Stem Cell Replacement Improves Expression of SMP30 in db/db Mice

Int J Mol Sci. 2015 Dec 16;16(12):29971-9. doi: 10.3390/ijms161226217.

Abstract

We have previously reported that replacing bone marrow stem cells may improve hyperglycemia and oxidative stress in db/db mice, a type 2 diabetic mouse model. Senescence marker protein 30 (SMP30) is an antioxidant protein that decreases with aging. However, it has not been clear whether SMP30 decreases in the livers of obese mice, and whether stem cell replacement would improve SMP30 expression in the liver. Bone marrow stem cells of db/db mice were replaced with the bone marrow stem cells of C57BL/6 mice. Plasma cytokine and insulin levels were measured, and glycogen content, expression of SMP30, and fibrosis in the liver were assessed. Our results showed that stem cell replacement increased the expression of SMP30 in the liver, resulting from decreased plasma inflammation cytokines and hyperinsulinemia in db/db mice. This is the first report that stem cell replacement increased the expression of SMP30 in the liver, and may help prevent fibrosis in the liver of db/db mice.

Keywords: SMP30; cytokines; fibrosis; stem cell replacement.

MeSH terms

  • Adiponectin / blood
  • Animals
  • Blood Glucose / metabolism
  • Blotting, Western
  • Body Weight
  • Calcium-Binding Proteins / metabolism*
  • Cytokines / blood
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / metabolism*
  • Immunohistochemistry
  • Insulin / blood
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Mice, Inbred C57BL
  • Pancreas / pathology
  • Sirtuin 1 / metabolism
  • Staining and Labeling
  • Stem Cell Transplantation*

Substances

  • Adiponectin
  • Blood Glucose
  • Calcium-Binding Proteins
  • Cytokines
  • Insulin
  • Intracellular Signaling Peptides and Proteins
  • Rgn protein, mouse
  • Sirtuin 1