The prostaglandin receptor EP4 suppresses colitis, mucosal damage and CD4 cell activation in the gut (original) (raw)
Exacerbation of colitis by indomethacin in mice treated with low-dose (3%) DSS. Administration of NSAIDs, the inhibitor of prostanoid synthesis, often triggers or worsens IBD in humans and is regarded as one of the major risk factors of IBD. To confirm the adverse effect of NSAIDs in mice, we added indomethacin to mice treated with low-dose (3%) DSS. Low-dose DSS-treatment of control C57BL/6 mice for 7 days evoked only marginal alterations in stool consistency and slight loss of the body weight, and there was no significant change in the diarrhea and hemoccult scores. Similarly, administration of indomethacin alone in the drinking water (4 mg/kg per day) did not cause significant body weight loss, diarrhea, or hemoccult in the stool (data not shown). When the mice were treated with indomethacin and 3% DSS in combination, however, they gradually lost weight, and their body weight loss was significant compared with the mice treated with 3% DSS alone on day 3 and thereafter (Figure 1a). The mice treated with indomethacin and 3% DSS also showed gradual onset of diarrhea, and the diarrhea score significantly increased compared with the mice treated with 3% DSS alone after day 2 (Figure 1b). Furthermore, the mice treated with indomethacin and 3% DSS developed acute onset of bloody stool. This symptom worsened gradually and, on day 4 and thereafter, most of mice in this group showed gross bleeding, while all of the mice treated with 3% DSS alone did not show hemoccult in the stool at all (Figure 1c). The macroscopic examination of the intestine revealed hemorrhagic redness of the whole large intestine in mice treated with indomethacin and 3% DSS (data not shown). In some cases, the distal portion of the ileum showed redness, while the stomach and jejunum always appeared intact. Upon histological examination, crypt damage, ulceration, and infiltration of inflammatory cells, including neutrophils and lymphocytes, were reproducibly observed in the colon of mice treated with indomethacin and 3% DSS (Figure 1e). The histological injury score was significantly increased in mice treated with indomethacin and 3% DSS when compared with the mice treated with 3% DSS alone (Figure 1d). Treatment with indomethacin and 3% DSS provoked significant leukocytosis and anemia when compared with treatment with 3% DSS alone (Figure 1, f and g). Moreover, splenomegaly was found in mice treated with indomethacin and 3% DSS in combination (Figure 1h). Flow cytometric analysis revealed that most of the splenocytes from mice treated with indomethacin and 3% DSS were TER119-positive cells (data not shown), indicating that extramedullary hematopoiesis occurred in the spleen to compensate for severe anemia.
Induction of colitis by indomethacin in mice treated with 3% DSS and suppression of this effect by dm-PGE2. (a–c) Wild-type C57BL/6 mice were treated with either 3% DSS alone (diamonds), 3% DSS and indomethacin (squares), or 3% DSS, indomethacin, and dm-PGE2 (triangles), and monitored for body weight loss (a), diarrhea (b), and hemoccult (c) for 7 days. (d and e) On day 7, the mice were sacrificed. The colon was dissected for histological analysis with H&E staining (e), and the histological injury scores were obtained (d). Blood was collected for measurement of the WBC number (f) and HCT (g). The weights of spleens of the sacrificed animals are shown (h). N, mice treated with vehicle; D, mice treated with 3% DSS alone; D+I, mice treated with 3% DSS and indomethacin; D+I+E, mice treated with 3% DSS, indomethacin, and dm-PGE2. Data in a–d and f–h are means ± SEM from six animals. *P < 0.05 versus D (Dunnett). #P < 0.05 versus D+I (Dunnett multiple comparison test). Scale bars, 200 μm in e.
