Alterations in expression of angiopoietins and the Tie-2 receptor in the retina of streptozotocin induced diabetic rats

Mol Vis. 2004 Aug 26:10:608-17.

Abstract

Purpose: The angiopoietin (Ang)/Tie-2 system may play a role in vascular integrity and angiogenesis. In this study, we investigated alterations of the gene expression of Ang-1 and Ang-2 in the retinas of streptozotocin (STZ) induced diabetic rats.

Methods: In situ hybridization, reverse transcriptase polymerase chain reaction (RT-PCR) and western blot analyses were performed to determine the mRNA and protein content for Ang-1 and Ang-2 and the Tie2 receptor in the retinas of STZ diabetic and age matched control rats.

Results: Using in situ hybridization analysis, Ang-1, Ang-2, and Tie2 mRNA expression was observed in the ganglion cell layer (GCL) and the inner nuclear layer (INL). While Ang-2 mRNA expression did not changed after 2 weeks, 1 month, or 3 months of STZ induced diabetes, it was increased in the GCL and slightly elevated in the INL after 6 months of diabetes. In contrast, Ang-1 and Tie2 mRNA expression was stable at every timepoint during 6 months of STZ induced diabetes. RT-PCR and western blot analyses confirmed the increase of Ang-2 expression after 6 months of diabetes. Furthermore, double staining of alpha-smooth muscle actin (alphaSMA) and Ang-2 mRNA demonstrated that the SMA positive cells surrounding Ang-2-expressing cells were decreased in the GCL.

Conclusions: Diabetes increases Ang-2 expression in the GCL accompanied by a reduction of alphaSMA positive perivascular cells. These changes may suggest a role for Ang-2 in the mechanism of pericyte loss in diabetic retinopathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiopoietin-1 / genetics*
  • Angiopoietin-1 / metabolism
  • Angiopoietin-2 / genetics*
  • Angiopoietin-2 / metabolism
  • Animals
  • Blotting, Western
  • Diabetes Mellitus, Experimental / metabolism*
  • Diabetic Retinopathy / metabolism*
  • Gene Expression Regulation*
  • Immunoenzyme Techniques
  • In Situ Hybridization
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, TIE-2 / genetics*
  • Receptor, TIE-2 / metabolism
  • Retina / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Angiopoietin-1
  • Angiopoietin-2
  • RNA, Messenger
  • Receptor, TIE-2