of the hematopoietic stem cell niche and control granulopoiesis.11 In addition to the pivotal role of neutrophil aging in homeostasis, this fundamental biological process has recently been identified to be required for neutrophils to fully develop their anti-infectious functions.12 13 To this end, neutrophils employ an autocrine, CXCL2-CXCR2-mediated mechanism that facilitates the release of their granular protein content.14 With respect to the potential of malignant tumors to produce such cytokines and to the protumorigenic properties of distinct granular proteins (eg, NE, MMP-9) of neutrophils, we hypothesize that aging of these immune cells in the circulation contributes to the progression of cancer.15
A detailed description of methods is provided in online supplemental information.
During all surgical and experimental procedures, animals were anesthetized using ketamine (100 mg/kg; Zoetis, Parsippany, New Jersey, USA) and xylazine (10 mg/kg; Bayer, Leverkusen, Germany).
Male C57BL/6NCrl, male C3H/HeNCrl, and female Balb/C mice were purchased from Charles River (Sulzfeld, Germany) aging 6–8 weeks (body weight of 15–18 g). Animals were housed under standard conditions (22°C±2°C, 30%–60% humidity, 12 hours light/dark cycle, lights on at 7 am) with access to food and water ad libitum.
A mouse squamous cell carcinoma cell line (SCC VII) and a mammary carcinoma cell line (4T1) were obtained from KL (Department of Radiotherapy and Radiation Oncology, LMU München, Munich, Germany). Cells were cultured in Roswell Park Memorial Institute (Thermo Fisher Scientific, Waltham, Massachusetts, USA) media, supplemented with 10% Fetal Bovine Serum (FBS) (Biochrom, Berlin, Germany) and 1% 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) (PromoCell, Heidelberg, Germany) at 37°C and 5% CO2. Mouse endothelial cells (bEnd.3) were purchased from American Type Culture Collection (Manassas, Virginia, USA) and cultured in DMEM (ATCC) supplemented with 10% FBS.
The trafficking of neutrophils to malignant tumors was analyzed in orthotopic syngeneic mouse models of 4T1 breast cancer (in female BALB/c mice) and of SCC VII head and neck squamous cell carcinoma (in male C3H mice) by multi-channel flow cytometry. Aged and non-aged neutrophils were differentiated by pulse-labeling with BrdU. In heterotopic models of these malignant tumors in the mouse auricle, interactions of neutrophils in the tumor microvasculature were further evaluated by multi-channel in vivo fluorescence microscopy. Responses of aged and non-aged neutrophils were differentiated by employing an adoptive cell transfer method.
To characterize the mechanisms underlying the trafficking of aged neutrophils in more detail, confocal microscopy and multiplex ELISA analyses as well as a mouse peritonitis assay and multi-channel in vivo fluorescence microscopy on the mouse cremaster muscle were employed. Phenotypic and functional properties of aged and non-aged neutrophils were assessed by multi-channel flow cytometry and different in vitro assays (cell activation, cell proliferation) using primary mouse neutrophils.
Data analysis was performed with the statistical software SigmaPlot for Windows (Jandel Scientific, Erkrath, Germany). After confirming normality and equal variance of data (using the Shapiro-Wilk and Brown-Forsythe tests), the one-way analysis of variance (ANOVA) test followed by the Dunnett test (>2 groups) or the t test (two groups) was used for the estimation of stochastic probability in intergroup comparisons. If normality and/or equal variance testing failed, the Kruskal-Wallis one-way ANOVA of ranks test followed by the Dunnett test (>2 groups) or the Mann-Whitney rank-sum test (two groups) was used. For survival estimation, the log-rank test was employed. Mean values and SEM are given. P values<0.05 were considered significant. A detailed report of the statistical analyses employed is provided in online supplemental file 2.
