Fibroblast growth factor 2 promotes endothelial differentiation of adipose tissue-derived stem cells

J Sex Med. 2009 Apr;6(4):967-979. doi: 10.1111/j.1743-6109.2008.01172.x. Epub 2008 Feb 4.

Abstract

Introduction: Adipose tissue-derived stem cells (ADSC) could potentially restore endothelial function in vasculogenic erectile dysfunction (ED). The mechanism for ADSC endothelial differentiation remained unidentified.

Aim: To test whether ADSC could differentiate into endothelial cells in the penis and to identify the underlying mechanism of ADSC endothelial differentiation.

Methods: For in vivo endothelial differentiation, ADSC were labeled with bromodeoxyuridine (BrdU), injected into rat corpora cavernosa, and localized by immunofluorescence and phase-contrast microscopy. For in vitro endothelial differentiation, ADSC were grown in endothelial growth medium 2 (EGM2), stained for endothelial markers CD31, von Willebrand Factor (vWF), and endothelial nitric oxide synthase (eNOS), and assessed for the ability to form tube-like structures in Matrigel and to endocytose acetylated low-density lipoprotein (Ac-LDL). To identify factors that promote ADSC endothelial differentiation, ADSC were grown in various media, each of which contained a specific combination of supplemental factors and assessed for LDL-uptake. PD173074, a selective inhibitor of fibroblast growth factor 2 (FGF2) receptor, was used to confirm the importance of FGF2 signaling for ADSC endothelial differentiation.

Main outcome measures: In vivo endothelial differentiation was assessed by immunofluorescence microscopy. In vitro endothelial differentiation was assessed by immunofluorescence, Matrigel tube formation, and Ac-LDL uptake.

Results: Injected ADSC were localized to the sinusoid endothelium, some of which stained positive for both BrdU and endothelial antigen rat endothelial cell antigen. ADSC proliferated at a faster rate in EGM2 than in standard DMEM, expressed endothelial markers CD31, vWF, and eNOS, formed tube-like structures in Matrigel, and endocytosed Ac-LDL. These properties were greatly diminished when ADSC were grown in the absence of FGF2 but were unaffected when grown in the absence of vascular endothelial growth factor, insulin-like growth factor, or epidermal growth factor. Furthermore, ADSC displayed similar endothelial properties when grown in FGF2-supplemented basic medium as in EGM2. Finally, blockade of FGF2 signaling with PD173074 abrogated ADSC endothelial differentiation.

Conclusions: ADSC could differentiate into endothelial cells in the penis. FGF2 signaling mediates ADSC endothelial differentiation.

Publication types

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

MeSH terms

  • Adipose Tissue / metabolism*
  • Animals
  • Bromodeoxyuridine / administration & dosage
  • Cell Differentiation*
  • Cell Proliferation
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / metabolism*
  • Endothelium, Vascular / pathology
  • Erectile Dysfunction / immunology
  • Erectile Dysfunction / pathology
  • Erectile Dysfunction / physiopathology*
  • Fibroblast Growth Factor 2 / metabolism*
  • Fluorescent Antibody Technique
  • In Vitro Techniques
  • Injections
  • Male
  • Nitric Oxide Synthase / metabolism
  • Platelet Endothelial Cell Adhesion Molecule-1 / immunology
  • Rats
  • Rats, Sprague-Dawley
  • Staining and Labeling
  • Stem Cells / metabolism*
  • von Willebrand Factor / metabolism

Substances

  • Platelet Endothelial Cell Adhesion Molecule-1
  • von Willebrand Factor
  • Fibroblast Growth Factor 2
  • Nitric Oxide Synthase
  • Bromodeoxyuridine