Hyalocyte proliferation and ECM accumulation modulated by bFGF and TGF-beta1

Graefes Arch Clin Exp Ophthalmol. 2008 Sep;246(9):1275-84. doi: 10.1007/s00417-008-0846-z. Epub 2008 May 7.

Abstract

Purpose: In cases of severe retinal diseases, the vitreous body has to be removed and replaced by a suitable biomaterial. Currently, however, no satisfying long-term vitreous substitute is in clinical use. A novel therapeutic concept represents the combination of hyalocytes with suitable biomaterials. The goal of the present study was to evaluate the potential of bFGF and TGF-beta1 as tools to control hyalocyte proliferation and the accumulation of extracellular matrix (ECM).

Methods: In vitro investigation on the influence of different concentrations of bFGF and TGF-beta1 on hyalocyte morphology, proliferation and ECM production.

Results: Both growth factors affected hyalocyte morphology; small, round cells could be observed after bFGF supplementation, whereas the cells appeared more completely spread when cultured with TGF-beta1. Hyalocyte proliferation was increased 3-fold by 10 ng/ml bFGF; 1 ng/ml TGF-beta1 in contrast reduced cell proliferation to about 40% of the control. Converse effects of the growth factors could also be observed on the ECM accumulation of hyalocytes; whereas bFGF halved ECM accumulation, TGF-beta1 enhanced the ECM production up to 3-fold. Precultivation of hyalocytes with bFGF for two passages had no influence on their subsequent accumulation of glycosaminoglycans (GAG). However, cells precultivated with bFGF exhibited a doubled accumulation of collagen compared to controls.

Conclusions: The observed opposite effects of bFGF and TGF-beta1 on hyalocyte proliferation and ECM accumulation may allow for the control of hyaloycte properties. Therefore, these two growth factors seem to be valuable tools towards the development of a cell-based vitreous substitute.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Cell Count
  • Cell Culture Techniques
  • Cell Proliferation / drug effects*
  • Collagen / metabolism
  • Extracellular Matrix / metabolism*
  • Fibroblast Growth Factor 2 / pharmacology*
  • Glycosaminoglycans / metabolism
  • Hydroxyproline / metabolism
  • Microscopy, Fluorescence
  • Swine
  • Tissue Engineering
  • Transforming Growth Factor beta1 / pharmacology*
  • Vitreous Body / cytology*
  • Vitreous Body / drug effects
  • Vitreous Body / metabolism

Substances

  • Actins
  • Glycosaminoglycans
  • Transforming Growth Factor beta1
  • Fibroblast Growth Factor 2
  • Collagen
  • Hydroxyproline