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E3 泛素连接酶 Nedd4-2 在内质网应激过程中发挥神经保护作用。

E3 ubiquitin ligase Nedd4-2 exerts neuroprotective effects during endoplasmic reticulum stress.

机构信息

Department of Molecular and Integrative Physiology, School of Molecular and Cellular Biology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

Neuroscience Program, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

出版信息

J Neurochem. 2022 Mar;160(6):613-624. doi: 10.1111/jnc.15567. Epub 2021 Dec 29.

Abstract

The neural precursor cell expressed developmentally down-regulated protein 4-like (Nedd4-2) is an E3 ubiquitin ligase critical for neurodevelopment and homeostasis of neural circuit excitability. While dysregulation of Nedd4-2 has been linked to elevated seizure susceptibility through impaired ubiquitination of multiple direct substrates, it remains largely unclear whether Nedd4-2 interconnects other cellular pathways that affect neuronal activity and seizure susceptibility. Here, we first showed that Nedd4-2 associates with the endoplasmic reticulum (ER) and regulates the expression of multiple ER-resident proteins. Furthermore, utilizing Nedd4-2 conditional knockout mice, we showed that Nedd4-2 is required for the maintenance of spontaneous neural activity and excitatory synapses following the induction of ER stress. When analyzing activation of the canonical pathways of ER stress response, we found that Nedd4-2 is required for phosphorylation of eIF2α. While phosphorylation of eIF2α has been shown to reduce seizure susceptibility, attempts to facilitate phosphorylation of eIF2α in Nedd4-2 conditional knockout mice failed to produce such a beneficial function, suggesting a role for Nedd4-2 in integrating the ER stress response to modulate seizure susceptibility. Altogether, our study demonstrates neuroprotective functions of Nedd4-2 during ER stress in neurons and could provide insight into neurological diseases in which the expression or activity of Nedd4-2 is impaired.

摘要

神经前体细胞发育下调蛋白 4 样物(Nedd4-2)是一种 E3 泛素连接酶,对神经发育和神经回路兴奋性的内稳态至关重要。虽然 Nedd4-2 的失调通过多种直接底物的泛素化受损与癫痫易感性升高有关,但它是否与影响神经元活动和癫痫易感性的其他细胞途径相互作用在很大程度上仍不清楚。在这里,我们首先表明 Nedd4-2 与内质网(ER)相关联,并调节多种 ER 驻留蛋白的表达。此外,利用 Nedd4-2 条件性敲除小鼠,我们表明 Nedd4-2 是维持 ER 应激诱导后自发性神经活动和兴奋性突触所必需的。在分析 ER 应激反应的经典途径的激活时,我们发现 Nedd4-2 是 eIF2α 磷酸化所必需的。虽然 eIF2α 的磷酸化已被证明可降低癫痫易感性,但在 Nedd4-2 条件性敲除小鼠中促进 eIF2α 的磷酸化的尝试未能产生这种有益的功能,这表明 Nedd4-2 在整合 ER 应激反应以调节癫痫易感性方面具有作用。总之,我们的研究表明 Nedd4-2 在神经元 ER 应激期间具有神经保护作用,并可为 Nedd4-2 的表达或活性受损的神经疾病提供见解。

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