Cellular localization and regulation of receptors and enzymes of the endocannabinoid system in intestinal and systemic inflammation
0000 0000 8988 2476grid.11598.34Pharmacology Section, Otto Loewi Research Center, Medical University of Graz, Universitätsplatz 4/I, 8010 Graz, Austria
grid.452216.6BioTechMed Graz, Graz, Austria
Abstract
Surveys suggest that Cannabis provides benefit for people with inflammatory bowel disease. However, mechanisms underlying beneficial effects are not clear. We performed in situ hybridization RNAscope® combined with immunohistochemistry to show cell-specific distribution and regulation of cannabinoid receptor 1 and 2 (CB1, CB2), G protein-coupled receptor 55 (GPR55), and monoacylglycerol lipase (MGL) mRNA in immune cells using murine models of intestinal and systemic inflammation. In healthy animals, the presence in enteric ganglia is high for CB1 mRNA, but low for CB2 and GPR55 mRNAs. MGL mRNA is predominant throughout the intestinal wall including myenteric neurons, epithelium, circular and longitudinal muscular layers, and the lamina propria. Within the immune system, B220+ cells exhibit high gene expression for CB2 while the expression of CB2 in F4/80+ and CD3+ cells is less prominent. In contrast, GPR55 mRNA is highly present in F4/80+ and CD3+ cells. qRT-PCR of total colonic segments shows that the expression of GPR55 and MGL genes drops during intestinal inflammation. Also at cellular levels, GPR55 and MGL gene expression is reduced in F4/80+, but not CD3+ cells. As to systemic inflammation, reduced gene expression of MGL is observed in ileum by qRT-PCR, while at cellular levels, altered gene expression is also seen for CB1 and GPR55 in CD3+ but not F4/80+ cells. In summary, our study reveals changes in gene expression of members of the endocannabinoid system in situ attesting particularly GPR55 and MGL a distinct cellular role in the regulation of the immune response to intestinal and systemic inflammation.
Electronic supplementary material
The online version of this article (10.1007/s00418-018-1719-0) contains supplementary material, which is available to authorized users.
Introduction
Knowledge of the endocannabinoid system (ECS) has immensely grown in the past few years. Its members, i.e., cannabinoid receptors, endocannabinoids and the enzymes that synthesize/degrade endocannabinoids, have become highly investigated targets [rev. in (Pertwee 2015)]. This molecular network has been recently coined “endocannabinoidome”, as more components have been added lately (Di Marzo and Piscitelli 2015). Apart from the brain, the gastrointestinal (GI) tract is one of the organs that contains key players of the ECS, including cannabinoid receptors (CB) 1 and 2 (CB1, CB2), G protein-coupled receptor 55 (GPR55) and the 2-arachidonoylglycerol (AG)-degrading enzyme monoacylglycerol lipase (MGL) [rev. in (Hasenoehrl et al. 2016)]. Functional tasks of the ECS in the GI tract comprise the control of the epithelial barrier (Cani et al. 2016; Karwad et al. 2017), the maintenance of immune homeostasis (Acharya et al. 2017), the regulation of motility, and the protection against inflammatory attacks (Schicho and Storr 2010). However, a clear understanding of how the ECS is regulated and which cell populations express these molecules during disease in situ is lacking. The GI tract is a heterogeneous organ, and therefore, accommodates the ECS in various cell types. CB1 and CB2 receptors, for instance, have been reported in the enteric nervous system and in epithelial and lamina propria cells (Wright et al. 2005, 2008). GPR55 has been located in enteric neurons and the colonic mucosa (Li et al. 2013). A recent study reported that GPR55 is involved in intraepithelial lymphocyte migration (Sumida et al. 2017). Little is known, however, about the cellular localization of GPR55 in the adaptive and innate immune system of the inflamed gut.
Much of the research progress on the ECS is hampered by a lack of specific tools, especially of antibodies against GPR55 and CB2, to detect their localization in different cell populations of the gut. As shown in several reports, antibodies against the CB2 receptor are likely unspecific (Baek et al. 2013; Cecyre et al. 2014; Marchalant et al. 2014). Commercially available antibodies against CB1 have also been evaluated, showing that unspecific staining may be an issue with CB1 antibodies as well (Grimsey et al. 2008). In intestinal tissue, commercially available GPR55 antibodies have been used for immunohistochemistry with more or less strict controls (Galiazzo et al. 2018; Li et al. 2013; Lin et al. 2011). However, most of them show a band in GPR55−/− mice at the right molecular weight (see online resource Fig. 1). The strongest indication for antibody specificity, therefore, is the absence of staining in the respective knockout mouse.