Gene expression of FPR1 and CXCR4 positively correlates with advanced tumor stages in human cancer
With respect to the capability of malignant tumors to produce cytokines promoting neutrophil aging and to the protumorigenic properties of distinct granular proteins of neutrophils, we hypothesize that aging of these immune cells in the circulation contributes to the progression of cancer. To prove this hypothesis, we first analyzed RNA microarray data from the METABRIC human breast cancer cohort (online supplemental figure S1A).16 Here, we found a significant positive correlation between the RNA expression levels of formyl peptide receptor 1 (FPR1), an established marker gene of neutrophils, and of CXCR4, whose gene product increases during neutrophil aging on the surface of these immune cells,10 with higher tumor stages. Conversely, RNA expression levels of CXCR2, whose gene product expression decreases during neutrophil aging on the surface of these immune cells,10 were slightly attenuated in advanced tumor stages (online supplemental figure S1B). Consequently, overall survival of patients with breast cancer with tumors exhibiting high RNA expression of FPR1 or CXCR4 was more impaired than that of patients with low tumor RNA expression of these molecules (online supplemental figure S1C). These bulk data suggest that neutrophil biological aging might promote cancer progression.
Tumor-released chemokines uncouple biological from chronological aging of circulating neutrophils in cancer
Since expression of CXCR2 and CXCR4 is not restricted to neutrophils, we sought to directly explore the aging process of circulating neutrophils in animal models of cancer. Toward a more general biological conception, we employed orthotopic, syngeneic mouse models of poorly immunogenic (SCC VII; head and neck squamous cell carcinoma (HNSCC)) and higher immunogenic (4T1 breast cancer) cancer at early, premetastatic stages. Multiplex ELISA analyses revealed distinct expression profiles of cytokines in the cell culture supernatants of these malignant tumor cell lines (figure 1A). Whereas these differences in the cytokine expression patterns were less pronounced in the corresponding lysate of solid neoplasms raised in mice, the amount of the released cytokines was essentially higher. Here, particularly ligands of the chemokine receptor CXCR2 including the chemokine CXCL2, which is known to promote biological aging of neutrophils,13 were detected. Accordingly, exposure to CXCL2 or to the supernatant of SCC VII or 4T1 tumor cells induced a significant increase in the surface expression of CXCR4 on neutrophils isolated from the peripheral blood of wild-type (WT) mice (figure 1B). This increase was significantly diminished on antibody blockade of CXCR2.
To analyze effects of these tumor-released signals on biological aging of circulating neutrophils, we subsequently evaluated the surface expression of the chemokine receptors L-selectin/CD62L, CXCR2, and CXCR4 (which gradually increase (CXCR4) or decrease (L-selectin/CD62L, CXCR2) with biological aging of these leukocytes in the systemic circulation under homeostatic conditions)12 13 17 18 on blood neutrophils in SCC VII or 4T1 tumor-bearing mice. Metabolic pulse labeling with BrdU further allowed us to determine the relative chronological age of these immune cells (figure 1C). In healthy tumor-free mice, cell surface expression of CXCR4 was significantly higher in chronologically aged (BrdUneg) than in non-aged (BrdUpos) blood neutrophils (figure 1D), whereas cell surface expression of L-selectin/CD62L and CXCR2 was significantly decreased (online supplemental figure S2). Most interestingly, expression of CXCR4, CXCR2, and L-selectin/CD62L (figure 1D, online supplemental figure S2) did not significantly differ between chronologically aged (BrdUneg) and non-aged (BrdUpos) circulating as well as tumor-associated neutrophils in tumor-bearing mice, suggesting that in early stages of cancer chronological and biological aging of neutrophils in the systemic circulation is uncoupled. Moreover, the average expression of CXCR4 was significantly elevated on total circulating neutrophils in tumor-bearing mice compared with total circulating neutrophils in healthy controls (figure 2A). Inversely, the average expression of L-selectin/CD62L and CXCR2 on total circulating neutrophils was significantly diminished in tumor-bearing mice compared with controls (online supplemental figure S3). However, the proportion of chronologically aged and non-aged neutrophils of total neutrophils as detected by BrdU pulse labeling did not vary between tumor-free and tumor-bearing animals (figure 2B), further indicating that in early cancer biological aging of circulating neutrophils is accelerated. Importantly, all neutrophils recruited to the tumors were mature (as indicated by normal cell size and segmented nuclear morphology; online supplemental figure S4), whereas only a small proportion of non-aged (BrdUpos) neutrophils in the peripheral blood of tumor-bearing animals exhibited band nuclei (indicative for less neutrophil maturity). This elevation in CXCR4 expression of neutrophils in tumor-bearing animals was almost completely abolished on antibody blockade of the aging-promoting chemokine receptor CXCR2 (figure 2A). Noteworthy, serum levels of CXCR2 ligands only slightly, but not significantly varied between tumor-bearing and tumor-free mice (online supplemental figure S5), pointing to activity of these chemokines in the immediate tumor microvasculature. Collectively, our data suggest that tumor-released CXCR2 ligands uncouple biological from chronological aging of circulating neutrophils in early cancer by promoting excessive biological aging of these immune cells.
