Mast cells are known effector cells in allergic and inflammatory diseases, but their precise roles in intestinal inflammation remain unknown. Here we show that activation of mast cells in intestinal inflammation is mediated by ATP-reactive P2X7 purinoceptors. We find an increase in the numbers of mast cells expressing P2X7 purinoceptors in the colons of mice with colitis and of patients with Crohn's disease. Treatment of mice with a P2X7 purinoceptor-specific antibody inhibits mast cell activation and subsequent intestinal inflammation. Similarly, intestinal inflammation is ameliorated in mast cell-deficient KitW-sh/W-sh mice, and reconstitution with wild-type, but not P2x7−/− mast cells results in susceptibility to inflammation. ATP-P2X7 purinoceptor-mediated activation of mast cells not only induces inflammatory cytokines, but also chemokines and leukotrienes, to recruit neutrophils and subsequently exacerbate intestinal inflammation. These findings reveal the role of P2X7 purinoceptor-mediated mast cell activation in both the initiation and exacerbation of intestinal inflammation.
Both active and quiescent immunity occur simultaneously to achieve immunological homoeostasis in the harshest of environments—namely, the intestine. Aberrant immune responses in the gut lead to the development of intestinal immune diseases such as colitis and food allergies1,2. Mast cells (MCs) are generally recognized as major effector cells of type 1 allergic diseases, as well as of inflammation, host defenses, innate and adaptive immune responses and homoeostatic responses3,4,5. Histological analyses of patients with, and murine models of, colitis have implicated the involvement of MCs in intestinal inflammation4,6, but the factors responsible for MC activation are not fully understood.
Several lines of evidence have demonstrated that release of extracellular ATP and ADP from injured, dying or activated cells acts as a danger signal by modulating various cellular functions via the activation of P2 purinoceptors7,8. P2 purinoceptors comprise P2X (P2X1–7) and P2Y receptors (P2Y1, 2, 4, 6, 11–14). P2X1–7 receptors are ATP-gated ion channels and specific for ATP, whereas P2Y receptors are G protein-coupled receptors that are specific for ADP, UTP and ATP7,8.
Stimulation by ATP or ADP through the P2 purinoceptors of macrophages and dendritic cells (DCs) results in the production of inflammatory cytokines; this can lead to the development of asthma, contact hypersensitivity or graft-versus-host disease9,10,11. MCs also express several P2 purinoceptors and release histamine, cytokines and chemokines upon nucleotide stimulation12. Although MCs are thought to be involved in intestinal inflammation, it is unclear whether extracellular nucleotides are required for this process.
Here, we used a newly established anti-MC monoclonal antibody (mAb) to identify activated MCs and found that extracellular ATP mediates MC activation through P2X7 purinoceptors to initiate and amplify intestinal inflammation. Consequently, obstruction of the ATP-P2X7 purinoceptor cascade could be used to inhibit gut inflammatory diseases.
Activated MCs in intestinal inflammation
Using a 2,4,6-trinitrobenzene sulphonic acid (TNBS)-induced colitis model, we first examined whether MCs were involved in intestinal inflammation. To assess MC activation in vivo, we established an mAb (clone: 5A9) specific for CD63, a marker of activated MCs13. We confirmed that our anti-CD63 mAb was reactive specifically to MCs activated by immunoglobulin (Ig)E plus relevant allergen or a calcium ionophore, and not to naïve and CD63-knocked down MCs (Supplementary Fig. S1). In the colons of TNBS-treated mice, increased numbers of CD63+-activated MCs were noted until day 3 post administration; the numbers then gradually decreased and reached a basal level on day 6 (Fig. 1a,b), indicating that MC activation was associated with the initiation phase of colitis development, as previously reported in a murine model and in patients with inflammatory bowel disease6,14. It has generally been accepted that the mechanistic basis of ulcerative colitis (UC) and Crohn's disease (CD) are different. Indeed, the pathogenic cytokines involved in the development of UC and CD are different2 and the genetic polymorphisms specific for UC and CD are also different15. In addition, the cytokines required for the development of MCs differ between humans (stem cell factor) and mice [interleukin (IL)-3 and stem cell factor]4. Thus, these different pathological environments may have led to differences in the requirement for, and involvement of, MCs in the development of inflammation. Therefore, we analysed MC numbers in both UD and CD patients, although we focused on the TNBS-induced colonic inflammation model. We detected increased numbers of MCs in the colons of patients with CD or UC (Fig. 1c,d). Thus, increased numbers of MCs in the colon is a characteristic of intestinal inflammation.
