Gli1-3 are expressed in the pancreatic stroma and expand during PDA progression

To determine GLI1-3 expression in human PDA, we analyzed epithelial and stromal samples isolated from PDA patients by laser-capture microdissection [40]. GLI1-3 are predominantly expressed in the stroma (Fig 1A–1C), while HH ligands are expressed in the epithelium (S1A Fig). HH receptors are also enriched in the stroma (S2B and S2C Fig), consistent with the paracrine manner of HH signaling in PDA [25,26,28,30,41]. Further, all three GLIs are expressed by multiple types of pre-cancerous lesions, including both pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMNs). Since the stroma consists of diverse cell types, we analyzed a recently published single-cell RNA sequencing dataset [42] to precisely determine which cellular compartments express GLI1-3. Gene expression analysis revealed that fibroblasts are the primary source of GLI1-3 in PDA (Fig 1D).

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Fig 1. Gli1-3 are expressed in the pancreatic stroma and expand during PDA progression.

(A–C). Epithelial vs. Stromal GLI expression in human IPMN tissue (green, n = 19 Epithelial, n = 12 Stromal), PanIN (blue, n = 26 Epithelial, n = 23 Stromal), and PDA (red, n = 197 Epithelial, n = 124 Stromal), determined by LCM-RNAseq [40]. (D) Expression of HH pathway components in human PDA (red, n = 16) and adjacent normal pancreas (blue, n = 3), determined by scRNAseq [42]. Dot size indicates frequency. Dot color intensity indicates expression level. Boxes outline ligands (purple), receptors (orange), and transcription factors (green). Arrow indicates GLI expression in fibroblasts. (E–H) Expression analysis of healthy (E-F), PanIN (G), and PDA (H) pancreata from Gli^lacZ reporter mice (n ≥ 3 for all genotypes). X-gal staining (E, G, H) in blue. Arrowheads indicate lacZ+ cells. Scale bar = 50μm. For immunofluorescent antibody analysis of healthy pancreata (F), antibodies detect β-Galactosidase (β-GAL, green) and fibroblasts (VIM, Red). DAPI (blue) denotes nuclei. Scale bar = 20 μm. Mouse drawing acquired from the open source repository SciDraw.io (doi.org/10.5281/zenodo.3925901).

https://doi.org/10.1371/journal.pgen.1010315.g001

Kras^LSL-G12D/+;Ptf1a^Cre/+ (KC) [43] and Kras^LSL-G12D/+; p53^LSL-R172H/+;Ptf1a^Cre/+ (KPC) [44] mouse models of PDA provide an opportunity to investigate disease progression in a system that faithfully recapitulates human disease. In both models, Cre expression by pancreatic progenitor cells activates oncogenic Kras [43,44]. Induction of acute pancreatitis (via caeruelin injections) synergizes with oncogenic Kras to produce widespread PanIN lesions in KC mice [45]. In KPC mice, CRE also drives the expression of a mutant p53 allele, leading to the spontaneous development of invasive pancreatic tumors [44]. To determine if Gli1-3 expression in mouse models is consistent with human disease, we utilized Gli-lacZ reporter mice [37,46,47]. X-gal staining (Fig 1E) and immunofluorescent (IF) detection of Beta Galactosidase (β-GAL; Figs 1F and S1D and S1E) in healthy mouse pancreata revealed that Gli1, Gli2, and Gli3 are all expressed by fibroblasts surrounding blood vessels and pancreatic ducts. Further, Gli2- and Gli3-expressing fibroblasts also surround acinar cell clusters (Fig 1E and 1F). Gli-lacZ reporter mice were then crossed into KC and KPC models of PDA. X-gal staining of Gli1-lacZ;KC, Gli2-lacZ;KC, and Gli3-lacZ;KC tissue revealed that all three Glis expand within the stroma at PanIN stages (Fig 1G), and immunofluorescent detection of β-GAL indicated that Gli expression remains restricted to pancreatic fibroblasts (S1F–S1I Fig). Further, Gli1-3 are expressed broadly within the tumor stroma of Gli-lacZ; KPC mice (Figs 1H and S1J). Together, these data demonstrate that the patterns of Gli expression observed in mouse models are consistent with human PDA.

Conditional Gli2 and Gli3 deletion in vivo restricts immunosuppressive macrophages and promotes T cell infiltration

The broad, stromal expression of Gli1-3 throughout disease progression raised the question of Gli function in PDA. While Gli1 has established roles in tissue recovery [39] and PanIN progression [48], the roles of stromal Gli2 and Gli3 during PDA progression are unknown. To target Gli2 and Gli3 in fibroblasts in vivo, we crossed the Pdgfrα^CreER-T2 allele [49] into Kras^FSF-G12D/+;Ptf1a^FlpO/+ (KF) [50] mice. In this combined KF;Pdgfrα^CreER-T2 model (Fig 2A), Ptf1a^FlpO/+ drives oncogenic Kras expression and PanIN formation in the pancreatic epithelium, allowing us to utilize a CreER to inducibly delete Gli in pancreatic fibroblasts. Adult KF;Pdgfrα^CreER-T2 mice were given tamoxifen daily for 5 days to induce recombination, followed by two days of caerulein injections to drive acute pancreatitis and initiate PanIN formation [51]. Mice were then harvested 3 weeks later once PanIN lesions established throughout the pancreas. Lineage tracing revealed that the Pdgfrα^CreER-T2 allele effectively labels the neoplastic stroma (S2A Fig), and reduces Gli2 and Gli3 expression by approximately 70% each in KF; Pdgfrα^CreER-T2; Gli2^fl/fl; Gli3^fl/fl (KF;Gli2/Gli3 cKO) mice (S2B Fig). Histologic analysis of KF;Gli2/Gli3 cKO mice revealed a disrupted stroma, including an increased number of stromal cells and a decrease in collagen deposition compared to KF; Gli2^fl/fl; Gli3^fl/fl (KF;Gli2/Gli3 WT) mice (Fig 2B and 2C). However, initial characterization of fibroblasts from KF;Gli2/Gli3 cKO mice revealed no inherent differences in proliferation compared to KF;Gli2/Gli3 WT mice (S2C Fig). To determine which stromal cell types change as a result of Gli2/Gli3 deletion, we performed flow cytometry analysis on KF;Gli2/Gli3 cKO and KF;Gli2/Gli3 WT tissue. Interestingly, we found that total immune cells increase following loss of Gli2 and Gli3, yet total myeloid cells decrease (Figs 2D and S2D and S2E). When we examined different subpopulations of immune cells (Figs 2E–2I and S2D and S2F–S2J), we found a significant reduction in macrophages in KF;Gli2/Gli3 cKO mice (Fig 2E). To assess which types of macrophages are impacted by the loss of Gli2/Gli3, we evaluated the expression of arginase 1 (ARG1), a marker of immunosuppressive tumor-associated macrophages (TAMs). Co-staining with ARG1 and the general macrophage marker F4/80 revealed a decrease in TAMs following the loss of Gli2 and Gli3 (Fig 2F). In contrast to this decrease in immunosuppressive TAMs, we found an increase in total T cells in KF;Gli2/Gli3 cKO mice (Figs 2G and S2D). Analysis of different T cell populations revealed that both CD4+ and CD8+ T cells increased following the loss of Gli2 and Gli3 (Figs 2H and 2I, and S2D and S2H–S2J). Together, these data suggest that fibroblast-specific Gli2/Gli3 deletion disrupts the immunosuppressive microenvironment in pancreatic neoplasia.