In this context, in situ hybridization (ISH) has proved to be a most valuable and highly specific alternative to demonstrate the presence and regulation of CB receptors (Li and Kim 2015). As PCR analysis of whole intestinal tissue does not reveal in which cells CB receptor regulation occurs, ISH can be combined with immunohistochemistry (IHC) in co-localization studies to identify the cells in which regulation of receptors takes place. We, therefore, localized and evaluated CB1, CB2, GPR55 and MGL gene expression (the official symbols of encoding genes are termed Cnr1, Cnr2, Gpr55 and Mgll) in mouse models of intestinal and systemic inflammation by a novel ISH technique (RNAscope®) with emphasis on the localization of GPR55. For co-localization with distinct immune cell populations, we used established T-cell, B-cell and macrophage markers. Intestinal inflammation in mice was induced by adding 2.5% dextran sulfate sodium (DSS) to the drinking water. DSS disrupts the epithelial barrier in the colon causing inflammation reminiscent of human ulcerative colitis (Eichele and Kharbanda 2017). Systemic inflammation was performed by treatment with lipopolysaccharide (LPS), a model that leads to intestinal barrier dysfunction (Han et al. 2004; Kimura et al. 1997), epithelial injury and a change in T cell populations (Liu et al. 2009). The specificity of the probes was tested in sections of the respective knockout mice (CB1−/−, CB2−/−, GPR55−/−, and MGL−/−).
Materials and methods
Animals
C57BL/6 mice obtained from Charles River (Sulzfeld, Germany) were used for the experiments. CB1−/− and MGL−/− mice were kindly provided by A. Zimmer and R. Zimmermann, respectively (Hasenoehrl et al. 2018; Taschler et al. 2011). CB2−/− mice were purchased from Jackson Laboratory (Bar Harbor, ME, USA) and GPR55−/− animals from the Mutant Mouse Resource & Research Center (MMRRC; University of North Carolina, Chapel Hill, NC; USA) (Hasenoehrl et al. 2018). Knockout mice with a C57BL/6 background served as negative controls for ISH and IHC. All mice were bred in our own facilities and housed in plastic cages with sawdust floors at constant temperature (22 °C) under a 12 h light/12 h dark cycle with standard lab food and water ad libitum. The experimental procedures were approved by the Austrian Federal Ministry of Science, Research and Economy (protocol numbers: BMWF- 66.010/0131-WF/V/3b/2014; BMWF-66.010/0044-WF/V/3b/2016) and performed in strict accordance with international guidelines.
Treatment of animals
DSS-induced intestinal inflammation
Colitis was induced in C57BL/6 mice by adding 2.5% DSS (MP Biomedicals, Illkirch, France) to their drinking water for 5 days and animals were killed on day 8 (Stancic et al. 2015).
LPS-induced systemic inflammation
C57BL/6 mice were treated with an intraperitoneal injection of 0.83 mg/kg LPS (Farzi et al. 2015) (Sigma, Vienna, Austria) or with PBS alone (vehicle) and killed 4 h later.
Tissue processing
Colon (DSS treatment) or ileum (LPS treatment) was harvested and cut in half. One piece of tissue was snap frozen in liquid N2 and stored at −80 °C until it was further processed for quantitative reverse transcription-polymerase chain reaction (qRT-PCR), the other half was fixed in acid free phosphate-buffered 10% formaldehyde solution (Roti®-Histofix 10%; pH 7, stabilized with methanol) for 16–24 h at room temperature.
RNA isolation and qRT-PCR
RNA was extracted from tissue samples using TRIzol (Life Technologies). Samples from DSS-treated animals were purified in an additional step with the “RNA clean up” protocol from the RNeasy kit and subsequently subjected to the Oligotex mRNA Mini Kit (both Qiagen) to remove remaining DSS that could inhibit subsequent qRT-PCR steps. All samples were treated with the DNA Removal Kit DNA-free (Life Technologies) and 2 µg of total RNA were reverse transcribed to cDNA using High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Carlsbad, USA).