To directly show the involvement of MCs in the development of intestinal inflammation, we used MC-deficient KitW-sh/W-sh mice. We confirmed that immunological and inflammatory symptoms induced by TNBS treatment were identical in KitW-sh/+ heterozygous and Kit+/+ homozygous mice; however, inflammatory symptoms, such as body weight loss, massive inflammatory cell infiltration and colon shortening, were restored in KitW-sh/W-sh mice but not in KitW-sh/+ heterozygous and Kit+/+ homozygous mice (Fig. 1e–h). Similarly, our histological and immunological analyses revealed that destruction of the colonic epithelial layer and infiltration by inflammatory cells—especially neutrophils, which were stained neutral pink and had lobulated nuclei,—were reduced in KitW-sh/W-sh mice (Fig. 1f,h,i). Moreover, inflammatory signs were ameliorated in KitW-sh/W-sh mice when we used other well-known inflammatory bowel disease models, such as the dextran sodium sulphate (DSS) colitis model (Fig. 2a–c). As the use of KitW-sh/W-sh mice as an MC-deficient model is controversial16,17, we also used the MC-specific enhancer-mediated toxin receptor-mediated conditional cell knockout (TRECK) system (Mas-TRECK mice)18. We confirmed that specific depletion of MCs ameliorated the inflammation in this DSS-induced colitis model (Fig. 2d–h). Our data indicate that activated MCs participate in the aggravation of intestinal inflammation.
Establishment of an inhibitory MC-specific mAb
IgE plus a relevant allergen induces MC activation; however, Rag-1−/− and Tcrβ−/−δ−/− mice showed inflammatory responses comparable to those in TNBS-induced intestinal inflammation (Supplementary Fig. S2a–d)19 and had increased numbers of CD63+-activated MCs in their colons (Supplementary Fig. S2e), suggesting that T and B cells are not involved in MC activation during colitis. We also found no increase in CD63 expression on MCs after stimulation with IL-18 and IL-33, which are known to be involved in colitis (Supplementary Fig. S2f)20,21.
We next tried to establish an anti-MC mAb that could ameliorate activated MC-mediated intestinal inflammation. We immunized rats with purified murine-activated colonic MCs, established hybridomas, performed flow cytometry to select hybridomas that produced mAbs that preferentially recognized colonic MCs and examined the hybridomas' ability to inhibit ovalbumin-induced food allergy22 or TNBS-induced intestinal inflammation (Supplementary Fig. S3). Among 2,000 clones, we obtained an anti-MC mAb (designated clone 1F11; rat IgG2b) that was strongly reactive to colonic MCs (Fig. 3a; Supplementary Fig. S3). In addition to colonic MCs, 1F11 mAb bound efficiently to peritoneal cavity-, lung- and bone marrow (BM)-derived MCs, but not to skin MCs (Fig. 3a). When tested with other immunocompetent cells in the colon, 1F11 mAb was weakly reactive to some CD3+ T cells, CD11c+ DCs and F4/80+ macrophages, but was not reactive to Gr-1+ granulocytes, IgA+ plasma cells or epithelial cells (ECs) (Fig. 3b).
To show the inhibitory function of 1F11 mAb in intestinal inflammation, mice were given 1F11 mAb (0.5 mg day−1 in a single dose) for 3 days, beginning 1 day before intrarectal administration of TNBS. 1F11 mAb treatment reduced the intestinal inflammation (Fig. 3c–g) and decreased the number of CD63+-activated MCs in 1F11 mAb-treated mice (Fig. 3h).
Targeting P2X7 receptors reduces intestinal inflammation
Mass spectrometry analyses of immunoprecipitants of MC cell lysates with 1F11 mAb showed that the P2X7 purinoceptor is recognized by 1F11 mAb (Supplementary Fig. S4a). The specificity of 1F11 mAb for the P2X7 purinoceptor was confirmed by its specific reactivity to cells transfected with P2X7 receptors but not with other types of P2X receptor (for example, P2X1 and P2X4; Supplementary Fig. S4b). MCs derived from P2x7−/− mice, however, were not recognized by 1F11 mAb (Supplementary Fig. S4c). Western blot and flow cytometric analysis showed that, among the several variants of P2X7 purinoceptors23, 1F11 mAb bound to variant a (full-length; Supplementary Fig. S4d,e). In contrast, variant c (possessing the ATP-binding portion but lacking the C-terminal region) was detected by western blot, but its surface expression was not detected by flow cytometry because of its defect in extracellular expression (Supplementary Fig. S4d,e)24. In addition, neither western blot nor flow cytometry detected variant d (lacking the ATP-binding portion; Supplementary Fig. S4d,e). These data strongly suggest that 1F11 mAb recognizes P2X7 receptors, specifically the ATP-binding portion. We also confirmed that 1F11 mAb had similar reactivity to that of a commercially available anti-P2X7 mAb (clone: Hano43; Supplementary Fig. S4f,g).
To evaluate whether 1F11 mAb directly affects MCs during ATP-mediated activation, we treated MCs with ATP in the presence of 1F11 mAb in vitro. 1F11 mAb treatment reduced the number of CD63+-activated MCs induced by ATP in a dose-dependent manner (Fig. 4a). High concentrations of extracellular ATP increased the cell permeability of the MCs12. Thus, uptake of Lucifer yellow was observed in ATP-stimulated MCs but was substantially impaired in 1F11 mAb-treated and P2x7−/− MCs (Fig. 4b,c).
