IL-4/IL-13 independent goblet cell hyperplasia in experimental helminth infections
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Intestinal mucus production by hyperplasic goblet cells is a striking pathological feature of many parasitic helminth infections and is related to intestinal protection and worm expulsion. Induction of goblet cell hyperplasia is associated with TH2 immune responses, which in helminth infections are controlled primarily by IL-13, and also IL-4. In the study presented here we examine the goblet cell hyperplasic response to three experimental parasitic helminth infections; namely Nippostrongylus brasiliensis, Syphacia obvelata and Schistosoma mansoni.
As expected N. brasiliensis infection induced a strong goblet cell hyperplasia dependent on IL-4/IL-13/IL-4Rα expression. In contrast, and despite previously published transiently elevated IL-4/IL-13 levels, S. obvelata infections did not increase goblet cell hyperplasia in the colon. Furthermore, induction of goblet cell hyperplasia in response to S. mansoni eggs traversing the intestine was equivalent between BALB/c, IL-4/IL-13-/- and IL-4Rα-/- mice.
Together these data demonstrate that intestinal goblet cell hyperplasia can be independent of TH2 immune responses associated with parasitic helminth infections.
KeywordsGoblet Cell Post Infection Helminth Infection Worm Burden Nematode Infection
The following abbreviations were used
periodic acid Schiff
Interleukin (IL)-4 and IL-13 are related cytokines and the dominant mediators of TH2 immune responses [1, 2, 3]. Signalling by both cytokines is dependent on binding to heterodimeric receptors containing the IL-4 receptor α chain (IL-4Rα). Ligand binding results in intracellular signalling pathways activating the TH2 defining transcription factors STAT-6 and/or GATA-3 [4, 5]. This polarisation to a TH2 immune response is essential for the successful resolution of a number of helminth infections [6, 7, 8, 9, 10].
Actual worm expulsion, in nematode infections, is associated with increased IL-13/IL-4Rα/STAT-6 dependent intestinal smooth muscle contractions, epithelial cell turnover and goblet cell hyperplasia [11, 12, 13]. Infections of IL-4-/-, IL-13-/-, IL-4Rα-/- and Stat 6-/- mice with the nematodes Trichuris muris, Heligmosomoides polygyrus and Nippostrongylus brasiliensis have demonstrated a positive relationship between polarisation to a TH2 immune response, goblet cell hyperplasia and worm expulsion [14, 15, 16, 17, 18, 19]. In support of a role for goblet cell derived mucus in worm expulsion in vitro experiments have demonstrated increased viscosity of mileu surrounding N. brasiliensis at an equivalent density to intestinal mucus inhibits worm movement . Moreover, isolation of the goblet cell secreted protein RELMβ/FIZZ2 and incubation with parasitic nematodes in vitro results in impaired chemotactic function in the worm . These observations have led to TH2 induced goblet cell hyperplasia being considered a key mechanistic factor in resolving gastrointestinal related nematode infections [22, 23, 24]
Intestinal goblet cell hyperplasia in Schistosoma mansoni (S. mansoni) infections is driven by parasite eggs traversing the intestine [8, 25], as opposed to nematode infections where adult worms residing in the intestine induce the goblet cell responses [8, 9, 26]. S. mansoni eggs produced by adults residing in the mesenteric venules move from the blood vessels through the intestine passing to the lumen. This movement of eggs generates considerable tissue damage as well as inducing a strong mucosal response in the intestine [8, 27]. As with nematode infections, S. mansoni induced mucus production has been considered to be TH2 dependant [22, 28, 29, 30].
In this study we examined goblet cell hyperplasia in response to infection with the nematodes N. brasiliensis and Syphacia obvelata and the trematode S. mansoni. As already published N. brasiliensis infection induced a goblet cell hyperplasic response dependent on IL-4/IL-13/IL-4Rα expression . However, infection with the nematode S. obvelata did not increase goblet cell hyperplasia in the host colon, irrespective of IL-4Rα expression. Such data demonstrates that IL-4Rα driven goblet cell hyperplasia may not be essential for the clearance of all gastro-intestinal nematode infections. Furthermore, we also show S. mansoni induced goblet cell hyperplasia to be independent of IL-4/IL-13 responsiveness. This data represents the first demonstration of goblet cell hyperplasia and mucus production in response to helminth infections being independent of IL-4/IL-13.