Suppression by exogenous PGE2 of the indomethacin-induced exacerbation of low-dose (3%) DSS-induced colitis. Indomethacin inhibited the production of prostanoids by inhibition of both COX-1 and COX-2. Because it was reported that the level of PGE2 was elevated locally in the intestine of IBD patients (10, 11), we wondered whether the exacerbation by indomethacin was due to the inhibition of PGE2 production. To address this point, we administered intraperitoneally a stable PGE2 analogue, dimethyl-PGE2 (dm-PGE2) to the mice treated with indomethacin and 3% DSS. Dm-PGE2 significantly suppressed the weight loss in mice treated with indomethacin and 3% DSS in combination alone (Figure 1a). Dm-PGE2 also prevented clinical symptoms, such as diarrhea and hemoccult, induced by indomethacin and 3% DSS. The diarrhea score was significantly improved on days 2, 3, 5, 6, and 7 (Figure 1b). The hemoccult score was also improved (Figure 1c). Moreover, dm-PGE2 ameliorated the histological findings of the colon induced by the treatment with indomethacin and 3% DSS. There was no epithelial cell loss, crypt damage, or inflammatory cell aggregation in the colon from mice administered with dm-PGE2 (Figure 1e). Consequently, dm-PGE2 significantly suppressed the histological injury score, when compared with the mice treated with indomethacin and 3% DSS (Figure 1d). Hematological evaluation showed that the treatment with dm-PGE2 corrected leukocytosis and anemia found with the treatment with indomethacin and 3% DSS in combination alone (Figure 1, f and g) and resolved the splenomegaly found in the mice treated with indomethacin and 3% DSS in combination alone (Figure 1h). These results suggest that the exacerbation of DSS-induced colitis by indomethacin was mostly, if not solely, due to the inhibition of endogenous PGE2 production.
Induction of severe colitis by 3% DSS in EP4-deficient mice but not in mice deficient in other prostanoid receptors. PGE2 elicits its physiological effects by acting on four different subtypes of EP receptors (9). Previously, we generated mice deficient in each EP subtype individually (14–16). To clarify which subtype of the EP receptor mediates the protective action of PGE2 in DSS-induced colitis, we subjected EP1–/–, EP2–/–, EP3–/–, and EP4–/– mice to 3% DSS treatment. C57BL/6 mice were used as controls for EP1–/–, EP2–/–, and EP3–/– mice, and the progeny of wild-type littermates (EP4+/+) in the mixed background of C57BL/6 and 129/Ola were used as controls for EP4–/– mice. These mice neither developed gastrointestinal inflammation spontaneously nor exhibited any clinical manifestations, such as diarrhea, fecal occult blood, or anemia, when they were raised under SPF conditions. When these animals were treated with 3% DSS, only EP4–/– mice developed severe bloody diarrhea and body weight loss, while the body weight loss, diarrhea, and hemoccult of EP1–/–, EP2–/–, and EP3–/– mice were similar to those of control C57BL/6 mice. EP4–/– mice treated with 3% DSS lost their weight progressively during the entire experimental period and significantly as compared with control EP4+/+ mice (Figure 2a). The diarrhea score of EP4–/– mice was significantly high compared with EP4+/+ mice (Figure 2b). These mice showed loose stool already on day 1, and some of them exhibited watery diarrhea after day 6. EP4–/– mice also showed hemoccult already on day 1, and most of them exhibited gross bleeding in the stool after day 6, yielding significantly higher hemoccult scores than the EP4+/+ mice throughout the experimental period (Figure 2c). The macroscopic finding of the intestine of EP4–/– mice treated with 3% DSS and sacrificed on day 7 showed edema and hemorrhagic redness all through the colon and cecum (Figure 2d). These mice also showed splenomegaly (data not shown). While the histological examination of the colon obtained from EP4+/+ mice treated with 3% DSS appeared normal, the histological results from EP4–/– mice treated with 3% DSS showed epithelial loss, crypt damage, partial ulceration, and infiltration of inflammatory cells (Figure 2e, upper and middle). The inflammatory cells included neutrophils, lymphocytes, and eosinophils as found at high magnification (Figure 2e, lower). Consistently, the histological injury score obtained from six EP4–/– mice was significantly higher than that from six control mice (Figure 2f). The time course of weight loss, the character of bloody diarrhea, and histological findings obtained from EP4–/– mice treated with 3% DSS were similar to those obtained from C57BL/6 mice treated with 3% DSS and indomethacin in combination. These findings suggest that the indomethacin-induced exacerbation of colitis was mostly, if not solely, due to its inhibition of the PGE2-EP4 signaling. To confirm this point further and to assess the contribution of prostanoids other than PGE2, we subjected mice deficient in either DP, FP, IP, or TP to the 3% DSS-induced colitis model. As shown in Figure 2, g and h, none of the DP–/–, IP–/–, FP–/–, and TP–/– mice developed body weight loss, diarrhea, or bloody stool to an extent similar to that found in EP4–/– mice. These results suggest that contribution of other prostanoids is, if present, much limited.
