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. 1991 Mar;15(2):103-8.
doi: 10.1007/BF00224462.

Vitronectin and proliferative intraocular disorders. II. Expression of cell surface receptors for fibronectin and vitronectin in periretinal membranes

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Vitronectin and proliferative intraocular disorders. II. Expression of cell surface receptors for fibronectin and vitronectin in periretinal membranes

M Weller et al. Int Ophthalmol. 1991 Mar.

Abstract

Several cell types participate in the formation of vitreoretinal traction membranes in proliferative intraocular disorders. The communication between these cells involves hormones, growth factors, and the interaction with extracellular matrix molecules. We have previously demonstrated a partial colocalisation of two potent mediators of cell attachment, fibronectin and vitronectin, in periretinal membranes from patients with proliferative vitreoretinopathy (PVR). We found a similar pattern of vitronectin and fibronectin deposition in proliferative diabetic retinopathy (PDR) (n = 6). Now we show the expression of the corresponding cell surface receptors, integrins, for fibronectin and vitronectin by proliferating cells in 22 periretinal membranes, including traumatic (n = 8) and idiopathic (n = 8) PVR as well as PDR membranes (n = 6). Integrins are membrane receptors for extracellular matrix macromolecules which are involved in such basic biological phenomena as embryogenesis and metastasis. Future studies on the pathogenesis of vitreoretinal proliferation will have to focus on the initiation, maintenance, and regulation of this intercellular communication network involving attachment proteins and integrins.

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References

    1. Graefes Arch Clin Exp Ophthalmol. 1988;226(3):294-8 - PubMed
    1. Dev Ophthalmol. 1989;16:54-74 - PubMed
    1. J Cell Biol. 1988 Sep;107(3):1225-30 - PubMed
    1. J Biol Chem. 1987 Dec 25;262(36):17294-8 - PubMed
    1. Arch Ophthalmol. 1984 Dec;102(12):1830-3 - PubMed

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