Abstract
The intestinal tract is a common site for different types of infections including viruses, bacteria, and helminths, each requiring specific modes of immune defense. The intestinal epithelium has a pivotal role in both immune initiation and effector stages, which are coordinated by immune-type specific cytokines such as IFNγ, IL-13 and IL-22. Here, we study intestinal epithelial immune responses using organoid image analysis based on a convolutional neural network, transcriptomic analysis, and in vivo infection models. We find that IL-22 and IL-13 both induce genes associated with goblet cells, but their phenotypes are dichotomous. Moreover, only IL-13 driven goblet cells are associated with classical NOTCH signaling. We further show that IL-13 induces BMP signaling, which acts in a negative feedback loop in immune type 2 driven tuft cell hyperplasia. This is associated with inhibiting Sox4 expression to putatively limit the tuft progenitor population. Blocking BMP signaling with the ALK2 inhibitor DMH1 interrupts the feedback loop, resulting in greater tuft cell numbers both in vitro and in vivo after infection with Nippostrongylus brasiliensis. Taken together, these novel aspects of cytokine effector responses reveal an unexpected and critical role for BMP signaling in type 2 immunity, which can be exploited to tailor epithelial immune responses.
Introduction
Gut infections remain a common threat for patients and are an immense burden on health systems worldwide (1). Resistance to intestinal pathogens relies on the capacity of the immune system to mount an appropriate response. For example, one requires a different type of response to intracellular viruses compared to extracellular pathogens including bacteria or parasites. Cytokines are key participants in polarizing the immune response by altering the cellular composition and state. Innate lymphoid cells (ILCs) are tissue resident immune cells which are early responders to infections and create a local cytokine environment. ILCs are classically divided into three groups and secrete IFNγ (group 1), IL-13 (group 2), and IL-22 (group 3), and which ILC subtype is dominant depends on the pathogenic challenge (2).
In addition to defining the immune landscape, cytokines directly affect intestinal epithelial cells (IECs) to drive immune-type specific responses (3). The intestinal epithelium consists of a single layer of cells and is responsible both for taking up nutrients as well as providing a protective barrier. One of the hallmarks of IECs is their rapid turnover (3-5 days), which allows for prompt cellular responses, for example, to expand goblet cells which can produce protective mucus. This plasticity of IECs makes them particularly well-suited to defend against pathogens (4).
In addition to responding to immune cues, the epithelium can also be involved in tailoring immune responses. For example, tuft cells, which are important for defending against parasitic helminths, are the main source of IL-25 to control ILC2 populations both in homeostasis and upon helminth infection (5–7). As tuft cells rapidly expand upon exposure to type 2 cytokines, they exemplify both how the intestinal epithelium changes upon an immune response and how it can partake in shaping it. Of note, tuft cells are not only important in immunity to helminth infections; activation of tuft cells by succinate is protective in a murine model of colitis, and reduced tuft cell numbers are found in patients with Crohn’s disease that have more severe inflammation (8). Thus, tuft cells have been gaining interest as important regulators of intestinal diseases (9), and the discovery of regulatory mechanisms could have clinical ramifications.
Intestinal organoids are self-organizing structures that are useful to study epithelial (stem) cell biology (10). They are particularly instructive to identify epithelial-intrinsic responses as they lack any other cell type normally present in vivo, such as fibroblasts. This also means their culture medium requires addition of growth factors normally supplied by fibroblasts, such as those that target pathways such as WNT and BMP. In addition, organoid cultures come with challenges as most metrics cannot capture the complexity of these large multicellular structures. To capture this complexity, a study used single cell RNA sequencing (scRNA-seq) to systemically compare single cell responses to cytokines of the three immune environments (3). However, there are still many unclear aspects to how cytokines induce epithelial responses, especially mechanistically. Here we combine quantitative imaging with bulk RNA-seq to define how cytokines intercept developmental pathways to instruct epithelial differentiation and maturation. Most prominently, we identify a feedback loop by which IL-13 induced tuft cell hyperplasia is self-limiting in a BMP-dependent manner, and confirm this in a murine helminth infection model using N. Brasiliensis.
Results
IFNγ, IL-13, and IL-22 uniquely affect organoid growth and morphology
Intestinal organoids grow as a morphologically heterogeneous population, where a fraction of organoids grow as immature “spheroids” and the rest form mature “budding” organoids. Lgr5+ stem cells and Paneth cells are found in the buds in budding organoids (mimicking crypts) while spheroids consist of less differentiated, proliferating cells (11). Building on our recent work on organoid segmentation (12), we here developed an automated image analysis pipeline that segments organoid objects from the background and subsequently classifies them into “spheroid” or “budding” categories based on a convolutional neural network (Fig. 1A). This includes an optional manual correction step for organoids that were difficult to automatically segment or classify (Fig. S1A). Comparing manually verified with automatically classified and segmented images had a good correlation in analysis of >20,000 organoids (Fig. S1B). Expectedly, we find that in time the number of spheroids decrease and appear darker in appearance, confirming that our systematic approach captures what is observed visually (Fig. S1C,D,E).
To mimic different types of immune responses, we treated organoids with key cytokines IFNγ, IL-13, or IL-22. As was previously found (13, 14), long term IL-22 or IFNγ treatment ultimately leads to organoid disintegration (Fig. S1F). At an earlier time point (day 2), this is characterized by a darker appearance, reduced percentage of spheroids, and an increased percentage of budding organoids (Fig. 1B,C and S1G). In contrast, a population of IL-13 treated organoids form large spheroids at day 2 (Fig. 1C and S1G).