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Fig 2. Conditional Gli2 and Gli3 deletion in vivo restricts immunosuppressive macrophages and promotes T cell infiltration.

A) Cartoon depicting experimental strategy. Adult KF; Pdgfrα^CreERt2/+; Gli2^fl/fl; Gli3^fl/fl (KF;Gli2/Gli3 cKO) mice were given tamoxifen (Tx, 200mg/kg) once a day for 5 days. Mice were then given 8 hourly injections of caerulein (C) over 2 days to induce pancreatitis. Pancreata were harvested 3 weeks later. B-C) H&E (B) and Gomori trichrome (C) staining of KF;Gli2/Gli3 cKO mice (right) and KF; Gli2^fl/fl; Gli3^fl/fl (KF;Gli2/Gli3 WT) mice (left). Arrowheads indicate dense pockets of stromal cells. D-E) Flow cytometry analysis of total immune cells (D) and macrophages (E) in KF;Gli2/Gli3 WT and KF;Gli2/Gli3 cKO mice. F) Immunofluorescent antibody detection (left) and quantitation (right) of macrophages (F4/80, red) expressing arginase 1 (ARG1, green). DAPI staining in blue. G-I) Flow cytometry analysis of total T cells (G), CD4+ T cells (H), and CD8+ T Cells (I). N ≥ 3 for all genotypes. All P-values were determined by un-paired t-test. Scale bars = 100μm. Mouse drawing acquired from the open source repository SciDraw.io (doi.org/10.5281/zenodo.3925901).

https://doi.org/10.1371/journal.pgen.1010315.g002

Since immune suppression plays a crucial role in PDA [14], we investigated whether loss of Gli2/Gli3 affects PanIN progression. However, caerulein administration in mutant Kras mice can synchronize and accelerate PanIN lesions [45]. We therefore utilized a spontaneous model in which KF;Gli2/Gli3 cKO mice were aged to 20 weeks, when spontaneous PanIN formation is expected (Fig 3A and 3B). KF;Gli2/Gli3 cKO mice present with reduced collagen deposition (Fig 3C and 3G) and a reduction in macrophage infiltration (Fig 3E and 3I). We also observed a trend toward increased cytoplasmic mucin, a feature of low-grade PanIN [52], in a majority of KF;Gli2/Gli3 cKO mice (Fig 3D and 3H). However, histopathological analysis of the PanIN lesions indicated no difference in PanIN progression between KF;Gli2/Gli3 cKO and KF;Gli2/Gli3 WT mice (Fig 3F). Thus, while loss of Gli2 and Gli3 in the fibroblasts significantly impairs ECM accumulation and reduces the relative proportion of macrophages, it is not sufficient to alter PanIN progression.

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Fig 3. Loss of stromal Gli2 and Gli3 reduces collagen deposition and macrophage infiltration in a spontaneous PanIN model.

A) Cartoon depicting experimental strategy. Adult KF;Gli2/Gli3 cKO mice were given tamoxifen (Tx, 200 mg/kg) once a day for 5 days. Pancreata were harvested at 20 weeks of age. B-D) Histological analysis of KF;Gli2/Gli3 cKO;LSL-tdTomato/+ (bottom) pancreata compared to KF;Gli2/Gli3 WT;LSL-tdTomato/+ tissue (top), including H&E (B), Gomori Trichrome (C), and PAS (D) staining. E) Immunofluorescent antibody detection of macrophages (F4/80, green). DAPI staining in blue. F) Pathology analysis of PanIN progression in KF;Gli2/Gli3 WT;LSL-tdTomato/+ (left) and KF;Gli2/Gli3 cKO;LSL-tdTomato/+ (right) mice. G-I) Quantitation of collagen deposition (G), mucin (H), and macrophages (I) in KF;Gli2/Gli3 WT;LSL-tdTomato/+ and KF;Gli2/Gli3 cKO;LSL-tdTomato/+ mice. J) Gli1 expression (yellow) in KF;Gli2/Gli3 WT (top) and KF;Gli2/Gli3 cKO mice (bottom), determined by RNAscope. Vimentin (VIM) staining in blue. Scale bar = 50 μm. N ≥ 3 for all genotypes. P-values were determined by un-paired t-test. Mouse drawing acquired from the open source repository SciDraw.io (doi.org/10.5281/zenodo.3925901).

https://doi.org/10.1371/journal.pgen.1010315.g003

Combined Gli1-3 deletion drives widespread tissue loss during PanIN progression

While validating our KF;Gli2/Gli3 cKO model, we were surprised to find that Gli1 expression is maintained following the loss of Gli2/Gli3 (Fig 3J). This contrasts with Gli2;Gli3 double mutant embryos, which lack Gli1 expression across multiple developing tissues [53]. We hypothesized that Gli1 could be functioning partially redundantly with Gli2 and Gli3, and that deleting all three Glis would accentuate the phenotypes we observed in KF;Gli2/Gli3 cKO mice. To test this, we utilized Gli1^CreERT2 mice [54], in which a CreER-t2 allele knocked into the endogenous Gli1 locus abolishes Gli1 expression while driving recombination in pancreatic fibroblasts [50]. Crossing this allele into KF mice enabled us to target Gli2 and Gli3 expression in Gli1-expressing fibroblasts during PanIN progression (Fig 4A). RNAscope analysis of KF; Gli1^{CreERT2/CreERT2}; Gli2^fl/fl; Gli3^fl/fl (KF;Gli1/Gli2/Gli3 KO) mice confirmed complete elimination of Gli1 (S3A Fig) and efficient conditional reduction of Gli3 (S3B Fig). Once validated, KF;Gli1/Gli2/Gli3 KO mice were aged to 20 weeks to evaluate spontaneous PanIN progression in the absence of Gli1-3.

Strikingly, combined Gli1/Gli2/Gli3 depletion leads to a dramatic loss of pancreas parenchyma, with concurrent pancreatic lipomatosis, or adipocyte accumulation in the pancreas (Figs 4B–4E and S3C). Pancreatic lipomatosis is observed following extensive acinar cell death [55,56]. Although no differences in cell death are detected between KF;Gli1/Gli2/Gli3 WT and KF;Gli1/Gli2/Gli3 KO tissue at the time of dissection (S3C Fig), the loss of acinar tissue likely occurred earlier in disease progression, resulting in the disrupted state of the pancreas following Gli deletion. Interestingly, the pancreata of Gli1/Gli2/Gli3 KO mice that do not express oncogenic Kras are grossly normal, and do not show any evidence of tissue loss or pancreatic lipomatosis (Fig 4D and 4E). Thus, the combined loss of Gli1/Gli2/Gli3 only compromises tissue integrity in the context of pancreatic carcinogenesis.

