Bal Natalia, Roshchin Matvey, Salozhin Sergey, Balaban Pavel
Institute of Higher Nervous Activity and Neurophysiology of RAS, 5A Butlerova St., Moscow, 117485, Russia.
Cell Mol Neurobiol. 2017 Jul;37(5):763-769. doi: 10.1007/s10571-016-0413-9. Epub 2016 Aug 5.
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.
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。