Gene expression of CB1, CB2, GPR55 and MGL was quantified using SsoAdvanced™ Universal SYBR® Green Supermix (Bio-Rad, Vienna, Austria). Validated primers were purchased from Bio-Rad and relative gene expression was assessed according to the 2−ΔΔCq method.
In situ hybridization (ISH) and immunohistochemistry (IHC)
Freshly harvested and fixed tissue was further processed for paraffin embedding according to standard procedures. Tissue was cut in 5 µm sections, baked at 60 °C for 1 h, de-waxed and rehydrated.
ISH
RNAscope® is an advanced ISH method where two adjacent probes (the so-called ZZ probes) are needed to bind to the target sequence to develop a signal. This method provides the possibility of detecting a low number of mRNAs in peripheral tissue due to a decreased background noise (Wang et al. 2012).
20 ZZ probes for murine CB1 (targeting bases 701–1792 of NM_007726.3), CB2 (targeting bases 291–719 of NM_009924.3), GPR55 (targeting bases 2–907 of NM_001033290.2) and 3 ZZ probes for MGL (targeting bases 703–849 of NM_001166251.1) (all purchased from Advanced Cell Diagnostics, ACD, Newark, USA) were used to detect the corresponding mRNAs in murine intestinal or systemic inflammation models. ISH (RNAscope® 2.5 HD brown or red kit for CB1, CB2 and GPR55 and BASEscope™ red kit for MGL, ACD) was performed according to manufacturer’s protocol. In brief, tissue sections were treated with H2O2 for 10 min, target retrieval was performed using the Brown FS3000 food steamer for 15 min, each step followed by washes in H2O dest. The next day, sections were digested with Protease Plus (for CB1, CB2 and GPR55) or Protease IV (MGL) at 40 °C for 20 min, washed, followed by incubation with the corresponding probes at 40 °C for 2 h. The procedure was continued according to the manufacturer’s protocol for RNAscope® or BASEscope™ (ACD). CB1, CB2, GPR55 and MGL were stained using 3,3′-diaminobenzidine (DAB; for brightfield) or FastRed (for brightfield and fluorescence, both dyes provided by ACD). Colonic or ileal sections from treated and untreated C57BL/6 mice and the corresponding knockout controls were put on one slide for comparison.
IHC
Antibodies against cell markers including CD3, CD4, CD8 and FoxP3 (for T-cell subtypes), F4/80 (for monocytes/macrophages), CD45R-B220 (for B lymphocytes), and neurofilament H and synaptophysin (for neuronal structures [axons/synapses]) were used to determine cell types co-localizing with mRNAs (see Table 1).
| Antigen/antibody (clone/cat no) | Provider | Specificity shown by | Dilution | Host/isotype |
|---|---|---|---|---|
| CD3 (ab5690) | Abcam, Cambridge, UK | WB (data sheet) | 1:1000 | Rabbit IgG pAb |
| CD4 (EPR19514/ ab183685) | Abcam, Cambridge, UK | WB, IP (data sheet) | 1:1000 | Rabbit IgG mAb |
| CD8 (ab203035) | Abcam, Cambridge, UK | WB (data sheet) | 1:2000 | Rabbit IgG pAb |
| FoxP3 (D6O8R/ #12653) | Cell Signaling Technology, Danvers, MA, USA | Flow cytometry (data sheet) | 1:200 | Rabbit IgG mAb |
| F4/80 (BM8/ sc-52664) | Santa Cruz Biotechnologies, Dallas, TX, USA | Comparison to CD68 (Shi 2010), data sheet reference) | 1:200 | Rat IgG2a, mAb |
| CD45R-B220 (RA3-6B2/ 14-0452-82) | Thermo Fisher Scientific, Waltham, MA, USA | Flow cytometry, WB (data sheet) | 1:250 | Rat IgG 2a, kappa, mAb |
| Neurofilament H(ab8135) | Abcam, Cambridge, UK | WB (data sheet) | 1:2000 | Rabbit IgG, pAb |
| Synaptophysin (SP11/ MA5-14532) | Thermo Fisher Scientific, Waltham, MA, USA | WB (data sheet) | 1:250 | Rabbit IgG, mAb |
| Biotinylated anti-rabbit IgG | Vector laboratories, Burlingame, CA, USA | Omission of primary Ab | 1:200 | Goat IgG |
| Biotinylated anti-rat IgG (BA-9401) | Vector laboratories, Burlingame, CA, USA | Enzyme immunoassay (data sheet) | 1:200 | Goat IgG |
| Anti-rabbit Alexa Fluor® 488 | Thermo Fisher Scientific, Waltham, MA, USA | Omission of primary Ab | 1:500 | Goat IgG |
Tissue sections were blocked in 0.1 M PBS containing 0.3% Triton X-100 and 5% goat serum (Sigma-Aldrich/ Merck, Darmstadt, Germany). First antibody in 0.1 M PBS containing 0.3% Triton X-100 and 1% goat serum was applied over night at 4 °C, IHC was performed using the Vectastain®ABC kit and Vector® VIP HRP substrate kit (both Vector Laboratories) according to the manufacturer’s protocol. Sections were counterstained with 1:5 dilutions of Gill’s II Hematoxylin or with Methyl green, washed, dried and mounted with Vectamount mounting medium (Vector Laboratories).
