一种新发现的DR5特异性拮抗肽对神经退行性疾病的意义

M. Heins, W. Quax
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引用次数: 3

摘要

大多数神经退行性疾病是炎症和神经元细胞死亡的结果。尽管许多细胞因子被认为参与了发病机制,但最近的研究表明TRAIL与神经元凋亡有关。TRAIL以其在许多癌细胞中诱导细胞凋亡的能力而闻名。正常情况下TRAIL不存在于中枢神经系统。然而,它是由β -淀粉样蛋白诱导的,并在可浸润中枢神经系统的感染巨噬细胞上上调。TRAIL可通过死亡受体DR4和DR5诱导细胞凋亡。DR5在神经元细胞上表达。特异性结合DR5的拮抗肽的鉴定为我们提供了一个有用的研究工具。小肽能以高亲和力和特异性结合靶点。此外,它们易于修改和进一步开发用于临床应用。因此,R2C16肽甚至可以作为先导肽用于开发神经退行性疾病的治疗药物,因为TRAIL的产生是在细胞紊乱中诱导的。关键词:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implications of a Newly Discovered DR5 Specific Antagonistic Peptide for Neurodegenerative Disorders
Abstract Most neurodegenerative disorders are the result of inflammation and neuronal cell death. Although many cytokines have been implied to be involved in the pathogenesis, recent studies have shown TRAIL to be responsible for neuronal apoptosis. TRAIL is best known for its ability to induce apoptosis in many cancer cells. Normally TRAIL is not present in the CNS. However, it is induced by β‐ amyloid protein and upregulated on infected macrophages which can infiltrate the CNS. TRAIL is able to induce apoptosis via death receptors DR4 and DR5. DR5 is shown to be expressed on neuronal cells. The identification of an antagonistic peptide that specifically binds DR5 provides us with a useful investigative tool. Small peptides can bind their targets with high affinity and specificity. In addition, they are easily modified and further developed for clinical application. So the peptide R2C16 might even be used as a lead peptide for the development of therapeutic agents in neurodegenerative scenario is that TRAIL production is induced in cells disorders. Keywords:
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