Ecole Nationale Vétérinaire d'Alfort, URO, 7 Avenue de Général De Gaulle, Paris, France.
Neurochem Int. 2010 Oct;57(3):278-87. doi: 10.1016/j.neuint.2010.06.006. Epub 2010 Jun 15.
Neuroprotection strategies in the retina aim at interference with regulatory mechanisms of cell death. To successfully target these mechanisms it is necessary to understand the molecular pathways activated in the degenerating retina. Induced retinal degeneration models, like the light damage model, give a synchronized response allowing their detailed investigation. In this study we exposed Fisher rats to a continuous white light. This induced a caspase-independent cell death in which the activation of cathepsin D has an important role via the activation of L-DNase II. Inhibition of this enzyme by intravitreal administration of pepstatin A protects photoreceptors indicating that this enzyme might be an interesting target for neuroprotection.
视网膜神经保护策略旨在干扰细胞死亡的调节机制。为了成功靶向这些机制,有必要了解在变性视网膜中激活的分子途径。诱导性视网膜变性模型,如光损伤模型,提供了同步反应,允许对其进行详细研究。在这项研究中,我们将 Fisher 大鼠暴露于连续的白光下。这诱导了一种 caspase 非依赖性细胞死亡,其中组织蛋白酶 D 的激活通过激活 L-DNase II 起重要作用。通过玻璃体内给予胃蛋白酶抑制剂 A 抑制这种酶可以保护光感受器,表明这种酶可能是神经保护的一个有趣靶点。