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载脂蛋白D过表达可保护小鼠免受红藻氨酸诱导的神经毒性。

Apolipoprotein D Overexpression Protects Against Kainate-Induced Neurotoxicity in Mice.

作者信息

Najyb Ouafa, Do Carmo Sonia, Alikashani Azadeh, Rassart Eric

机构信息

Laboratoire de Biologie Moléculaire, Département des Sciences Biologiques, Centre BioMed, Université du Québec à Montréal, Case Postale 8888, Succursale Centre-ville, Montréal, QC, H3C-3P8, Canada.

Department of Pharmacology and Therapeutics, McGill University, Montreal, QC, Canada.

出版信息

Mol Neurobiol. 2017 Aug;54(6):3948-3963. doi: 10.1007/s12035-016-9920-4. Epub 2016 Jun 7.

Abstract

Excitotoxicity due to the excessive activation of glutamatergic receptors leads to neuronal dysfunction and death. Excitotoxicity has been implicated in the pathogenesis of a myriad of neurodegenerative diseases with distinct etiologies such as Alzheimer's and Parkinson's. Numerous studies link apolipoprotein D (apoD), a secreted glycoprotein highly expressed in the central nervous system (CNS), to maintain and protect neurons in various mouse models of acute stress and neurodegeneration. Here, we used a mouse model overexpressing human apoD in neurons (H-apoD Tg) to test the neuroprotective effects of apoD in the kainic acid (KA)-lesioned hippocampus. Our results show that apoD overexpression in H-apoD Tg mice induces an increased resistance to KA-induced seizures, significantly attenuates inflammatory responses and confers protection against KA-induced cell apoptosis in the hippocampus. The apoD-mediated protection against KA-induced toxicity is imputable in part to increased plasma membrane Ca2+ ATPase type 2 expression (1.7-fold), decreased N-methyl-D-aspartate receptor (NMDAR) subunit NR2B levels (30 %) and lipid metabolism alterations. Indeed, we demonstrate that apoD can attenuate intracellular cholesterol content in primary hippocampal neurons and in brain of H-apoD Tg mice. In addition, apoD can be internalised by neurons and this internalisation is accentuated in ageing and injury conditions. Our results provide additional mechanistic information on the apoD-mediated neuroprotection in neurodegenerative conditions.

摘要

由于谷氨酸能受体过度激活导致的兴奋性毒性会引发神经元功能障碍和死亡。兴奋性毒性与多种病因各异的神经退行性疾病的发病机制有关,如阿尔茨海默病和帕金森病。大量研究表明,载脂蛋白D(apoD)是一种在中枢神经系统(CNS)中高度表达的分泌型糖蛋白,在各种急性应激和神经退行性变的小鼠模型中具有维持和保护神经元的作用。在此,我们使用在神经元中过表达人apoD的小鼠模型(H-apoD Tg)来测试apoD在 kainic 酸(KA)损伤的海马体中的神经保护作用。我们的结果表明,H-apoD Tg 小鼠中 apoD 的过表达诱导了对 KA 诱导的癫痫发作的抵抗力增加,显著减轻了炎症反应,并对海马体中 KA 诱导的细胞凋亡具有保护作用。apoD 介导的对 KA 诱导毒性的保护作用部分归因于质膜 Ca2+ ATPase 2 型表达增加(1.7 倍)、N-甲基-D-天冬氨酸受体(NMDAR)亚基 NR2B 水平降低(30%)以及脂质代谢改变。事实上,我们证明 apoD 可以降低原代海马神经元和 H-apoD Tg 小鼠大脑中的细胞内胆固醇含量。此外,apoD 可以被神经元内化,并且这种内化在衰老和损伤条件下会加剧。我们的结果为 apoD 在神经退行性疾病中介导的神经保护作用提供了更多的机制信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b316/7091089/342401a70f38/12035_2016_9920_Fig1_HTML.jpg

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