Tuft cells are a specific epithelial cell type involved in type 2 immunity, and induced by IL-13 (6, 7). Tuft cells in organoids share the characteristic shape and F-actin brush with their in vivo counterparts (Fig. S2A) (15). We next combined our classification setup with confocal imaging to automatically quantify tuft cells in organoid subtypes. This configuration allows for classification and counting of tuft cells in hundreds of organoids and supports both automatic estimates of tuft cell number and a more accurate manually curated count (Fig. S2B). Indeed, we find that tuft cells primarily appear in budding organoids both in control and IL-13-treated conditions (Fig. S2C,D,E). Together, these data show that classification of organoids combined with confocal imaging provides a tractable measure of epithelial cellular responses.
IFNγ, IL-13, and IL-22 uniquely affect RNA expression in organoids in a manner aligned to in vivo infection profiles
To assess in detail how IFNγ, IL-13, and IL-22 affect intestinal epithelial cells we performed bulk RNA-seq on organoids treated with indicated cytokines for 24 hours compared to untreated controls (Fig. 1D). The different cytokines showed up-regulation of unique genes that grouped separately in a PCA plot, and each cytokine induced different GO-terms, highlighting the different effector responses required to each type of immune response (Fig. 1E,F, S3A-D).
To investigate to what degree cytokines control the epithelial response in vivo, we performed RNA-seq on intestinal epithelium from mice infected with Nippostrongylus brasiliensis or Citrobacter rodentium, which are classical intestinal infection models for a parasitic and extracellular bacterial infection respectively (Fig. S4A). Intestinal epithelium infected with N. brasiliensis did show the expected induction of tuft cells (Fig. S4C,D,E) and had up-regulation of GO terms associated with wound healing (Fig. S4F). Intestinal epithelium infected with C. rodentium had up-regulation of GO-terms associated with inflammatory response (Fig. S4G). We found that epithelium from duodenum isolated from N. brasiliensis infected mice was similar to IL-13 treated-organoids (Fig. 1G). In contrast, colonic epithelium isolated from C. rodentium infected mice aligned with IL-22- and IFNγ-treated organoids using gene set enrichment analysis (GSEA) (Fig. 1G). A caveat to the analysis of C. rodentium analysis is that this epithelium is isolated from colon and not small intestine. The correlation with IL-13 induced genes in N. brasiliensis infected epithelium and IL-22 induced genes in C. rodentium infected intestinal epithelium aligns with the standard model of the involvement of these cytokines in specific immune responses and indicates that treating intestinal organoids with cytokines provide a relevant model to, in part, mimic in vivo epithelial responses.
IL-13 and IL-22 induce different gene signatures in goblet cells
To test the effect of IFNγ, IL-13 and IL-22 on cell lineage differentiation, we used cell-type specific gene signatures acquired through scRNAseq (16). GSEA revealed that these cytokines broadly affect intestinal cell lineage differentiation in an expected manner (Fig. 2A). For example, giving IL-13 to organoids induced a tuft cell signature, supported by tuft cell staining in vitro (Fig. S2C) and in vivo upon N. brasiliensis infection (Fig. S4C,D,E). In addition, both IL-13 and IL-22 induced a goblet-cell associated gene signature (Fig. 2A). However, close examination showed that each cytokine induced a different set of goblet-cell genes with relatively little overlap both after 24 and 72 hours of cytokine stimulation (Fig. 2B, S5A), see supplementary file 2 for complete gene lists. This is exemplified by goblet cell markers Muc2 and Clca1 being specifically induced by IL-13 whereas another goblet cell marker, RELMβ (Retnlb), was induced more strongly by IL-22 (Fig. 2C, S5B). Even though not all mucins are goblet cell specific (17), we found mucin genes to have different expression patterns between IL-13 and IL-22 treatment (Fig. S5C). Confocal staining confirms that MUC2 was induced by IL-13 (Fig. 2D,F), and that RELMβ was more strongly induced by IL-22 (Fig. 2E,G). We noted that IL-22 induced (RELMβ+) goblet cells also looked different from those induced by IL-13 and often lacked large granule-like structures (Fig. 2E). To determine if these cells where positive for Muc2 by mRNA, we combined staining of Muc2 by RNAscope with MUC2 protein staining (Fig. S5D). We found that IL-22 led to the expansion of Muc2-high cells with patterns mimicking (RELMβ+) staining (Fig. S5D). These cells also had low MUC2 protein levels. Canonical differentiation of goblet cells occurs through inhibition of NOTCH and relies on transcription factors ATOH1 and SPDEF (18). Indeed, IL-13 induced Atoh1 and Spdef, however, IL-22 did not, indicating that IL-22 induces goblet cell genes in a non-typical manner (Fig. 2H, S5E). It is not clear from these results what mechanism leads to induction of IL-22 dependent goblet cell, but RNAseq of early time points after IL-22 stimulation show that Relmβ is induced after just a few hours and GSEA of IL-22 specific goblet cell genes show significant enrichment after just 4 hours (Fig. S5F, 2I). These results indicate that IL-22 specific goblet cell genes are relative direct targets of IL-22. Furthermore, GO-term analysis of the goblet cell genes uniquely induced by IL-13 and IL-22 revealed different terms, for example, “response to endoplasmatic stress” was the top GO term associated with goblet cell genes induced by IL-22 (Fig. S5G,H). Taken together, we propose that cytokine-driven goblet cell responses are linked to their function. IL-13 would primarily induce mucus to aid in parasite clearance whereas IL-22 responses are characterized by induction of antimicrobials to kill extracellular pathogens. More specifically, IL-13 leads to a quantitative increase in relative goblet cell numbers, whereas IL-22 treatment leads to a change in qualitative goblet cellular state including the induction of high levels of RELMβ.
