Open Access

Abnormalities in endocrine and immune cells are correlated in dextran‑sulfate‑sodium‑induced colitis in rats

  • Authors:
    • Magdy El‑Salhy
    • Jan Gunnar Hatlebakk
    • Odd Helge Gilja
  • View Affiliations

  • Published online on: December 12, 2016     https://doi.org/10.3892/mmr.2016.6023
  • Pages:12-20
  • Copyright: © El‑Salhy et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

The interaction between the gut hormones and the immune system has been suggested to serve an important role in the pathophysiology of inflammatory bowel disease. The aims of the present study were to elucidate the possible abnormalities in the colonic endocrine cells in rats with dextran sodium sulfate (DSS)‑induced colitis, and to determine whether they are correlated with alterations in the immune cells. A total of 24 male Wistar rats were divided into two groups: Control and DSS‑induced colitis. Colonic tissues were harvested via postmortem laparotomy from all of the animals at the end of the experimental period, and fixed and sectioned for histology. The colonic endocrine and immune cells in those tissue samples were immunostained and their densities quantified by computerized image analysis. The densities of chromogranin A, serotonin, peptide YY and oxyntomodulin cells were significantly higher, and those of pancreatic peptide and somatostatin cells were lower in rats with DSS‑induced colitis than in the controls. The densities of mucosal leukocytes, T and B lymphocytes, macrophages/monocytes, and mast cells were significantly higher than in the controls, and these changes were closely associated with the aforementioned changes in all endocrine cell types. These observations indicate an interaction between intestinal hormones and the immune system as represented by immune cells.

Introduction

The etiology of inflammatory bowel disease (IBD) remains unclear (13). There are three main forms of IBD, ulcerative colitis (UC), Crohn's disease (CD) and microscopic colitis (MC), which exhibit differences in prevalence, clinical course and prognosis (36). While the onset of UC and CD occurs predominantly in individuals <40 years, the onset of MC occurs in those >60 years (3,7). In addition to the morbidity caused by IBD, it considerably reduces the quality of life of patients (3,5,6).

The gastrointestinal endocrine cells are a component of the local regulatory system of the gut, the neuroendocrine system (NES) (8), which also includes the enteric nervous system (8). The NES regulates gastrointestinal motility, secretion, absorption, cell proliferation, visceral sensitivity, local immune defense and appetite (8,9). Abnormalities in several intestinal endocrine cells have been reported in IBD (1029). It is believed that the interaction between the hormones secreted by the gut endocrine cells and the immune system serve a major role in the pathophysiology of the IBD (30,31).

The primary aim of the present study was to establish the presence of abnormalities in the colonic endocrine cells following dextran sulfate sodium (DSS)-induced colitis in rats, which closely mimics human UC (32). Furthermore, the existence of a correlation between any colonic endocrine cell abnormalities and changes in the densities of various types of immune cells was determined.

Materials and methods

Rats

A total 24 male Wistar rats (age, 12 weeks; Hannover GALAS; Taconic Biosciences, Lille Skensved, Denmark) with a mean body weight of 280 g (range, 231–380 g) were housed in Macrolon III cages with water and food available ad libitum. They were fed a standard diet (B & K Universal, Nittedal, Norway) consisting of cereal products (88.5%), soy protein (6%), animal protein (2.5%), soy oil (0.5%), and vitamin, mineral and amino-acid supplements (2.5%). The animals were maintained at a temperature of 21±1°C and a relative humidity of 55±5%, and under a 12/12-h light/dark cycle.

The animals were left to acclimatize in the animal house for 7 days prior to the experiment, and were then divided into 2 groups of 12 animals each: Control and DDS-induced colitis (DSS group). Animals in the control group were provided with normal drinking water for 7 days, while those in the DDS-colitis group were instead provided with distilled water containing 5% DSS (molecular weight, 40 kDa; prepared daily; TdB Consultancy AB, Uppsala, Sweden) for 7 days, according to a previously described protocol (33,34). All of the animals were monitored twice daily and were weighed once daily. Animals that showed any signs of pain were given a subcutaneous, 1 ml injection of Temgesic solution (containing 0.3 g/ml Temgesic; Merck Millipore, Darmstadt, Germany).

At the end of the 7-day period, the animals were sacrificed by CO2 inhalation, and the colon was dissected out via a postmortem laparotomy. Tissue samples were collected from the lower part of the colon for further, histopathological and immunohistochemical examinations.

The local ethical committee for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes approved the study protocols (project no. 20124629).

Histopathology and immunohistochemistry

The tissue samples were fixed overnight in 4% buffered paraformaldehyde, embedded in paraffin and then sectioned at a thickness of 5 mm. The sections were deparaffinized and then stained with hematoxylin-eosin, or immunostained using the ultraView Universal DAB Detection kit (version 1.02.0018, Ventana Medical Systems, Inc., Basel, Switzerland) and the BenchMark Ultra IHC/ISH staining module (Ventana Medical Systems, Inc.).