Microscopy
Brightfield images were taken using a Zeiss Axiophot (100x/1.30 Plan-Neofluar objective with oil immersion; Carl Zeiss AG, Oberkochen, Germany) equipped with a high resolution CCD camera (coolsnap cf from Photometrics®, Tuscon, AZ, USA; images: 1392 × 1040 pixels; 24 bit) and MCID™ Analysis software 7.0 (InterFocus Imaging Ltd, Linton, England), or an Olympus BX41 microscope (objectives: 20x/0.75, UPlanSApo; 40x/0.95, UPlanSApo; 100x/1.40, UplanSApo with oil immersion) and an Olympus UC 90 digital camera; images: 1688 × 1353 pixel; 24 bit connected with Olympus CellSense® standard 1.17 imaging software (Olympus, Vienna, Austria).
Fluorescence images were taken by an Olympus IX70 (objectives: 10x UPlanFl) connected with an Olympus MT20 light source (150W xenon arc burner) and a Hamamatsu ORCA-ER digital camera (1344 × 1024 pixels; Hamamatsu Photonics K.K., Japan). Olympus xcellence® imaging analysis software 1.1 was used for acquiring images (1344 × 1024 pixels, 24 bit). The following fluorescence filters were used: for Fast Red (U-M41007 cube): DM568, excitation filter 540–560, barrier filter 575–645; for Alexa 488 (modified U-MNIBA cube): DM 505, excitation filter BP470-490, barrier filter BA515-550; for DAPI (Olympus DAPI Filter MT20): DM 409, excitation filter 378/52 (MT20 light source), barrier filter HC Quadband Filter 432. Contrast, brightness and color balance of images were adjusted using Corel Photo Paint®.
Quantification of ISH gene expression
Tissues to be compared were mounted on one slide to be processed together for ISH and IHC.
A semi-quantitative histological scoring method was chosen based on ACD scoring criteria for RNAscope® to count and compare gene expression in different cell types and between control and diseased animal tissue. In brief, about 100 cells per tissue/mouse (3 mice/ treatment) were evaluated. Only cells with a visible nucleus and a clearly confined cell body were taken into account. Dots in each cell were counted and cells were allocated to one of five groups. Group 0 means no expression, group 1 is 1–3 dots, group 2 is 4–9 dots or 1 cluster, group 3 is 10–15 dots or few clusters, group 4 is > 15 dots or many clusters. The columns in the graphs indicate the percentage of cells in each group (sum of all groups per treatment equals 100%).
Statistics
ISH: Data are shown as mean +/– standard error of the mean (SEM) with three mice (ISH) or five–ten mice (qRT-PCR) per experimental group. Statistical analysis was done using GraphPad Prism 5.03 (GraphPad Software, La Jolla, CA, USA). Cell counts were compared by two-way analysis of variance followed by Bonferroni multiple comparison post hoc analysis. Gene expression was compared by unpaired two-tailed Student’s t test. P values < 0.05 were considered significant and denoted with 1, 2 or 3 asterisks when lower than 0.05, 0.01 or 0.001, respectively.
