Roles of stem cell factor on loss of interstitial cells of Cajal in bladder of diabetic rats

Urology. 2011 Dec;78(6):1443.e1-6. doi: 10.1016/j.urology.2011.08.019. Epub 2011 Oct 13.

Abstract

Objective: To explore the roles of stem cell factor (SCF) on the loss of interstitial cells (ICCs) in the bladder of diabetic rats, which have not been investigated.

Methods: The rats were assigned to 3 groups: normal control rats, diabetic rats, and SCF-treated diabetic rats. The diabetic rat model was created using a streptozotocin (60 mg/kg) intraperitoneal injection. The SCF and c-kit levels in bladder tissue were determined using reverse transcriptase-polymerase chain reaction and Western blot analysis. The quantity of ICCs as represented by c-kit-positive cells was examined by image analysis of immunofluorescence staining.

Results: Compared with the control rats, the diabetic rats exhibited a significant decrease in the SCF levels and c-kit expression and number of ICCs in the bladder tissues. All these impaired parameters were effectively restored to the control level after exogenous SCF treatment.

Conclusion: These findings suggest that the loss of ICCs in the bladder tissue of diabetic rats can be attributed to a deficiency in endogenous SCF. The beneficial effect of exogenous SCF on diabetic depletion of ICCs could provide a theoretical rationale for the use of SCF as a potential therapeutic drug in treating patients with diabetes-related voiding dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diabetes Mellitus, Experimental / metabolism*
  • Female
  • Interstitial Cells of Cajal / cytology
  • Interstitial Cells of Cajal / drug effects
  • Interstitial Cells of Cajal / metabolism*
  • Proto-Oncogene Proteins c-kit / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Statistics, Nonparametric
  • Stem Cell Factor / metabolism*
  • Stem Cell Factor / pharmacology
  • Streptozocin
  • Urinary Bladder / cytology
  • Urinary Bladder / drug effects
  • Urinary Bladder / metabolism*

Substances

  • Stem Cell Factor
  • Streptozocin
  • Proto-Oncogene Proteins c-kit