Walsh Desmond T, Montero Rosa M, Bresciani Laura G, Jen Angela Y T, Leclercq Pascale D, Saunders Debbie, EL-Amir Ahmed N, Gbadamoshi Lukemann, Gentleman Stephen M, Jen Ling-Sun
Department of Neuroinflammation, Division of Neuroscience and Psychological Medicine, London, W6 8RF, United Kingdom.
Neurobiol Dis. 2002 Jun;10(1):20-7. doi: 10.1006/nbdi.2002.0485.
We have studied the neurotoxicity of amyloid-beta (Abeta) after a single unilateral intravitreal injection. Within the retina apoptotic cells were seen throughout the photoreceptor layer and the inner nuclear layer but not in the ganglion cell layer at 48 h after injection of Abeta(1-42) compared to vehicle control and control peptide. At 5 months, there was a significant reduction in total cell numbers in the ganglion cell layer in Nissl stained retinas. There was glial cell dysfunction with upregulation of glial fibrillary acidic protein and a reduction in the expression of Müller cell associated proteins in the injected retinas. These results suggest an indirect cytotoxic effect of Abeta on retinal neurons and an important role for dysfunction of Müller glia in mediating Abeta neurotoxicity.
我们研究了单次单侧玻璃体内注射β-淀粉样蛋白(Aβ)后的神经毒性。与载体对照和对照肽相比,注射Aβ(1-42)后48小时,视网膜内可见整个光感受器层和内核层有凋亡细胞,但神经节细胞层未见。5个月时,尼氏染色视网膜的神经节细胞层总细胞数显著减少。注射的视网膜中存在胶质细胞功能障碍,胶质纤维酸性蛋白上调,Müller细胞相关蛋白表达降低。这些结果表明Aβ对视网膜神经元有间接细胞毒性作用,且Müller胶质细胞功能障碍在介导Aβ神经毒性中起重要作用。