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通过自噬诱导使用NeuroHeal对受损新生运动神经元进行新型神经保护治疗。

Novel neuroprotective therapy with NeuroHeal by autophagy induction for damaged neonatal motoneurons.

作者信息

Romeo-Guitart David, Marcos-DeJuana César, Marmolejo-Martínez-Artesero Sara, Navarro Xavier, Casas Caty

机构信息

Institut de Neurociències (INc) and Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona (UAB), & Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Bellaterra, Barcelona, Spain.

出版信息

Theranostics. 2020 Apr 6;10(11):5154-5168. doi: 10.7150/thno.43765. eCollection 2020.

DOI:10.7150/thno.43765
PMID:32308774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7163445/
Abstract

: Protective mechanisms allow healthy neurons to cope with diverse stresses. Excessive damage as well as aging can lead to defective functioning of these mechanisms. We recently designed NeuroHeal using artificial intelligence with the goal of bolstering endogenous neuroprotective mechanisms. Understanding the key nodes involved in neuroprotection will allow us to identify even more effective strategies for treatment of neurodegenerative diseases. : We used a model of peripheral nerve axotomy in rat pups, that induces retrograde apoptotic death of motoneurons. Nourishing mothers received treatment with vehicle, NeuroHeal or NeuroHeal plus nicotinamide, an inhibitor of sirtuins, and analysis of the pups were performed by immunohistochemistry, electron microscopy, and immunoblotting. , the post-translational status of proteins of interest was detailed using organotypic spinal cord cultures and genetic modifications in cell lines to unravel the neuroprotective mechanisms involved. : We found that the concomitant activation of the NAD-dependent deacetylase SIRT1 and the PI3K/AKT signaling pathway converge to increase the presence of deacetylated and phosphorylated FOXO3a, a transcription factor, in the nucleus. This favors the activation of autophagy, a pro-survival process, and prevents pro-apoptotic PARP1/2 cleavage. : NeuroHeal is a neuroprotective agent for neonatal motoneurons that fine-tunes autophagy on by converging SIRT1/AKT/FOXO3a axis. NeuroHeal is a combo of repurposed drugs that allow its readiness for prospective pediatric use.

摘要

保护机制使健康的神经元能够应对各种压力。过度损伤以及衰老会导致这些机制功能失调。我们最近利用人工智能设计了NeuroHeal,旨在增强内源性神经保护机制。了解神经保护中涉及的关键节点将使我们能够确定更有效的神经退行性疾病治疗策略。

我们使用了幼鼠外周神经轴突切断模型,该模型可诱导运动神经元逆行凋亡死亡。喂养幼鼠的母鼠接受了载体、NeuroHeal或NeuroHeal加烟酰胺(一种沉默调节蛋白抑制剂)的治疗,并通过免疫组织化学、电子显微镜和免疫印迹对幼鼠进行分析。此外,利用脊髓器官型培养和细胞系基因改造详细研究了相关蛋白的翻译后状态,以阐明其中涉及的神经保护机制。

我们发现,NAD依赖的去乙酰化酶SIRT1和PI3K/AKT信号通路的协同激活会使转录因子FOXO3a的去乙酰化和磷酸化形式在细胞核中的含量增加。这有利于自噬(一种促生存过程)的激活,并防止促凋亡的PARP1/2裂解。

NeuroHeal是一种针对新生运动神经元的神经保护剂,它通过汇聚SIRT1/AKT/FOXO3a轴来微调自噬。NeuroHeal是一种由重新利用的药物组成的组合药物,使其可用于未来的儿科应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3069/7163445/13209dada83b/thnov10p5154g006.jpg
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Biomedicines. 2021 Aug 18;9(8):1039. doi: 10.3390/biomedicines9081039.
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