In addition to disrupted tissue architecture, the pancreata of KF;Gli1/Gli2/Gli3 KO mice feature an increase in macrophages compared to KF;Gli1/Gli2/Gli3 WT mice (Fig 4F and 4G), in contrast to the decrease in macrophages observed in KF;Gli2/Gli3 cKO tissue (cf. Fig 2E). We did not find any difference in T cell number between KF;Gli1/Gli2/Gli3 KO and KF;Gli1/Gli2/Gli3 WT mice (Fig 4F and 4H). Thus, a baseline level of Gli activity is necessary to maintain pancreas integrity during PanIN progression. Further, total ablation of Gli promotes macrophage infiltration, suggesting that macrophages are sensitive to subtle changes in GLI activity in fibroblasts.

Loss of Gli2 and Gli3 reduces tumor growth through the recruitment of NK cells

To study the role of Gli1/Gli2/Gli3 in tumor growth, we performed tumor implantation experiments with Gli KO pancreatic fibroblasts (Fig 5A). Since germline Gli2 and Gli3 mutants die perinatally [57,58], we utilized Gli^fl/fll mice to derive fibroblast lines from the adult pancreas. Once established, fibroblast lines were infected with either a GFP-expressing adenovirus (WT lines) or a Cre-expressing adenovirus (Gli KO), and Gli deletion was validated by qPCR and western blot (S4A–S4D Fig). Both Gli2/Gli3 KO and Gli1/Gli2/Gli3 KO pancreatic fibroblasts are unresponsive to HH stimulation, while parental line controls remain HH responsive (S4E and S4F Fig). Gli KO fibroblasts were co-injected with KPC-derived tumor cells [59] into the flanks of nude mice, which lack functional T and B cells. Consistent with previous findings [18,60], co-injecting tumor cells with WT fibroblasts produces larger tumors than tumor cells alone (Fig 5B). In contrast, co-injecting Gli2/Gli3 KO fibroblasts with tumor cells fails to promote tumor growth, and produces tumors that are significantly smaller than tumors co-injected with WT fibroblasts (Fig 5B). Given the detrimental effects observed when Gli1, Gli2, and Gli3 are deleted at PanIN stages (Fig 4), we next tested how Gli1/Gli2/Gli3 KO fibroblasts impact invasive tumor growth. Strikingly, co-injection of tumor cells with Gli1/Gli2/Gli3 KO fibroblasts promotes tumor growth to the same degree as parental Gli1 KO fibroblasts and WT control fibroblasts (Fig 5C, cf. Fig 5B). Thus, while reduction of Gli restrains tumor growth, total ablation of Gli promotes tumor growth.

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Fig 4. Combined Gli1-3 deletion drives widespread tissue loss during PanIN progression.

A) Cartoon depicting experimental strategy. Adult KF; Gli1^{CreERT2/CreERT2}; Gli2^fl/fl; Gli3^fl/fl (KF;Gli1/Gli2/Gli3 KO) mice were given tamoxifen (Tx, 200mg/kg) once a day for 5 days. Pancreata were harvested at 20 weeks of age. B-E) Histological analysis of KF; Gli2^fl/fl; Gli3^fl/fl (KF;Gli1/Gli2/Gli3 WT) (left) and KF;Gli1/Gli2/Gli3 KO (right) mice, including H&E staining (B), Gomori trichrome (C, quantified in D), and fat area (E). Green shaded area outlines intestinal tissue (In). Pancreas tissue (Pa) and Lymph nodes (Ln) annotated accordingly. Scale bar = 500μm. P-values determined by ordinary one-way ANOVA with Tukey’s multiple comparisons test. F-H) Immunofluorescent antibody detection (F) and quantitation (G-H) of macrophages (F4/80) and T cells (CD3) in KF;Gli1/Gli2/Gli3 WT and KF;Gli1/Gli2/Gli3 KO mice. Inset scale bar = 10μm. All other scale bars = 100μm. P-values were determined by unpaired t-test. N ≥ 3 for all genotypes. Mouse drawing acquired from the open source repository SciDraw.io (doi.org/10.5281/zenodo.3925901).

https://doi.org/10.1371/journal.pgen.1010315.g004

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Fig 5. Loss of Gli2 and Gli3 reduces tumor growth through the recruitment of NK cells.

A) Cartoon depicting experimental strategy. Tumor cells were injected subcutaneously either alone or in combination with pancreatic fibroblasts into nude mice. (B-C) Volume (mm³) of implanted tumors over time. Tumor cells were injected alone (gray), or co-injected with WT (black), Gli2/3 KO (red), Gli1 KO (blue), or Gli1/Gli2/Gli3 KO (purple) pancreatic fibroblasts. Displayed p-values compare Gli KO fibroblasts to their corresponding parental line control. (D-F) Flow cytometry analysis of total immune cells (D), MDSCs (E), or NK cells (F) in subcutaneous tumors. (G) Cartoon depicting experimental strategy for NK cell depletion experiment. Animals were either treated with an IgG control or an anti-NK cell depleting antibody (anti-asialo GM1). (H) Volume (mm³) of implanted tumors following NK Cell depletion. P-values determined by ordinary one-way ANOVA with Tukey’s multiple comparison test. The displayed p-values compare Tumor + Gli2/Gli3 KO + anti-NK conditions to Tumor + WT + IgG conditions. For all analyses, n ≥ 5 tumors for each experimental condition. Mouse drawing acquired from the open source repository SciDraw.io (doi.org/10.5281/zenodo.3925901).

https://doi.org/10.1371/journal.pgen.1010315.g005

We next wanted to determine why Gli2/Gli3 KO fibroblasts fail to promote tumor growth. To confirm that Gli2/Gli3 KO fibroblasts persist in this transplantation model, we analyzed harvested tumors for the presence of a tdTomato reporter allele expressed by Gli2/Gli3 KO fibroblasts. TdTomato expression was detected by IF in tumors from our Gli2/Gli3 KO fibroblast condition (S5A Fig), confirming that the decrease in tumor growth was not simply due to the death of injected fibroblasts. We next assessed whether Gli2/Gli3 KO fibroblasts impacted the growth of tumor cells directly. However, we found no differences in tumor cell proliferation nor cell death between Gli2/Gli3 KO and WT conditions (S5B and S5C Fig). We also did not find any differences between fibroblast nor endothelial cell abundance across our experimental conditions (S5D and S5E Fig). Given the connection between Gli expression and immune infiltration that we observed at PanIN stages, we next investigated whether this reduction in tumor growth was due to altered recruitment of immune cells. We found no difference in total immune cells between our different experimental conditions (Fig 5D). However, when we analyzed different subpopulations of immune cells (Figs 5E and 5F, and S5F and S5G), we determined that Gli2/Gli3 deletion in fibroblasts leads to a decrease in MDSCs and an increase in NK cells (Fig 5E and 5F). Interestingly, Gli2 KO, Gli3 KO, and Gli1/Gli2/Gli3 KO fibroblasts do not impact MDSC nor NK cell infiltration (S5H–S5J and S6A–S6L Figs), indicating that this effect on immune infiltration is specific to Gli2/Gli3 KO fibroblasts.