As many cell types (MCs, T cells and DCs) express P2X7 receptors (Fig. 3b), we then asked whether the P2X7 receptors on MCs were responsible for the MC-mediated intestinal inflammation in vivo by analysing MC-deficient KitW-sh/W-sh mice reconstituted with P2x7+/+ or P2x7−/− MCs. We confirmed that reconstituted MCs were present in the colon and maintained P2X7 expression (Supplementary Fig. S5). Like wild-type mice, KitW-sh/W-sh mice reconstituted with P2x7+/+ MCs showed severe inflammatory responses when treated with TNBS. However, these inflammatory responses were ameliorated when KitW-sh/W-sh mice were reconstituted with P2x7−/− MCs; the amelioration included inhibition of neutrophil infiltration and MC activation (Figs 1 and 5a–f).
We next analysed whether the MCs in UC or CD patients expressed P2X7. Although increased number of MCs were observed in the colons of both UC and CD patients (Fig. 1c,d), P2X7 purinoceptors were expressed by the MCs in CD patients but not by those in UC patients or healthy volunteers (Fig. 5g,h). Thus, it is likely that P2X7 purinoceptor-mediated MC activation also occurs in the human colon, especially in CD patients.
To examine whether ATP was extracellularly released at high concentrations at inflammatory sites, we next measured ATP release from inflammatory colonic tissues. An elevated level of ATP release from the colon tissue was noted in TNBS-treated mice (Fig. 6a). In addition, intrarectal administration of non-hydrolyzable ATP (adenosine 5′-O-(3-thio) triphosphate and O-(4-benzoyl)benzoyl adenosine 5′-triphosphate) led to MC activation in the colonic tissue, similar to the effect of TNBS treatment (Fig. 6b). In contrast, intrarectal administration of other P2Y receptor agonists did not increase colonic MC activation (Fig. 6b). These findings indicate that inflammatory stimuli induce the extracellular release of ATP, which in turn leads to P2X7-dependent MC activation in the colon and subsequent exacerbation of intestinal inflammation.
P2X7 signalling activates the caspase-1 inflammasome to induce the production of IL-1β and IL-18 (ref. 25). IL-1β production is also mediated by MC proteases, such as chymases26. We therefore examined whether MCs produced IL-1β via P2X7 receptor activation, and if so whether this production was caspase-1-dependent. IL-1β production was decreased when P2X7-deficient MCs were stimulated with ATP, whereas substantial amounts of IL-1β were produced in caspase-1-deficient MCs (Supplementary Fig. S6), indicating that IL-1β production was P2X7-dependent but caspase-1-independent. In line with this finding, body weight changes were noted in KitW-sh/W-sh mice reconstituted with caspase-1−/− MCs (Fig. 5a). These results suggest that MC-dependent inflammation through P2X7 purinoceptors is not dependent on caspase-1-mediated IL-1β or IL-18 production.
An autocrine loop of ATP conversion mediates MC activation
In addition to ATP, other nucleotides (for example, extracellular ADP) act as signals to induce inflammatory responses27. We confirmed that MCs are activated by high concentrations of ADP and ATP (Fig. 7a,b). Extracellular ATP is hydrolysed by ectonucleoside triphosphate diphosphohydrolases (CD39) to ADP and AMP; it is then further hydrolysed by ecto-5′-nucleotidase (CD73) to adenosine, which has anti-inflammatory functions27. Colonic MCs expressed CD39 but not CD73 (Supplementary Fig. S7a,b), indicating that MCs can convert ATP to ADP but not to adenosine. We therefore examined the involvement of ADP-reactive P2Y purinoceptors and found that P2Y1 and P2Y12 were highly expressed on colonic MCs (Fig. 7c). However, inhibitors of P2Y1 and P2Y12 receptors, as well as knockdown of the P2Y12 receptor, had no effect on the induction of CD63+-activated MCs (Fig. 7d,e; Supplementary Fig. S8a). Similarly, intestinal inflammation, as well as activation of colonic MCs, was unaffected in clopidogrel (a P2Y12 receptor inhibitor)-treated mice (Supplementary Fig. S8b–d). These data indicate that although P2Y1 and P2Y12 were expressed on MCs neither P2Y1 nor P2Y12 purinoceptors mediate ADP-dependent CD63+ MC induction.
It is generally accepted that P2X7 purinoceptors specifically recognize ATP7, but we found that they were also involved in ADP-mediated MC activation. Indeed, no activation was noted in P2x7−/− MCs when they were stimulated with ADP (Fig. 7f), leading us to hypothesize that ADP promotes ATP release from MCs and their subsequent stimulation. To test this hypothesis, we measured the expression of pannexin-1, connexin 43 and connexin 32, which are ATP-releasing hemichannels, during cell activation28,29. The hemichannels were rarely expressed on the colonic MCs (Fig. 7g), and no inhibitory effect was observed when the MCs were treated with ADP in the presence of hemichannel inhibitors (flufenamic acid and carbenoxolone). However, cell activation was inhibited by P2X7 antagonists [oxidized ATP (OxATP), pyridoxal-phosphate-6-azophenyl-2′,4′-disulfonate and 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid disodium salt hydrate] (Fig. 7h). To further exclude the possibility that ADP triggers ATP release, we stimulated MCs with another P2Y ligand (UTP); we found that UTP did not induce MC activation (Fig. 7b).