BMP signaling is associated with IL-13 and limits tuft cell differentiation in vitro
We were interested in how cytokines control mechanisms that define cell fate in the intestinal epithelium. Intestinal epithelium relies on NOTCH-, WNT-, BMP- and HIPPO-signaling to maintain homeostatic differentiation of cell lineages. We hypothesized that cytokines may use these developmental pathways in directing epithelial cell differentiation. We generated gene sets for these different pathways from published transcriptome datasets (19–22). GSEA analysis revealed that cytokines, and in particular IL-13 and IL-22, alter transcription of genes normally associated with HIPPO, NOTCH, and BMP pathways (Fig. 3A).
We were somewhat surprised to find a strong enrichment of BMP signaling upon IL-13 treatment. BMP members are traditionally expressed by mesenchymal cells, so it is unclear how IL-13 may induce BMP signaling. Nonetheless, established BMP target genes Id1 and Id3 (20), are upregulated specifically after IL-13 treatment (Fig. 3B). Next, we assessed the expression pattern of the TGF-β family members and surprisingly found that IL-13 robustly induced Bmp2 and Bmp8b but not any other members (Fig. 3C, S6A). The change in the Bmp2 gene also was reflected with an increase of BMP2 protein secreted by organoids stimulated with IL-13 (Fig. 3D). In support, there was also an increase of Bmp2 during a N. brasiliensis infection (Fig. 3E). Interestingly, Haber et al. lists Bmp2 as a bona fide tuft cell marker in their gene sets from plate-based scRNAseq of small intestinal epithelium (Fig. 3F) (16). The connection between tuft cells and IL-13 signaling is further highlighted by the fact that tuft cells specifically expressed high levels of IL13ra1 as noted by Haber et al., whereas IL4ra or other cytokine receptors did not have such skewed cell-type specific receptor expression (Fig. S6B-D). In addition, tuft cells have increased pSTAT6 levels compared to other lineages (23). To test whether BMP signaling affects tuft cell differentiation, we compared organoids grown in normal EGF, NOGGIN, and RSPO (ENR) media with organoids grown without the presence of the BMP antagonist NOGGIN (ER media). Thus, taking away the obstructing factor for BMP activation. Organoids grown with NOGGIN in the media showed enrichment for a tuft cell signature and had higher expression of established tuft cell markers (Fig. 3G,H). Furthermore, antibody staining of the tuft cell marker DCLK1 revealed higher levels of tuft cells in organoids grown in the presence of NOGGIN (Fig. 3I,J).
BMP signaling acts as a feedback loop to limit tuft cell expansion
Tuft cells are crucial mediators of parasitic immunity. In a feed-forward loop, tuft cells amplify ILC2s by expressing IL-25, and ILC2s, in turn, express IL-13 to expand tuft cells (5–7). Our findings so far may suggest a novel mechanism that IL-13 treatment induces an epithelial-intrinsic feedback loop mediated by BMP signaling. To further investigate this, we tested the ALK2 (BMP type I receptor) inhibitor dorsomorphin homolog 1 (DMH1) in combination with IL-13 (24) (Fig. 4A). We found that DMH1 completely blocked the induction of canonical BMP target genes Id1 and Id3 (Fig. 4B), but did not affect IL-13-induced Bmp2 expression (Fig. 4C). Furthermore, the overall enrichment of BMP signaling target genes by IL-13 is blocked by DMH1, without modulating the effect of IL-13 on HIPPO or NOTCH target genes (Fig. 4D). Although DMH1 in itself did not change expression of tuft cell-associated genes such as Dclk1, Pou2f3, Trpm5, and Alox5, it did increase the expression of these genes when combined with IL-13 (Fig. 4E). The tuft cell marker gene Il25 could not be detected in our RNAseq, but we did see an increase in Il25 in IL-13+DMH1 treatmed compared to DMH1 alone when we tested this separately by qPCR (Fig. S7A). In support, the tuft cell gene signature was enriched in IL-13 + DMH1 compared to IL-13 by GSEA analysis while no other cell type gene signature was altered (Fig. 4F). Confocal staining confirmed the specific enrichment of tuft cells upon combination treatment of IL-13 and DMH1 (Fig. 4G,H,I). In addition, we noted that IL-13 also induced expression of the TGF-β induced gene Tgfbi, independently of ALK2 (Fig. 4J), and this also occurred after N. brasiliensis infection (Fig. 4K). BMP signaling is complex and is mediated by multiple receptors. For example, BMP2 can activate both SMAD1/5/8 (BMP) and SMAD2/3 (TGF-β) signaling (25). Therefore, we decided to also test SB525334, an inhibitor for the TGF-β type I receptor ALK5. Just as seen with DMH1, we see an increase in IL-13 induced tuft cells in organoids treated with SB525334 in a dose-dependent manner (Fig. 4L, S7B,C). Together, this supports a model in which activation of BMP and/or TGF-β signaling limits IL-13-induced tuft cell differentiation, thus, providing a feedback loop to limit tuft cell expansion during immune responses.