We were surprised to find that total myeloid cells and macrophages do not change following the loss of Gli2/Gli3 in our tumor implantation experiments (S5F and S5G Fig), in contrast to our KF;Gli2/Gli3 cKO model (cf. Figs 2E and S2E). We wondered if this difference could be due to the different genetic strains between our experimental systems, as KF;Gli2/Gli3 cKO mice are fully immune competent and possess functional T cells, while nude mice do not. We hypothesized that the loss of Gli2/Gli3 leads to a decrease in immunosuppressive myeloid cells (MDSCs/macrophages) and an increase in cytotoxic immune cells (T cells/NK cells), and the exact cell types involved depend on the model system. We therefore suspected that in the absence of T cells, the enhanced NK cell recruitment in our Gli2/Gli3 KO condition was responsible for antagonizing tumor growth. To test whether this infiltration of NK cells suppresses tumor growth, tumor-bearing mice were treated with an NK cell-depleting antibody (anti-asialo GM1; Figs 5G and S6M–S6P). Tumor growth following co-injection with WT fibroblasts is unaffected by NK cell depletion (Fig 5H), presumably due to NK cells already being excluded from the microenvironment. In contrast, depleting NK cells in tumors co-injected with Gli2/Gli3 KO fibroblasts rescues tumor growth, and the resulting tumors are equivalent in size to tumors co-injected with WT fibroblasts (Fig 5H). These data reveal that the loss of Gli2/Gli3 in fibroblasts restricts tumor growth through the recruitment of NK cells.

Gli activity in fibroblasts directly controls macrophage and T cell migration

To further investigate GLI2/GLI3 function in the pancreatic TME, we transcriptionally profiled Gli2/Gli3 KO pancreatic fibroblasts by RNA sequencing (RNAseq). RNAseq analysis identified over 2,200 differentially expressed genes in Gli2/Gli3 KO fibroblasts compared to WT fibroblasts (S1 Supplemental File). When we filtered the data for membrane-bound and secreted factors [61], we detected a number of differentially expressed ECM components and receptors (S7A and S7B Fig), consistent with the impaired ECM deposition we observe following the loss of Gli2 and Gli3 in vivo (cf. Fig 2C). Further, we detected several cytokines that are upregulated in Gli2/Gli3 KO fibroblasts (Figs 6A and S7A). Specifically, Ccl5 and Cxcl10, two genes encoding T cell and NK cell chemoattractants [62–64], are increased in Gli2/Gli3 KO fibroblasts (Fig 6A). Further, two myeloid-modulating cytokines, Il6 and Il11, [65,66] are reduced in Gli2/Gli3 KO fibroblasts (Fig 6A). We validated these changes in cytokine expression by qPCR (Fig 6B). To determine if these transcriptional changes in Gli2/Gli3 KO fibroblasts are maintained in vivo, we analyzed cytokine expression in KF;Gli2/Gli3 cKO mice by RNAscope. While Il6 expression in fibroblasts is heterogeneous (as expected from previous work [67]), we detected PDPN+ fibroblasts with high Il6 expression in our KF;Gli2/Gli3 WT mice (Fig 6C and 6D). In contrast, no PDPN+ fibroblasts with high Il6 expression were detected in KF;Gli2/Gli3 cKO mice (Fig 6C and 6D), indicating that Gli2 and Gli3 deletion restricts Il6 expression in vivo.

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Fig 6. Gli1-3 in fibroblasts directly control macrophage and T cell migration.

A) Differential expression of cytokines in Gli2/Gli3 WT and Gli2/Gli3 KO fibroblasts, as determined by RNA sequencing. B) qPCR analysis of Ccl5 (left) and Il6 (center) and Il11 (right) in Gli2/Gli3 WT and Gli2/Gli3 KO fibroblasts. C) Il6 expression (red) by fibroblasts (PDPN, green) in KF;Gli2/Gli3 WT and KF;Gli2/Gli3 cKO mice, as determined by RNAscope. Scale bar = 50 μm D) Quantification of high Il6-expressing fields of view in in KF;Gli2/Gli3 WT and KF;Gli2/Gli3 cKO mice (n = 3 for each genotype). High Il6 expression defined as an integrated density value (for the Il6 probe channel) >2300000. P-values for (B) and (D) determined by un-paired T test. E) Cartoon depicting macrophage migration assay experimental strategy. Macrophages and Gli KO fibroblasts are separated by an 8μm pore transwell membrane, and macrophages are allowed to migrate through the membrane for 12h. (F-I) Quantitation of macrophage migration following co-culture with WT fibroblasts (F-I), Gli2 KO fibroblasts (F), Gli3 KO fibroblasts (G), Gli2/Gli3 KO fibroblasts (H), Gli1 KO fibroblasts (I), and Gli1/Gli2/Gli3 KO fibroblasts (I). J) Quantitation of T cell migration following co-culture with WT, Gli2/Gli3 KO, and Gli1/Gli2/Gli3 KO fibroblasts. Recombinant CXCL12 (100 ng/ml) added to media was used as a positive control. P-values for (F-J) were determined by ordinary one-way ANOVA with Tukey’s multiple comparison test.

https://doi.org/10.1371/journal.pgen.1010315.g006

Although these changes cytokine expression are consistent with the decrease in macrophages and increase in T cells observed in vivo, it remained unclear whether Gli2/Gli3 deletion in fibroblasts impacted the function of these immune cells directly. To investigate the interaction between fibroblasts and macrophages mechanistically, we performed macrophage migration assays [68], in which macrophages were placed above fibroblasts on a transwell membrane, and allowed to migrate for 12 hours (Fig 6E). WT fibroblasts consistently promote macrophage migration compared to media alone (Fig 6F–6I). Loss of Gli2 alone does not affect macrophage migration (Fig 6F), while loss of Gli3 alone leads to a partial reduction of macrophage migration (Fig 6G). In contrast, Gli2/Gli3 KO fibroblasts reduce macrophage migration to near baseline levels (Fig 6H). This reduction in macrophage migration is consistent across multiple macrophage phenotypes, including M0, M1, M2, and TAMs (S7C Fig). Interestingly, Gli1/Gli2/Gli3 KO fibroblasts promote macrophage migration to a significantly greater degree than either WT or Gli1 KO parental line control fibroblasts (Fig 6I). These data are consistent with what we observe in vivo (cf. Fig 4G), indicating that the increase in macrophage infiltration in KF;Gli1/Gli2/Gli3 KO mice is directly due to the loss of Gli1/Gli2/Gli3 in fibroblasts. Further, these Gli-dependent effects on macrophages are mediated by secreted factors, as conditioned media from WT and Gli KO fibroblasts recapitulate the effects observed in fibroblast co-culture experiments (S7D Fig). Together, our data indicate that Gli-mediated cytokine expression directly regulates macrophage infiltration in PDA.

