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Immunohistochemical localization of NGF BDNF and their receptors in a normal and AMD-like rat retina

机译:NGFBDNF及其受体在正常和AMD样大鼠视网膜中的免疫组织化学定位

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摘要

BackgroundAge-related macular degeneration (AMD) is a major cause of blindness in developed countries, and the molecular pathogenesis of AMD is poorly understood. A large body of evidence has corroborated the key role of neurotrophins in development, proliferation, differentiation, and survival of retinal cells. Neurotrophin deprivation has been proposed to contribute to retinal-cell death associated with neurodegenerative diseases. Little is known about the expression of the immature form of neurotrophins (proneurotrophins) and their mature form [e.g., nerve growth factor (proNGF and mNGF) and brain-derived neurotrophic factor (proBDNF and mBDNF)] in the retina during physiological aging and against the background of AMD. In addition, cell-specific localization of proteins NGF and BDNF in the retina during AMD development is not clear. Here, we evaluated contributions of the age-related alterations in the neurotrophin system to the development of AMD-like retinopathy in OXYS rats.
机译:背景技术与年龄相关的黄斑变性(AMD)是发达国家失明的主要原因,对AMD的分子发病机理了解甚少。大量证据证实了神经营养蛋白在视网膜细胞发育,增殖,分化和存活中的关键作用。已提出剥夺神经营养蛋白可导致与神经退行性疾病相关的视网膜细胞死亡。生理衰老期间,视网膜中神经营养蛋白(神经营养因子)的未成熟形式及其成熟形式(例如神经生长因子(proNGF和mNGF)和脑源性神经营养因子(proBDNF和mBDNF))的表达尚不清楚。 AMD的背景。此外,尚不清楚AMD发育过程中视网膜蛋白NGF和BDNF的细胞特异性定位。在这里,我们评估了神经营养蛋白系统中与年龄有关的变化对OXYS大鼠AMD样视网膜病发展的贡献。

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