For immunostaining, the sections were incubated with one of the following primary antibodies for 32 min at 37°C: Monoclonal mouse anti-N-terminal of purified chromogranin A (CgA; cat. no. M869; Dako, Glostrup, Denmark) diluted 1:1,000, monoclonal mouse antiserotonin (cat. no. 5HT-209; Dako) diluted 1:1,200, polyclonal antiporcine peptide YY (PYY; cat. no. PYY 11A; Alpha Diagnostic International, San Antonio, TX, USA) diluted 1:1,400, polyclonal rabbit antisynthetic human pancreatic polypeptide (PP; cat. no. #114; Diagnostic BioSystems, Pleasanton, CA, USA) diluted 1:800, polyclonal rabbit antiporcine oxyntomodulin ‘glicentin/enteroglucagon’ (cat. no. BP508; Acris Antibodies GmbH, Herford, Germany) diluted 1:400, polyclonal rabbit antisynthetic human somatostatin (cat. no. A566; Dako) diluted 1:200, monoclonal mouse antihuman CD45 (cat. no. M0701; Dako) diluted 1:100, monoclonal mouse antihuman CD5 (cat. no. IS082; Dako) diluted 1:200, monoclonal mouse antihuman CD57 (cat. no. IS647; Dako) diluted 1:100, monoclonal mouse antihuman CD23 (cat. no. IS781; Dako) diluted 1:100, monoclonal mouse antihuman CD68 (cat. no. M0814; Dako) diluted 1:100 and monoclonal mouse antihuman mast-cell tryptase (cat. no. M7052; Dako) diluted 1:100. CD45 is considered a common leukocyte antigen and is expressed exclusively on cells of the hematopoietic system and their progenitors. CD5 is expressed on B and T lymphocytes, CD57 is expressed by subsets of natural killer cells and CD8+ lymphocytes, and by a small proportion of CD4+/CD45R0+ T lymphocytes, CD23 is expressed on B lymphocytes, CD68 labels human monocytes, macrophages, and myeloid cells, and mast-cell tryptase is expressed predominantly in mast cells (35).

Quantification of endocrine and immune cells

The endocrine and immune cells were quantified by counting each cell type in 10 randomly chosen microscopic fields. Measurements were performed on a computer linked to a microscope (BX43; Olympus Corporation, Tokyo, Japan) that was equipped with a digital camera (DP26; Olympus Corporation), and using cellSens imaging software (version 1.7; Olympus Corporation). The number of endocrine cells in the epithelial lining of the intestinal lumen and immune cells in the lamina propria of each field were counted on a computer screen, and the area of the epithelial cells was determined by manual drawing using the computer mouse. A 40X objective was used, for which each frame (field) on the monitor represented a tissue area of 0.035 mm2. The data are presented as density measurements (i.e., the number of endocrine cells/mm2 epithelium, and the number of immune cells per field). Immunostained sections were coded and mixed, and measurements were made by the same person (Professor Magdy El-Salhy), who was blind to the identity of the sections.

Statistical analysis

Differences between the control and DSS groups were tested using the Mann-Whitney nonparametric test. The existence of a correlation between abnormalities/alterations in the densities of endocrine cells and immune cells was determined using the nonparametric Spearman's correlation test. The data are presented as the mean ± standard error, and P<0.05 was considered to indicate a statistically significant difference.

Results

The histopathological examinations of the colonic tissues produced normal results in the control group, whereas the DSS group had severe-to-moderate inflammation with disturbed mucosal architecture, crypt abscesses, edema, bleeding and infiltration of immune cells into the mucosa and submucosa.

Endocrine cells

The densities of CgA, serotonin, PYY and enteroglucagon cells were all significantly higher in the DDS group (333.1±34.7, 61.8±6.5, 115.6±5.9 and 85.7±9.0 cells/mm2 epithelium, respectively) than in the control group (117.4±20.7, 40.7±5.5, 86.0±1.5 and 42.9±3.3 cells/mm2 epithelium; P<0.0001, P=0.0006, P=0.002 and P=0.0003, respectively; Figs. 13). Conversely, the densities of PP and somatostatin cells were significantly higher in the control group (62.4±3.1 and 43.4±3.2 cells/mm2 epithelium, respectively) than in the DSS group (40.3±3.7 and 28.6±2.7 cells/mm2 epithelium, respectively; P=0.0002 and 0.007, respectively; Figs. 1 and 4).

Immune cells

The densities of all of the immune cell types were significantly higher in the DDS group than in the control group (Figs. 58): Leukocytes, 5.9±0.4 vs. 23.3±2.2 cells/field (P<0.0001); B/T lymphocytes, 7.8±0.8 vs. 23.8±1.6 cells/field (P<0.0001); T lymphocytes, 6.8±0.7 vs. 26.6±2.9 cells/field (P<0.0001); and B lymphocytes, 9.8±0.6 vs. 22.1±2.3 cells/field (P<0.0001).