To determine if this effect is conserved in human fibroblasts, we performed macrophage migration assays with human pancreatic stellate cells (hPSCs) [7]. We confirmed that hPSCs are HH-responsive, and upregulate the HH target genes GLI1 and PTCH1 in response to HH stimulation (S7E and S7F Fig). In addition, hPSCs promote macrophage migration to a similar degree as WT mouse fibroblasts (S7G Fig). Thus, human pancreatic fibroblasts are both HH-responsive and directly promote macrophage migration.

We next investigated the consequence of fibroblast-specific Gli deletion on T cells. We first evaluated whether Gli expression regulates T cell differentiation and polarization. Our in vivo data indicate that fibroblast-specific Gli2/Gli3 deletion leads to a subtle (and not statistically significant) increase in regulatory T cells (Tregs, S2H Fig). Since Tregs regulate immune suppression in PDA through cross-talk with fibroblasts [61], we investigated whether loss of Gli in fibroblasts impacts Treg differentiation. While T cells co-cultured with Gli2/Gli3 KO fibroblasts do not significantly increase expression of the Treg marker Foxp3, T cells co-cultured with Gli1/Gli2/Gli3 KO fibroblasts do significantly upregulate Foxp3 (S8A Fig). These data are consistent with the notion that Gli1/Gli2/Gli3 KO fibroblasts promote immune suppression, as suggested by enhanced macrophage infiltration both in vitro and in vivo (Figs 4G and 6I). Notably, the expression of functional Treg markers associated with an immunosuppressive phenotype (including Il10 and Tgfb) is not significantly altered across our different Gli KO fibroblast lines (S8B and S8C Fig). These data indicate that fibroblasts regulate T cell differentiation into Tregs in a GLI-dependent fashion, but do not affect the gene expression pattern of established Tregs.

To determine if the loss of Gli in fibroblasts directly regulates T cell infiltration, we performed transwell T cell migration assays with our Gli KO fibroblast lines. While WT fibroblasts do not impact T cell migration, Gli2/Gli3 KO fibroblasts promote T cell migration to the same degree as a potent T cell chemoattractant, CXCL12 (SDF1α) (Fig 6J). In contrast, Gli1/Gli2/Gli3 KO fibroblasts do not promote T cell migration, as the degree of migration is comparable to media alone (Fig 6J). Together, these data corroborate the phenotypes we observe in vivo, and reveal that fibroblasts directly regulate the migration of both macrophages and T cells through GLI-dependent expression of cytokines.

Tumor-supporting and tumor-restricting roles for HH in PDA

Unraveling the role of HH signaling in PDA has proven challenging, as reports have described contradictory roles for the pathway in pancreatic cancer [15,18–20]. However, these seemingly conflicting findings may be an accurate reflection of the complicated and nuanced biology at play in this disease. Our data support a model in which reduced HH signaling promotes tumor growth, while total ablation of HH pathway activity reduces it. Subtle differences in how the pathway is manipulated alters the levels of HH signaling, and tip the scales towards tumor-promoting or tumor-restricting effects.

Our data provide evidence that the activity of multiple transcription factors regulate PDA progression, a theme that has been seen at all levels of the HH signaling pathway. For example, multiple HH ligands (Shh and Ihh) are expressed in PDA [19,28,35], and while loss of a single ligand promotes tumor growth [19,20], the absence of both Ihh and Shh reduces tumor growth [35]. Importantly, this decrease in tumor growth is only seen in a HH-sensitized model (when host mice lack one copy of Gli1), further demonstrating that severe inhibition of HH, not slight reduction, is necessary to reduce tumor growth. Similarly, multiple HH co-receptors (Gas1, Boc, Cdon) regulate pancreatic tumor growth [18]. While loss of two receptors (Gas1 and Boc) promote tumor growth, deleting all three co-receptors reduces tumor growth [18]. These patterns of tumor growth in Gas^-/-;Boc^-/- and Gas1^-/-;Boc^-/-;Cdon^-/- tumors also coincide with increased and decreased vasculature, respectively, indicating that subtle differences in HH signaling levels impact multiple compartments within the TME. Together, these data from throughout the pathway indicate that slight reduction of HH signaling promotes disease progression, while severe inhibition restrains it.

Taken alone, the reduction of tumor growth following severe inhibition of HH signaling would indicate that HH solely supports tumor growth. However, our data also indicate that activation of HH can be protective. Loss of GLI repressor (via Gli3 deletion) reduces the migration of macrophages and decreases tumor growth, demonstrating that HH activation can antagonize PDA. This finding is consistent with previous work, in which pharmacological activation of HH signaling via Smoothened agonist (SAG21k) led to decreased proliferation/abundance of PanIN lesions [20]. Thus, HH has the ability to both promote and restrict tumor growth, and the net effect depends on the levels of HH pathway activity.

Beyond the importance of signaling levels, HH pathway components have functions outside of canonical signal transduction. While the primary role of GLIs is to regulate levels of HH signaling, growing evidence indicates that GLIs also influence PDA through HH-independent mechanisms. Although the canonical HH response is restricted to fibroblasts, tumor cells can aberrantly activate GLIs. Non-canonical upregulation of GLI2 causes tumor cells to adopt a more basal subtype, leading to an increase in mesenchymal markers and a decrease in epithelial markers [69]. This finding is consistent with previous work from our group, where ectopic expression of constitutively active GLI2 drove the formation of undifferentiated tumors [70]. Conversely, antagonizing GLI targets in tumor cells either by knocking down Gli1 [41] or over-expressing a constitutive GLI3 repressor [71] increases tumor cell death and reduces colony formation. Thus, GLI activity can promote tumor growth in epithelial cells in a cell-autonomous, HH-independent manner.

While aberrant upregulation of GLI promotes tumor cell growth, our single-cell and laser capture RNA sequencing analysis indicate that GLIs are predominantly expressed in the stroma. Therefore, in this study we focused our attention on the role of GLI1-3 in the stroma. However, even within the stroma there are non-canonical functions for HH pathway components. For example, genetic deletion of Smo in pancreatic fibroblasts eliminates the HH-response, but leads to the aberrant activation of AKT [72,73]. AKT is then able to stabilize GLI2 in fibroblasts, which in turn promotes epithelial cell growth via TGF-α secretion [72]. These HH-independent roles for GLIs open up the possibility that the phenotypes we observe in Gli KO fibroblasts could be due to a combination of both canonical as well as non-canonical GLI functions. Exploring this possibility requires a deeper investigation into GLI targets in PDA.