IL-13 activates BMP signaling in stem cells
To gain further insight into what role BMP signaling plays in the effect of IL-13 on the intestinal epithelium we stimulated small intestinal organoids with IL-13 for 1, 4, 8 and 24 hours with and without DMH1 (Fig. 5A). We found that IL-13 itself rapidly affects the transcriptome with 91 significantly changed genes after 1 hour compared to untreated, and 770 genes after 8 hours (p<0.01). In contrast, comparing DMH1+IL-13 vs. IL-13 we found a slower response with only 13 significantly changed genes after 8 hours, but 188 genes after 24 hours (p<0.01) (Fig. 5B). This suggests that BMP target genes are not early response genes upon IL-13 treatment. In accordance, we find that Bmp2 and Bmp8b is rapidly induced after 1 hour (Fig. 5C, S8A), whereas maximal upregulation of canonical BMP target genes Id1 and Id3 and TGF-β target gene Tgfbi occurs only after 24 hours (Fig. 5D, S8B). Together, we propose that IL-13 mediated BMP signaling is mediated by rapid induction of BMP family members such as Bmp2 and Bmp8b to subsequently activate BMP receptors.
We have found that BMP signaling limits IL-13-mediated tuft cell expansion (Fig. 4 and 5). To determine the cellular sequence of events, we downloaded and re-analyzed a scRNAseq data set from small intestinal organoids that were treated with IL-13 (Fig. 5E) (3). We split the tuft cell population in two, and by RNA velocity analysis we found that there is a tuft progenitor (with closer proximity to the stem cell population) and a mature tuft cell population (Fig. 5F). The mature tuft cells have a high expression of Dclk1, Pou2f3 is expressed in both populations, and Sox4 is specific for tuft cell progenitors (Fig. 5G). The trancription factor Sox4 has previously been found to be important in tuft cell development (26). Although Sox4 has been associated with the intestinal stem cell signature (27), in this dataset it is more highly correlated with progenitor tuft cells (Fig. 5G). Qi et al. found that mice with an inducible epithelial specific knock out of Bmpr1a (ALK3) had up-regulation of Sox4 expression in Lgr5+ stem cells and that Sox4 is down-regulated in Lgr5+ stem cells from intestinal organoids stimulated with BMP4 (20), indicating that BMP signaling might actively regulate the amount of Sox4 positive tuft cell progenitors. To investigate where BMP signaling affected tuft cell development we plotted Id1 and Id3 expression and found them to be specifically induced in stem cells by IL-13 (Fig. 5H). Furthermore, Sox4 is rapidly induced by IL-13 before it returns to homeostasis levels after 24 hours and this down-regulation is not seen in 24 hours of IL-13 stimulation with DMH1 (Fig. 5I). This result is supported by our 72 hour stimulation data where we see an up-regulation of Sox4 in IL-13 + DMH1 compared to IL-13 (Fig. 5J). We were not able to associate receptor (Acvr1) expression to stem cells specifically (Fig. S8C), so how stem-cell enriched responses occur is unclear. In summary, these data indicate a model where IL-13 induces differentiation of stem cells into tuft cell progenitors positive for Sox4. At the same time, IL-13 induces production of BMP signaling molecules, which act on stem cells and inhibits them from developing into Sox4 positive tuft cell progenitors.
BMP signaling restricts N. brasiliensis induced tuft cell expansion in vivo
Organoid work allows us to study intestinal epithelial mechanisms in isolation. However, in vivo there are many additional cell types that together orchestrate immunity to infection. To investigate the role of ALK2 signaling in N. brasiliensis-induced tuft cell hyperplasia, we injected mice with either DMH1 or its solvent (DMSO) intraperitoneally every other day starting one day before infection (Fig. 6A). Confocal staining of DCLK1 revealed an increase in the number of tuft cells at both day 6 and day 8 after infection when comparing DMH1-treated to DMSO-treated animals (Fig. 6B,C). The increase in tuft cells was also associated with a non-significant increase in Il25 but not Il13 (Fig. S9A). No difference was found in RELMβ or UEA1 (goblet) positive cells, indicating that the difference is specific to tuft cells (Fig. 6D-F).
To test if BMP/TGF-β signalling is altered during infection we performed pSMAD2 staining (Fig. 7A,B). We found that there was a significant induction of nuclear pSMAD2 levels in crypt cells of infected mice compared to uninfected mice, and that this induction required ALK2 signalling as it did not occur in DMH1-treated mice (Fig. 7A,B). Based on our organoid work, we proposed that BMP/TGF-β signalling leads to repression of Sox4 (Fig. 5G,I,J). Indeed we find a reduction of crypt-base located Sox4 levels after infection and this repression did not occur in DMH1-treated animals (Fig. 7C,D). As reported by others, we found Sox4 enriched at the stem cell zone (26, 27), however, the reduction of Sox4 did not lead to a reduction of numbers of intestinal stem cells, as measured by counting OLFM4+ cells in crypts (Fig. 7E,F). Nor did it affect crypt proliferation as assessed by Ki67 staining (Fig. S9B,C) or apoptosis as assessed with cleaved Caspase3 staining (Fig. S9D,E). Finally, we investigated the association between Bmp2 and tuft cells in vivo by using RNAscope probes for Bmp2 and Dclk1 we found Bmp2 to be associated with tuft cells in the crypt (Fig. 7G,H). This association is not exclusive to tuft cells as we do see Bmp2 in non-tuft cells, especially in the villus tip, a conclusion which is supported by the association of Bmp2 with both enterocytes and tuft cells in organoids stimulated with IL-13 from scRNAseq data from (3) (Fig 7I). Taken together, these results suggest that BMP/TGF-β signaling restricts N. brasiliensis dependent tuft cell expansion in vivo by controlling Sox4 expression.
