Hyperglycemia causes cellular senescence via a SGLT2- and p21-dependent pathway in proximal tubules in the early stage of diabetic nephropathy

J Diabetes Complications. 2014 Sep-Oct;28(5):604-11. doi: 10.1016/j.jdiacomp.2014.05.010. Epub 2014 Jun 4.

Abstract

Aims: Kidney cells in patients with diabetic nephropathy are reported to be senescent. However, the mechanisms that regulate cellular senescence in the diabetic kidney are still unknown. In the present study, we evaluated the contribution of high glucose to renal cell senescence in streptozotocin (STZ)-induced diabetic mice.

Methods: Non-diabetic and streptozotocin (STZ, 10mgkg(-1)day(-1) for 7days, i.p.)-induced type 1 diabetic C57BL/6J mice and cultured human proximal tubular cells were used in this study.

Results: Hyperglycemia dramatically increased the renal expression of p21 but not other CDK inhibitors such as p16 and p27 at 4weeks after STZ injection. These changes were accompanied by an increase in senescence-associated β-galactosidase staining in tubular epithelial cells. Administration of insulin at doses that maintained normoglycemia or mild hypoglycemia suppressed the changes induced by STZ. Insulin did not affect the senescent markers in non-diabetic mice. Exposure of cultured human proximal tubular cells to 25mmol/L, but not 8mmol/L, glucose medium increased the expression of senescence markers, which was suppressed by knock-down of p21 or sodium glucose cotransporter (SGLT) 2.

Conclusions: These results suggest that hyperglycemia causes tubular senescence via a SGLT2- and p21-dependent pathway in the type 1 diabetic kidney.

Keywords: Cellular senescence; Diabetic nephropathy; Insulin; Proximal tubular cells; Sodium glucose cotransporter 2; p21.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Cellular Senescence* / genetics
  • Cyclin-Dependent Kinase Inhibitor p21 / physiology*
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / physiopathology
  • Diabetes Mellitus, Type 1 / complications
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / metabolism
  • Diabetes Mellitus, Type 1 / physiopathology
  • Diabetic Nephropathies* / complications
  • Diabetic Nephropathies* / genetics
  • Diabetic Nephropathies* / metabolism
  • Diabetic Nephropathies* / physiopathology
  • Disease Progression
  • Hyperglycemia / complications
  • Hyperglycemia / genetics
  • Hyperglycemia / physiopathology*
  • Kidney Tubules, Proximal* / metabolism
  • Kidney Tubules, Proximal* / physiopathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Signal Transduction / physiology
  • Sodium-Glucose Transporter 2 / physiology*
  • Streptozocin

Substances

  • Cyclin-Dependent Kinase Inhibitor p21
  • Slc5a2 protein, mouse
  • Sodium-Glucose Transporter 2
  • Streptozocin