Hyperglycemia induces abnormal gene expression in hematopoietic stem cells and their progeny in diabetic neuropathy

FEBS Lett. 2014 Mar 18;588(6):1080-6. doi: 10.1016/j.febslet.2014.02.030. Epub 2014 Feb 25.

Abstract

Diabetic peripheral neuropathy is a major chronic diabetic complication. We have previously shown that in type 1 diabetic streptozotocin-treated mice, insulin- and TNF-α co-expressing bone marrow-derived cells (BMDCs) induced by hyperglycemia travel to nerve tissues where they fuse with nerve cells, causing premature apoptosis and nerve dysfunction. Here we show that similar BMDCs also occur in type 2 diabetic high-fat diet (HFD) mice. Furthermore, we found that hyperglycemia induces the co-expression of insulin and TNF-α in c-kit(+)Sca-1(+)lineage(-) (KSL) progenitor cells, which maintain the same expression pattern in the progeny, which in turn participates in the fusion with neurons when transferred to normoglycemic animals.

Keywords: Cell–cell fusion; Hematopoietic stem cell; Hyperglycemia; Neuropathy; Stem cell abnormalities.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow / metabolism
  • Bone Marrow / pathology
  • Bone Marrow Transplantation
  • Cell Fusion
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / metabolism*
  • Diabetes Mellitus, Experimental / pathology
  • Diabetes Mellitus, Type 1 / complications
  • Diabetes Mellitus, Type 1 / metabolism*
  • Diabetes Mellitus, Type 1 / pathology
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / pathology
  • Diabetic Neuropathies / metabolism*
  • Diabetic Neuropathies / pathology
  • Diet, High-Fat / adverse effects
  • Ganglia, Spinal / pathology
  • Gene Expression
  • Hematopoietic Stem Cells / physiology*
  • Hyperglycemia / genetics
  • Hyperglycemia / metabolism*
  • Hyperglycemia / pathology
  • Insulin / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Neurons / physiology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Insulin
  • Tumor Necrosis Factor-alpha