Discussion
The intestinal epithelium is capable of rapidly altering its cellular composition to defend against pathogens. Here, we provide a comprehensive comparison of how different immune responses mechanistically drive changes in the intestinal epithelium. Specifically, we find that key cytokines associated with different modes of immunity influence developmental pathways to guide changes in epithelial composition.
In recent years, tuft cells have been identified as regulators of intestinal health in general (9), and have taken center stage in the defense against helminth infections specifically (28). They express receptors that help them detect helminths, which together with type 2 cytokines results in their expansion (29, 30). This culminates in a feed forward loop where tuft cell derived IL-25 activates ILC2s and ILC2 derived IL-13 induces tuft cell differentiation (5–7). There are limits to this feed-forward loop though. For example, a putative epithelial-intrinsic PGD2-CRTH2 axis counteracts the IL-13-induced epithelial response (31), and ILC2-expressed CISH blocks ILC2 activation, which in turn limits tuft cell expansion (32). Other, competing, cytokines can also affect this loop as IL-22 inhibits IL-13 induced tuft cell responses (33). Finally, pathogens may also take part. Two studies recently showed that Heligmosomoides polygyrus secreted products can inhibit tuft cell expansion, likely by reprogramming epithelium towards a fetal-like state (34, 35).
Here, we identify that intestinal-epithelial intrinsic Bmp signaling can act as a brake on IL-13-induced tuft cell expansion (Fig. 4). We attribute this feedback mechanism to BMP/TGF-β signaling in general rather than a single BMP protein as we found both Bmp2 and Bmp8b to be induced by IL-13 in organoids. In further support, the ALK5 inhibitor SB525334 show a similar ability as the ALK2 inhibitor DMH1 to increase tuft cell numbers upon IL-13 treatment. Our data indicate that the IL-13-mediated tuft cell hyperplasia is limited by BMP/TGF-β-dependent inhibition of Sox4. Sox4 + tuft cell progenitors are thus initially expanded by IL-13, and then repressed by BMP signalling. It is paradoxical that inhibition of BMP signaling can affect intestinal epithelial stem cells since the crypt is surrounded by BMP antagonists (36). However, these BMP antagonists incompletely block BMP signaling as some pSMAD1/5/8 activation is still found in LGR5+ stem cells (20), and we observed a distinct increase of pSMAD2 in intestinal crypts upon infection with N. brasiliensis (Fig. 7). Furthermore, our experiments comparing IL-13 and IL-13+DMH1 are done in the presence of NOGGIN, a BMP inhibitor, indicating these crypt inhibitors only partly inhibit BMP signaling.
In addition to our findings regarding cytokine-driven tuft cell expansion, we also provide data suggesting that both IL-13 and IL-22 induce goblet cell gene signatures, but that these are different (Fig. 2). There have been conflicting reports in whether IL-22 influence goblet cell levels in intestinal epithelium. Some studies find that the number of MUC2+ cells are unchanged or reduced upon IL-22 treatment (37, 38), however, a study that over express the IL-22 inhibitor IL-22BP in the gut found a reduction in goblet cells (39) and IL-22 knock out mice infected with N. brasiliensis have reduction in goblet cell induction as measured by Periodic acid schiff (PAS) staining (40). Additionally, the goblet-cell effector RELMβ is critical for resistance against both bacterial and helminth infections (41–43). We hypothesize that the difference between IL-13 and IL-22 induced goblet cells is related to the type of immune response. Immunity to parasites requires a ‘weep and sweep’ response, in which goblet cells play an essential role by secreting mucus (weeping) to facilitate the expulsion of helminths (44), whereas other responses may rely less on the induction of mucus and expansion of goblet cell numbers. Instead, we find that IL-22 rapidly induces goblet-cell specific ER stress response genes, which corroborates recent work that identified a pathologically relevant role for IL-22 (45).
Overall, our approach of stimulating intestinal organoids with cytokines has revealed that developmental pathways underlie the cellular compositional changes that occur as part of immune responses taking place in the intestine. In support, a recent study showed that Il17ra signalling in intestinal stem cells induces ATOH1, thereby inducing secretory cells through NOTCH signalling (46). These changes have been confirmed using relevant in vivo models of infection or inflammation. It is important to balance both active immunity/inflammation with resolution of inflammation, and many immunopathologies reflect the importance of maintaining this balance. The discovery of an innate BMP-driven brake on IL-13 induced immune changes suggest that targeting this pathway may therefore be a useful tool to aid resolution of inflammation in clinically relevant diseases.
Supplementary Material
Acknowledgments
We thank the animal care (CoMed) and imaging (CMIC) core facilities that assisted in this work (NTNU). Part of the RNA-seq was done by the Genomics Core Facility at NTNU, which receives funding from the Faculty of Medicine and Health Sciences and Central Norway Regional Health Authority. This work was financially supported by the Norwegian Research Council (Centre of Excellence grant 223255/F50, and ‘Young Research Talent’ 274760 to MJO) and the Norwegian Cancer Society (182767 to MJO). This work was supported by the Wellcome Trust through Investigator Awards to RMM (Ref 106122 and 219530), and the Wellcome Trust core-funded Wellcome Centre for Integrative Parasitology (Ref 104111).