Correlation between endocrine and immune cells

The Spearman correlation coefficients and P-values between different endocrine cell types and various immune cells are summarized in Table I. The abnormalities in CgA, serotonin, PYY, and enteroglucagon cells were identified to be positively correlated with the alterations of all types of immune cells, while a negative correlation was observed for PP and somatostatin cells.

Table I.

Summary of the Spearman correlation coefficient (r) and P values between different endocrine cell types and various immune cells.

Table I.

Summary of the Spearman correlation coefficient (r) and P values between different endocrine cell types and various immune cells.

Immune cell type

Endocrine cell typeLeukocytesB/T lymphocytesT lymphocytesB lymphocytes Macrophages/monocytesMast cells
Chromogranin Ar=0.8r=0.7r=0.6r=0.7r=0.8r=0.7
P=0.006P=0.009P=0.03P=0.008P=0.0009P=0.008
Serotoninr=0.7r=0.7r=0.8r=0.8r=0.8r=0.7
P=0.007P=0.004P=0.004P=0.006P=0.004P=0.008
Peptide YYr=0.6r=0.6r=0.7r=0.6r=0.7r=0.7
P=0.03P=0.04P=0.02P=0.03P=0.02P=0.02
Enteroglucagonr=0.6r=0.8r=0.8r=0.7r=0.7r=0.9
P=0.04P=0.006P=0.006P=0.02P=0.02P=0.0005
Pancreatic peptider=−0.7r=−0.7r=−0.8r=0.7r=−0.7r=0.7
P=0.006P=0.007P=0.001P=0.01P=0.006P=0.006
Somatostatinr=−0.7r=−0.6r=−0.6r=−0.8r=−0.5r=−0.8
P=0.01P=0.02P=0.02P=0.0009P=0.006P=0.0007

Discussion

Animal models of IBD are either those with chemically induced colitis or mutant (knockout) mice (7,32,3639). Although neither of these models accurately mimic human IBD, they are useful tools towards understanding the pathophysiological mechanisms underlying IBD (32). DSS-induced colitis is a mixed Th1/Th2 cytokine-mediated colitis (40,41) and is considered be a model for UC with clinical and morphological features similar to that of human UC (32,42,43). However, DSS-induced colitis lacks the chronicity seen in human UC (32).

The present study identified that the densities of all of the colonic endocrine cell types were affected in rats with DSS-induced colitis. Furthermore, the abnormalities in the colonic endocrine cells were closely correlated with the alterations in several immune-cell types following the induction of colitis. These observations lend support to the hypothesized role of gut hormones in immune activation and inflammation (30,31,44).

CgA belongs to the family of granins (45,46), and is localized to the stomach and small and large intestines (4750). It is commonly used as a marker for gastrointestinal and endocrine tumor cells (51,52). The increase in CgA-immunoreactive cells observed in the present study could reflect an increase in the cell density of the total colonic endocrine cells following the induction of colitis. This observation is in line with the previously reported increases in CgA cells in UC and CD (10,23). However, CgA itself inhibits the vascular leakage caused by tumor necrosis factor α (53). Furthermore, CgA-derived peptides reduce the release of interleukin (IL)-16 and IL-5, hence reducing the number of lymphocytes at inflammatory sites and thus the proinflammatory action of lymphocytes and monocytes (5456). The increase in the density of CgA cells reported herein was closely associated with the increase in immune cells. Taking into consideration the known interaction between CgA and immune cells, this increase in CgA density is likely a response defense mechanism against inflammation.

Serotonin is a potent hormone that exerts several effects at its numerous receptor types. Thus, it stimulates gastric and intestinal motility, modulates visceral sensitivity, and stimulates intestinal secretion (8,57). The present observation of an increased density of colonic serotonin cells in DSS-induced colitis relative to healthy controls is in agreement with previously published observations in patients with UC, CD and MC, and in animal models of colitis (10,12,5860). However, additional studies identified that the serotonin cell density reduced in UC and remained unchanged in CD (61,62). It has been reported that serotonin serves an important role in intestinal inflammation (30,54). Thus, the number of serotonin cells has been reported to be reduced in mice lacking the T-lymphocyte receptors (54), IL-13 receptors have been localized on serotonin cells (63), and serotonin receptors have been observed in lymphocytes, monocytes, macrophages and dendritic cells (64). In addition, serotonin affects the proliferation of lymphocytes, protects natural killer cells, inhibits the apoptosis of immune cells, and promotes the recruitment of T cells (6568). Thus, the fact that the increase in serotonin-cell density in DSS-induced colitis was to be closely associated with the increased densities of the immune-cell types was expected.

