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Study on Changes in Endogenous Stem Cells in the Salivary Gland of Streptozotocin-induced Diabetic Rats

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Type1 diabetes mellitus (DM) is generally known to be caused by destruction of insulin-producing pancreatic β cells or an immune-related problem. Polydipsia is a representative symptom of DM, and it has been reported that this condition is closely related to xerostomia and is considered that hyposalivation from the salivary gland results in this phenomenon. Although various studies have reported that induction of diabetes reduces endogenous stem cells in other organs (heart, brain etc.), diabetes-related changes in endogenous stem cells in the salivary gland have not yet been well established. Therefore, in this study, to verify the change in salivary gland stem cells after diabetes, salivary gland tissues in the control and diabetes-induced groups were processed by histochemistry (Masson’s trichrome staining) for morphological analysis, TUNEL assay for cell death, and immunohistochemistry (Ki-67 and c-Kit) for cell proliferation and maturation. Diabetes induced by STZ leads to vacuolization, apoptosis, and reduction in proliferating cells/salivary gland stem cells in salivary glands of rats. This result suggests that diabetes may be associated with reduction in salivary gland function such as degeneration and inhibition of regeneration in the salivary gland.

Abstract

Type1 diabetes mellitus (DM) is generally known to be caused by destruction of insulin-producing pancreatic β cells or an immune-related problem. Polydipsia is a representative symptom of DM, and it has been reported that this condition is closely related to xerostomia and is considered that hyposalivation from the salivary gland results in this phenomenon. Although various studies have reported that induction of diabetes reduces endogenous stem cells in other organs (heart, brain etc.), diabetes-related changes in endogenous stem cells in the salivary gland have not yet been well established. Therefore, in this study, to verify the change in salivary gland stem cells after diabetes, salivary gland tissues in the control and diabetes-induced groups were processed by histochemistry (Masson’s trichrome staining) for morphological analysis, TUNEL assay for cell death, and immunohistochemistry (Ki-67 and c-Kit) for cell proliferation and maturation. Diabetes induced by STZ leads to vacuolization, apoptosis, and reduction in proliferating cells/salivary gland stem cells in salivary glands of rats. This result suggests that diabetes may be associated with reduction in salivary gland function such as degeneration and inhibition of regeneration in the salivary gland.

참고문헌 (20)

  1. Mark A Atkinson, "Type 1 diabetes", The Lancet, 383(9911), pp.69~82 (2014), Elsevier BV[DOI]
  2. S. Mahay, "Streptozotocin-induced type 1 diabetes mellitus alters the morphology, secretory function and acyl lipid contents in the isolated rat parotid salivary gland", Molecular and Cellular Biochemistry, 261(1), pp.175~181 (2004), Springer Nature[DOI]
  3. Kim EJ, "Diabetes", pp.211~215 (1992), Korea medical book publishing company
  4. Moore PA, "Type 1 diabetes mellitus, xerostomia, and salivary flow rates. Oral Surgery, Oral Medicine, Oral Pathology", Oral Radiology, and Endodontology, 92, pp.281~291 (2001)[DOI]
  5. Michael W. J. Dodds, "Salivary alterations in type 2 (non-insulin-dependent) diabetes mellitus and hypertension", Community Dentistry and Oral Epidemiology, 28(5), pp.373~381 (2000), Wiley[DOI]
  6. Renata S. Leite, "Oral Health and Type 2 Diabetes", The American Journal of the Medical Sciences, 345(4), pp.271~273 (2013), Elsevier BV[DOI]
  7. Fedirko NV, "Changes in functioning of rat submandibular salivary gland under streptozotocin-induced diabetes are associated with alterations of ca 2 signaling and ca 2 transporting pumps", Biochimica Et Biophysica Acta (BBA)-Molecular Basis of Disease, 1762, pp.294~303 (2006), Elsevier BV[DOI]
  8. Keitaro Satoh, "E2f1-deficient NOD", SCID mice have dry mouth due to a change of acinar, Pflügers Archiv - European Journal of Physiology, pp.2013, 465(2)[DOI]
  9. J. M. Slack, "Stem Cells in Epithelial Tissues", Science, 287(5457), pp.1431~1433 (2000), American Association for the Advancement of Science (AAAS)[DOI]
  10. Christopher S. Potten, "The small intestine as a model for evaluating adult tissue stem cell drug targets1", Cell Proliferation, 36(3), pp.115~129 (2003), Wiley[DOI]
  11. Atsushi Suzuki, "Clonal identification and characterization of self-renewing pluripotent stem cells in the developing liver", The Journal of Cell Biology, 156(1), pp.173~184 (2002), Rockefeller University Press[DOI]
  12. Ashleigh S. Boyd, "Concise Review: Immune Recognition of Induced Pluripotent Stem Cells", STEM CELLS, 30(5), pp.797~803 (2012), Wiley[DOI]
  13. Isabelle M. A. Lombaert, "Rescue of Salivary Gland Function after Stem Cell Transplantation in Irradiated Glands", PLoS ONE, 3(4), pp.e2063~ (2008), Public Library of Science (PLoS)[DOI]
  14. Catherine Andre, "Sequence Analysis of Two Genomic Regions Containing the KIT and the FMS Receptor Tyrosine Kinase Genes", Genomics, 39(2), pp.216~226 (1997), Elsevier BV[DOI]
  15. Kevin G. Leong, "Generation of a prostate from a single adult stem cell", Nature, 456(7223), pp.804~808 (2008), Springer Nature[DOI]
  16. Charlotte E. Edling, "c-Kit—A hematopoietic cell essential receptor tyrosine kinase", The International Journal of Biochemistry & Cell Biology, 39(11), pp.1995~1998 (2007), Elsevier BV[DOI]
  17. Christopher A. Sullivan, "Chemoradiation-Induced Cell Loss in Human Submandibular Glands", The Laryngoscope, 115(6), pp.958~964 (2005), Wiley[DOI]
  18. M. Rota, "Diabetes Promotes Cardiac Stem Cell Aging and Heart Failure, Which Are Prevented by Deletion of the p66shc Gene", Circulation Research, 99(1), pp.42~52 (2006), Ovid Technologies (Wolters Kluwer Health)[DOI]
  19. W.-J. Zhang, "Impairment of hippocampal neurogenesis in streptozotocin-treated diabetic rats", Acta Neurologica Scandinavica, 117(3), pp.205~210 (2008), Wiley[DOI]
  20. J. Beauquis, "Prominently decreased hippocampal neurogenesis in a spontaneous model of type 1 diabetes, the nonobese diabetic mouse", Experimental Neurology, 210(2), pp.359~367 (2008), Elsevier BV[DOI]

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