The authors have no conflicting financial interests.
Code and data availability
Code for brightfield and confocal analysis: https://github.com/havardtl/coco
Sequencing data is deposited in the ArrayExpress database (http://www.ebi.ac.uk/arrayexpress) under the following accession numbers:
RNAseq of small intestinal organoids treated with cytokines for 24 hours: E-MTAB-9182
RNAseq of duodenal intestinal epithelium from mice infected with N. brasiliensis: E-MTAB-9183
RNAseq of colon intestinal epithelium from mice infected with C. rodentium: E-MTAB-9184
RNAseq of small intestinal organoids treated for 72 hours with IL-13, IL-22 and DMH1: E-MTAB-9185
RNAseq of small intestinal organoids treated with IL-13 for 0h, 1h, 4h, 8h and 24h with and without DMH1: E-MTAB-10455
RNAseq of small intestinal organoids treated with IL-22 for 0h, 1h and 4h: E-MTAB-11273
References
- 1.Kirk MD, Pires SM, Black RE, Caipo M, Crump JA, Devleesschauwer B, Döpfer D, Fazil A, Fischer-Walker CL, Hald T, Hall AJ, et al. PLOS Medicine. Vol. 12. Public Library of Science; 2015. Dec, e1001921. ISSN: 1549-1676. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Spits H, Artis D, Colonna M, Diefenbach A, Di Santo JP, Eberl G, Koyasu S, Locksley RM, McKenzie ANJ, Mebius RE, Powrie F, et al. Nature Reviews Immunology. 2. Vol. 13. Nature Publishing Group; 2013. Feb, pp. 145–149. ISSN: 1474-1741. [DOI] [PubMed] [Google Scholar]
- 3.Biton M, Haber AL, Rogel N, Burgin G, Beyaz S, Schnell A, Ashenberg O, Su C-W, Smillie C, Shekhar K, Chen Z, et al. Cell. 2018 Nov;175:1307–1320.:e22. doi: 10.1016/j.cell.2018.10.008. ISSN: 00928674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Tetteh PW, Farin HF, Clevers H. Trends in Cell Biology. 2015 Feb;25:100–108. doi: 10.1016/j.tcb.2014.09.003. ISSN: 09628924. [DOI] [PubMed] [Google Scholar]
- 5.Howitt MR, Lavoie S, Michaud M, Blum AM, Tran SV, Weinstock JV, Gallini CA, Redding K, Margolskee RF, Osborne LC, Artis D, et al. Science. 2016 Mar;351:1329–1333. doi: 10.1126/science.aaf1648. ISSN: 0036-8075, 1095-9203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Gerbe F, Sidot E, Smyth DJ, Ohmoto M, Matsumoto I, Dardalhon V, Cesses P, Garnier L, Pouzolles M, Brulin B, Bruschi M, et al. Nature. 7585. Vol. 529. Nature Publishing Group; 2016. Jan, pp. 226–230. ISSN: 1476-4687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.von Moltke J, Ji M, Liang H-E, Locksley RM. Nature. 7585. Vol. 529. Nature Publishing Group; 2016. Jan, pp. 221–225. ISSN: 1476-4687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Banerjee A, Herring CA, Chen B, Kim H, Simmons AJ, Southard-Smith AN, Allaman MM, White JR, Macedonia MC, Mckinley ET, Ramirez-Solano MA, et al. Gastroenterology. Vol. 159. Elsevier; 2020. Dec, pp. 2101–2115.e5. ISSN: 0016-5085, 1528-0012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Hendel SK, Kellermann L, Hausmann A, Bindslev N, Jensen KB, Nielsen OH. Frontiers in Immunology. 2022;13 doi: 10.3389/fimmu.2022.822867. ISSN: 1664-3224. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Dedhia PH, Bertaux-Skeirik N, Zavros Y, Spence JR. Gastroenterology. Vol. 150. Elsevier; 2016. May, pp. 1098–1112. ISSN: 0016-5085, 1528-0012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Serra D, Mayr U, Boni A, Lukonin I, Rempfler M, Meylan LC, Stadler MB, Strnad P, Papasaikas P, Vischi D, Waldt A, et al. Nature. 2019 Apr;1 doi: 10.1038/s41586-019-1146-y. ISSN: 1476-4687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Ostrop J, Zwiggelaar RT, Pedersen M Terndrup, Gerbe F, Bösl K, Lindholm HT, Díez-Sánchez A, Parmar N, Radetzki S, von Kries JP, Jay P, et al. Frontiers in Cell and Developmental Biology. Vol. 8. Frontiers; 2021. ISSN: 2296-634X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Lindemans CA, Calafiore M, Mertelsmann AM, O’Connor MH, Dudakov JA, Jenq RR, Velardi E, Young LF, Smith OM, Lawrence G, Ivanov JA, et al. Nature. 2015 Dec;528:560–564. doi: 10.1038/nature16460. ISSN: 1476-4687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Farin HF, Karthaus WR, Kujala P, Rakhshandehroo M, Schwank G, Vries RGJ, Kalkhoven E, Nieuwenhuis EES, Clevers H. Journal of Experimental Medicine. 2014 June;211:1393–1405. doi: 10.1084/jem.20130753. ISSN: 0022-1007, 1540-9538. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Gerbe F, van Es JH, Makrini L, Brulin B, Mellitzer G, Robine S, Romagnolo B, Shroyer NF, Bourgaux J-F, Pignodel C, Clevers H, et al. Journal of Cell Biology. 