Here we describe the coordinated roles of all three GLIs in vivo within the context of PDA progression. Our data demonstrate that manipulating GLI has both tumor-promoting and tumor-restricting effects, depending on their combinatorial activity. However, the transcriptional mechanisms driving these different phenotypes remain unclear. Our RNA sequencing analysis of Gli2/Gli3 KO fibroblasts indicates that the coordinated activity of GLI2 and GLI3 drive a transcriptional program that shapes the extracellular and immune landscape of PDA. Further, pervious work has identified a number of transcriptional targets of GLI1 in pancreatic fibroblasts, including Il6, Il8, Mcp-1, M-csf [39,48]. However, the degree of overlap between GLI1, GLI2, and GLI3 transcriptional targets in PDA is still unknown. In addition, it is possible that GLI target genes may change at different stages of disease progression. Fortunately, the development of ChIP-capable tags on endogenous Gli alleles (e.g., 3xFlag-Gli3) [74] provides an opportunity to define GLI target genes in vivo. Future studies could utilize ChIP-capable GLI1-3 proteins to define shared and unique GLI target genes, and evaluate how GLI-driven transcriptional programs change throughout PDA progression. Building out this transcriptional roadmap could help identify the HH targets responsible for driving tumor-promoting versus tumor-restricting programs in PDA, opening up new, more targeted avenues for potential therapies.

Hedgehog-Immune crosstalk

Fibroblasts play a crucial role in regulating immune infiltration in PDA, and are essential in driving immune-suppression [13,14,61]. Further, growing evidence supports the notion that HH signaling regulates immune infiltration in pancreatic cancer. Prior work has demonstrated that Gli1 drives the expression of immune-modulatory cytokines [39,48]. More recently, pharmacological inhibition of SMO (via LDE225) in tumor-bearing mice was shown to increase the recruitment of immunosuppressive macrophages and decrease the relative proportion of cytotoxic T cells [35]. Our data confirms that disrupting HH signaling dramatically alters immune infiltration in the context of PDA progression. However, combined loss of Gli2 and Gli3 decreases the recruitment immunosuppressive macrophages and increases the recruitment of cytotoxic T cells. At first glance these results seem surprising, as both LDE225-treated and Gli2/Gli3 KO fibroblasts do not respond to HH. This discrepancy raises the question: why does SMO inhibition and Gli deletion drive such divergent immune phenotypes?

One essential difference between these two experimental systems is the combinatorial activity of the GLIs. Although Gli2/Gli3 KO pancreatic fibroblasts do not upregulate target genes following HH stimulation, we found that a baseline level of Gli1 expression is maintained in these cells. As a result, some GLI target genes could still be bound by this baseline level of GLI-activator in the absence of Gli2 and Gli3. In contrast, LDE225 treatment effectively eliminates Gli1 expression in pancreatic fibroblasts [35], leading to a fully “HH Off” state. Thus, genetic loss of Gli2 and Gli3 represents a different level of HH pathway activity compared to LDE225-treated pancreatic fibroblasts. Given the evidence that different levels of HH activity drive radically different phenotypes in PDA [18], it is not surprising that we see distinct immune phenotypes between Gli2/Gli3 cKO and LDE225-treated mice. Notably, when we eliminate all three Glis, we observe patterns of immune infiltration that are more consistent with LDE225 treatment, presumably due to the elimination of redundant GLI-activator.

Beyond the compensatory actions of GLI-activators, Gli2/Gli3 KO fibroblasts fundamentally differ from LDE225-treated cells due to the loss of Gli3. We see in our system that loss of Gli3 alone is sufficient to partially reduce the migration of macrophages. This indicates that in the context of PDA progression, de-repression of GLI target genes is an important force in regulating immune infiltration. In our Gli2/Gli3 KO fibroblasts, the absence of a repressor combined with the presence of an activator (GLI1) has the potential to drive substantial transcriptional activity, even in the absence of a HH response. Together, these data emphasize the importance of combinatorial GLI activity in regulating disease progression, and reveal how subtle differences in HH transcriptional activity can dramatically shape the immune landscape of PDA. These findings also provide further rationale for defining GLI-activator versus GLI-repressor transcriptional targets throughout PDA progression.

In addition to demonstrating the differences between pharmacological and genetic manipulation of HH signaling, these studies reveal how the role of HH in regulating immune infiltration changes at different stages of disease. In the present study, Gli was deleted in fibroblasts prior to the formation of PanIN lesions (KF mice) or before exposure to tumor cells (tumor implantation experiments). Therefore, our data reveal how the immune landscape of PDA develops in the absence of normal HH activity. In contrast, pharmacological inhibition in tumor-bearing mice demonstrate the impact of removing HH signaling from an established disease [35]. Prior research has demonstrated that disrupting HH signaling in fibroblasts has different consequences on PDA progression depending on the stage of disease studied [48,75]. It is therefore likely that the role of HH on the immune system also evolves throughout PDA progression, and that some of the differences we observe reflect a shift in HH’s role. Fortunately, the inducible nature of the KF; Pdgfrα^CreER-T2;Gli2^fl/fl; Gli3^fl/fl mouse model could be leveraged to delete Gli after the formation of PanIN lesions, directly testing the role of Gli in established pancreatic disease. Thus, this experimental system provides new opportunities to evaluate the role of HH signaling at multiple stages of PDA.

Although our study provides new insight into Gli-mediated regulation of immune infiltration in PDA, many open questions remain. One outstanding question is how GLIs regulate the balance of CAF subtypes in PDA. A growing body of work is revealing the heterogeneity of pancreatic fibroblasts, and demonstrating that different populations have distinct roles in the context of pancreatic cancer [23,67,76,77]. Further, pharmacological inhibition of HH changes the balance of inflammatory CAFs (iCAFs) and myofibroblastic CAFs (myCAFs) in vivo, resulting in a more immunosuppressive microenvironment [35]. Given the ability of GLIs to fine-tune HH responses in pancreatic fibroblasts, a natural next question is how different GLIs influence the relative proportion of CAFs in PDA. Our expression analysis in vitro and in vivo demonstrates that loss of Gli2/Gli3 reduces Il6 expression, a key marker of iCAFs. A reduction in iCAFs would be consistent with the reduction in immunosuppressive immune cells that we observe in vivo. However, more in-depth analysis will be necessary to explore the potential connections between GLIs and fibroblast heterogeneity.

Overall, our data indicate that all three GLIs play a central role in PDA progression. The reduction in immunosuppression following Gli2/Gli3 deletion warrants further exploration into the transcriptional networks downstream of Gli. Identifying and targeting these mechanisms of immunosuppression could provide new avenues for future therapies, potentially enhancing the efficacy of immunotherapy in this challenging disease.

