Experimental tractional retinal detachment: an immunohistochemical study

This study investigated the pathogenesis of tractional retinal detachment associated with proliferative vitreoretinopathy in an experimental model, using immunohistochemical staining. To produce tractional retinal detachment in rabbit eyes, homologous cultured fibroblasts obtained from the gluteal m...

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Bibliographic Details
Published inEuropean journal of ophthalmology Vol. 8; no. 2; p. 112
Main Authors Basmak, H, Isiksoy, S, Topbas, S, Artan, S, Yurdakul, S
Format Journal Article
LanguageEnglish
Published United States 01.04.1998
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Summary:This study investigated the pathogenesis of tractional retinal detachment associated with proliferative vitreoretinopathy in an experimental model, using immunohistochemical staining. To produce tractional retinal detachment in rabbit eyes, homologous cultured fibroblasts obtained from the gluteal muscle fascia were injected intravitreously. Right eyes of 20 rabbits in the study group, and 7 rabbits in the control group were followed for 26 days at weekly intervals with indirect ophthalmoscopy and fundus photographs. During the follow-up period grade III tractional retinal detachment developed in 11 eyes, grade II in six, and grade 1 in three eyes. The spindle-shaped cells contributed predominantly to the development of epiretinal membrane, and a smaller number of round small and large cells. In 10/17 grade II and III eyes, spindle-shaped cells had vimentin, 7/10 had actin, 5/17 had GFAP, 4/17 had S-100 protein immunoreactivity. Round small and large cells expressed S-100 protein, GFAP and actin in 5/17 eyes. Epiretinal membrane appeared to be formed by spindle-shaped fibroblast-like cells and small and large round glia-like cells. Actin positivity of spindle-shaped and round cells was taken as a marker of contractile elements of the cells and their locomotional features. These features are believed to be involved in contraction of the membrane and retinal detachment.
ISSN:1120-6721
DOI:10.1177/112067219800800211