PYY and oxyntomodulin are colocalized in the same endocrine cell type (69,70). However, the degree of that colocalization differs according to the animal species (70). PYY delays gastric emptying, and is a key mediator of the ileal brake. It also inhibits gastric and pancreatic secretion, and stimulates the absorption of water and electrolytes (71). Oxyntomodulin has an incretin effect, inhibits gastric and pancreatic secretions, and reduces gastric motility (8). PYY and oxyntomodulin have been previously observed to exhibit anorexigenic effects (72), and the present observation of increased PYY and oxyntomodulin cell densities is in agreement with previous observations in UC and IL-2 gene knockout mice (10,59). Whereas the increase in the oxyntomodulin cell density identified is in line with previous observations in IL-2 knockout mice, it disagrees with observations in UC, where oxyntomodulin cell density was unchanged (10,59). The close correlation between the increase in PYY and oxyntomodulin cell densities with the increase in the densities of the immune cells identified in the current study indicates an interaction between the endocrine and immune systems.

PP stimulates gastric acid secretion and the motility of the stomach and small intestine, and relaxes the gallbladder (8). Somatostatin inhibits intestinal contraction, and gut exocrine and neuroendocrine secretions (8). In addition, somatostatin inhibits lymphocyte proliferation, immunoglobulin synthesis and neutrophil elastase release (7377). The reduction in PP cell density observed in the present investigation is in line with what has been reported in UC and CD (10). Although the reduction in somatostatin cell density in DSS-induced colitis observed in the current study is also in line with previous publications on UC and CD (28,29), it is in disagreement with a study in which the density of somatostatin cells was observed to be unchanged in these conditions (10). As for the other endocrine cell types assessed in the current study, the correlation between the alterations in the PP and somatostatin cell densities points to their involvement in the inflammatory process.

A potential interaction is suggested between inflammation as indicated by the increase in immune cells and the colonic endocrine cells. It is possible that the increase in serotonin and the reduction in somatostatin cell densities results from inflammation, and that the changes in CgA, PYY, oxyntomodulin and PP cells are secondary responses to the changes in serotonin and somatostatin. Cytokines appear to serve a significant role in the proliferation and differentiation of intestinal stem cells (7880). It is suggested that inflammation with increased cytokine production increases the serotonin and reduces the somatostatin cell densities by affecting their early progenitors, and that these alterations would result in increased gastrointestinal motility and secretion in addition to visceral hypersensitivity. As a compensatory defense, an increase in PYY and oxyntomodulin, and a reduction in PP would slow gastrointestinal motility and reduce gastrointestinal secretions. The increase in CgA, which appears to have anti-inflammatory effects, may simply reflect the total increase in colonic endocrine cells or another defensive action against inflammation (30).

The induction of colitis by DSS in rats affects all of the colonic endocrine cells. Given the available data on the interactions between hormones and the immune system, it can be hypothesized that inflammation induces the proliferation of serotonin cells and inhibits that of somatostatin cells, in response to which there is a secondary change in the densities of CgA, PYY, oxyntomodulin and PP cells. The close correlation between the changes in all endocrine cell types and immune cells emphasizes the importance of the role of interactions between the intestinal hormone and immune systems in the pathophysiology of intestinal inflammation.

Acknowledgements

The current study was supported by grants from Helse-Fonna (grant no. 40415), and Helse-Vest (grant no. 911978), Norway.

References

1 

Danese S and Fiocchi C: Etiopathogenesis of inflammatory bowel diseases. World J Gastroenterol. 12:4807–4812. 2006.PubMed/NCBI

2 

Nunes T, Fiorino G, Danese S and Sans M: Familial aggregation in inflammatory bowel disease: Is it genes or environment? World J Gastroenterol. 17:2715–2722. 2011. View Article : Google Scholar : PubMed/NCBI

3 

El-Salhy M, Gundersen D, Hatlebakk JG and Hausken T: Clinical presentation, diagnosis, pathogenesis and treatment options for lymphocytic colitis (Review). Int J Mol Med. 32:263–270. 2013.PubMed/NCBI

4 

Prantera C and Marconi S: Glucocorticosteroids in the treatment of inflammatory bowel disease and approaches to minimizing systemic activity. Therap Adv Gastroenterol. 6:137–156. 2013. View Article : Google Scholar : PubMed/NCBI

5 

Podolsky DK: Inflammatory bowel disease. N Engl J Med. 347:417–429. 2002. View Article : Google Scholar : PubMed/NCBI

6 

Podolsky DK: The current future understanding of inflammatory bowel disease. Best Pract Res Clin Gastroenterol. 16:933–943. 2002. View Article : Google Scholar : PubMed/NCBI

7 

Carter MJ, Lobo AJ and Travis SP: IBD Section, British Society of Gastroenterology: Guidelines for the management of inflammatory bowel disease in adults. Gut. 53:Suppl 5. V1–16. 2004. View Article : Google Scholar : PubMed/NCBI

8 

El-Salhy M, Seim I, Chopin L, Gundersen D, Hatlebakk JG and Hausken T: Irritable bowel syndrome: The role of gut neuroendocrine peptides. Front Biosci (Elite Ed). 4:2783–2800. 2012.PubMed/NCBI

9 

Wu T, Rayner CK, Young RL and Horowitz M: Gut motility and enteroendocrine secretion. Curr Opin Pharmacol. 13:928–934. 2013. View Article : Google Scholar : PubMed/NCBI