Excessive aging of neutrophils promotes their migration to malignant tumors
To directly elucidate the fate of excessively aging neutrophils in cancer, we isolated aged neutrophils from tumor-free mice treated with blocking anti-P-selectin and anti-E-selectin antibodies which effectively interferes with the elimination of chronologically (and biologically) aged neutrophils in bone marrow, liver, and spleen, thereby enriching BrdUneg CXCR4hi (aged) neutrophils in the systemic circulation (90.2%±2.6% aged neutrophils of total neutrophils). In addition, we isolated non-aged neutrophils from tumor-free mice treated with isotype control antibodies in which most circulating aged neutrophils are physiologically eliminated,12 13 17 18 resulting in only 21.6%±1.5% of BrdUneg CXCR4hi aged neutrophils of total neutrophils. After differential ex vivo fluorescence labeling and subsequent adoptive transfer of these two different cell fractions into recipient mice heterotopically bearing SCC VII or 4T1 tumors, multi-channel in vivo microscopy unveiled that particularly aged neutrophils accumulate in the tumor microvasculature (figure 2C). Immunostaining and confocal microscopy on tissue sections from orthotopic 4T1 and SCC VII tumors further demonstrated a robust infiltration of neutrophils into the malignant neoplasms (figure 2D). The majority of these neutrophils was represented by chronologically aged (BrdUneg) neutrophils as evidenced by multi-channel flow cytometry analyses of the tumor lysates (figure 2E). These data indicate that excessive biological aging of neutrophils supports the migration of these immune cells to malignant tumors.
Activation of the NLRP3 inflammasome by tumor-released DAMPs induces the trafficking of excessively aging neutrophils to malignant tumors
Damage-associated molecular patterns (DAMPs) such as S100A8/9, high mobility group box 1 (HMGB1), or uric acid are released from damaged cells under a variety of pathological conditions including cancer and have been implicated in leukocyte trafficking.19 Consequently, these DAMPs might mediate the recruitment of excessively aging neutrophils in cancer to malignant tumors. In further experiments, we document that intraperitoneal stimulation with monosodium urate (MSU) and—to a lesser degree—with S100A8/9 but not with HMGB1 induces the recruitment of mature neutrophils (as indicated by segmented nuclear morphology of these cells; data not shown) and/or classical monocytes (cMOs), but not of non-classical monocytes (ncMOs), to the peritoneal cavity (online supplemental figure S6A). Importantly, in the supernatant of SCC VII and 4T1 tumor cells, we only detected large amounts of uric acid (figure 3A), whereas HMGB1 levels were low and S100A8/9 was not present (not shown). Exposure of the tumor cell supernatants to (toll-like receptor) TLR-2 or TLR-4 (principal receptors of HMGB1) reporter cells, however, did not induce a positive signal in these cells (figure 3B). In contrast, exposure of MSU potently activated peritoneal macrophages as indicated by a significant increase in the production of interleukin (IL)-1β (figure 3C). Accordingly, we detected strong expression of IL-1β and other inflammatory cytokines such as tumor necrosis factor (TNF) in SCC VII and 4T1 tumors (which include macrophages) grown in mice, but barely in the underlying tumor cells (figure 1A).
