Modulate immune system activity at the gut mucosa initially was analyzed by measuring 15900046 cytokine gene expression in small intestinal tissue. Mice were administered GRA or vehicle alone by oral gavage. Ten hours post-treatment, total RNA was extracted from sections of the 
gut taken ,one cm from the gastroduodenal junction, or the ileum, and changes in cytokine gene transcription were measured by RT-qPCR using a Mouse Inflammatory Cytokine array. In the initial experiment, ten genes were up-regulated in GRA-treated mice .2-fold over vehicle-treated controls. These genes, listed in Table 1, plus one additional gene of interest, CCL21b, were chosen to design custom arrays. The same pattern of up-regulated chemokine and chemokine ML 240 price receptor transcripts was observed in multiple repetitions of the experiment, and was similar regardless of whether RNA was extracted from duodenal or ileal tissue. GRA-induced transcripts included chemokine receptor CXCR5 and its ligand CXCL13, receptor CCR7 and its ligands CCL19 and CCL21b, and receptors CCR6 and CCR9. Increased transcription of genes encoding the ligands for CCR6 and CCR9 (CCL20 
and CCL25, respectively) did not meet the established cut-off of .2-fold Docosahexaenoyl ethanolamide web change, although CCL20 was moderately up-regulated in the original full array (1.6 fold, data not shown). Lymphotoxin A (Lta) and lymphotoxin B (Ltb) also were up-regulated in GRA-treated animals. IFN-c and IL-10 were moderately increased in the first experiment, but induction was not consistent between multiple experiments. Some variability between mice in terms of the presence or absence of a response was observed. However, the pattern was reproducible with respect to both the transcripts that were induced and the relative magnitude of expression in all mice that responded, and these genes never were up-regulated in vehicle-treated controls. Expression of genes encoding these chemokine receptors and their corresponding ligands is consistent with signals known to be required for lymphocyte recruitment to the intestinal mucosa, and with formation and maturation of B cell-rich isolated lymphoid follicles (ILF, ([24,25], see below). To test whether enteric rotavirus infection affected induction of these genes by GRA, mice were infected for 18 hours with murine rotavirus strain EW prior to administration of GRA. The same pattern of gene expression was observed (Table 1), indicating virus replication does not modulate the signal-inducing activity of GRA early post-infection. These results suggest GRA likely has a direct effect on specific cellular targets in the small intestinal mucosa that results in coordinated chemokine and receptor gene expression.Cxcr5 Ccl19 Ccr6 Ccr7 Ccr9 Cxcl13 IFNc Il10 Lta Ltb Ccl21bDuodenum 30.0 3.4 9.4 5.3 2.6 4.2 2.6 2.6 6.8 4.2 NDIleum 21.0 15.7 12.5 10.4 2.2 4.6 1.4 1.6 8.5 6.2 3.+EW 23.4 13.8 9.8 6.4 1.3 7.1 ND 1.3 4.3 4.1 2.Representative data are shown for RNA isolated from duodenal or ileal tissue. Data shown for duodenal tissue are from the initial full array. Data from ileal sections from uninfected and EW infected mice were obtained with the custom array. Data are presented as fold-increase over mock-treated controls. ND ?not done. doi:10.1371/journal.pone.0049491.tImmune Cell Populations Induced in MLNs and PPs by GRAThe observed pattern of chemokine and receptor gene expression led us to examine the effects of GRA on immune cell populations at mucosal inductive sites. Mice were administered GRA or vehicle and infecte.Modulate immune system activity at the gut mucosa initially was analyzed by measuring 15900046 cytokine gene expression in small intestinal tissue. Mice were administered GRA or vehicle alone by oral gavage. Ten hours post-treatment, total RNA was extracted from sections of the gut taken ,one cm from the gastroduodenal junction, or the ileum, and changes in cytokine gene transcription were measured by RT-qPCR using a Mouse Inflammatory Cytokine array. In the initial experiment, ten genes were up-regulated in GRA-treated mice .2-fold over vehicle-treated controls. These genes, listed in Table 1, plus one additional gene of interest, CCL21b, were chosen to design custom arrays. The same pattern of up-regulated chemokine and chemokine receptor transcripts was observed in multiple repetitions of the experiment, and was similar regardless of whether RNA was extracted from duodenal or ileal tissue. GRA-induced transcripts included chemokine receptor CXCR5 and its ligand CXCL13, receptor CCR7 and its ligands CCL19 and CCL21b, and receptors CCR6 and CCR9. Increased transcription of genes encoding the ligands for CCR6 and CCR9 (CCL20 and CCL25, respectively) did not meet the established cut-off of .2-fold change, although CCL20 was moderately up-regulated in the original full array (1.6 fold, data not shown). Lymphotoxin A (Lta) and lymphotoxin B (Ltb) also were up-regulated in GRA-treated animals. IFN-c and IL-10 were moderately increased in the first experiment, but induction was not consistent between multiple experiments. Some variability between mice in terms of the presence or absence of a response was observed. However, the pattern was reproducible with respect to both the transcripts that were induced and the relative magnitude of expression in all mice that responded, and these genes never were up-regulated in vehicle-treated controls. Expression of genes encoding these chemokine receptors and their corresponding ligands is consistent with signals known to be required for lymphocyte recruitment to the intestinal mucosa, and with formation and maturation of B cell-rich isolated lymphoid follicles (ILF, ([24,25], see below). To test whether enteric rotavirus infection affected induction of these genes by GRA, mice were infected for 18 hours with murine rotavirus strain EW prior to administration of GRA. The same pattern of gene expression was observed (Table 1), indicating virus replication does not modulate the signal-inducing activity of GRA early post-infection. These results suggest GRA likely has a direct effect on specific cellular targets in the small intestinal mucosa that results in coordinated chemokine and receptor gene expression.Cxcr5 Ccl19 Ccr6 Ccr7 Ccr9 Cxcl13 IFNc Il10 Lta Ltb Ccl21bDuodenum 30.0 3.4 9.4 5.3 2.6 4.2 2.6 2.6 6.8 4.2 NDIleum 21.0 15.7 12.5 10.4 2.2 4.6 1.4 1.6 8.5 6.2 3.+EW 23.4 13.8 9.8 6.4 1.3 7.1 ND 1.3 4.3 4.1 2.Representative data are shown for RNA isolated from duodenal or ileal tissue. Data shown for duodenal tissue are from the initial full array. Data from ileal sections from uninfected and EW infected mice were obtained with the custom array. Data are presented as fold-increase over mock-treated controls. ND ?not done. doi:10.1371/journal.pone.0049491.tImmune Cell Populations Induced in MLNs and PPs by GRAThe observed pattern of chemokine and receptor gene expression led us to examine the effects of GRA on immune cell populations at mucosal inductive sites. Mice were administered GRA or vehicle and infecte.