N. brasiliensis infection induces IL-4/IL-13 dependent goblet cell hyperplasia while S. obvelata infection does not induce goblet cell hyperplasia
Examination of IL-4/IL-13 dependent goblet cell hyperplasic responses in the intestinal niches utilised by the nematodes N. brasiliensis and S. obvelata infections was carried out in BALB/c, IL-4/IL-13-/-, IL-4-/- and IL-4Rα-/- mice.
Together these data demonstrate that S. obvelata infections do not induce a colonic mucus response even though levels of IL-4 and other TH2 cytokines are significantly increased 
Schistosoma mansoni induces goblet cell hyperplasia in the intestine in an IL-4/IL-13 independent manner
Our data demonstrates that (i) goblet cell hyperplasia is dependent on helminth species and (ii) IL-4/IL-13 responsiveness is not required for induction of S. mansoni egg induced goblet cell hyperplasia.
It has previously been demonstrated that N. brasiliensis  and S. obvelata  infected IL-4-/-, IL-13-/- and IL-4Rα-/- mice have impaired worm expulsion, while in S. mansoni infections IL-4/IL-13 signalling is essential for host survival . A common feature of both N. brasiliensis and S. mansoni infections is the hosts' goblet cell hyperplasic response to the parasite. Such responses have previously been considered to be dependent, in part at least, on the hosts TH2 polarised immune response [9, 32]. From the data presented here and in other studies this does indeed appear to be the case in N. brasiliensis infections[6, 8, 9]. Work on other parasitic nematode models such a T. muris also show a TH2 dependent worm expulsion and goblet cell response . However, in this study we have demonstrated that this may not be the case for all intestinal nematode infections.
Following oral infection with S. obvelata eggs, larvae emerge in the hosts small intestine at 7 day PI . From here the larvae migrate, mature and establish the definitive infection in the hosts cecum and colon. We found the hosts TH2 immune response to peak at day 7 PI and then decreases from at least day 14 PI. Previous work has shown that by day 35 PI this response is undetectable . Together, these data demonstrate a transient TH2 response to this infection. TH2 responses in other intestinal nematode infections result in strong goblet cell hyperplasic responses [14, 17, 18, 19]. However, mice infected with S. obvelata failed to generate hyperplasic goblet cell responses, suggesting that TH2 induction of intestinal mucus responses is not a common feature of intestinal nematode infections, or that the TH2 response needs to be sustained. Other factors such as prostaglandins , cholinergic  and non-cholinergic  agonist may also play a role. Additionally, the different niches occupied by various species of parasitic nematodes could effect the host response to them . S. obvelata infections do not cause major pathology in the intestine  as opposed to N. brasiliensis and T. muris which cause considerable histological damage to the hosts intestinal architecture [9, 22]. Such differences in worm pathogenicity may explain the lack of a goblet cell response in S. obvelata infections, irrespective of the hosts TH2 polarisation .
S. mansoni infection induces a strong TH2 response initiated by worm egg production at week 4 PI and persists throughout the infection . Associated with this are significant levels of goblet cell hyperplasia in the intestine [25, 31]. S. mansoni egg antigens have previously been shown to also induce goblet cell hyperplasia in the lung in a IL-4Rα dependent manner . However the role of IL-4Rα in goblet cell hyperplasia in the intestine during the live infection has not been shown. An explanation for the IL-4Rα independent hyperplasia described here could be the mode of S. mansoni infection and its interaction with the hosts' tissue. S. mansoni eggs cause pathology from the adventitial surface of the intestine, as opposed to nematodes driving the pathology from the lumen. We propose that the severe tissue damage resulting from the eggs migration from the adventitial surface to the lumen is capable of initiating a goblet cell response, independently of IL-4 and IL-13 signalling during S. mansoni infection.
In addition to IL-4/IL-13 other cytokines may act to induce goblet cells hyperplasia. IL-9 and IL-5 have previously been shown to play a role in directly inducing IL-4/IL-13 independent goblet cell hyperplasia in lung models [38, 39]. IL-9 overexpressing transgenic mice infected with S. mansoni do have increased goblet cell hyperplasia . However IL-9 transgenic mice also had increased IL-4 and IL-13 compared to wild type mice, and therefore it cannot be concluded that IL-9 directly increases goblet cell hyperplasia. Furthermore IL-9 levels are decreased in N. brasiliensis infected IL-4Rα-/- mice . As such IL-4/IL-13 independent intestinal goblet cell hyperplasia may not be due to increased IL-9. No clear reports linking IL-5 to goblet cell hyperplasia during S. mansoni infection have reported. As IL-4Rα-/- mice have decreased IL-5 expression it is also unlikely that IL-5 induces intestinal goblet cell hyperplasia in S. mansoni infections .