We then tested whether ADP was converted to ATP by ATP-converting enzymes such as ecto-adenylate kinase, ATP synthase and nucleoside diphosphokinase30. To test the involvement of these enzymes, we used inhibitors of ecto-adenylate kinase (diadenosine pentaphosphate; AD2P5), ATP synthase (oligomycin; oligo) and nucleoside diphosphokinase (UDP), and we found that inhibition of ecto-adenylate kinase and ATP synthase, but not nucleoside diphosphokinase, reduced ADP- as well as ATP-dependent MC activation (Fig. 7h,i). Neither AD2P5 nor oligo inhibited MC activation induced by the crosslinking of IgE with relevant allergen (Fig. 7i). Among the adenylate kinases, adenylate kinase 1 (AK1) and AK2 were expressed in colonic MCs, and the expression of AK2 was much higher than that of AK1 (Supplementary Fig. S9a). As with AD2P5 treatment, knockdown of AK2, but not AK1, led to the inhibition of both ADP- and ATP-mediated MC activation (Supplementary Fig. S9b). These results indicate that P2X7 purinoceptors have an important role in the activation of MCs by ATP, including ATP derived from ADP by the action of ecto-enzymes such as ATP synthase and AK2.
Neutrophil infiltration by MC-derived mediators
Evaluation of MC activation on the basis of CD63 expression is an important criterion13; however, degranulation is not absolutely associated with cytokine production31. Therefore, we measured MC production of an array of inflammatory cytokine, chemokine and lipid mediators to additionally elucidate the role of P2X7 purinoceptor-mediated MC activation in the development of intestinal inflammation. Stimulation of MCs with ATP induced the production of inflammatory cytokines such as IL-6, tumour necrosis factor (TNF)α and oncostatin M32; this induction was not observed in P2x7−/− MCs or in wild-type MCs treated with 1F11 mAb (Fig. 8a,b).
We showed that neutrophil infiltration into the colon was mediated by MC activation (Fig. 1h,i), and a previous study suggested that neutrophil infiltration is a potential target in colitis treatment33. Consistent with these findings, ATP stimulation induced MCs, but not P2x7−/− MCs, to produce leukotrienes (LTs; LT C4/D4/E4), which are associated with the translocation of 5-lipoxygenase (5-LO) into the nucleus—an important step for LT synthesis in MCs34 (Fig. 8c,d). Also, chemokine gene array analysis demonstrated that ATP stimulation of MCs induced the expression of chemokines, including CCL2, CCL7 and CXCL2 (Fig. 8e–g), and 1F11 mAb treatment or P2X7 deficiency resulted in decreased CCL2 production from MCs activated by ATP but not by IgE plus allergen (Fig. 8g). Furthermore, KitW-sh/W-sh mice showed decreased levels of both CCL2 and IL-1β in the colon tissue, but the production levels of these molecules recovered when the mice were reconstituted with wild-type MCs (Supplementary Fig. S10a). As neutrophils express the corresponding chemokine receptors, it is likely that ATP-dependent MC activation induced inflammatory neutrophil infiltration into the colon from the peripheral blood (Supplementary Fig. S10b,c), given the high level of TNFα production by the neutrophils (Supplementary Fig. S10d). These results indicate that ATP-dependent MC activation has key roles in the induction of inflammatory responses (by inducing inflammatory cytokines) and in the exacerbation of inflammatory responses (by inducing LTs and chemokines to recruit TNFα-producing neutrophils to the colon).
Here, we showed that MCs have a critical role in the severity of colitis through their interaction with ATP and P2X7 purinoceptors. These interactions not only induce MC-mediated inflammatory responses but also exacerbate them by promoting neutrophil infiltration. Indeed, MC-deficient mice reconstitution with wild-type, but not P2x7−/−, MCs resulted in neutrophil infiltration and severe inflammatory responses, together with increased production of IL-1β, LTs and CCL2 (Figs 5 and 8, and Supplementary Fig. S10). KitWsh/Wsh mice spontaneously show elevated levels of neutrophils in their spleens35; however, we confirmed that the neutrophil levels were the same as those in the colons of Kit+/+, KitWsh/+ and KitWsh/Wsh mice under naïve conditions (Fig. 1h,i). To exclude the possible involvement of other immunological defects in KitWsh/Wsh mice, such as the involvement of the Corin gene, which is associated with type II transmembrane serine protease35, we further confirmed the amelioration of intestinal inflammation in conditional MC-deficient mice (Fig. 2d–h). These findings strongly suggest that P2X7 on MCs has a pivotal role in the development of murine and human intestinal inflammation.
