Article ID Journal Published Year Pages File Type
4012352 Experimental Eye Research 2007 13 Pages PDF
Abstract

Reactive astrocytes in glaucomatous optic nerve changes are characterized by an increased expression of αB-crystallin and transforming growth factor-beta (TGF-β). In the pathogenesis of glaucomatous optic nerve damage, ischemia/reperfusion injury may play an important role. The goal of the present study was to determine the influence of hypoxia/reoxygenation and TGF-β on the expression of αB-crystallin in cultured human astrocytes of the optic nerve head (ONH). Cultured human astrocytes were incubated under hypoxic conditions (1% O2 for 4–12 h) with subsequent reoxygenation (12–24 h). Additionally, cells were treated with 1.0 ng/ml TGF-β1 and TGF-β2 for 12–48 h. Expression of αB-crystallin was examined by Northern- and Western-blotting. Levels of TGF-β1 and TGF-β2 were analyzed by RT-PCR analysis and ELISA. The effect of TGF-β blocking on the hypoxia/reoxygenation modulated expression of αB-crystallin was investigated by simultaneous incubation with neutralizing antibodies against TGF-β during the reoxygenation phase. Hypoxia/reoxygenation increased the expression of αB-crystallin at the mRNA (2.8- to 3.1-fold) and protein level (1.8- to 2.1-fold). Treatment with 1.0 ng/ml TGF-β1 and TGF-β2 for 12–48 h markedly enhanced αB-crystallin mRNA expression approximately three- to fourfold. Using Western blot analysis, this increase ranged from 2 to 3 times. Both cytokines showed a twofold increase after 12 and 24 h of reoxygenation at the mRNA and a two- to threefold increase at the protein level. Simultaneous treatment with neutralizing antibodies against both TGF-β isoforms prevented the hypoxia/reoxygenation-mediated elevation of αB-crystallin. The process of hypoxia/reoxygenation is capable of inducing the expression of αB-crystallin and TGF-ß in cultured ONH astrocytes. Therefore, optimization of conditions leading to hypoxia/reoxygenation in the ONH of glaucomatous patients may help to lower the incidence of characteristic changes in the optic nerve.

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