Induction of severe colitis by 3% DSS in EP4-deficient mice and not in mice deficient in other prostanoid receptors. (a–c) Wild-type C57BL/6 (filled circles), EP1–/– (filled triangles), EP2–/– (filled squares), EP3–/– (open circles), EP4+/+ (open triangles), and EP4–/– (open squares) mice were treated with 3% DSS for 7 days and monitored for body weight loss (a), diarrhea (b), and hemoccult (c). The numbers of mice used in this experiment were 25 (C57BL/6), 7 (EP1–/–), 10 (EP2–/–), 14 (EP3–/–), 16 (EP4–/–), and 12 (EP4+/+). (d–f) On day 7, EP4+/+ and EP4–/– mice treated with 3% DSS were sacrificed. The macroscopic examination of the large intestine is shown (d). The colon was dissected for histological analysis with H&E staining (e), and the histological injury scores were obtained (f). (g and h) Body weight loss (g) and clinical scores (h) of mice deficient in DP, FP, IP, and TP in 3% DSS colitis. DP–/–, FP+/+, FP–/–, IP–/–, and TP–/– mice were treated with 3% DSS for 7 days and monitored for body weight, diarrhea, and hemoccult. The body weight loss and clinical scores (diarrhea score plus hemoccult score) of these mice are compared with those of EP4+/+, EP4–/–, and C57BL/6 wild-type mice. The numbers of mice used in this experiment were 12 (EP4+/+), 16 (EP4–/–), 18 (C57BL/6), 11 (DP–/–), 5 (FP+/+), 4 (FP–/–), 8 (IP–/–), and 5 (TP–/–). Data in a–c and f–h are means ± SEM. *P < 0.05 versus EP4+/+ (t test) in a–c. Scale bars, 1 cm in d; 200 μm in upper and middle panel of e; 40 μm in lower panel of e.
Reproduction of the EP4–/– phenotype in wild-type mice by administration of the EP4 antagonist. To confirm that the above phenotype of EP4–/– mice is due to the lack of EP4 receptor, we used an EP4-selective antagonist, AE3-208 (Figure 3a, left). AE3-208 was added to 3% DSS in the drinking water and administered to C57BL/6 mice for 7 days. The mice treated with the EP4 antagonist and 3% DSS together showed severe weight loss and bloody diarrhea. Significant differences in the weight loss and the diarrhea and hemoccult scores were found between these mice and mice treated with 3% DSS alone (Figure 3b). Consistently, the histological injury score of mice treated with the EP4 antagonist and 3% DSS in combination was also significantly high compared with those treated with 3% DSS alone (Figure 3c). To verify the specificity of AE3-208 in vivo, we applied this compound to EP4–/– mice together with 3% DSS. AE3-208 did not exacerbate the colitis further in EP4–/– mice; the body weight loss of 10.2% ± 4.2% and 8.7% ± 3.2%, the diarrhea score of 1.3 ± 0.3 and 1.8 ± 0.3, and the hemoccult score of 3.3 ± 0.5 and 3.3 ± 0.5 were observed on day 7 in EP4–/– mice treated with AE3-208 and untreated EP4–/– mice, respectively (n = 5, each).