Results
Specificity of the ISH probes
ISH RNAscope® and ISH/IHC were performed to determine detailed cellular localizations of mRNA and to investigate, if changes in gene expression by DSS and LPS treatment can be detected on a cellular level in situ. To evaluate the kit performance and the quality of the fixed tissue, we first performed ISH RNAscope® using the positive (PPIB) and negative (bacterial dapB) probes provided by the manufacturer. The positive probe produced visible ISH staining on all tissues, while the negative probe showed no ISH staining (not shown). Pretreatment conditions were adjusted to minimize tissue digestion and background while maintaining highest possible positive ISH signal. To confirm the specificity of the target probes, untreated CB1−/−, CB2−/−, GPR55−/− and MGL−/− mice were used and compared to healthy or treated wild type mice. CB1, CB2 and GPR55 probes, used with the standard RNAscope® kit, showed no staining at all or only minimal background staining (see online resource Fig. 2). Initially, all RNAscope® probes were detected using the brown detection kit. To better distinguish between ISH and IHC stainings, we switched to the red detection kit for some selected targets. MGL, detected by the highly sensitive red BASEscope™ kit, resulted in only minimal background staining in the corresponding knockout tissue.
Colon/ DSS-induced colitis
Localization and extent of CB1 gene expression markedly differs from CB2 gene expression in the murine colon
The regulation of CB1 and CB2 at the cellular level in situ during inflammation is still unexplored and the localization of CB2 receptors in the colon has been conflicting so far. Therefore, CB1 and CB2 gene expression and localization in healthy and DSS-treated mice was investigated using ISH RNAscope®. In healthy tissue, CB1 gene expression was prominent in enteric ganglia (Fig. 1a), but was also seen in lymph follicles (Fig. 1b), and in epithelial and lamina propria cells (Fig. 1c). Contrary to CB1, CB2 mRNA was heavily expressed in lymph follicles (Fig. 1e) but only marginally in the myenteric plexus (Fig. 1d) and the epithelium (Fig. 1f) of healthy colon. qRT-PCR showed that CB1 and CB2 mRNA levels were not altered in total tissue of DSS-treated mice (Fig. 2a, b), as compared to healthy animals. Likewise, no differences in CB1 and CB2 mRNA levels were found on the cellular level using scoring criteria as described in the Methods (data not shown). To investigate if CB1 mRNA staining in the muscle layers was of neuronal or muscular origin, we stained for neuronal structures using synaptophysin and neurofilament H (NFH). Some CB1 mRNA co-localized with synaptophysin (Fig. 1g) and NFH in ganglia (Fig. 1h, i). CB1 mRNA was also found in the longitudinal muscle layer and did not co-localize with the neuronal markers (Fig. 1g, arrows), indicating CB1 gene expression in the longitudinal muscle cells themselves. CB2 mRNA highly co-localized with the B-cell marker B220+ (Fig. 1j). Some CB2 gene expression was also found in F4/80+ (Fig. 1k) and CD3+ cells (Fig. 1l).
The MGL gene is highly expressed in healthy and to a lesser degree in DSS-treated mice
MGL gene expression was found in colonic mucosa, epithelial cells, lamina propria cells, myenteric ganglia and particularly in muscle layers of healthy mice (Fig. 3a–c). In DSS-treated animals, qRT-PCR showed that overall MGL gene expression was reduced (Fig. 2c). This reduction was particularly visible in the epithelium and the circular muscle layer of ISH-stained colon sections (Fig. 3d). To investigate the source of MGL mRNA in the muscle layers, we performed double ISH/immunofluorescence with MGL and synaptophysin (Fig. 3e) or NFH (not shown). While little co-localization of MGL mRNA with synaptophysin was detectable (Fig. 3e, arrows), most of the MGL mRNA staining did not overlap with synaptophysin/NFH. To determine the cell type responsible for MGL gene expression in the lamina propria, we co-stained for MGL/CD3 (Fig. 3f) and F4/80 (Fig. 3g, h). While the majority of CD3+ cells were negative for MGL gene expression, over 80% of F4/80+ cells did express MGL in healthy animals (Fig. 3i).
