Scientific article
German

Myofibroblastes et membranes fibrovasculaires rétiniennes

Published inKlinische Monatsblätter für Augenheilkunde, vol. 212, no. 5, p. 356-358
Publication date1998
Abstract

INTRODUCTION: Epiretinal tissue proliferations occurring during the evolution of ischemic microangiopathies or preretinal diseases are tough to cause retinal detachment by traction mechanisms. Cellular migration/proliferations and finally contraction are tough to be the pathogenic element. Myofibroblasts are contractile cells having features intermediate between those of the fibroblasts and smooth muscle. We conducted a study to explore whether such cells are present in preretinal membranes. MATERIALS AND METHODS: 8 membranes, preelevated during vitrectomy for proliferative vitreoretinopathy or diabetic proliferative vitreoretinopathy, were analysed with immunostaining technique searching for alpha-actine smooth muscle, desmine, which are specific markers for myofibroblasts and TGF-beta1, that is considered as the mean factor promoting the transformation of fibroblasts into myofibroblasts. RESULTS: All the histological preparation showed abundant staining with antibody against alpha-actine smooth muscle, desmine and TGF-beta1. CONCLUSIONS: Myofibroblasts are one of the major cellular element of preretinal membranes. They are scattered throughout the membrane and seem to account for their contractile properties.

Keywords
  • Actins/metabolism
  • Cell Division/ physiology
  • Cell Movement/physiology
  • Desmin/metabolism
  • Diabetic Retinopathy/ pathology
  • Epiretinal Membrane/ pathology
  • Fibroblasts/pathology
  • Humans
  • Myosins/metabolism
  • Retinal Detachment/pathology
  • Transforming Growth Factor beta/metabolism
  • Vitreoretinopathy, Proliferative/ pathology
Citation (ISO format)
POURNARAS, C. J. et al. Myofibroblastes et membranes fibrovasculaires rétiniennes. In: Klinische Monatsblätter für Augenheilkunde, 1998, vol. 212, n° 5, p. 356–358. doi: 10.1055/s-2008-1034905
Identifiers
Journal ISSN0023-2165
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