10 

El-Salhy M, Danielsson A, Stenling R and Grimelius L: Colonic endocrine cells in inflammatory bowel disease. J Intern Med. 242:413–419. 1997. View Article : Google Scholar : PubMed/NCBI

11 

El-Salhy M, Gundersen D, Hatlebakk JG and Hausken T: Chromogranin a cell density as a diagnostic marker for lymphocytic colitis. Dig Dis Sci. 57:3154–3159. 2012. View Article : Google Scholar : PubMed/NCBI

12 

El-Salhy M, Gundersen D, Hatlebakk JG and Hausken T: High densities of serotonin and peptide YY cells in the colon of patients with lymphocytic colitis. World J Gastroenterol. 18:6070–6075. 2012. View Article : Google Scholar : PubMed/NCBI

13 

El-Salhy M, Lomholt-Beck B and Gundersen TD: High chromogranin A cell density in the colon of patients with lymphocytic colitis. Mol Med Rep. 4:603–605. 2011.PubMed/NCBI

14 

Moran GW, Pennock J and McLaughlin JT: Enteroendocrine cells in terminal ileal Crohn's disease. J Crohns Colitis. 6:871–880. 2012. View Article : Google Scholar : PubMed/NCBI

15 

Moran GW, Leslie FC and McLaughlin JT: Crohn's disease affecting the small bowel is associated with reduced appetite and elevated levels of circulating gut peptides. Clin Nutr. 32:404–411. 2013. View Article : Google Scholar : PubMed/NCBI

16 

Besterman HS, Mallinson CN, Modigliani R, Christofides ND, Pera A, Ponti V, Sarson DL and Bloom SR: Gut hormones in inflammatory bowel disease. Scand J Gastroenterol. 18:845–852. 1983. View Article : Google Scholar : PubMed/NCBI

17 

El-Salhy M, Mazzawi T, Gundersen D, Hatlebakk JG and Hausken T: The role of peptide YY in gastrointestinal diseases and disorders (review). Int J Mol Med. 31:275–282. 2013.PubMed/NCBI

18 

Hirotani Y, Mikajiri K, Ikeda K, Myotoku M and Kurokawa N: Changes of the peptide YY levels in the intestinal tissue of rats with experimental colitis following oral administration of mesalazine and prednisolone. Yakugaku Zasshi. 128:1347–1353. 2008. View Article : Google Scholar : PubMed/NCBI

19 

Vona-Davis LC and McFadden DW: NPY family of hormones: Clinical relevance and potential use in gastrointestinal disease. Curr Top Med Chem. 7:1710–1720. 2007. View Article : Google Scholar : PubMed/NCBI

20 

El-Salhy M, Suhr O and Danielsson A: Peptide YY in gastrointestinal disorders. Peptides. 23:397–402. 2002. View Article : Google Scholar : PubMed/NCBI

21 

Tari A, Teshima H, Sumii K, Haruma K, Ohgoshi H, Yoshihara M, Kajiyama G and Miyachi Y: Peptide YY abnormalities in patients with ulcerative colitis. Jpn J Med. 27:49–55. 1988. View Article : Google Scholar : PubMed/NCBI

22 

Sciola V, Massironi S, Conte D, Caprioli F, Ferrero S, Ciafardini C, Peracchi M, Bardella MT and Piodi L: Plasma chromogranin a in patients with inflammatory bowel disease. Inflamm Bowel Dis. 15:867–871. 2009. View Article : Google Scholar : PubMed/NCBI

23 

Bishop AE, Pietroletti R, Taat CW, Brummelkamp WH and Polak JM: Increased populations of endocrine cells in Crohn's ileitis. Virchows Arch A Pathol Anat Histopathol. 410:391–396. 1987. View Article : Google Scholar : PubMed/NCBI

24 

Manocha M and Khan WI: Serotonin and GI disorders: An update on clinical and experimental studies. Clin Transl Gastroenterol. 3:e132012. View Article : Google Scholar : PubMed/NCBI

25 

Stoyanova II and Gulubova MV: Mast cells and inflammatory mediators in chronic ulcerative colitis. Acta Histochem. 104:185–192. 2002. View Article : Google Scholar : PubMed/NCBI

26 

Yamamoto H, Morise K, Kusugami K, Furusawa A, Konagaya T, Nishio Y, Kaneko H, Uchida K, Nagai H, Mitsuma T and Nagura H: Abnormal neuropeptide concentration in rectal mucosa of patients with inflammatory bowel disease. J Gastroenterol. 31:525–532. 1996. View Article : Google Scholar : PubMed/NCBI

27 

Payer J, Huorka M, Duris I, Mikulecky M, Kratochvílová H, Ondrejka P and Lukác L: Plasma somatostatin levels in ulcerative colitis. Hepatogastroenterology. 41:552–553. 1994.PubMed/NCBI