Effect of EP4-selective drugs on DSS-induced colitis. (a) Structures of ONO-AE3-208 (left) and ONO-AE1-734 (right). (b and c) Reproduction of the EP4–/– phenotype in wild-type mice by administration of an EP4 antagonist. AE3-208, an EP4 antagonist, was added to 3% DSS in the drinking water and administered to C57BL/6 mice for 7 days. Body weight loss, diarrhea, and hemoccult scores on day 7 of 3% DSS-treated mice administered with vehicle (open bars) or AE3-208 (closed bars) is shown in b, and histological injury scores of the colon are shown in c. (d–f) Amelioration of high-dose (7%) DSS-induced colitis by an EP4 agonist. High-dose (7%) DSS was administered to C57BL/6 mice together with vehicle or AE1-734, an EP4 agonist, for 7 days. Body weight loss, diarrhea, and hemoccult scores on day 7 of 7% DSS-treated mice with vehicle (open bars) or the EP4 agonist (closed bars) are shown in d, and H&E staining of the colon (f) and the histological injury scores (e) are shown. Data are means ± SEM from five to ten mice. *P < 0.05 versus mice treated with 3% or 7% DSS alone (t test). Scale bars, 200 μm in f.
Amelioration of high-dose (7%) DSS-induced colitis by an EP4 agonist. Because the above study showed that the EP4 antagonist exacerbated low-dose DSS-induced colitis, we wondered whether an EP4 agonist ameliorates severe colitis. To examine this issue, we used the colitis induced by high-dose DSS as a model. Administration of high-dose (7%) DSS in the drinking water to wild-type mice induced fulminant colitis characterized by the bloody diarrhea and loss of body weight; the body weight loss, diarrhea score, and hemoccult score on day 7 were 9.8% ± 2.7%, 2.2 ± 0.1, and 3.8 ± 0.2, respectively (Figure 3d). Upon histological examination, epithelial loss, goblet cell loss, and aggregation of inflammatory cells were observed in the mice treated with 7% DSS (Figure 3f). When we administered an EP4 agonist, AE1-734 (Figure 3a, right), subcutaneously twice a day to 7% DSS-treated mice, we found that the EP4 agonist significantly suppressed the weight loss and bloody diarrhea induced by 7% DSS treatment in C57BL/6 mice. The body weight loss, diarrhea score, and hemoccult score on day 7 were 3.3% ± 1.0% versus 9.8% ± 2.7%, 1.1 ± 0.3 versus 2.2 ± 0.1, and 1.4 ± 0.4 versus 3.8 ± 0.2, respectively (Figure 3d). Upon histological examination, there were neither loss of epithelial and goblet cells nor aggregation of inflammatory cells in the colon of the mice treated with the EP4 agonist in addition to 7% DSS (Figure 3f). Consistently, the EP4 agonist lowered the histological injury score to 7.5 ± 1.1 from 22.3 ± 3.5 found in mice treated with 7% DSS alone (Figure 3e). This preventive action of AE1-734 was most likely due to stimulation of the EP4 receptor, because administration of this compound to EP4–/– mice treated with 7% DSS did not ameliorate any symptoms of the colitis throughout the experi-mental period. The body weight loss, the diarrhea score, and the hemoccult score on day 7 were 23.4% ± 1.4% and 22.0% ± 2.2%, 4.0 ± 0.0 and 4.0 ± 0.0, and 4.0 ± 0.0 and 4.0 ± 0.0 for EP4–/– mice treated with AE1-734 and untreated EP4–/– mice, respectively (n = 5, each).
