首页> 外文期刊>Neural regeneration research >Release of interleukin-10 and neurotrophic factors in the choroid plexus: possible inductors of neurogenesis following copolymer-1 immunization after cerebral ischemia
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Release of interleukin-10 and neurotrophic factors in the choroid plexus: possible inductors of neurogenesis following copolymer-1 immunization after cerebral ischemia

机译:脉络丛中白细胞介素10和神经营养因子的释放:脑缺血后copolymer-1免疫后神经发生的可能诱导剂

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Copolymer-1 (Cop-1) is a peptide with immunomodulatory properties, approved by the Food and Drug Administration of United States in the treatment of multiple sclerosis. Cop-1 has been shown to exert neuroprotective effects and induce neurogenesis in cerebral ischemia models. Nevertheless, the mechanism involved in the neurogenic action of this compound remains unknown. The choroid plexus (CP) is a network of cells that constitute the interphase between the immune and central nervous systems, with the ability to mediate neurogenesis through the release of cytokines and growth factors. Therefore, the CP could play a role in Cop-1-induced neurogenesis. In order to determine the participation of the CP in the induction of neurogenesis after Cop-1 immunization, we evaluated the gene expression of various growth factors (brain-derived neurotrophic factor, insulin-like growth factor 1, neurotrophin-3) and cytokines (tumor necrosis factor alpha, interferon-gamma, interleukin-4 (IL-4), IL-10 and IL-17), in the CP at 14 days after ischemia. Furthermore, we analyzed the correlation between the expression of these genes and neurogenesis. Our results showed that Cop-1 was capable of stimulating an upregulation in the expression of the genes encoding for brain-derived neurotrophic factor, insulin-like growth factor 1, neurotrophin-3 and IL-10 in the CP, which correlated with an increase in neurogenesis in the subventricular and subgranular zone. As well, we observed a downregulation of IL-17 gene expression. This study demonstrates the effect of Cop-1 on the expression of growth factors and IL-10 in the CP, in the same way, presents a possible mechanism involved in the neurogenic effect of Cop-1.
机译:共聚物1(Cop-1)是一种具有免疫调节特性的肽,已获得美国食品药品监督管理局的批准用于治疗多发性硬化症。已经证明Cop-1在脑缺血模型中发挥神经保护作用并诱导神经发生。然而,该化合物的神经源性作用所涉及的机制仍然未知。脉络丛(CP)是构成免疫系统和中枢神经系统之间相间细胞的网络,具有通过释放细胞因子和生长因子介导神经发生的能力。因此,CP可能在Cop-1诱导的神经发生中起作用。为了确定CP在Cop-1免疫后参与神经发生的诱导,我们评估了各种生长因子(脑源性神经营养因子,胰岛素样生长因子1,neurotrophin-3)和细胞因子(缺血后14天CP中的肿瘤坏死因子α,干扰素-γ,白介素4(IL-4),IL-10和IL-17)。此外,我们分析了这些基因的表达与神经发生之间的相关性。我们的研究结果表明,Cop-1能够刺激CP中编码脑源性神经营养因子,胰岛素样生长因子1,neurotrophin-3和IL-10的基因的表达上调,这与增加有关。在脑室下和颗粒下区域的神经发生。同样,我们观察到IL-17基因表达的下调。这项研究表明,Cop-1对CP中生长因子和IL-10表达的影响,以同样的方式,提出了可能的机制参与Cop-1的神经源性作用。

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