Therapeutic efficiency of adipose-derived mesenchymal stem cells in healing of experimentally induced gastric ulcers in rats.

Safaa A Hassan, Amal Taha Abou Elghait, Zainab S Abdelqader, Fatma Y Meligy
Author Information
  1. Safaa A Hassan: Histology and Cell Biology Department, Faculty of Medicine, Assiut University, Assiut, Egypt. ORCID
  2. Amal Taha Abou Elghait: Histology and Cell Biology Department, Faculty of Medicine, Assiut University, Assiut, Egypt. ORCID
  3. Zainab S Abdelqader: Histology and Cell Biology Department, Faculty of Medicine, Assiut University, Assiut, Egypt. ORCID
  4. Fatma Y Meligy: Histology and Cell Biology Department, Faculty of Medicine, Assiut University, Assiut, Egypt. ORCID

Abstract

Gastric (peptic) ulcer is a major gastrointestinal disorder with high morbidity and mortality. While several drugs have been used to treat gastric ulcers, such as proton pump inhibitor-based triple therapy for eradication, but hey result in adverse side effects. Therefore, development of new alternative therapies is desirable. Many recent studies have shown that mesenchymal stem cells (MSCs) might have an enhancing effect on the ulcerated gastric mucosa. The aim of this study is to evaluate the efficacy of MSCs in the treatment of indomethacin-induced gastric ulcer, and to compare it with the normal ulcer autohealing. This work was performed on 36 adult male albino rats, divided into four groups: Group I (control group), Group II (ulcer group), Group III (autohealing group), and Group IV (stem cells-treated group). The histological changes of gastric mucosa were examined in sections stained with H&E using light microscope for expression of vascular endothelial growth factors (VEGF) and proliferating cell nuclear antigen (PCNA) in immunohistochemical stained sections using image analyzer. The results from MSCs-treated group revealed restoration of the normal architecture of the gastric mucosa with comparison to the autohealing group which showed excessive granulation tissue and heavy cellular infiltration with disorganized architecture of the fundic mucosa. Immunohistochemical examination showed strong expression of both VEGF and PCNA in the MSCs-treated group. So it was concluded that MSCs accelerate gastric ulcer healing when injected intraperitoneally, compared to autohealing process which showed delayed healing.

Keywords

References

  1. Aust Fam Physician. 2006 Sep;35(9):719-21 [PMID: 16969445]
  2. Gastroenterology. 2002 Feb;122(2):458-68 [PMID: 11832460]
  3. Anal Cell Pathol. 1998;16(4):185-92 [PMID: 9762365]
  4. World J Gastroenterol. 2012 Apr 7;18(13):1479-84 [PMID: 22509079]
  5. Biores Open Access. 2012 Aug;1(4):174-83 [PMID: 23514846]
  6. Gastroenterology. 2009 Mar;136(3):978-89 [PMID: 19135996]
  7. Cell Prolif. 2013 Feb;46(1):10-22 [PMID: 23163975]
  8. Curr Opin Gastroenterol. 1999 Nov;15(6):463-72 [PMID: 17023992]
  9. Inflammation. 2010 Aug;33(4):224-34 [PMID: 20084447]
  10. Exp Hematol. 2001 Feb;29(2):244-55 [PMID: 11166464]
  11. In Vitro Cell Dev Biol Anim. 2012 Apr;48(4):203-15 [PMID: 22396125]
  12. PLoS One. 2013 Sep 13;8(9):e74468 [PMID: 24058571]
  13. Cell Stem Cell. 2008 Feb 7;2(2):141-50 [PMID: 18371435]
  14. Circulation. 2002 Jan 1;105(1):93-8 [PMID: 11772882]
  15. Scand J Gastroenterol Suppl. 1985;110:11-24 [PMID: 2862697]
  16. Gut. 2013 Aug;62(8):1098-9 [PMID: 23263523]
  17. Blood. 2007 Nov 15;110(10):3499-506 [PMID: 17664353]
  18. Keio J Med. 2003 Jun;52(2):134-7 [PMID: 12862366]
  19. Gastroenterology. 2000 Sep;119(3):706-14 [PMID: 10982765]
  20. Nat Neurosci. 2012 Jun;15(6):862-70 [PMID: 22610068]
  21. Mt Sinai J Med. 2000 Jan;67(1):41-53 [PMID: 10677782]
  22. Cell Tissue Res. 2017 Aug;369(2):245-253 [PMID: 28413860]
  23. Gastroenterology. 2005 Oct;129(4):1171-8 [PMID: 16230071]
  24. Chin Med J (Engl). 2012 Mar;125(6):1169-74 [PMID: 22613549]
  25. J Cell Biochem. 1991 Nov;47(3):219-23 [PMID: 1791186]
  26. Am J Physiol Gastrointest Liver Physiol. 2008 Mar;294(3):G778-86 [PMID: 18202110]
  27. Int J Stem Cells. 2014 May;7(1):1-11 [PMID: 24921022]
  28. Gastroenterology. 2008 Jan;134(1):281-91 [PMID: 18045590]
  29. Nat Rev Immunol. 2009 May;9(5):324-37 [PMID: 19390566]
  30. J Physiol Biochem. 2013 Sep;69(3):527-37 [PMID: 23456451]
  31. J Cell Physiol. 2006 Dec;209(3):905-11 [PMID: 16972272]
  32. Stem Cell Res Ther. 2017 Jan 28;8(1):20 [PMID: 28129776]
  33. Nat Med. 1999 Dec;5(12):1418-23 [PMID: 10581086]
  34. Curr Opin Gastroenterol. 2007 Nov;23(6):607-16 [PMID: 17906436]
  35. Cell Mol Immunol. 2012 Nov;9(6):473-81 [PMID: 23085948]
  36. Indian J Physiol Pharmacol. 2007 Apr-Jun;51(2):131-40 [PMID: 18175656]
  37. Tissue Cell. 2015 Jun;47(3):273-83 [PMID: 25882756]
  38. Tissue Eng. 2007 Apr;13(4):767-73 [PMID: 17432951]
  39. Neurobiol Aging. 2015 Oct;36(10):2885-92 [PMID: 26242706]
  40. Am J Physiol Gastrointest Liver Physiol. 2001 May;280(5):G922-9 [PMID: 11292601]
  41. Prim Care. 2011 Sep;38(3):383-94, vii [PMID: 21872087]
  42. J Cell Biochem. 2009 Apr 15;106(6):984-91 [PMID: 19229871]
  43. J Nutr Biochem. 2007 Sep;18(9):567-79 [PMID: 17360173]
  44. Cytotechnology. 2012 Oct;64(5):511-21 [PMID: 22328147]
  45. J Cell Mol Med. 2009 Nov-Dec;13(11-12):4385-402 [PMID: 19602034]
  46. Cancer Res. 2007 Oct 1;67(19):9142-9 [PMID: 17909019]
  47. Arch Int Pharmacodyn Ther. 1985 May;275(1):123-38 [PMID: 2862848]
  48. Biochem Biophys Res Commun. 1997 Oct 29;239(3):639-44 [PMID: 9367820]
  49. Organogenesis. 2010 Jan-Mar;6(1):11-4 [PMID: 20592860]
  50. Neural Regen Res. 2020 Jan;15(1):75-77 [PMID: 31535654]
  51. Mol Ther. 2009 Oct;17(10):1799-803 [PMID: 19602999]
  52. Expert Opin Biol Ther. 2015 Apr;15(4):477-9 [PMID: 25539087]
  53. Bull Mem Acad R Med Belg. 2001;156(3-4):175-84; discussion 185 [PMID: 11789398]

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