Impaired mucosal integrity in mice with the EP4 deficiency. The above studies taken together have suggested that the PGE2-EP4 signaling plays a critical role in protection of DSS-induced colitis. To obtain a mechanistic insight into the protective action of the PGE2-EP4 signaling, we first used FITC-dextran assay and evaluated the mucosal barrier function in the induction phase of colitis. The EP4 antagonist (AE3-208) was administered in the drinking water (10 mg/kg/day) to C57BL/6 mice 1 day before and throughout the treatment of 3% DSS. Twenty-four hours after DSS treatment, FITC-dextran was given orally, and 4 hours later blood was drawn. The serum level of FITC-dextran in the mice treated with the EP4 antagonist and DSS was significantly higher than that in nontreated mice, while that in mice treated with 3% DSS alone or AE1-734 alone was not significantly higher than that in nontreated mice (Figure 4a). We also administered FITC-dextran orally to EP4+/+ and EP4–/– mice treated with 3% DSS for 1 day. Four hours after FITC-dextran administration we excised the colon for fluorescent microscopic examination. The colon from EP4–/– mice treated with 3% DSS showed significant infiltration of FITC-dextran into submucosa, while no infiltration was found in that from EP4+/+ mice (Figure 4b).
Impaired mucosal integrity caused by the EP4-deficiency. (a) Effect of the EP4 antagonist. C57BL/6 mice were treated with either vehicle (None), 3% DSS alone, AE3-208 (EP4 antagonist) alone, or 3% DSS and AE3-208 in combination for 1 day. FITC-dextran was administered by mouth, and the serum level was measured 4 hours later. Data are means ± SEM from six mice per group. *P < 0.05 versus the vehicle-treated mice (t test). (b) DSS-induced submucosal infiltration of FITC-dextran in EP4-deficient mice. FITC-dextran was administered by mouth to EP4+/+ and EP4–/– mice pretreated with 3% DSS for 1 day. Four hours later the colon was excised and subjected to fluorescent microscopic examination. Scale bars, 1 mm.
Impaired epithelial regeneration and enhanced CD4+ T cell activation in mice treated with an EP4 antagonist during the recovery period after high-dose DSS-induced colitis. The results above revealed that the PGE2-EP4 signaling is important in the maintenance of the mucosal barrier in induction of colitis. This impairment of the mucosal barrier would lead to the exposure of submucosa to luminal antigens. We next examined whether EP4 plays a role in prevention of the disease progression and/or in repair of epithelial damage. Since EP4 was reported to be expressed on epithelial cells in the large intestine (27), we hypothesized that the intestinal epithelial growth after injury was modulated by the PGE2-EP4 signaling. To clarify this point, we used the BrdU incorporation assay. After high-dose (7%) DSS treatment for 7 days, mice were treated with or without the EP4 antagonist (AE3-208) in the absence of DSS treatment for 3 days and sacrificed. BrdU was added intraperitoneally 2 hours before sacrifice. While the vehicle-treated mice quickly recovered from the weight loss and bloody diarrhea, the EP4 antagonist–treated mice continued to exhibit severe colitis (data not shown). The histological results from the H&E-stained colon from the vehicle-treated mice appeared normal, while those from the EP4 antagonist–treated mice showed that epithelial and crypt loss remained as that seen in the colon from mice treated with 7% DSS for 7 days (Figure 5, a and b). Moreover, in the mice treated with the EP4 antagonist, infiltration of inflammatory cells, including lymphocytes and neutrophils in submucosa, became more pronounced (Figure 5c). As for BrdU staining, a number of positive cells were found in the crypt epithelium of the colon from the vehicle-treated mice, suggesting that repair from epithelial damage was occurring (Figure 5, d and e). On the other hand, in mice treated with the EP4 antagonist after DSS treatment, BrdU-positive epithelial cells were barely detected, indicating that the PGE2-EP4 signal blockade suppressed epithelial regeneration (Figure 5, f and g). On the other hand, there existed a large number of BrdU-positive mononuclear cells in the submucosal area of the EP4 antagonist–treated mice (Figure 5, f and h). Immunohistochemistry showed that CD4+ T cells comprised the majority of these inflammatory cells (Figure 5i). This pronounced infiltration of CD4+ T cells was not seen in the colons from mice treated with 7% DSS for 7 days (data not shown). CD8- or B220-positive cells were also seen, but they did not make clusters as did CD4+ cells but were scattered all over the lamina propria (Figure 5, j and k). Neutrophils and macrophages were also detected (data not shown). Most of the infiltrated cells were also stained positive with anti–IFN-γ Ab, while IFN-γ–positive cells were found only occasionally in the submucosa from the vehicle-treated mice (Figure 5, l and m). These results suggest that the activation of T cells occurred upon prolonged PGE2-EP4 signal blockade.