Ethics statement

All experiments performed in this study were approved by the University of Michigan Institutional Animal Care and Use Committee (IACUC), the University of Michigan Institutional Biosafety Committee (IBC), and the University of Michigan Institutional Review Boards (IRB).

Laser-capture microdissection and RNA sequencing (LCM-RNAseq)

LCM-RNAseq was performed and analyzed by Maurer and colleagues [40]. Briefly, samples underwent laser capture microdissection using a PALM MicroBeam microscope (Zeiss). RNA libraries were generated using the Obation RNAseq System V2 kit (NuGEN), and sequenced to a depth of 30 million, 100 bp, single-end reads.

Single-cell RNA sequencing (scRNAseq)

scRNAseq data were generated and processed as previously described [42]. Briefly, processed data were normalized using the Seurat (V4) [78] pipeline in R with a scale factor of 10,000 and the LogNormalize normalization method. Variable genes were identified using FindVariableFeatures. Data were scaled and centered using linear regression and principal component analysis (PCA) was run with the RunPCA function using the defined variable genes. Genes in the HH pathway were displayed as a Dot Plot analysis.

X-gal staining

Pancreata were dissected in chilled 1x PBS (pH 7.4). Tissue samples were collected for RNA isolation and histology, and the remaining tissue was fixed (4% PFA) on ice for 1h. Pancreata were washed 3x5min in PBS and transferred to a PBS+30% sucrose solution overnight at 4°C. The next day, half of the 30% sucrose was removed and replaced with OCT embedding medium, and placed on a rocker at 4°C for 1h. This process was repeated twice, and then the tissue was transferred to 100% OCT for 1h. Tissues were embedded in OCT and sectioned on a Leica CM1950 cryostat (12μm sections). β-Galactosidase activity was detected with X-gal staining solution [5 mM K3Fe(CN)6, 5 mM K4Fe(CN)6, 2 mM MgCl2, 0.01% Na deoxycholate, 0.02% NP-40, 1 mg/ml X-gal] and stained for 2 – 36h at 37°C. After staining, the sections were washed 3x5min in PBS and counterstained with Nuclear Fast Red for 5min. Sections were dehydrated 70% ethanol, 95% ethanol, 100% ethanol and 100% xylene) and mounted with coverslips using Permount Mounting Medium (Thermo Fisher Scientific).

Immunofluorescence

Tissues were dissected/processed as described above. Frozen sections were warmed to room temperature (RT), then baked at 60°C for 10min. Sections were washed 3x5min in PBS and blocked in blocking buffer [3% bovine serum albumin, 1% heat-inactivated sheep serum, 0.1% Triton X-100 in PBS] for 1h at RT. Paraffin sections were rehydrated (100% xylene, 100% ethanol, 95% ethanol, DI water) and underwent citric acid antigen retrieval (Vector Laboratories, H-3300) for 10min at 92°C. Paraffin sections were washed 3x5min with DI water, 3x5min with PBS, and blocked for 1h at RT in PBS+1% BSA. All sections were incubated with primary antibodies overnight at 4°C in a humidified chamber. Primary antibodies are listed in S1 Table. Secondary antibodies were diluted in blocking buffer and incubated for 1h at RT, followed by 3x5min washes in PBS. All secondary antibodies were used at a 1:500 dilution. Nuclei were labeled with DAPI for 10min at RT. Slides were mounted with coverslips using Immu-mount aqueous mounting medium (for frozen sections) or Permount Mounting Medium (for paraffin sections). Sections were visualized on a Leica SP5X upright confocal or a Nikon E800 epifluorescent microscope. For quantitation, 3–5 fields of view were imaged per section and analyzed using FIJI (version 2.0.0-rc-69/1.52p).

Subcutaneous tumor growth assays

1 x 10⁵ 7940b tumor cells were mixed with 5 x 10⁵ fibroblasts, resuspended in a 50:50 mix of serum-free media [DMEM+1% Pen/Step] and Matrigel (Corning 354234). Two fibroblast clones (in equal numbers) were used in each injection to reduce the impact of clonal variability. Cells were injected subcutaneously into the flanks of NU/J mice (Jackson Laboratory Stock No: 002019). Tumors were measured every other day with calipers, and animals were sacrificed after 10 days. For NK cell depletion experiments, 10μl of anti-asialo GM1 (Wako 986–10001) or an equivalent volume of normal Rabbit IgG control (R&D AB-105-C) was diluted 1:10 in sterile PBS and injected intraperitoneally. Injections were given 24h before tumor implantation, on the day of tumor implantation, and once every three days for the remainder of the experiment.

Flow cytometry

Single-cell suspensions of tissue were prepared as previously described [79]. Flow cytometry was performed either on a BioRad Ze5 Analyzer or a MoFLo Astrios cell sorter, and data were analyzed with FlowJo v10 Software. Values for all flow cytometry data displayed as a percentage of total cells. Antibodies used for flow cytometry are listed in S2 Table.

Histology

Tissue samples were fixed in 10% neutral buffered formalin (Thermo Fisher 245–685) overnight at RT. Samples were washed 3x5min in PBS, moved to 70% ethanol, and then processed for paraffin embedding. 5μm sections were collected and used for histological analysis. Hematoxylin and eosin (H&E) and Gomori Trichrome stain were performed according to standard protocols.

Macrophage migration assays

Bone marrow cells were isolated as described previously [80] and plated in a 50–50 mixture of complete media [DMEM F12 + 10% Calf Serum + 1% Pen/Step] and tumor cell (7940b) conditioned media. Cells were supplemented with 750μl of 50–50 media every other day for a total of 6 days. On day 5, 2.5 x 10⁵ total fibroblasts were plated into each well of a 12-well plate. Two fibroblast clones (in equal numbers) were used for all conditions. Once cells adhered to the plates (after 8h), the media was replaced with low (0.1%) serum media. On day 6, macrophages were removed from plates with 0.25% Trypsin-EDTA (Gibco 25200–056) and scraping, and resuspended in low serum media. 4 x 10⁵ macrophages were plated onto each transwell insert (8μm pore size, Thermo Scientific 140656) above fibroblast wells. After 12h, remaining macrophages were removed from the top of the transwells with a cotton swab, and the membranes were fixed (4% PFA) for 10min at RT, followed by 3x5 min PBS washes. Membranes were stained with DAPI for 10min at RT, washed 3x5 min in PBS, and removed from the transwells with a scalpel. Membranes were then mounted onto slides with Immu-mount aqueous mounting medium, coverslipped, and imaged as described above.