P2X7 purinoceptors are expressed on T cells, DCs, macrophages and ECs9,10,11,25,36. In a recent study, ATP/P2X7-mediated signalling inhibited the generation and function of regulatory T cells and ATP stimulation led to their conversion into Th17 cells via an IL-6-dependent pathway; thus, the P2X7 antagonist OxATP inhibited colitis37. In that study, ATP/P2X7-mediated regulation of regulatory T cells was involved in the chronic phase of intestinal inflammation, which takes about 4 weeks for disease development37. Similarly, ATP-mediated DC activation occurs in the chronic phase of intestinal inflammation through the preferential induction of Th17 cells, although whether this is mediated by P2X7 remains to be seen38. In contrast, ATP/P2X7-mediated MC activation in our model was important in the development of T-cell-independent acute colitis, which occurs within 1 week. Thus, our study and those of others37,38 complement each other by reflecting the complicated pathological aspects and kinetics of the acute and chronic phases of intestinal inflammation mediated by ATP and P2X7.
We also found that the expression level of P2X7 receptors differed depending on the tissue and animal species. First, colonic MCs expressed high levels of P2X7, but skin MCs did not (Fig. 3a). Second, in contrast to MCs, some macrophages (for example, microglia and RAW264.7 cells) expressed higher levels of P2X7 than did colonic macrophages (Fig. 3b and data not shown). Third, among the several types of immunocompetent cell in the colon, MCs expressed the highest levels of P2X7 (Fig. 3a,b). Fourth, we found P2X7 expression on human colonic ECs, but not on murine colonic ECs (Figs 3b and 5g). In addition, as reported previously36, P2X7 expression on ECs was downregulated in the colons of CD patients; instead, CD patients showed increased numbers of P2X7+ MCs in their colons (Fig. 5g,h). It is important to note that, like murine MCs, human lung MCs express functional P2X7 (ref. 39). Therefore, although we must recognize the similarities and differences between mouse and human intestinal inflammation and MC distribution, ATP/P2X7-mediated MC activation seems to have a major role in the development of intestinal inflammation.
We found elevated levels of extracellular ATP in the colons of TNBS-treated mice (Fig. 6a). This high ATP concentration was most likely achieved by a combination or cascade of several ATP production pathways (for example, cell injury or lysis7, pattern recognition receptor-mediated activation of monocytes40 and commensal bacteria38). In our tissue culture system, we detected elevated release of ATP (40 μM) in the inflamed colon compared with the control (Fig. 6); however, at least 100 μM ATP was required for MC activation in vitro in the single cell culture system (Fig. 7b). This disparity likely reflects the differences in the culture conditions. Unlike in the single cell culture system, the concentration of secreted ATP in the tissue culture system could have been diluted in the culture medium, or ATP could have been consumed rapidly by activated inflammatory cells in the tissue. Alternatively, a lack of commensal bacteria-derived ATP in the tissue culture system as a result of the inclusion of antibiotics may have reduced the ATP level. Another possibility is that the abundant endogenous ATP-degrading enzymes (for example, CD39) in the colon tissue may have degraded some of the ATP. In support of this idea, a suppressive role for CD39 in intestinal inflammation has been reported41.
We found that ADP-reactive P2Y1 and P2Y12 receptors were expressed on colonic MCs (Fig. 7c), but inhibition or knockdown of these receptors did not suppress the CD63 expression (Fig. 7d,e; Supplementary Fig. S8a). In previous studies, stimulation of MCs with ADP (0.05–50 μM) has led to calcium influx via the P2Y1- but not the P2Y12-mediated pathway42, whereas our results indicate that CD63 expression required a higher concentration of ADP and was not suppressed by a P2Y1 inhibitor (Fig. 7b,d). This finding indicates that P2Y purinoceptors are not involved in the induction of CD63+-activated MCs that is mediated by high concentrations of ADP. However, we found that adenylate kinase and ATP synthase converted ADP back to ATP, which subsequently induced P2X7 purinoceptor-dependent MC activation. A similar conversion of ADP to ATP has been reported for endothelial cells27. Among adenylate kinases, AK2 was highly expressed on MCs and had a pivotal role in the conversion of ADP to ATP (Supplementary Fig. S9a,b). As another P2Y ligand (UTP) did not induce MC activation (Fig. 7b), our findings suggest that ADP could be converted into ATP by AK2 and ATP synthase, and that this ATP subsequently activates MCs through P2X7 purinoceptors. In addition, colonic MCs do not express ecto-5′-nucleotidase (CD73), an enzyme that degrades ADP into adenosine, which has anti-inflammatory effects in intestinal inflammation43. Therefore, our study indicates that MCs express CD39, adenylate kinases and ATP synthase, but not CD73, to preferentially convert ADP to ATP for the exacerbation of inflammatory responses through P2X7 purinoceptors.