Impaired epithelial proliferation and enhanced CD4+ T cell proliferation in mice treated with an EP4 antagonist. Mice pretreated with 7% DSS for 7 days were then administered with either vehicle (a, d, e, and l) or the EP4 antagonist (AE3-208) (b, c, f–k, and m) for 3 days without DSS and sacrificed. BrdU was added intraperitoneally 2 hours before sacrifice. The colon was dissected for histological examination with H&E staining (a–c) and immunohistochemical analysis for BrdU (d–h), CD4 (i), CD8 (j), B220 (k), and IFN-γ (l and m). (e and g) Enlarged figures of d and f, respectively, showing the epithelial area; (h) an enlarged figure of f showing the submucosal area. (i–m) The submucosal area. Scale bars, 200 μm in a, b, d, f; 100 μm in c, e, g, h; 40 μm in i–m.
Downregulation of LPMNC proliferation and Th1 cytokine production by the PGE2-EP4 signaling. The results above showed that the enhanced proliferation of CD4+ T cells in the lamina propria occurred with prolonged inhibition of the EP4 signaling in colitis. EP4 was reported to be present on CD4+ T cells in the submucosa of the large intestine (27). These findings taken together suggest that EP4 activation may downregulate the proliferation of CD4+ T cells to modulate immunological response in the lamina propria. To examine this issue, we isolated LPMNCs from C57BL/6 mice and examined the effect of the EP4 agonist and antagonist on their proliferative response by measuring [3H] thymidine incorporation. LPMNCs treated with the EP4 antagonist (AE3-208) or indomethacin exerted a significant increase in the proliferative response compared with those treated with vehicle (Figure 6a). There was no additive effect of the EP4 antagonist and indomethacin in combination compared with the EP4 antagonist alone or indomethacin alone. The addition of the EP4 agonist suppressed the increase in the proliferative response by indomethacin (Figure 6a), while it did not suppress the proliferation of LPMNCs without indomethacin treatment (data not shown). Control experiments using LPMNCs from EP4–/– mice showed that the EP4 agonist and antagonist, as well as indomethacin, did not affect the proliferative response (Figure 6b). These results suggest that stimulation of the proliferative response of wild-type LPMNCs by the EP4 antagonist or indomethacin was due to the inhibition of the action of endogenous PGE2 on the EP4 receptor of these cells. This experiment thus clearly corroborates the immunosuppressive action of EP4 on LPMNCs and suggests that the enhanced proliferation of CD4+ T cells seen in the colitis of the animals treated with the EP4 antagonist AE3-208 was caused by prolonged inhibition of the EP4 signaling in T cells. We next examined the effect of the EP4 signaling on cytokine production. We either incubated LPMNCs for 72 hours without stimulation or stimulated them for 72 hours with LPS or LPS and ConA in combination and examined the effects of the EP4 agonist or antagonist on the levels of Th1 cytokines produced under these conditions. In all cases, the levels of IFN-γ significantly increased with the treatment of the EP4 antagonist and decreased with the EP4 agonist (AE1-734) treatment (Figure 6c). Similarly, the levels of IL-2 in the culture medium significantly increased with the EP4 antagonist treatment and decreased with the EP4 agonist treatment (Figure 6d). These results suggest that the PGE2-EP4 signaling regulates the proliferation and Th1 cytokine production of LPMNCs.