2011 Mar;192:767–780. doi: 10.1083/jcb.201010127. ISSN: 0021-9525. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Haber AL, Biton M, Rogel N, Herbst RH, Shekhar K, Smillie C, Burgin G, Delorey TM, Howitt MR, Katz Y, Tirosh I, et al. Nature. 2017 Nov;551:333–339. doi: 10.1038/nature24489. ISSN: 0028-0836, 1476-4687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Pelaseyed T, Bergström JH, Gustafsson JK, Ermund A, Birchenough GMH, Schütte A, van der Post S, Svensson F, Rodríguez-Piñeiro AM, Nyström EE, Wising C, et al. Immunological reviews. 2014 July;260:8–20. doi: 10.1111/imr.12182. ISSN: 0105-2896. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Noah TK, Kazanjian A, Whitsett J, Shroyer NF. Experimental Cell Research. 2010 Feb;316:452–465. doi: 10.1016/j.yexcr.2009.09.020. ISSN: 0014-4827. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Gregorieff A, Liu Y, Inanlou MR, Khomchuk Y, Wrana JL. Nature. 2015 Oct;526:715–718. doi: 10.1038/nature15382. ISSN: 0028-0836, 1476-4687. [DOI] [PubMed] [Google Scholar]
- 20.Qi Z, Li Y, Zhao B, Xu C, Liu Y, Li H, Zhang B, Wang X, Yang X, Xie W, Li B, et al. Nature Communications. 2017 Jan;8 doi: 10.1038/ncomms13824. ISSN: 2041-1723. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Yin X, Farin HF, van Es JH, Clevers H, Langer R, Karp JM. Nature Methods. 2014 Jan;11:106–112. doi: 10.1038/nmeth.2737. ISSN: 1548-7091, 1548-7105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Kim T-H, Li F, Ferreiro-Neira I, Ho L-L, Luyten A, Nalapareddy K, Long H, Verzi M, Shivdasani RA. Nature. 2014 Feb;506:511–515. doi: 10.1038/nature12903. ISSN: 0028-0836, 1476-4687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Herring CA, Banerjee A, McKinley ET, Simmons AJ, Ping J, Roland JT, Franklin JL, Liu Q, Gerdes MJ, Coffey RJ, Lau KS. Cell Systems. 2018 Jan;6:37–51.:e9. doi: 10.1016/j.cels.2017.10.012. ISSN: 2405-4712. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Mohedas AH, Xing X, Armstrong KA, Bullock AN, Cuny GD, Yu PB. ACS Chemical Biology. Vol. 8. American Chemical Society; 2013. Jun, pp. 1291–1302. ISSN: 1554-8929. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Holtzhausen A, Golzio C, How T, Lee Y-H, Schiemann WP, Katsanis N, Blobe GC. The FASEB Journal. 2014;28:1248–1267. doi: 10.1096/fj.13-239178. ISSN: 1530-6860. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Gracz AD, Samsa LA, Fordham MJ, Trotier DC, Zwarycz B, Lo Y-H, Bao K, Starmer J, Raab JR, Shroyer NF, Reinhardt RL, et al. Gastroenterology. 2018 Nov;155:1508–1523.:e10. doi: 10.1053/j.gastro.2018.07.023. ISSN: 0016-5085. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Muñoz J, Stange DE, Schepers AG, Wetering Mvd, Koo B-K, Itzkovitz S, Volckmann R, Kung KS, Koster J, Radulescu S, Myant K, et al. The EMBO Journal. 2012 July;31:3079–3091. doi: 10.1038/emboj.2012.166. ISSN: 0261-4189, 1460-2075. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Schneider C, O’Leary CE, Locksley RM. Nature Reviews Immunology. 2019 Sept;19:584–593. doi: 10.1038/s41577-019-0176-x. ISSN: 1474-1741. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Schneider C, O’Leary CE, von Moltke J, Liang H-E, Ang QY, Turnbaugh PJ, Radhakrishnan S, Pellizzon M, Ma A, Locksley RM. Cell. 2018 July;174:271–284.:e14. doi: 10.1016/j.cell.2018.05.014. ISSN: 0092-8674, 1097-4172. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Nadjsombati MS, McGinty JW, Lyons-Cohen MR, Jaffe JB, DiPeso L, Schneider C, Miller CN, Pollack JL, Nagana Gowda G, Fontana MF, Erle DJ, et al. Immunity. 2018 July;49:33–41.:e7. doi: 10.1016/j.immuni.2018.06.016. ISSN: 10747613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Oyesola OO, Shanahan MT, Kanke M, Mooney BM, Webb LM, Smita S, Matheson MK, Campioli P, Pham D, Früh SP, McGinty JW, et al. Journal of Experimental Medicine. 2021 July;218:e20202178. doi: 10.1084/jem.20202178. ISSN: 0022-1007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Kotas ME, Mroz NM, Koga S, Liang H-E, Schroeder AW, Ricardo-Gonzalez RR, Schneider C, Locksley RM. Mucosal Immunology. 6. Vol. 14. Nature Publishing Group; 2021. Nov, pp. 1295–1305. ISSN: 1935-3456. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Fu Z, Dean JW, Xiong L, Dougherty MW, Oliff KN, Chen Z-mE, Jobin C, Garrett TJ, Zhou L. Nature Communications. 