Here, we showed that colitis aggravated by P2X7-mediated activation of MCs was independent of the inflammasome pathway, and that P2X7-mediated activation of MCs promoted TNFα production by effector cells to further promote intestinal inflammation44. Our findings also suggest that MCs exacerbate inflammation by recruiting neutrophils to produce abundant TNFα, but less IL-10 than is produced by other cells (for example, eosinophils, DCs and macrophages; Supplementary Fig. S10d). This neutrophil recruitment was mediated by the production of IL-1β, LTs and chemokines, which are potential targets for the treatment of colitis. Mice with experimentally induced colitis that lack CXCR2 or 5-LO (a key enzyme for converting arachidonic acid to LTs), as well as mice treated with inhibitors of CCR2, CXCR2 or 5-LO, show reduced inflammation and less neutrophil recruitment in their colons33,45,46. Moreover, given that ATP promotes neutrophil migration47, it is possible that P2X7-dependent LT and chemokine production, as well as ATP generation via AK2 and ATP synthase from MCs, could amplify neutrophil infiltration of the colon. These data collectively indicate that MCs are key factors in the induction of intestinal inflammation and also recruit neutrophils to heighten inflammatory responses. P2X7-dependent MC activation could, therefore, be a target for the treatment of intestinal inflammation.
Mice and human samples
Female C57BL/6 mice were purchased from CLEA Japan. Rag1−/− and P2x7−/− mice were obtained from Jackson Laboratory (Bar Harbour, ME, USA). MC-deficient KitW-sh/W-sh mice were obtained from Dr H. Suto (Atopy Research Center, Juntendo University, Japan). For the conditional MC-deficient analysis, Mas-TRECK tg mice were injected intraperitoneally with 250 ng of diphtheria toxin for 5 consecutive days and then with 150 ng every other day18. Caspase-1−/− mice were backcrossed with C57BL/6 mice; F5 mice were used for this experiment48. All mice were maintained under specific-pathogen-free conditions at the Experimental Animal Facility of the Institute of Medical Science, the University of Tokyo. All experiments were approved by the Animal Care and Use Committee of the University of Tokyo.
MC reconstitution was performed as described previously49. Briefly, BM-derived MCs were obtained from P2x7+/+, P2x7−/− or caspase-1−/− mice as described previously22. BM-derived MCs (5×106) were intravenously transferred to KitW-sh/W-sh mice at two time points (0 and 14 days). The reconstituted mice were used 3 months after the last transfer.
Colon specimens from UC and CD patients and healthy volunteers were obtained by endoscopic biopsy at Osaka University Hospital. All subjects provided written informed consent, and the study protocol was approved by the Ethics Committee of Osaka University Graduate School of Medicine (no. 08243) and the Institute of Medical Science, The University of Tokyo (no. 20-67-0331).
For TNBS-induced colitis, anaesthetized mice (18–22 g) were sensitized with 2.5% TNBS (Sigma-Aldrich) together with acetone and olive oil50. After 1 week, after a 3-h fast, the mice were given 100 μl of 2.5% TNBS in 50% ethanol via a flexible feeding tube that maintained their heads in a vertical position for 10 min. The control group received only 50% ethanol. Weight changes were recorded daily, and tissues were collected for histological analysis and isolation of mononuclear cells from the colonic lamina propria. For mAb treatment, mice were injected intraperitoneally with 0.5 mg of mAb (1F11 or an isotype control) 1 day before being given TNBS/EtOH intrarectally. mAb administration was continued for 3 days. For P2Y12 inhibition with clopidogrel sulphate, (Wako, Osaka, Japan), mice received clopidogrel (0.5 mg ml−1) in their drinking water from 3 days before intrarectal administration of TNBS/EtOH until the end of the study50. For DSS-induced colitis, mice were given 3.5% DSS (Wako, for C57BL/6) or 2.5% DSS (MP Biomedicals, Illkirch, France, for Mas-TRECK tg mice) in their drinking water for 5 days and their body weights were monitored daily50. In some experiments, non-hydrolysable ATP (adenosine 5′-O-(3-thio) triphosphate and O-(4-benzoyl)benzoyl adenosine 5′-triphosphate) or UDP-glucose (0.25 mg in 50% EtOH) was intrarectally administered and the effects were analysed 2 days later.
In vitro MC stimulation and inhibition
BM-derived MCs (2.5×105) were cultured with various concentrations of adenosine, ADP, ATP, UTP or anti-DNP-IgE with DNP-human serum albumin. Adenosine-3-phosphate 5-phosphosulfate (0.25 mM), carbenoxolone (10 μM), flufenamic acid (100 μM), pyridoxal-phosphate-6-azophenyl-2′,4′-disulfonate (100 μM), 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid disodium salt hydrate (100 μM), OxATP (0.5 mM), AD2P5 (1 mM), oligo (10 or 100 μM) or UDP (100 μM) was added to the cells for the inhibition assay27,28,40,51. All reagents were purchased from Sigma-Aldrich (St Louis, MO, USA, purity was ≥ 95%). 5-LO (BD Pharmingen, Franklin Lakes, NJ, USA) was stained after permeabilization with 0.2% Triton-X100 for 10 min; nuclei were stained with 4′,6-diamidino-2-phenyl indole.