Our results demonstrate for the first time that intestinal goblet cell hyperplasia in response to parasitic helminth infections can occur independently of IL-4/IL-13 signalling and that intestinal nematode infections may not always induce a goblet cell response.
IL-4-/-  IL-4/13-/- and IL-4Rα-/-  mice were generated on a BALB/c background. BALB/c mice were used as controls in all experiments. All mice were age and sex matched. Mice were kept in the Health Science Faculty animal unit of the University of Cape Town (UCT), in individually ventilated cages under specific-pathogen-free (SPF) conditions. All experiments were performed in accordance with guidelines laid down by the Animal Ethics Research Board of UCT (Cape Town, South Africa).
Parasites and infection
Infection and recovery of S. obvelata were performed as previously described . Briefly, eggs of S. obvelata used for infection were collected from the caeca of naturally infected mice (IL-4/13-/-, and IL-4Rα-/-) maintained in barrier facilities. The caeca were collected in 0.65% NaCl, cut open, and submerged in a gauze mesh at the mouth of a conical flask for 1 to 2 h at 37°C to allow the worms to migrate out. Worm burdens were assessed on various days post infection. After being washed in 0.65% NaCl, worms were crushed and their eggs were isolated by passage through 70 μm nylon cell strainers (BD Falcon, BD Biosciences, Belgium). Each mouse was inoculated orally with 500 eggs using oral dosing cannulae (VetTech, Cheshire, United Kingdom).
N. brasiliensis nematodes were kindly provided by Klaus Erb, (Wurzberg, Germany). Mice were subcutaneously injected with 750 L3 larvae of N. brasiliensis. Analysis of numbers of adult worm numbers in the intestine was determined as previously described .
Naïve sex-matched mice from 6 to 10 weeks of age were percutaneously infected with 70 to 80 live cercariae of a Puerto Rican strain of S. mansoni obtained from infected Biomphalaria glabrata snails. Eight weeks post infection the intestine was surgically removed. Ileum and colon were removed 2 cm proximal and 0.5 cm distal to the caecum, respectively . Approximately 2 cm of tissue was weighed and digested in 5 ml of 5% potassium hydroxide overnight at 37°C. The digests were vortexed and centrifuged at 100 g for 5 min to pellet eggs. The supernatant was aspirated until 1–2 mls remained. The eggs were vortexed and counted in 50 μl in triplicate. The counts were presented as eggs per gram of tissue as previously described [43, 44]
Tissue samples were fixed in a neutral buffered formalin solution. Following embedding in paraffin, samples were cut into 5–7 μm sections. Sections were stained with periodic acid Schiff reagent (PAS). The number of positively stained cells per five villi or crypts was counted by light microscopy for small intestine or colon, respectively. All samples were randomized and counted in a blinded manner. Photomicrographs were captured using a Nikon 5.0 Mega Pixels Color Digital Camera (Digital SIGHT DS-SMc).
Splenocyte restimulation and IL-4 cytokine ELISA
Single cell splenocyte suspensions were prepared from spleens removed from infected (days 7 and 14 PI) and uninfected mice. 1 × 106 splenocytes per ml were cultured in IMDM (Gibco) media supplemented with 10% fetal calf serum (Gibco) for 72 h at 37°C in 96 well plates pre-coated with either PBS or 20 mg/ml anti-CD3 (clone 145-2C11). Cells were then centrifuged at 1200 rpm for 5 min and the supernatants collected. Supernatent IL-4 concentrations were then determined by ELISA as described previously .
Data are presented as means ± standard error of the mean (SEM), and the significant differences were determined using Student's t test (Prism software ).
This work was supported by grants from the Welcome Trust, (UK), National Research Foundation (South Africa), The Royal Society, (UK) and MRC (South Africa). B.D. is a postdoctoral researcher of the Fonds National de la Recherche Scientifique (FNRS). For technical assistance we would like to thank Mrs Marilyn Tyler, Mrs Wendy green, Mr Reagan Peterson and Mrs Zenaria Abbas. Dr Natalie Nieuwenhuizen and Mrs J. Claire Hoving are thanked for critically readying the manuscript.
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