DAMP-mediated synthesis of IL-1β and, in turn, of other cytokines is mainly regulated through different multimeric intracellular protein complexes termed inflammasomes.20 To identify specific inflammasomes mediating responses of aged neutrophils, we performed another set of experiments. Intraperitoneal application of an activator of the nucleotide oligomerization domain-like receptor pyrin domain-containing-3 (NLRP3; alum crystals) inflammasome, but not of the NLRP1 (muramyl dipeptide), the absent in melanoma 2 (AIM2; dA:dT), or the NLRC4 (flagellin) inflammasomes, elicited significant responses of neutrophils and cMOs, but not of ncMOs (figure 3D). The majority of neutrophils recruited on NLRP3 inflammasome activation was represented by aged (BrdUneg) neutrophils.
Employing multi-channel in vivo microscopy in our heterotopic models of SCC VII HNSCC and 4T1 breast cancer, we further found a significant increase in numbers of intravascularly rolling (SCC VII) and, later on, firmly adherent (SCC VII and 4T1) neutrophils in the tumor microvasculature over the experimental period of 7 days (figure 3E,F). This increase in numbers of rolling and firmly adherent neutrophils was completely abolished on application of a highly specific NLRP3 inflammasome inhibitor. In addition, neutrophilia in 4T1 tumor-bearing mice was abrogated on NLRP3 inflammasome inhibition (online supplemental figure S6B). Hence, the NLRP3 inflammasome controls the trafficking of excessively aging neutrophils to malignant lesions.
To further decipher the mechanisms underlying NLRP3 inflammasome-dependent neutrophil responses, we employed more reductionist model systems. Using immunostaining and confocal microscopy on cremasteric tissue whole mounts, we observed a significant increase in the expression of ICAM-1/CD54, but not of VCAM-1/CD106, on endothelial cells of postcapillary venules on intrascrotal stimulation with NLRP3 inflammasome-activating alum crystals compared with unstimulated controls (figure 4). Multi-channel in vivo microscopy on the mouse cremaster muscle further revealed a significant increase in numbers of intravascularly adherent, but not of rolling neutrophils, 6 hours after intrascrotal application of alum crystals compared with controls (figure 4B). In this context, activation of the NLRP3 inflammasome in peritoneal macrophages induced the synthesis of IL-1β (and, in turn, of various inflammatory cytokines; figure 4C). However, exposure of alum crystals to microvascular endothelial cells did not induce surface expression of adhesion and signaling molecules—in contrast to the cytokine TNF (figure 4D). Similarly, direct stimulation with PMA, but not with NLRP3 inflammasome-activating alum crystals, elicited surface expression of the integrin CD11b/Mac-1 (but not of CD11a/LFA-1 or VLA-4/CD49d) on neutrophils isolated from the peripheral blood of WT mice (figure 4E). Subsequent binding of ICAM-1/CD54-Fc to aged, but not to non-aged neutrophils, was significantly elevated on exposure to PMA, but not to alum crystals (figure 4F). Thus, activation of the NLRP3 inflammasome in perivascular macrophages induces the synthesis of inflammatory mediators that upregulate adhesion and signaling molecules on the surface of microvascular endothelial cells, in turn promoting the trafficking of aged neutrophils to the perivascular space.
Excessively aging neutrophils support tumor growth
Tumor-bearing animals exhibit excessively aging neutrophils in their peripheral blood (figures 1 and 2, online supplemental figure S2). To characterize the role of these excessively aging neutrophils for tumor progression, we first performed experiments in neutropenic mice which orthotopically developed SCC VII or 4T1 tumors. Antibody-mediated depletion of neutrophils prevented infiltration of the tumors by these immune cells and significantly reduced tumor growth compared with animals treated with isotype control antibodies(figure 5A). In line with our previous results, neutrophil recruitment into the malignant lesions was completely suppressed on blockade of the NLRP3 inflammasome (figure 5B). In contrast, blockade of the aging-promoting chemokine receptor CXCR2 or the aging-inhibiting chemokine receptor CXCR413 did not significantly alter neutrophil migration into the tumors. However, counteracting neutrophil trafficking (by NLRP3 inhibition) or neutrophil aging (by CXCR2 blockade) attenuated tumor progression, whereas supporting neutrophil aging (by blockade of CXCR4) even enhanced tumor growth in SCC VII HNSCC and 4T1 breast cancer (figure 5C). Importantly, direct exposure of NLRP3 activating alum crystals or of the NLRP3 inhibitor as well as of blocking antibodies directed against CXCR2 or of the CXCR4 inhibitor did not significantly change the proliferation of SCC VII or 4T1 tumor cells in vitro (figure 5D). Although we cannot exclude that these interventions might additionally alter processes independent from neutrophil biological aging or recruitment, our data strongly suggest that excessively aging neutrophils promote cancer progression.
