Stem cell transplantation increases antioxidant effects in diabetic mice

Int J Biol Sci. 2012;8(10):1335-44. doi: 10.7150/ijbs.4654. Epub 2012 Oct 27.

Abstract

Intra bone marrow-bone marrow transplantation (IBM- BMT) + thymus transplantation (TT) has been shown to reduce the incidence of graft versus host disease (GVHD) and restore donor-derived T cell function. In addition, an increase in insulin sensitivity occurred in db/db mice after IBM-BMT+TT treatment. Heme oxygenase (HO)-1 is a stress inducible enzyme which exert antioxidant, antiapoptotic, and immune-modulating properties. We examined whether IBM-BMT+TT could modulate the expression of HO-1 in the kidneys of db/db mice. Six-week-old db/db mice with blood glucose levels higher than 250 mg/dl were treated with IBM-BMT+TT. Six weeks later, the db/db mice showed decreased body weight, blood glucose levels and insulin, and increased plasma adiponectin levels. The upregulation of HO-1 was associated with significantly (p<0.05) increased levels of peNOS and pAKT, but decreased levels of iNOS in the kidneys of db/db mice. Plasma creatinine levels also decreased (p<0.05), and the expression of type IV collagen was improved. Thus IBM-BMT+TT unregulated the expression of HO-1, peNOS and pAKT, while decreasing iNOS levels in the kidney of db/db mice. This was associated with an improvement in renal function.

Keywords: HO-1; IBM-BMT+TT; antioxidant; diabetic nephropathy..

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • AMP-Activated Protein Kinases
  • Animals
  • Antioxidants / metabolism*
  • Blood Glucose
  • Body Weight
  • Bone Marrow Transplantation*
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / therapy*
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / metabolism*
  • Insulin / metabolism
  • Kidney / metabolism
  • Kidney / pathology
  • Lymphocytes / physiology
  • Mice
  • Nitric Oxide Synthase / genetics
  • Nitric Oxide Synthase / metabolism
  • Pancreas / metabolism
  • Pancreas / pathology
  • Phosphorylation
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Stem Cell Transplantation*
  • Thymus Gland / pathology
  • Thymus Gland / transplantation
  • Up-Regulation

Substances

  • Antioxidants
  • Blood Glucose
  • Insulin
  • Nitric Oxide Synthase
  • Heme Oxygenase-1
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Stk11 protein, mouse
  • AMP-Activated Protein Kinases