Murine double minute-2 mediates exercise-induced angiogenesis in adipose tissue of diet-induced obese mice

Microvasc Res. 2020 Jul:130:104003. doi: 10.1016/j.mvr.2020.104003. Epub 2020 Mar 19.

Abstract

Objective: This study aimed to determine the effects of physical exercise on the angio-adaptive response in adipose tissue following weight loss in a mouse model of diet-induced obesity. We hypothesized that physical exercise stimulates angiogenesis through the regulation of Vascular endothelial growth factor-A (VEGF-A) pro-/Thrombospondin-1 (TSP-1) anti-angiogenic signal under the control of the Murine double-minute 2/Forkhead box Os (Mdm2/FoxOs) axis, as reported in skeletal muscle.

Methods: We studied the effects of 7 weeks-voluntary exercise (Ex) in C57Bl/6 control or diet-induced obese (HFS) mice on vascularization of white adipose tissue (AT).

Results: Diet-induced obese sedentary (HFSsed) mice presented a powerful angiostatic control in all adipose tissues, under FoxOs protein regulation, leading to capillary rarefaction. Exercise increased expression of Mdm2, repressing the angiostatic control in favor of adipose vascular regrowth in normal chow (NCex) and HFSex mice. This phenomenon was associated with adipocytes microenvironment improvement, such as decreased adipocytes hypertrophy and adipose tissue inflammation. In addition, adipose angiogenesis stimulation by exercise through Mdm2 pro-angiogenic action, improved visceral adipose insulin sensitivity, activated browning process within subcutaneous adipose tissue (ScWAT) and decreased ectopic fat deposition (muscle, heart and liver) in obese HFSex mice. The overall result of this approach of therapy by physical exercise is an improvement of all systemic cardiometabolic parameters.

Conclusions: These data demonstrated the therapeutic efficacy of physical exercise against obesity-associated pathologies, and also offer new prospects for molecular therapies targeting the adipose angio-adaptation in obese humans.

Keywords: Adipose tissue; Angiogenesis; Browning; FoxO-1; Inflammation; Mdm-2; Physical activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown / metabolism
  • Adipocytes, Brown / pathology
  • Adipocytes, White / metabolism*
  • Adipocytes, White / pathology
  • Adipose Tissue, White / blood supply*
  • Adipose Tissue, White / metabolism*
  • Adipose Tissue, White / pathology
  • Animals
  • Cellular Microenvironment
  • Diet, High-Fat*
  • Disease Models, Animal
  • Exercise Therapy*
  • Forkhead Box Protein O1 / metabolism
  • Forkhead Box Protein O3 / metabolism
  • Male
  • Mice, Inbred C57BL
  • Neovascularization, Physiologic*
  • Obesity / metabolism
  • Obesity / pathology
  • Obesity / physiopathology
  • Obesity / therapy*
  • Proto-Oncogene Proteins c-mdm2 / metabolism*
  • Signal Transduction
  • Thrombospondin 1 / metabolism
  • Tissue Culture Techniques
  • Vascular Endothelial Growth Factor A / metabolism
  • Weight Loss

Substances

  • Forkhead Box Protein O1
  • Forkhead Box Protein O3
  • FoxO3 protein, mouse
  • Foxo1 protein, mouse
  • Thrombospondin 1
  • Vascular Endothelial Growth Factor A
  • Thbs1 protein, mouse
  • vascular endothelial growth factor A, mouse
  • Mdm2 protein, mouse
  • Proto-Oncogene Proteins c-mdm2