Excessively aging neutrophils stimulate cancer cell proliferation via release of NE
Under homeostatic conditions, neutrophils progressively release their protein content from intracellular granules when aging in the circulation. This process initially renders these innate immune cells highly reactive for their fight against invading pathogens, before they ultimately become ‘disarmed’ to prevent unwanted collateral damage.14 Extending these observations, the granularity of chronologically aged (BrdUneg) neutrophils in the peripheral blood was slightly lower than that in non-aged (BrdUpos) neutrophils in both tumor-free and and tumor-bearing animals (online supplemental figure S7A). Most interestingly, these differences were dramatically enhanced in neutrophils isolated from malignant tumors, strongly suggesting that particularly aging tumor-associated neutrophils release their protein content.
To further define the protumorigenic potential of excessively aging neutrophils, we determined the expression of key molecules supposed to mediate antitumorigenic and protumorigenic effects of these immune cells.8 Employing multi-channel flow cytometry on neutrophils isolated from the peripheral blood of mice, we primarily detected higher surface levels of NE, but also of MMP-9, VEGF, CCL3, CCL5, and arginase-1 on aged neutrophils compared with non-aged neutrophils(figure 6A), complementing recent data on enhanced MMP-9 release and NE activity in aged neutrophils compared with non-aged neutrophils.21 Furthermore, neutrophils in tumors exhibited slightly higher NE surface levels than neutrophils in the peripheral blood (online supplemental figure S7B). Accordingly, exposure of the supernatant of excessively aging blood neutrophils isolated from tumor-bearing mice to SCC VII HNSCC or 4T1 breast cancer cells (figure 6B), but not to mouse microvascular endothelial cells (figure 6C), induced a significant increase in the proliferation of these tumor cells in vitro compared with non-aged and physiologically aged neutrophils isolated from tumor-free mice. This increase was significantly reduced on application of an NE inhibitor (figure 6B).
Excessively aging neutrophils do not alter tumor angiogenesis or T cell recruitment
Furthermore, migration of microvascular endothelial cells did not significantly differ on exposure to the supernatant of tumor-primed neutrophils or of healthy control neutrophils in an in vitro scratch assay (figure 6D). Consequently, antibody-mediated depletion of neutrophils did not significantly alter vessel density as well as the number of branches or junctions in the vessel network of SCC VII or 4T1 tumors as evidenced by multi-channel in vivo microscopy in our heterotopic cancer models (figure 6E). Moreover, neutrophil depletion did not significantly alter numbers of CD4+ or CD8+ T cells in the malignant lesions (figure 6F) as well as the proliferation of these immune cells (determined by Ki-67 immunostaining; online supplemental figure S8), collectively suggesting that excessive aging of neutrophils in cancer particularly promotes NE-dependent tumor cell proliferation.
In tumors derived from the squamous cell carcinoma cell line SCC VII (‘poorly immunogenic’), expectedly less neutrophil (figure 5A) and lymphocyte (figure 6F) responses were observed compared with tumors derived from the breast cancer cell line 4T1 (‘higher immunogenic’). In addition, neutrophil counts were higher in the peripheral blood of (particularly orthotopically) 4T1 tumor-bearing animals than those of SCC VII tumor-bearing animals (online supplemental table S1). These differences in immunogenicity might be explained—inter alia—by the different chemokine expression patterns of 4T1 and SCC VII tumors including the chemokine CCL24 (attracting eosinophils, neutrophils, and T cells), the chemokine CCL19 (activating lymphocytes), or the chemokine CCL12 (attracting eosinophils, monocytes, and T lymphocytes; figure 1A). Consequently, all the above reported results were found to be more pronounced in 4T1 tumors than in SCC VII tumors.