28 

Watanabe T, Kubota Y, Sawada T and Muto T: Distribution and quantification of somatostatin in inflammatory disease. Dis Colon Rectum. 35:488–494. 1992. View Article : Google Scholar : PubMed/NCBI

29 

Koch TR, Carney JA, Morris VA and Go VL: Somatostatin in the idiopathic inflammatory bowel diseases. Dis Colon Rectum. 31:198–203. 1988. View Article : Google Scholar : PubMed/NCBI

30 

Khan WI and Ghia JE: Gut hormones: Emerging role in immune activation and inflammation. Clin Exp Immunol. 161:19–27. 2010.PubMed/NCBI

31 

Margolis KG and Gershon MD: Neuropeptides and inflammatory bowel disease. Curr Opin Gastroenterol. 25:503–511. 2009. View Article : Google Scholar : PubMed/NCBI

32 

Elson CO, Sartor RB, Tennyson GS and Riddell RH: Experimental models of inflammatory bowel disease. Gastroenterology. 109:1344–1367. 1995. View Article : Google Scholar : PubMed/NCBI

33 

Grimstad T, Bjørndal B, Cacabelos D, Aasprong OG, Omdal R, Svardal A, Bohov P, Pamplona R, Portero-Otin M, Berge RK and Hausken T: A salmon peptide diet alleviates experimental colitis as compared with fish oil. J Nutr Sci. 2:e22013. View Article : Google Scholar : PubMed/NCBI

34 

Stucchi AF, Shofer S, Leeman S, Materne O, Beer E, McClung J, Shebani K, Moore F, O'Brien M and Becker JM: NK-1 antagonist reduces colonic inflammation and oxidative stress in dextran sulfate-induced colitis in rats. Am J Physiol Gastrointest Liver Physiol. 279:G1298–G1306. 2000.PubMed/NCBI

35 

El-Salhy M, Mazzawi T, Umezawa K and Gilja OH: Enteroendocrine cells, stem cells and differentiation progenitors in rats with TNBS-induced colitis. Int J Mol Med. Oct 24–2016.(Epub ahead of print).

36 

Saleh M and Elson CO: Experimental inflammatory bowel disease: Insights into the host-microbiota dialog. Immunity. 34:293–302. 2011. View Article : Google Scholar : PubMed/NCBI

37 

Sands BE: New therapies for the treatment of inflammatory bowel disease. Surg Clin North Am. 86:1045–1064. 2006. View Article : Google Scholar : PubMed/NCBI

38 

Lopez A, Billioud V, Peyrin-Biroulet C and Peyrin-Biroulet L: Adherence to anti-TNF therapy in inflammatory bowel diseases: A systematic review. Inflamm Bowel Dis. 19:1528–1533. 2013. View Article : Google Scholar : PubMed/NCBI

39 

Danese S, Semeraro S, Armuzzi A, Papa A and Gasbarrini A: Biological therapies for inflammatory bowel disease: Research drives clinics. Mini Rev Med Chem. 6:771–784. 2006. View Article : Google Scholar : PubMed/NCBI

40 

Motomura Y, Ghia JE, Wang H, Akiho H, El-Sharkawy RT, Collins M, Wan Y, McLaughlin JT and Khan WI: Enterochromaffin cell and 5-hydroxytryptamine responses to the same infectious agent differ in Th1 and Th2 dominant environments. Gut. 57:475–481. 2008.PubMed/NCBI

41 

Wirtz S, Neufert C, Weigmann B and Neurath MF: Chemically induced mouse models of intestinal inflammation. Nat Protoc. 2:541–546. 2007. View Article : Google Scholar : PubMed/NCBI

42 

Dieleman LA, Palmen MJ, Akol H, Bloemena E, Peña AS, Meuwissen SG and Van Rees EP: Chronic experimental colitis induced by dextran sulphate sodium (DSS) is characterized by Th1 and Th2 cytokines. Clin Exp Immunol. 114:385–391. 1998. View Article : Google Scholar : PubMed/NCBI

43 

Low D, Nguyen DD and Mizoguchi E: Animal models of ulcerative colitis and their application in drug research. Drug Des Devel Ther. 7:1341–1357. 2013.PubMed/NCBI

44 

Öhman L, Tornblom H and Simrén M: Crosstalk at the mucosal border: Importance of the gut microenvironment in IBS. Nat Rev Gastroenterol Hepatol. 12:36–49. 2015.PubMed/NCBI

45 

Buffa R, Maré P, Gini A and Salvadore M: Chromogranins A and B and secretogranin II in hormonally identified endocrine cells of the gut and the pancreas. Basic Appl Histochem. 32:471–484. 1988.PubMed/NCBI

46 

Eiden LE: Is chromogranin a prohormone? Nature. 325:3011987. View Article : Google Scholar : PubMed/NCBI

47 

Buffa R, Capella C, Fontana P, Usellini L and Solcia E: Types of endocrine cells in the human colon and rectum. Cell Tissue Res. 192:227–240. 1978.PubMed/NCBI

