Dmytriyeva Oksana, Pankratova Stanislava, Korshunova Irina, Walmod Peter S
Laboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Research Laboratory for Stereology and Neuroscience, Bispebjerg-Frederiksberg Hospital, Copenhagen University Hospital, Copenhagen, Denmark.
Laboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Juliane Marie Centret, Rigshospitalet (Copenhagen University Hospital), Copenhagen, Denmark.
Mediators Inflamm. 2016;2016:1346390. doi: 10.1155/2016/1346390. Epub 2016 Nov 21.
The cytokine erythropoietin (EPO) stimulates proliferation and differentiation of erythroid progenitor cells. Moreover, EPO has neuroprotective, anti-inflammatory, and antioxidative effects, but the use of EPO as a neuroprotective agent is hampered by its erythropoietic activity. We have recently designed the synthetic, dendrimeric peptide, Epobis, derived from the sequence of human EPO. This peptide binds the EPO receptor and promotes neuritogenesis and neuronal cell survival. Here we demonstrate that Epobis promotes neuritogenesis in primary motoneurons and has anti-inflammatory effects as demonstrated by its ability to decrease TNF release from activated AMJ2-C8 macrophages and rat primary microglia. When administered systemically Epobis is detectable in both plasma and cerebrospinal fluid, demonstrating that the peptide crosses the blood-brain barrier. Importantly, Epobis is not erythropoietic, but systemic administration of Epobis in rats delays the clinical signs of experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis, and the peptide has long-term, but not short-term, effects on working memory, detected as an improved social memory 3 days after administration. These data reveal Epobis to be a nonerythropoietic and neuroprotective EPO receptor agonist with anti-inflammatory and memory enhancing properties.
细胞因子促红细胞生成素(EPO)可刺激红系祖细胞的增殖和分化。此外,EPO还具有神经保护、抗炎和抗氧化作用,但其促红细胞生成活性限制了它作为神经保护剂的应用。我们最近设计了一种合成的树枝状肽Epobis,它源自人EPO的序列。这种肽能结合EPO受体,促进神经突生长和神经元细胞存活。在此我们证明,Epobis可促进原代运动神经元的神经突生长,并具有抗炎作用,这体现在它能够减少活化的AMJ2-C8巨噬细胞和大鼠原代小胶质细胞释放肿瘤坏死因子(TNF)。全身给药后,血浆和脑脊液中均可检测到Epobis,这表明该肽能够穿过血脑屏障。重要的是,Epobis不具有促红细胞生成作用,但在大鼠中全身给予Epobis可延缓实验性自身免疫性脑脊髓炎(一种多发性硬化症的动物模型)的临床症状,并且该肽对工作记忆具有长期而非短期的影响,给药3天后可检测到社交记忆得到改善。这些数据表明Epobis是一种不具有促红细胞生成作用的神经保护剂,是具有抗炎和增强记忆特性的EPO受体激动剂。