Aging of neutrophils in the systemic circulation is critical for the pivotal function of these innate immune cells in homeostasis and host defense against invading pathogens.11–13 Recent experimental data in metastatic cancer21 and own analyses of the METABRIC human breast cancer cohort, however, suggest that neutrophils exhibiting a phenotype reminiscent of aged neutrophils promote advanced stages of malignant disease. Whether and how neutrophil aging contributes to local tumor growth remains obscure.
To directly evaluate the effect of solid malignancies on aging of circulating neutrophils, we employed orthotopic, syngeneic mouse models of poorly (SCC VII HNSCC) and higher immunogenic (4T1 breast cancer) tumors at early, premetastatic stages.22 In the tumor cell culture supernatants and the corresponding solid tumors raised in mice, we identified distinct expression patterns of cytokines in SCC VII and 4T1. Among these molecular factors, particularly ligands of the chemokine receptor CXCR2, including the chemokine CXCL2, were found to be enriched in both SCC VII and 4T1. Previously, CXCL2 has been reported to mediate phenotypic and functional changes related to chronological aging of neutrophils (‘biological aging’) under homeostatic conditions in an autocrine manner,13 in addition to its well-known chemotactic properties.23 We therefore hypothesized that these tumor-released molecular signals promote such age-related changes in circulating neutrophils.
To prove this hypothesis, we isolated neutrophils from the peripheral blood of tumor-bearing or tumor-free mice and determined cell surface expression levels of CXCR4, which are known to robustly increase with chronological cell aging under both homeostatic and inflammatory conditions (whereas expression levels of CD62L/L-selectin and CXCR2 decrease).12 18 As opposed to healthy tumor-free animals, however, expression of CXCR2, CXCR4, and CD62L/L-selectin did not significantly vary between chronologically aged and chronologically non-aged neutrophils in tumor-bearing mice, indicating that in early cancer biological aging of circulating neutrophils is uncoupled from chronological aging. Importantly, the overall expression of CXCR4 on blood neutrophils from tumor-bearing mice was significantly higher compared with non-diseased animals, whereas the proportion of chronologically aged neutrophils of total neutrophils remained stable. These data further point to excessive biological aging of neutrophils in cancer. In line with these results, the elevation in the expression of CXCR4 on circulating neutrophils in tumor-bearing mice was substantially reduced on blockade of the aging-promoting chemokine receptor CXCR2, collectively suggesting that CXCR2 ligands released by malignant tumors uncouple biological from chronological aging of neutrophils in the systemic circulation by promoting excessive biological aging of these immune cells. Notably, serum levels of CXCR2 ligands did not grossly differ between tumor-bearing and tumor-free mice in these early disease states which might be due to cytokine buffering activity of erythrocytes.24 Consequently, circulating neutrophils might encounter higher local concentrations of these tumor-released chemokines when passing the tumor microenvironment, where these immune cells are thought to be retained for an extended period of time.25 26
Chronological aging of neutrophils induces considerable changes in their molecular repertoire that enable them to rapidly migrate to the site of injury or infection.12 The fate of excessively (biologically) aged neutrophils in cancer remains elusive. In vivo microscopy in the heterotopic mouse models of HNSCC and breast cancer demonstrated that preferentially adoptively transferred aged neutrophils accumulate in the tumor microvasculature of tumor-bearing recipient mice. In line with these observations, metabolic pulse-labeling experiments in the orthotopic tumor models further revealed that particularly neutrophils with a high relative chronological age infiltrate and reside in malignant tumors. Hence, aging of circulating neutrophils in cancer effectively supports the recruitment of these immune cells into malignant tumors. These findings might be explained by previous reports documenting that aged neutrophils are highly reactive due to increased surface levels of integrins in high affinity confirmation on these immune cells facilitating endothelial interactions in the inflamed microvasculature.12 18