48 

Curry WJ, Johnston CF, Hutton JC, Arden SD, Rutherford NG, Shaw C and Buchanan KD: The tissue distribution of rat chromogranin A-derived peptides: Evidence for differential tissue processing from sequence specific antisera. Histochemistry. 96:531–538. 1991. View Article : Google Scholar : PubMed/NCBI

49 

Portela-Gomes GM and Stridsberg M: Selective processing of chromogranin A in the different islet cells in human pancreas. J Histochem Cytochem. 49:483–490. 2001. View Article : Google Scholar : PubMed/NCBI

50 

Portela-Gomes GM and Stridsberg M: Chromogranin A in the human gastrointestinal tract: An immunocytochemical study with region-specific antibodies. J Histochem Cytochem. 50:1487–1492. 2002. View Article : Google Scholar : PubMed/NCBI

51 

Taupenot L, Harper KL and O'Connor DT: The chromogranin-secretogranin family. N Engl J Med. 348:1134–1149. 2003. View Article : Google Scholar : PubMed/NCBI

52 

Wiedenmann B and Huttner WB: Synaptophysin and chromogranins/secretogranins-widespread constituents of distinct types of neuroendocrine vesicles and new tools in tumor diagnosis. Virchows Arch B Cell Pathol Incl Mol Pathol. 58:95–121. 1989. View Article : Google Scholar : PubMed/NCBI

53 

Ferrero E, Magni E, Curnis F, Villa A, Ferrero ME and Corti A: Regulation of endothelial cell shape and barrier function by chromogranin A. Ann N Y Acad Sci. 971:355–358. 2002. View Article : Google Scholar : PubMed/NCBI

54 

Spiller R: Serotonin and GI clinical disorders. Neuropharmacology. 55:1072–1080. 2008. View Article : Google Scholar : PubMed/NCBI

55 

Egger M, Beer AG, Theurl M, Schgoer W, Hotter B, Tatarczyk T, Vasiljevic D, Frauscher S, Marksteiner J, Patsch JR, et al: Monocyte migration: A novel effect and signaling pathways of catestatin. Eur J Pharmacol. 598:104–111. 2008. View Article : Google Scholar : PubMed/NCBI

56 

Feistritzer C, Mosheimer BA, Colleselli D, Wiedermann CJ and Kahler CM: Effects of the neuropeptide secretoneurin on natural killer cell migration and cytokine release. Regul Pept. 126:195–201. 2005. View Article : Google Scholar : PubMed/NCBI

57 

El-Salhy M, Gundersen D, Hatlebakk JG and Hausken T: Irritable bowel syndrome: Diagnosis, pathogenesis and treatment options. Nova Science Publishers, Inc.; New York: 2012

58 

Bertrand PP and Bertrand RL: Serotonin release and uptake in the gastrointestinal tract. Auton Neurosci. 153:47–57. 2010. View Article : Google Scholar : PubMed/NCBI

59 

Qian BF, El-Salhy M, Melgar S, Hammarstrom ML and Danielsson A: Neuroendocrine changes in colon of mice with a disrupted IL-2 gene. Clin Exp Immunol. 120:424–433. 2000. View Article : Google Scholar : PubMed/NCBI

60 

Oshima S, Fujimura M and Fukimiya M: Changes in number of serotonin-containing cells and serotonin levels in the intestinal mucosa of rats with colitis induced by dextran sodium sulfate. Histochem Cell Biol. 112:257–263. 1999. View Article : Google Scholar : PubMed/NCBI

61 

Coates MD, Mahoney CR, Linden DR, Sampson JE, Chen J, Blaszyk H, Crowell MD, Sharkey KA, Gershon MD, Mawe GM and Moses PL: Molecular defects in mucosal serotonin content and decreased serotonin reuptake transporter in ulcerative colitis and irritable bowel syndrome. Gastroenterology. 126:1657–1664. 2004. View Article : Google Scholar : PubMed/NCBI

62 

Sjolund K, Schaffalitzky OB, Muckadell DE, Fahrenkrug J, Håkanson R, Peterson BG and Sundler F: Peptide-containing nerve fibres in the gut wall in Crohn's disease. Gut. 24:724–733. 1983. View Article : Google Scholar : PubMed/NCBI

63 

Wang H, Steeds J, Motomura Y, Deng Y, Verma-Gandhu M, El-Sharkawy RT, McLaughlin JT, Grencis RK and Khan WI: CD4+ T cell-mediated immunological control of enterochromaffin cell hyperplasia and 5-hydroxytryptamine production in enteric infection. Gut. 56:949–957. 2007. View Article : Google Scholar : PubMed/NCBI

64 

Cloëz-Tayarani I and Changeux JP: Nicotine and serotonin in immune regulation and inflammatory processes: A perspective. J Leukoc Biol. 81:599–606. 2007.PubMed/NCBI