T cell differentiation and migration assays

1 x 10⁵ total fibroblasts were plated into each well of a 24-well plate in complete media [DMEM + 10% CS + 1% Pen/Strep]. Two fibroblast clones (in equal numbers) were used for all conditions. 8 h later, the media was replaced with 1% serum media [DMEM + 1% CS + 1% Pen/Strep]. The next morning, single cell suspensions were made from the spleens of BL6 mice, and total T cells were isolated by MACS according to the manufacturer’s instructions (Miltenyi Biotec 130-042-401). T cells in suspension were bound by Biotin-conjugated anti-CD3 antibody (R&D BAM4841), and captured in a magnetic column with anti-Biotin microbeads. Isolated T cells were resuspended in 1% serum media and 2.5 x 10⁵ T cells were added to the top of each transwell. For differentiation assays, 0.4μm pore transwell membranes were used. For migration assays, 5μm pore transwell membranes were used. 100 ng/ml CXCL12 (SDF1α, R&D 460-SD-010) added to the bottom chamber was used as a positive control in migration assays. Plates were returned to the cell culture incubator under standard cell culture conditions for 6.5 h. At the end of differentiation assays, T cells were collected from the top chamber and lysed for RNA isolation (see below). At the end of migration assays, migrated T cells were collected from the bottom chamber, spun down, and counted with a hemocytometer.

RNAscope

RNAscope was performed as described previously [81]. Briefly, paraffin sections were baked at 60°C for 1h, and then stored overnight at RT. Fluorescent RNAscope was performed according to the manufacturer’s protocol (ACD: 323100-USM). Samples underwent antigen retrieval for 15min, followed by a 12min protease digestion. TSA fluorophores (Akoya biosciences NEL744001KT and NEL745E001KT) were diluted 1:2000 in TSA dilution buffer. Following HRP blocking, slides were washed 3x5 min in PBS and blocked in 0.1% PBS-Tween20 + 5% Normal Donkey Serum for 1h at RT. Primary antibody incubation, secondary antibody incubation, and the subsequent processing, imaging, and quantitation was performed as described above.

Western blot analysis

20μg of protein was separated on an SDS-polyacrylamide gel (5% GLI2, 7.5% GLI3) for 30min at 80V followed by 90min at 100V. Gels were transferred to an Immuno-Blot PVDF membrane (Bio-Rad; Cat #1620177), blocked with western blocking buffer (30g BSA, 2ml 10% NaN3, Q.S. 1L TBST) for 5min, and probed with antibody diluted in western blocking buffer. Membranes were washed for 3x5min in TBST and then probed with secondary antibody for 1h at RT. Membranes were then washed 12x5min at RT. Protein was detected by fluorescence, using ECL Primer Western Blotting Detection Reagents (RPN2232) developed on a Konica Minolta SRX-101A Medical Film Processor. All primary and secondary antibodies are listed in S3 and S4 Tables, respectively.

Cell culture

All cell lines were maintained at 37°C and 5% CO₂, and were kept in standard media (DMEM + 10% Calf Serum + 1% Pen/Strep) unless noted otherwise. The human pancreatic stellate cell (hPSC) line has been previously published [7], and was generously provided by C.A. Lyssiotis. Mouse fibroblast lines were established through the outgrowth method [82]. Briefly, pancreata were isolated from adult mice under sterile conditions. Pancreata were minced mechanically and digested for 15min at 37°C in 1 mg/ml collagenase (Sigma C9263, diluted in sterile Hank’s Balanced Salt Solution—HBSS). Standard media was added to inactivate the enzymatic digestion, and samples were passed through a 70μm cell strainer, resuspended in standard media, and plated onto tissue culture plates coated in 0.1% gelatin. Primary cells (less than 3 passages) were frozen and stored, and kept separate from immortalized lines. Following immortalization, fibroblasts were infected with adenovirus (Control: Ad5 CMV-eGFP and Lenti dsRed; cKO: Ad5 CMV-eGFP and Ad5 CMV-Cre) at an MOI of 500–2000. Successfully infected cells were isolated by flow cytometry and screened by qPCR and western blot for recombination efficacy. Cell lines were tested for mycoplasma before running experiments. For HH signaling assays, 5 x 10⁵ fibroblasts were plated in each well of a 6-well plate in standard media. 24h after plating, the media was replaced with low (0.1%) serum media. 24h later, the media was replaced with 1.5ml of low serum media + 600 nM of Smoothened agonist (SAG) or vehicle control (DMSO). 24h later, a supplemental dose of SAG/vehicle was added directly to each well to a final concentration of 600 nM. 24h later, the cells were lysed and analyzed for HH target gene expression.

RNA isolation

Snap-frozen tissue samples were pre-treated with RNAlater-ICE (Invitrogen AM7030) according to the manufacturer’s instructions. Tissue samples and bulk RNA sequencing samples were lysed in Buffer RLT + 1% BME and processed with the Qiagen RNeasy Mini Kit (Qiagen 74104) according to the manufacturer’s instructions. For all other applications, RNA isolation was performed using the PureLink RNA Mini Kit (Invitrogen 12183025) according to the manufacturer’s instructions. All samples were eluted in ultrapure water, and RNA quality was determined using a NanoDrop One (Thermo Scientific ND-ONE-W).

qPCR

cDNA was generated from 0.5–2μg of RNA using the Applied Biosystems High Capacity cDNA Reverse Transcription Kit (Thermo Fisher 4368814) according to the manufacturer’s instructions. qPCR reactions were run using PowerUp SYBR Green Master Mix (Applied Biosystems A25742) and the primers listed in S5 Table in a StepOnePlus Real-time PCR System (Applied Biosystems 4376600). Gene expression was normalized to Cyclophilin unless stated otherwise. Relative expression was calculated using the 2(^−ddCT) method.

Animal models

All mice were housed in specific pathogen-free facilities at the University of Michigan. Gli1^lacZ [46], Gli2^lacZ [37], Gli3^lacZ [47], Ptf1a^Cre (p48^Cre) [83], Kras^LSL-G12D [43], Ptf1a^FlpO (p48^FlpO) [84], Kras^FSF-G12D [85], Pdgfrα^CreERt2 [49], Gli2^fl/fl [86], Gli3^fl/fl [87], LSL-tdTomato [88], Gli1^CreERt2 [54] mice have all been described previously. To induce Cre recombination, tamoxifen (Sigma T5648) was administered to mice at a dose of 200 mg/kg once per day for 5 days by oral gavage. To induce acute pancreatitis in 6–8 week old KC and KF mice, 8 hourly i.p. injections of caerulein (Sigma C9026) were administered at a dose of 75μg/kg over two consecutive days. Caerulein-treated mice were harvested 3 weeks after their final dose. KF mice used in aging experiments were not given caerulein, and were dissected once the mice reached 20 weeks of age. KPC mice were monitored daily by abdominal palpitation and dissected once the mice reached humane endpoint.

Statistical analysis

All statistical analysis was performed using Graphpad Prism software. For quantitative analysis, each data point represents an independent biological replicate. Information such as sample size, P value, and the statistical test used is stated in the figure legend. Significant P-values are indicated with one or multiple asterisks according to the following convention: * = p ≤ 0.05, ** = p ≤ 0.01, *** = p ≤ 0.001, **** = p ≤ 0.0001, ns = p > 0.05.