Chemokine production varies widely between different cancer entities including SCC VII and 4T1 tumors. DAMPs such S100A8/9, HMGB1, or uric acid, however, are constantly released on cell injury under pathological conditions, including oncological disorders.19 In our experiments, we found that SCC VII as well as 4T1 cancer cells abundantly produce uric acid and—to a much lesser degree—HMGB1, but not S100A8/A9. In principle, these two detectable DAMPs are able to potently recruit aged neutrophils. However, the supernatants of these tumor cells did not activate TLR-2 or TLR-4 reporter cells, suggesting that HGMB1 (which mediates cell activation primarily via these receptors) is not dominant in regulating neutrophil trafficking to these malignant lesions. Since MSU is known to serve as a potent activator of the NLRP3 inflammasome, facilitating the synthesis of IL-1β and other inflammatory mediators,20 we assumed that inflammasome activation in the tumor environment controls the trafficking of excessively aging neutrophils to malignant tumors. In line with this assumption, activation of the NLRP3 inflammasome potently elicited responses of neutrophils in reductionist in vivo assays. Mechanistically, NLRP3 stimulation promoted neutrophil–endothelial cell interactions via the production of various cytokines and chemokines in macrophages capable of activating microvascular endothelial cells, but did neither directly activate endothelial cells nor neutrophils. Consequently, application of a highly specific NLRP3 inflammasome inhibitor almost completely abrogated neutrophilia and accumulation of excessively aging neutrophils in malignant tumors, but did not alter biological aging of these immune cells as indicated by unchanged surface expression levels of CXCR4. Taken together, our data suggest that activation of the NLRP3 inflammasome in (peritumoral) macrophages promotes the trafficking of excessively aging neutrophils to malignant lesions. Importantly, different malignancies exhibit specific spatiotemporal activation patterns of inflammasomes in tumor cells and their environment which might cause the previously published multifaceted (and also controversial) functions of this intracellular protein complex in different tumor entities.27–29 Specifically, the enormous phenotypic and functional heterogeneity of macrophages and endothelial cells in different tissues, pathologies, and disease states might contribute to these divergent results.
Next, we sought to characterize the effect of excessively aging neutrophils on the progression of malignant tumors. We found that antibody-mediated depletion of these immune cells significantly reduces the growth of tumors in experimental HNSCC and breast cancer. Similar results were obtained on inhibition of NLRP3 inflammasome-dependent neutrophil infiltration of these malignant lesions, indicating that excessively aging neutrophils support tumor growth. Although initial studies were not able to delineate a functional role of neutrophils in cancer models,30 our findings are in line with the majority of previously published experimental work reporting tumor-promoting properties of neutrophils.31 32 Accordingly, chemotherapy-induced neutropenia in patients with cancer was found to be associated with a favorable disease outcome,33 whereas application of granulocyte-colony stimulating factor to neutropenic individuals34 as well as high neutrophil-lymphocyte ratios in the peripheral blood or high neutrophil numbers in tumors35 are related to poor survival rates in oncological disorders. Noteworthy, aged neutrophils have recently been shown to promote thrombosis,13 suggesting that these specifically primed immune cells might also contribute to dreaded comorbidities of patients with cancer .36 37
To characterize age-related effects of neutrophils on tumor growth in more detail, we directly manipulated the aging process of circulating neutrophils in tumor-bearing mice. Blockade of the CXCL2 receptor CXCR2, which interferes with neutrophil biological aging,13 reduced tumor growth and—in line with recent observations38 and most probably due to the downregulation of CXCR2 on excessively aging neutrophils—did not significantly affect neutrophil trafficking into malignant lesions or directly modulate tumor cell proliferation. In contrast, blockade of the CXCL12-CXCR4 axis by a CXCR4 inhibitor (which supports the mobilization of non-aged neutrophils from the bone marrow into the systemic circulation, interferes with the recruitment of aged neutrophils back to bone marrow, liver, and spleen as well as directly promotes neutrophil aging13 39) even slightly enhanced tumor growth, again without altering neutrophil infiltration of the neoplasms or directly affecting tumor cell proliferation. Thus, our experimental findings indicate that excessive aging of neutrophils in the periphery renders these immune cells protumorigenic. Interestingly, however, inhibition of CXCR4 signaling has recently been reported to interfere with responses of protumorigenic neutrophils in a zebrafish xenotransplantation model of breast cancer40 as well as of immunosuppressive Ly6Clow monocytes in experimental colorectal cancer,41 pointing to distinct roles of this chemokine receptor, which can also be expressed by tumor cells, in different types of cancer.