GPR55 mRNA is present in T-cells and macrophages of healthy murine colon
GPR55 gene expression was detected in epithelial cells (Fig. 4a), cells of the lamina propria (Fig. 4b) and lymph follicles (Fig. 4c). GPR55 mRNA was only marginally found in neurons of the myenteric plexus (Fig. 4d). No GPR55 gene expression was found in the muscular layers of the colon (not shown). To further determine the cell type of highly expressing cells in the lamina propria, we co-stained for T-cell markers and for the monocyte/macrophage marker F4/80 in healthy tissue. The GPR55 gene was highly expressed in CD3+ (Fig. 4e) and F4/80+ cells (Fig. 4i, j). All subpopulations of T-cells were positive for GPR55 mRNA staining, i.e., CD4+ (Fig. 4f), FoxP3+ T regulatory (Fig. 4g), and CD8+ cells (Fig. 4h).
MGL and GPR55 gene expression is particularly altered in F4/80+ cells of DSS-treated mice
According to qRT-PCR, levels of CB1 and CB2 mRNAs from the entire colon wall did not significantly change in intestinal inflammation, whereas GPR55 and MGL gene expression decreased in DSS-treated versus vehicle-treated mice (Fig. 2c, d). While part of this could be explained due to damaged epithelial cells, we asked whether reduction could have also occurred in immune cells. Interestingly, scoring of GPR55 and MGL gene expression in CD3+ cells revealed no changes (not shown). However, MGL (Fig. 3h, i) and GPR55 (Fig. 4j, k) clearly showed reduced gene expression in F4/80+ cells after DSS treatment as compared to healthy animals (MGL: Fig. 3g; GPR55: Fig. 4i).
Ileum/LPS-induced systemic inflammation
CB1 gene expression is slightly altered at the cellular level, whereas no changes for CB2 gene expression were observed in ileum after LPS treatment
High CB1 gene expression was detected in the submucosal and the myenteric plexus (Fig. 5a) and in isolated cells of the epithelium, probably neuroendocrine cells (Fig. 5d). Low expression was found in the lamina propria, in lymph follicles, and the rest of the epithelium (Fig. 5b, c). By use of qRT-PCR of total ileal tissue, no differences in CB1 RNA levels were found between healthy and LPS-treated animals (Fig. 2e). Only a small amount of CD3+ cells co-localized with CB1 (Fig. 5d, arrows) which was slightly reduced after LPS treatment (Fig. 5e, f). CB2 mRNA staining was only marginal in the myenteric plexus (Fig. 6a) but was detectable in lymph follicles co-localizing with CD3+, though only with a weak ISH signal (Fig. 6b); however, CB2 mRNA was also seen in CD3+ cells of the lamina propria (Fig. 6d, e) and in F4/80+ cells of healthy (Fig. 6f) and LPS-treated animals (Fig. 6g). No significant differences in CB2 gene expression exist between healthy and LPS-treated animals as shown by qRT-PCR (Fig. 2f) and by quantification in CD3+ cells (Fig. 6c).
MGL gene expression is reduced in ileum of LPS-treated mice
MGL mRNA staining was detected in the epithelium, lamina propria cells (Fig. 7a, b), myenteric ganglia and the muscle layers (Fig. 7c, d). Total gene expression of MGL, as determined by qRT-PCR, was decreased in the ileum of LPS-treated versus healthy animals (Fig. 2g). This corroborates the observation that staining of MGL mRNA in muscle layers is lower in LPS-treated (Fig. 7d) versus healthy mice (Fig. 7c). In addition, CD3+ cells showed a slight reduction of already low levels of MGL gene expression (Fig. 7e–g). For quantification in CD3+ cells, see Fig. 7g. No differences were found between F4/80+ cells of healthy (Fig. 7e) and LPS-treated mice (Fig. 7f).
GPR55 mRNA highly co-localizes with T-cell and macrophage markers in the ileum of healthy and LPS-treated mice
In healthy mice, strong GPR55 mRNA staining was found in the ileal lamina propria (Fig. 8a), crypt epithelial cells (Fig. 8b) and lymph follicles (Fig. 8c). Levels of GPR55 mRNA seemed to be lower in ileal villi (Fig. 8a) than crypts (Fig. 8b). Very low expression was detected in neurons of myenteric ganglia (Fig. 8d). GPR55 ISH was combined with IHC to determine specific immune cells and investigate possible gene expression changes within immune cells. Like in the colon, there was a strong expression of the GPR55 gene in CD3+ cells (Fig. 8e, f) which could be also detected in all investigated T-cell subpopulations (Fig. 8h–k, n, o) and F4/80+ cells (Fig. 8l, m).