Cell preparation and flow cytometry
ECs and lamina propria mononuclear cells were isolated from the colon, as described previously52. For flow cytometric analysis, cells were incubated with 5 μg ml−1 of an anti-CD16/32 antibody (10 μg ml−1, Fc block, BD Pharmingen) for 5 min and stained for 30 min at 4 °C with fluorescence-labeled Abs specific for c-kit (0.2 μg ml−1), Gr-1 (0.4 μg ml−1), CD4 (1 μg ml−1), CD11b (0.2 μg ml−1), CD11c (0.4 μg ml−1), CD39 (0.4 μg ml−1), CD45 (0.4 μg ml−1), IgA (10 μg ml−1), B220 (0.4 μg ml−1; BD Pharmingen), CCR3 (2 μg ml−1), CXCR2 (4 μg ml−1; R&D Systems, Minneapolis, MN, USA), FcεRIα (0.4 μg ml−1), CD73 (0.4 μg ml−1), TLR2 (10 μg ml−1; eBioscience, San Diego, CA, USA), F4/80 (20 μg ml−1), CCR2 (10 μg ml−1), P2X7 (Hano43; 2 μg ml−1,Serotec, UK) or CCR1 (10 μg ml−1, Abnova, Taiwan). Flow cytometric analysis and cell sorting were performed by using FACSCalibur and FACSAria (BD Biosciences, Franklin Lakes, NJ, USA), respectively. Sorted cells were stained with May-Giemsa stain in some experiments. Colonic MCs and BM-derived MCs were prepared as described elsewhere22.
Establishment of an anti-P2X7 mAb (1F11) and an anti-CD63 mAb
The procedure used to establish MC-specific mAbs is shown as a flowchart in Supplementary Figure S3. Briefly, c-kit+ FcεRIα+ MCs were obtained as described previously22 from the colons of mice that exhibited allergic diarrhoea. Purified colonic MCs (106 cells) were injected into the footpads of Sprague Dawley rats seven times, as described previously53. Lymphocytes were isolated from the spleen and inguinal lymph nodes and fused with P3X63-AG8.653 myeloma cells (CRL-1580; American Type Culture Collection, Manassas, VA, USA). The reactivity of each hybridoma to the colonic MCs was examined by means of flow cytometry. To identify antigens recognized by the mAbs, immunoprecipitation was performed with the mAbs, followed by Liquid chromatography–mass spectrometry analysis, as described previously53. Antigen specificity was confirmed by transfecting CHO cells with plasmids that encoded the murine P2X7 receptor and CD63.
Measurements of membrane permeability and inflammatory mediators
To assess membrane permeability, BM-derived MCs were washed twice with phosphate-buffered saline (PBS) and incubated with 1 mg ml−1 Lucifer yellow (Sigma-Aldrich) containing 250 μM sulfinpyrazone (Sigma-Aldrich). The MCs were then stimulated with 0.5 mM ATP (Sigma-Aldrich) for 15 min, as described elsewhere12. In the inhibition assay, 1 or 10 μg ml−1 of 1F11 mAb or the control antibody (Rat IgG2b) was added before ATP stimulation. The fluorescence signal of Lucifer yellow was determined by using fluorescence microscopy (BZ9000, Keyence, Osaka, Japan) and flow cytometry.
To measure the production of cytokines, chemokines and LTs from MCs, BM-derived MCs (2.5×105) were stimulated with 2.5 mM ATP for 30 min, after which the supernatants were collected. Chemokine and cytokine production was detected with an inflammatory cytokine kit (BD Pharmingen). For IL-1β measurement, BM-derived MCs from wild-type, P2x7−/− and caspase-1−/− mice were stimulated with 0.1 μg ml−1 of LPS for 4 h, followed by ADP or ATP stimulation. LT C4/D4/E4 production was detected by use of an enzyme-linked immunosorbent assay (GE Healthcare Bio-Science, NJ, USA). For ATP, cytokine and chemokine measurements from the colon tissue, the colon tissues were isolated from mice 2 days after intrarectal administration of TNBS. Released ATP was measured by culturing colon tissues at 100 mg of tissue per 100 μl of RPMI1640 medium for 3 h and using a luminescence ATP detection system (PerkinElmer, Norwalk, CT, USA).
Immunoprecipitation and western blotting
Cell lysates obtained from BM-derived MCs or CHO transfectants (mouse P2X7 variants a, c and d and flag-mP2X7s, cloned from C57BL/6 mice) were analysed by western blotting and immunoprecipitation with 1F11 mAb or the control Ab. Membranes were probed with an anti-flag and a polyclonal rabbit anti-P2X7 antibody (Sigma-Aldrich).