1. Vol. 12. Nature Publishing Group; 2021. Jul, p. 4462. ISSN: 2041-1723. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Drurey C, Lindholm HT, Coakley G, Poveda MC, Löser S, Doolan R, Gerbe F, Jay P, Harris N, Oudhoff MJ, Maizels RM. Journal of Experimental Medicine. 2021 Nov;219:e20211140. doi: 10.1084/jem.20211140. ISSN: 0022-1007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Karo-Atar D, Ouladan S, Javkar T, Joumier L, Matheson MK, Merritt S, Westfall S, Rochette A, Gentile ME, Fontes G, Fonseca GJ, et al. Direct reprogramming of the intestinal epithelium by parasitic helminths subverts type 2 immunity, en, tech rep. 2021 Sept;:2021.09.25.461778. Section: New Results Type: article (bioRxiv)
- 36.Kosinski C, Li VSW, Chan ASY, Zhang J, Ho C, Tsui WY, Chan TL, Mifflin RC, Powell DW, Yuen ST, Leung SY, et al. Proceedings of the National Academy of Sciences. Vol. 104. National Academy of Sciences Section: Biological Sciences; 2007. Sept, pp. 15418–15423. ISSN: 0027-8424, 1091-6490. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Zhang X, Liu S, Wang Y, Hu H, Li L, Wu Y, Cao D, Cai Y, Zhang J, Zhang X. International Journal of Molecular Medicine. Vol. 43. Spandidos Publications; 2019. Apr, pp. 1657–1668. ISSN: 1107-3756. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Zha J-M, Li H-S, Lin Q, Kuo W-T, Jiang Z-H, Tsai P-Y, Ding N, Wu J, Xu S-F, Wang Y-T, Pan J, et al. Cellular and Molecular Gastroenterology and Hepatology. 2019 Jan;7:255–274. doi: 10.1016/j.jcmgh.2018.09.006. ISSN: 2352-345X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Sugimoto K, Ogawa A, Mizoguchi E, Shimomura Y, Andoh A, Bhan AK, Blumberg RS, Xavier RJ, Mizoguchi A. Journal of Clinical Investigation. 2008 Jan;:JCI33194. doi: 10.1172/JCI33194. ISSN: 0021-9738. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Turner J-E, Stockinger B, Helmby H. PLOS Pathogens. Vol. 9. Public Library of Science; 2013. Oct, e1003698. ISSN: 1553-7374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Artis D, Wang ML, Keilbaugh SA, He W, Brenes M, Swain GP, Knight PA, Donaldson DD, Lazar MA, Miller HRP, Schad GA, et al. Proceedings of the National Academy of Sciences. Vol. 101. National Academy of Sciences Section: Biological Sciences; 2004. Sept, pp. 13596–13600. ISBN: 9780404034108, ISSN: 0027-8424, 1091-6490. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Propheter DC, Chara AL, Harris TA, Ruhn KA, Hooper LV. Proceedings of the National Academy of Sciences. 2017 Oct;114:11027–11033. doi: 10.1073/pnas.1711395114. ISSN: 0027-8424, 1091-6490. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Bergstrom KSB, Morampudi V, Chan JM, Bhinder G, Lau J, Yang H, Ma C, Huang T, Ryz N, Sham HP, Zarepour M, et al. Baumler AJ, editor. PLOS Pathogens. 2015 Aug;11:e1005108. doi: 10.1371/journal.ppat.1005108. ISSN: 1553-7374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Gause WC, Rothlin C, Loke P. Nature Reviews Immunology. Nature Publishing Group; 2020. May, pp. 1–12. ISSN: 1474-1741. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Powell N, Pantazi E, Pavlidis P, Tsakmaki A, Li K, Yang F, Parker A, Pin C, Cozzetto D, Minns D, Stolarczyk E, et al. Gut. Vol. 69. BMJ Publishing Group Section: Recent advances in basic science; 2020. Mar, pp. 578–590. ISSN: 0017-5749, 1468-3288. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Lin X, Gaudino SJ, Jang KK, Bahadur T, Singh A, Banerjee A, Beaupre M, Chu T, Wong HT, Kim C-K, Kempen C, et al. Immunity. 2022 Feb;55:237–253.:e8. doi: 10.1016/j.immuni.2021.12.016. ISSN: 1074-7613. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
Code for brightfield and confocal analysis: https://github.com/havardtl/coco
Sequencing data is deposited in the ArrayExpress database (http://www.ebi.ac.uk/arrayexpress) under the following accession numbers:
RNAseq of small intestinal organoids treated with cytokines for 24 hours: E-MTAB-9182
RNAseq of duodenal intestinal epithelium from mice infected with N. brasiliensis: E-MTAB-9183
RNAseq of colon intestinal epithelium from mice infected with C. rodentium: E-MTAB-9184
RNAseq of small intestinal organoids treated for 72 hours with IL-13, IL-22 and DMH1: E-MTAB-9185
RNAseq of small intestinal organoids treated with IL-13 for 0h, 1h, 4h, 8h and 24h with and without DMH1: E-MTAB-10455
RNAseq of small intestinal organoids treated with IL-22 for 0h, 1h and 4h: E-MTAB-11273