GPR55 is markedly reduced in CD3+ cells in LPS-treated mice
Although qRT-PCR of ileal tissue from LPS-treated mice showed significant expressional changes only for the MGL gene but not for the other genes investigated, the detailed cellular scoring of GPR55 revealed that in contrast to DSS-induced colitis, gene expression of GPR55 in the ileum was lowered in CD3+ cells (see graph in Fig. 8), but did not change in F4/80+ cells (not shown).
Discussion
Several surveys performed in recent years have indicated that people suffering from inflammatory bowel disease (IBD) are using Cannabis to relieve pain and other symptoms associated with the disease [rev. in (Hasenoehrl et al. 2017)]. A small clinical trial in which Cannabis caused moderate symptom relief in Crohn’s patients seems to confirm this (Naftali et al. 2013). Other than these reports, little evidence yet exists whether Cannabis or cannabinoids are protective against IBD in humans. In contrast, a high number of reports describe beneficial effects of cannabinoids in preclinical models of intestinal inflammation [rev. in (Hasenoehrl et al. 2016)].
In our study, we used ISH RNAscope® combined with IHC to identify and quantify gene expression of receptors and enzymes of the ECS in cells of the ileal and colonic wall of mice exposed to DSS and LPS. It is commonly believed that the ECS is an entity that controls homeostasis in the gut and that levels of its receptors are thought to increase during an inflammatory attack. The goal was to measure gene expression of CB1, CB2, GPR55 and MGL and to delineate the cell types responding to the inflammation. The ISH probes against CB1, CB2, GPR55 and MGL were all tested in the respective knockout mouse providing a strong proof for the specificity of the probes, something which is missing for many antibodies used against cannabinoid receptors.
CB1 and CB2 mRNA in the colon and the ileum
First, we showed detailed localization of these receptors in the bowel wall, confirming that CB1 is largely present in enteric neurons (Duncan et al. 2005) and only moderately in the epithelial lining. CB1 mRNA was also detectable in the longitudinal muscle layer (but hardly in the circular layer) where it does not co-localize with synaptophysin. Extra-neuronal localization of CB1 mRNA in the longitudinal muscle layer, therefore, is of interest with regard to a recent article that describes myogenic, besides neurogenic, relaxant effects of CB1 agonists in longitudinal muscle myenteric plexus preparations (LMMP) of the guinea pig (Donnerer and Liebmann 2018). qRT-PCR of whole colonic segments and quantification of CB1/CB2 mRNA in single cells of ISH/IHC stainings revealed little differences between control and DSS- or LPS-treated animals. In the latter, CB1 gene expression in CD3+ cells was even more reduced compared to an already very low expression in healthy mice (Fig. 5f). Although CB1 receptors are important in the regeneration of epithelial cells (Wright et al. 2005), upregulation of CB1 may not be necessary for the regenerative process. It is also possible that a later time point than the one chosen in our experiments might have been more accurate to measure CB1 mRNA, as regeneration and re-epithelization after a bout of DSS may take several weeks (Perse and Cerar 2012). A recent study also highlighted that the presence of CB1 in epithelial cells is crucial for the regulation of intestinal permeability (Karwad et al. 2017). However, it is not yet clear how CB1 contributes to permeability during inflammation because activation of CB1 by anandamide and 2-AG, applied to the basolateral membrane of Caco-2 cells, have shown opposing effects (Karwad et al. 2017).
The CB2 receptor showed only little gene expression in myenteric neurons and the epithelium of the colon. However, mouse models of colitis show improvement in the presence of CB2 through apoptosis of T-cells (Singh et al. 2012) and through inhibition of the NLRP3 inflammasome in macrophages (Ke et al. 2016). A role in the protection of CB2 expressing immune cells against inflammation is, therefore, quite likely. As observed in the qRT-PCR, the presence of CB2 mRNA was not increased in whole bowel wall of the DSS and LPS model in comparison with the untreated animals. In contrast, CB2 mRNA was described to be upregulated in a TNBS colitis model (Storr et al. 2009). This discrepancy may lie in the different models that were used. Unlike the DSS model, the TNBS colitis model is caused by an immune response to the hapten TNBS, and therefore, differs from the DSS model, which is bacterially driven (Eichele and Kharbanda 2017). It is unclear if and how the strong presence of CB2 in B-cells found in our study could contribute to an amelioration of the inflammation because the presence of T- and B-cells were previously thought not to be needed for the development of acute DSS colitis (Dieleman et al. 1994). However, later studies showed that the CB2 receptor is critical for the formation of T- and B-cells (Ziring et al. 2006), and also for the homing and retention of marginal zone B lineage cells (Basu et al. 2011). More recent reports have revealed that B cells can protect from DSS colitis in cooperation with Tregs (Wang et al. 2015). CB2 receptors on B cells, therefore, could participate in the protection against intestinal inflammation.
