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Gen Physiol Biophys. 2015 Oct;34(4):337-52. doi: 10.4149/gpb_2015024.
2
GluN2B-Containing NMDA Receptors Regulate AMPA Receptor Traffic through Anchoring of the Synaptic Proteasome.含GluN2B的N-甲基-D-天冬氨酸受体通过突触蛋白酶体的锚定调节α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体的转运。
J Neurosci. 2015 Jun 3;35(22):8462-79. doi: 10.1523/JNEUROSCI.3567-14.2015.
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Proteasomes. A molecular census of 26S proteasomes in intact neurons.蛋白酶体。完整神经元中 26S 蛋白酶体的分子普查。
Science. 2015 Jan 23;347(6220):439-42. doi: 10.1126/science.1261197.
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Protein degradation and protein synthesis in long-term memory formation.长期记忆形成中的蛋白质降解和蛋白质合成。
Front Mol Neurosci. 2014 Jun 26;7:61. doi: 10.3389/fnmol.2014.00061. eCollection 2014.
5
Nitric oxide is necessary for labilization of a consolidated context memory during reconsolidation in terrestrial snails.一氧化氮对于陆地蜗牛再巩固过程中巩固的情境记忆的不稳定化是必需的。
Eur J Neurosci. 2014 Sep;40(6):2963-70. doi: 10.1111/ejn.12642. Epub 2014 Jun 7.
6
pT305-CaMKII stabilizes a learning-induced increase in AMPA receptors for ongoing memory consolidation after classical conditioning.pT305-CaMKII稳定了经典条件反射后持续记忆巩固过程中由学习引起的AMPA受体增加。
Nat Commun. 2014 May 30;5:3967. doi: 10.1038/ncomms4967.
7
S-nitrosylation regulates mitochondrial quality control via activation of parkin.S-亚硝基化通过激活 parkin 调节线粒体质量控制。
Sci Rep. 2013;3:2202. doi: 10.1038/srep02202.
8
Double dissociation of the requirement for GluN2B- and GluN2A-containing NMDA receptors in the destabilization and restabilization of a reconsolidating memory.在重新巩固的记忆的不稳定性和再稳定性中,需要 GluN2B 和 GluN2A 两种 NMDA 受体的双重分离。
J Neurosci. 2013 Jan 16;33(3):1109-15. doi: 10.1523/JNEUROSCI.3273-12.2013.
9
A cellular model of memory reconsolidation involves reactivation-induced destabilization and restabilization at the sensorimotor synapse in Aplysia.在海兔中,记忆再巩固的细胞模型涉及到感觉运动突触的再激活诱导不稳定性和再稳定。
Proc Natl Acad Sci U S A. 2012 Aug 28;109(35):14200-5. doi: 10.1073/pnas.1211997109. Epub 2012 Aug 14.
10
Activity-dependent actin dynamics are required for the maintenance of long-term plasticity and for synaptic capture.依赖活动的肌动蛋白动力学对于维持长期可塑性和突触捕获是必需的。
Eur J Neurosci. 2012 Jan;35(2):195-206. doi: 10.1111/j.1460-9568.2011.07955.x.

一氧化氮上调神经元中的蛋白酶体蛋白降解。

Nitric Oxide Upregulates Proteasomal Protein Degradation in Neurons.

作者信息

Bal Natalia, Roshchin Matvey, Salozhin Sergey, Balaban Pavel

机构信息

Institute of Higher Nervous Activity and Neurophysiology of RAS, 5A Butlerova St., Moscow, 117485, Russia.

出版信息

Cell Mol Neurobiol. 2017 Jul;37(5):763-769. doi: 10.1007/s10571-016-0413-9. Epub 2016 Aug 5.

DOI:10.1007/s10571-016-0413-9
PMID:27495161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11482057/
Abstract

Nitric oxide (NO) is involved in many neuronal functions such as neuromodulation and intracellular signaling. Recent studies have demonstrated that nitric oxide is involved in regulation of proteasomal protein degradation. However, its role in neuronal protein degradation still remains unclear. In our study, we investigated the influence of endogenous nitric oxide production in this process. We have shown that nitric oxide synthase blockade prevents decline of the Ub-GFP fluorescence (GFP-based proteasomal protein degradation reporter) in neuronal processes of the cultured hippocampal neurons. It suggests that nitric oxide may regulate ubiquitin-dependent proteasomal protein degradation in neurons. Also, we have confirmed that the NO synthesis blockade alone significantly impairs long-term potentiation, and demonstrated for the first time that simultaneous blockade of the NO and proteins synthesis leads to the long-term potentiation amplitude rescue to the control values. Obtained results suggest that nitric oxide is involved in the protein degradation in proteasomes in physiological conditions.

摘要

一氧化氮(NO)参与多种神经元功能,如神经调节和细胞内信号传导。最近的研究表明,一氧化氮参与蛋白酶体蛋白降解的调节。然而,其在神经元蛋白降解中的作用仍不清楚。在我们的研究中,我们调查了内源性一氧化氮产生在此过程中的影响。我们已经表明,一氧化氮合酶阻断可防止培养的海马神经元的神经突中Ub-GFP荧光(基于GFP的蛋白酶体蛋白降解报告基因)下降。这表明一氧化氮可能调节神经元中泛素依赖性蛋白酶体蛋白降解。此外,我们已经证实,单独的NO合成阻断会显著损害长时程增强,并且首次证明同时阻断NO和蛋白合成会导致长时程增强幅度恢复到对照值。获得的结果表明,在生理条件下,一氧化氮参与蛋白酶体中的蛋白降解。