Colonic tissues were fixed in 4% paraformaldehyde and embedded in paraffin. Tissue sections (5 μm) were stained with haematoxylin and eosin solution, as described previously22. For the detection of MCs and P2X7 expression in human specimens, colonic tissue sections were stained with antibodies for MC tryptase and P2X7 purinoceptors (Alomone Laboratories, Jerusalem, Israel).
shRNA plasmid construction and lentiviral transduction
For the construction of shRNA expression lentivirus vector plasmids, a series of oligonucleotide pairs were synthesized, as listed below. Each oligo pair was annealed and cloned into pmU654. Each mU6-shRNA cassette was then subcloned into the ΔU3 sequence of the 3′-LTR of the lentivirus vector plasmid pLCG to generate pLCG-shCD63 (sense: 5′-TTTGATTCTTGCTGCATCAACATAGCTTCCTGTCACTATGTTGATGCAGCAAGAATCTTTTTTG-3′, antisense: 5′-AATTCAAAAAAGATTCTTGCTGCATCAACATAGTGACAGGAAGCTATGTTGATGCAGCAAGAAT-3′), pLCG-shP2Y12 (sense: 5′-TTTGATCTACTAATGATTCTAACTGCTTCCTGTCACAGTTAGAATCATTAGTAGATCTTTTTTG-3′, antisense: 5′-AATTCAAAAAAGATCTACTAATGATTCTAACTGTGACAGGAAGCAGTTAGAATCATTAGTAGAT-3′) and pLCG-shAK1 (sense: 5′-TTTGCGAGAAGATTGTACAGAAATGCTTCCTGTCACATTTCTGTACAATCTTCTCGCTTTTTTG-3′, antisense: 5′-AATTCAAAAAAGCGAGAAGATTGTACAGAAATGTGACAGGAAGCATTTCTGTACAATCTTCTCG-3′) and pLCG-shAK2 (sense: 5′-TTTTGGAGCTAATTGAGAAGAATTGCTTCCTGTCACAATTCTTCTCAATTAGCTCCATTTTTTG-3′, antisense: 5′-AATTCAAAAAATGGAGCTAATTGAGAAGAATTGTGACAGGAAGCAATTCTTCTCAATTAGCTCC-3′).
To obtain lentivirus-encoding green fluorescent protein (as a reporter gene) and shRNA for CD63, 293FT cells (6×105) were transfected with pLP1, pLP2, pLP-VSVG and pLCG-shRNA by using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) as per the manufacturer's protocol (Invitrogen). After 24- and 48-h incubations, lentivirus-encoding shRNA was collected.
BM-derived MCs (1×106) or MC/9 cells were transduced with shRNA expression lentivirus stock in the presence of 8 μg ml−1 Polybrene (Sigma-Aldrich)55. After 24 h, the cells were washed and green fluorescent protein-positive cells were sorted by FACSAria and used for subsequent experiments.
Total RNA was prepared by using TRIzol (Invitrogen) and reverse transcribed by use of Superscript VILO (Invitrogen), as described. Quantitative reverse transcription–PCR was performed with the LightCycler 480 II (Roche, Mannheim, Germany) and the Universal Probe Library (Roche). Primer sequences are listed in Supplementary Table S1.
Statistical analysis was performed by using the unpaired two-tailed Student's t-test and Welch's t-test. The data are presented as means±s.e.m.
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We thank Drs T. Kitamura and J. Kitaura (The University of Tokyo) for discussions and for providing reagents; Dr H. Suto (Juntendo University) for providing KitW-sh/W-sh mice; Dr S. Nakae (The University of Tokyo) for advice on analysing KitW-sh/W-sh mice; Drs S. Ohmi, M. Oyama, H. Hata and C. Takamura (The University of Tokyo) for protein analysis; and Dr A. Uozumi, I. Ishikawa and M. Mejima (The University of Tokyo), Drs F. Ishikawa and Y. Saito (RCAI) for technical advice. This work was supported by grants from: the Ministry of Education, Science, Sports and Technology of Japan (Grant-in Aid for Scientific Research S (23229004 to H.K.), for Young Scientists A (22689015 to J.K.), for Scientific Research on Innovative Areas (23116506 to J.K.), for Scientific Research on Priority Areas (19059003 to H.K.), for Challenging Exploratory Research (24659217 to J.K.), Leading-edge Research Infrastructure Program (J.K. and H.K.); the Young Researcher Overseas Visits Program for Vitalizing Brain Circulation of the Japan Society for the Promotion of Science (JSPS; J.K., H.K., Y.K., T.N.), and for JSPS Fellows (021-07124 to Y.K.); the Ministry of Health and Welfare of Japan (J.K. and H.K.); the Global Center of Excellence Program of the Center of Education and Research for Advanced Genome-based Medicine (H.K.); the Program for Promotion of Basic and Applied Research for Innovations in Bio-oriented Industry (BRAIN to J.K.); and the Yakult Bio-Science Foundation (J.K.).
The authors declare no competing financial interests.
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Kurashima, Y., Amiya, T., Nochi, T. et al. Extracellular ATP mediates mast cell-dependent intestinal inflammation through P2X7 purinoceptors. Nat Commun 3, 1034 (2012). https://doi.org/10.1038/ncomms2023
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