According to the previously reported antitumorigenic and protumorigenic properties of neutrophils,8 the existence of distinct phenotypes of neutrophils has been proposed. Following the classification for macrophages, an antitumorigenic ‘N1’ and a protumorigenic ‘N2’ phenotype have been defined by specific surface protein expression signatures.42 We here identified that aging of neutrophils is associated with a more protumorigenic state, as indicated by increased surface expression of NE, MMP-9, VEGF, chemokines CCL3 or CCL5, and arginase-1 on these immune cells. These findings are in line with recent reports on the progressive release of neutrophil granular proteins during physiological aging of these immune cells in the circulation.14 Most interestingly, we found that this loss of granularity in aging neutrophils is also present in the circulation of tumor-bearing animals and, moreover, is particularly pronounced in tumor-associated neutrophils. In accordance with these observations, we were able to demonstrate that excessively aging neutrophils potently stimulate the proliferation of tumor cells in vitro. These effects were dependent on NE, which has previously been identified to degrade insulin receptor substrate 1 in the endosomal compartment of tumor cells on intracellular uptake of this protease. As a consequence of these events, interactions of phosphoinositide 3-kinase (PI3K) and platelet-derived growth factor receptor increase, thereby skewing the PI3K axis toward tumor cell proliferation. Furthermore, NE is supposed to upregulate mitogen-activated protein kinases, further enhancing the proliferation of tumor cells.5 43–46 In contrast, neutrophils from tumor-bearing mice did not significantly alter the proliferation or migration of microvascular endothelial cells in vitro and neutrophil-depletion did not affect the formation of the tumor vessel network in vivo. These data indicate that excessively aging neutrophils in cancer might be functionally different from the subset of CD49dhigh VEGFR1high CXCR4high neutrophils identified to support vascularization of non-vascularized hypoxic tissue47 48 or MMP9high VEGFhigh CXCR4high neutrophils that promote angiogenesis in experimental melanoma or fibrosarcoma.49 Likewise, lymphocyte infiltration of malignant tumors as well as the proliferation of these immune cells was not affected in the absence of excessively aging neutrophils, collectively suggesting that these protumorigenic neutrophils do not exhibit significant immunosuppressive properties as myeloid-derived suppressor cells, but promote tumor progression through NE-dependent stimulation of tumor cell proliferation.
Our experimental findings uncover a previously unknown self-sustaining mechanism of malignant tumors in uncoupling biological from chronological aging of circulating neutrophils. In contrast to the beneficial role of neutrophil aging in homeostasis and host defense against invading pathogens, excessive biological aging of these immune cells in cancer endows them with potent protumorigenic properties—a mechanism that is more pronounced in higher than in poorly immunogenic tumors. Interference with this aberrant process effectively compromises the progression of malignancies and might therefore provide a novel strategy for the treatment of oncological disorders. This translational approach seems to be particularly promising since first clinical trials employing inhibitors of the aging-promoting chemokine receptor CXCR2 on neutrophils reported positive results in patients with breast cancer.50
Data availability statement
All data relevant to the study are included in the article or uploaded as supplementary information.
Patient consent for publication
All animal experiments were approved by the local governmental authorities (‘Regierung von Oberbayern’) and conducted according to the guidelines to ensure animal welfare.
Data presented in this manuscript are part of the doctoral thesis of LAM. The authors thank Claudia Fahney for excellent technical assistance.
Contributors LAM, FH, JBS, RH, BS, GZ, and TV performed experiments and data analyses. MC, OG, FK, LH, SB, TV, and KL contributed to the writing of the manuscript. BU and CR conceived the study, supervised experiments, and wrote the manuscript. BU and CAR serve as guarantors.
Funding This study was supported by Deutsche Forschungsgemeinschaft (DFG), Sonderforschungsbereich (SFB) 914, projects B03 (to CAR) and B06 (to KL).
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.