T-cadherin deficiency increases vascular vulnerability in T2DM through impaired NO bioactivity

Cardiovasc Diabetol. 2017 Jan 19;16(1):12. doi: 10.1186/s12933-016-0488-0.

Abstract

Background: Endothelial dysfunction plays a critical role in the development of type 2 diabetes (T2DM). T-cadherin (T-cad) has gained recognition as a regulator of endothelial cell (EC) function. The present study examined whether T-cad deficiency increases vascular vulnerability in T2DM.

Methods: Vascular segments were isolated from WT or T-cad knockout mice. Endothelial function, total NO accumulation, and the expression of T-cad related proteins were determined.

Results: Ach and acidified NaNO2 induced similar vasorelaxation in WT groups. T-cad KO mice exhibited normal response to acidified NaNO2, but manifested markedly reduced response to Ach. NO accumulation was also decreased in T-cad KO group. T-cad expression was reduced in WT mice fed 8 weeks of high fat diet (HFD). Furthermore, exacerbated reduction of vasorelaxation was observed in T-cad KO mice fed 8 weeks of HFD.

Conclusions: In the current study, we provide the first in vivo evidence that T-cadherin deficiency causes endothelial dysfunction in T2DM vascular segments, suggesting the involvement of T-cad deficiency in T2DM pathogenesis.

Keywords: Endothelial cell; Endothelial dysfunction; NO bioactivity; T-cadherin; T2DM; Vascular ring.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta / drug effects
  • Aorta / metabolism
  • Cadherins / deficiency*
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / physiopathology
  • Diet, High-Fat / adverse effects
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism*
  • Male
  • Mice
  • Mice, Knockout
  • Nitric Oxide / metabolism*
  • Organ Culture Techniques
  • Vasodilation / drug effects
  • Vasodilation / physiology
  • Vasodilator Agents / pharmacology

Substances

  • Cadherins
  • H-cadherin
  • Vasodilator Agents
  • Nitric Oxide