GPR55 mRNA in the colon and the ileum
By use of a GPR55 antagonist and GPR55−/− mice, we previously detected a pro-inflammatory role of GPR55 in DSS and TNBS inflammation models (Stancic et al. 2015). In the present study, we also focused on GPR55 in immune cells. We observed that mRNA levels of GPR55 in whole colon segments were diminished in DSS mice as compared to controls while in LPS-treated mice, no significant changes were noticed. In line with previous results (Li et al. 2013), we also observed that GPR55 mRNA levels were higher in the ileum than in the colon (online resource Fig. 1d). Unlike CB1, GPR55 mRNA showed the prominent presence in epithelial cells, and even more in lamina propria cells, such as macrophages and T-cells. But like CB2 (and contrary to CB1), the GPR55 gene is only little expressed in the myenteric plexus. Most changes, i.e., reductions, in GPR55 gene expression were observed in T-cells during LPS-induced inflammation, while in DSS-induced inflammation, a reduction in GPR55 gene expression was predominant rather in F4/80+ cells. This is well in line with previous results we obtained in the azoxymethane + DSS cancer model, in which genetic knockout of GPR55 led to a substantially altered T- and myeloid-derived suppressor cell (MDSC) profile when compared to wild-type mice (Hasenoehrl et al. 2018). Additionally, we could previously show that treatment with a GPR55 antagonist leads to reduced influx of lymphocytes and macrophages into the inflamed colon in the DSS model (Stancic et al. 2015). The GPR55 receptor, therefore, seems to primarily act in immune cells during inflammatory attacks in the GI tract.
Presence of MGL mRNA
MGL is a key enzyme in the degradation of 2-AG, and therefore, a well characterized member of the ECS (Grabner et al. 2017). Pharmacologic inhibition of MGL has been shown to improve TNBS-induced colitis (Alhouayek et al. 2011). Inhibition of MGL also protects from LPS-induced lung injury (Costola-de-Souza et al. 2013). We found that the presence of MGL mRNA was decreased in DSS mice and after LPS treatment, and since MGL inhibition protects from injury, a decrease in MGL in the disease models could very well be part of a protective mechanism. Contrary to previous reports (Duncan et al. 2008), we observed MGL gene expression in the smooth muscle layer of the GI tract, indicating that MGL is expressed in smooth muscle cells themselves although the presence in resident macrophages cannot be excluded (Wehner and Engel 2017). However, owing to the abundance of MGL gene expression seen in the longitudinal muscle layer which is devoid of resident macrophages (Wehner and Engel 2017) as well as the observation that most of MGL mRNA does not co-localize with synaptophysin (Fig. 3e), MGL is likely expressed in the smooth myocytes themselves.
To conclude, RNAscope® ISH technique combined with IHC is an extremely valuable method for identifying gene expression and regulation of receptors and enzymes at a single cell basis in situ, as demonstrated by the response of the ECS to intestinal and systemic inflammation. Alterations in the gene expression of GPR55 and MGL in CD3+ lymphocytes and F4/80+ macrophages indicate that these two components of the ECS are an important part of the innate and adaptive immune response to the inflammatory attack. An upregulation of CB1 and CB2, often suggested as part of a homeostatic response of the ECS to injury, was not observed.
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Acknowledgements
Open access funding provided by Medical University of Graz. Thanks to Veronika Pommer for expert technical assistance.
Funding
The study was supported by the Austrian Science Fund (P30144 to RS).
Notes
Conflict of interest
The authors declare that they have no conflicts of interest.
Research involving animal participants
All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.