65 

Stefulj J, Cicin-Sain L, Schauenstein K and Jernej B: Serotonin and immune response: Effect of the amine on in vitro proliferation of rat lymphocytes. Neuroimmunomodulation. 9:103–108. 2001. View Article : Google Scholar : PubMed/NCBI

66 

Betten A, Dahlgren C, Hermodsson S and Hellstrand K: Serotonin protects NK cells against oxidatively induced functional inhibition and apoptosis. J Leukoc Biol. 70:65–72. 2001.PubMed/NCBI

67 

Laberge S, Cruikshank WW, Beer DJ and Center DM: Secretion of IL-16 (lymphocyte chemoattractant factor) from serotonin-stimulated CD8+ T cells in vitro. J Immunol. 156:310–315. 1996.PubMed/NCBI

68 

Soga F, Katoh N, Inoue T and Kishimoto S: Serotonin activates human monocytes and prevents apoptosis. J Invest Dermatol. 127:1947–1955. 2007. View Article : Google Scholar : PubMed/NCBI

69 

Spångéus A, Forsgren S and el-Salhy M: Does diabetic state affect co-localization of peptide YY and enteroglucagon in colonic endocrine cells? Histol Histopathol. 15:37–41. 2000.PubMed/NCBI

70 

Pyarokhil AH, Ishihara M, Sasaki M and Kitamura N: The developmental plasticity of colocalization pattern of peptide YY and glucagon-like peptide-1 in the endocrine cells of bovine rectum. Biomed Res. 33:35–38. 2012. View Article : Google Scholar : PubMed/NCBI

71 

El-Salhy M, Gundersen D, Gilja OH, Hatlebakk JG and Hausken T: Is irritable bowel syndrome an organic disorder? World J Gastroenterol. 20:384–400. 2014. View Article : Google Scholar : PubMed/NCBI

72 

El-Salhy M, Gundersen D, Hatlebakk JG and Hausken T: Diet and irritable bowel syndrome, with a focus on appetite-regulating hormonesNutrition in the prevention and treatment of abdominal obesity. Watson RR: Elsevier; San Diego: pp. 5–16G. 2014

73 

Payan DG, Hess CA and Goetzl EJ: Inhibition by somatostatin of the proliferation of T-lymphocytes and Molt-4 lymphoblasts. Cell Immunol. 84:433–438. 1984. View Article : Google Scholar : PubMed/NCBI

74 

Adeyemi EO, Savage AP, Bloom SR and Hodgson HJ: Somatostatin inhibits neutrophil elastase release in vitro. Peptides. 11:869–871. 1990. View Article : Google Scholar : PubMed/NCBI

75 

Stanisz AM, Befus D and Bienenstock J: Differential effects of vasoactive intestinal peptide, substance P, and somatostatin on immunoglobulin synthesis and proliferations by lymphocytes from Peyer's patches, mesenteric lymph nodes, and spleen. J Immunol. 136:152–156. 1986.PubMed/NCBI

76 

Scicchitano R, Dazin P, Bienenstock J, Payan DG and Stanisz AM: Distribution of somatostatin receptors on murine spleen and Peyer's patch T and B lymphocytes. Brain Behav Immun. 1:173–184. 1987. View Article : Google Scholar : PubMed/NCBI

77 

Scicchitano R, Stanisz AM, Payan DG, Kiyono H, McGhee JR and Bienenstock J: Expression of substance P and somatostatin receptors on a T helper cell line. Adv Exp Med Biol 216A. 185–190. 1987.

78 

Montgomery RK and Breault DT: Small intestinal stem cell markers. J Anat. 213:52–58. 2008. View Article : Google Scholar : PubMed/NCBI

79 

Potten CS: Stem cells in gastrointestinal epithelium: Numbers, characteristics and death. Philos Trans R Soc Lond B Biol Sci. 353:821–830. 1998. View Article : Google Scholar : PubMed/NCBI

80 

Potten CS: Interleukin-11 protects the clonogenic stem cells in murine small-intestinal crypts from impairment of their reproductive capacity by radiation. Int J Cancer. 62:356–361. 1995. View Article : Google Scholar : PubMed/NCBI

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January 2017
Volume 15 Issue 1

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APA
El‑Salhy, M., Hatlebakk, J.G., & Gilja, O.H. (2017). Abnormalities in endocrine and immune cells are correlated in dextran‑sulfate‑sodium‑induced colitis in rats. Molecular Medicine Reports, 15, 12-20. https://doi.org/10.3892/mmr.2016.6023
MLA
El‑Salhy, M., Hatlebakk, J. G., Gilja, O. H."Abnormalities in endocrine and immune cells are correlated in dextran‑sulfate‑sodium‑induced colitis in rats". Molecular Medicine Reports 15.1 (2017): 12-20.
Chicago
El‑Salhy, M., Hatlebakk, J. G., Gilja, O. H."Abnormalities in endocrine and immune cells are correlated in dextran‑sulfate‑sodium‑induced colitis in rats". Molecular Medicine Reports 15, no. 1 (2017): 12-20. https://doi.org/10.3892/mmr.2016.6023