Modulation of the LPMNC proliferation and Th1 cytokine production by EP4 signaling. (a and b) LPMNCs were prepared from C57BL/6 mice (a) or from EP4–/– mice (b), cultured with either vehicle (None), the EP4 antagonist (AE3-208), the EP4 agonist (AE1-734), or indomethacin (IND) either alone or in indicated combination, and examined for the proliferation by measuring [3H] thymidine uptake. Data are means ± SEM (n = 3). *P < 0.05 versus None (Tukey multiple comparison test). #P < 0.05 versus IND (Tukey multiple comparison test). (c and d) LPMNCs were stimulated for 72 hours with vehicle, LPS, or LPS and ConA in combination in the presence of vehicle (None), the EP4 antagonist (AE3-208), or the EP4 agonist (AE1-734), and the levels of IFN-γ (c) and IL-2 (d) in the culture medium were measured with an ELISA kit. Data are means ± SEM (n = 3). *P < 0.05 versus None (Dunnett multiple comparison test).
Elevated expression of genes associated with immune response and reduced expression of genes with mucosal repair and remodeling in the colon of EP4-deficient mice. To evaluate the functions of the EP4 signaling in more detail at the molecular level, we employed the DNA microarray analysis and compared the gene expression profiles of the colon between EP4–/– mice and EP4+/+ mice treated either with vehicle or low-dose (3%) DSS for 7 days. We tested about 10,000 genetic loci as identified UNIGENE clusters. After exclusion of expressed sequence tags (ESTs), we detected 30 genes that showed more than twofold increase and 53 genes that showed more than twofold decrease of expression in the vehicle-treated EP4–/– mice as compared with the vehicle-treated EP4+/+ mice. Representative genes are shown in the upper panel of Table 1. Gene expression profiles revealed that EP4–/– mice had reduced expression of genes involved in tissue defense, remodeling, and immunosuppression, such as NOV protein, angiogenin-3 precursor, intelectin, and TGF-β, and had increased expression of genes involved in tissue destruction, such as matrix metalloproteinase, and genes induced by IFN-γ, such as mig, guanylate nucleotide–binding protein, and indoleamine 2,3-dioxygenase. These results suggest that although EP4–/– mice appeared normal, both clinically and histologically without overt insults, they already have signs of intestinal injury or infection. To explore the possibility that other prostanoid receptors may be upregulated in compensation for the EP4 absence, we also examined expression of other prostanoid receptor genes. Among the seven other receptors, only the DP receptor showed a significant increase in expression (Table 1, upper panel). We next compared the gene expression profiles of the colon from EP4–/– and EP4+/+ mice treated with 3% DSS. After exclusion of ESTs, we detected 388 genes that showed more than threefold increase and 79 genes that showed more than threefold decrease of expression in EP4–/– mice as compared with EP4+/+ mice. Since the histological results of 3% DSS-treated EP4–/– mice showed epithelial loss and inflammatory cell aggregation, we focused on genes related to epithelial repair and chemokine families. EP4–/– mice treated with 3% DSS showed decreased expression of genes of epidermal growth factor (EGF) and EGF-binding proteins and increased expression of genes of chemokine families, such as ENA78, fractalkine, MCP-1, and RANTES (Table 1, the middle panel). Moreover, we examined whether the DSS treatment affected expression of genes of the prostanoid receptors and found that the expression of the gene for EP4 as well as that for DP significantly increased with DSS treatment in wild-type mice (Table 1, the lower panel).
Gene expression profile of the colon analyzed by the DNA microarray