慢性应激损害蓝斑神经元增加天冬酰胺内肽酶活性的自抑制作用。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-10-09 DOI:10.7554/eLife.106362
Hiroki Toyoda, Doyun Kim, Byeong Geon Koh, Tomomi Sano, Takashi Kanematsu, Seog Bae Oh, Youngnam Kang
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引用次数: 0

摘要

蓝斑(LC)损伤与焦虑/抑郁和阿尔茨海默病(AD)有关。胞浆内去甲肾上腺素(NA)浓度和单胺氧化酶A (MAO-A)活性的增加通过MAO-A产生NA代谢物3,4-二羟基苯基乙醇醛(DOPEGAL)而引发LC损伤。然而,尽管胞浆中几乎不存在NA,而NA仅由多巴胺通过多巴胺-β-羟化酶在细胞质囊泡中产生,但NA如何在LC神经元的体细胞/树突胞浆中积累尚未得到解决。由于自分泌释放的NA的再吸收是NA积累的主要来源,我们研究了慢性应激是否以及如何增加伴随NA自分泌的spike活性。LC神经元的过度兴奋通常是通过α 2a -肾上腺素能受体(AR)偶联自分泌释放NA的内向整流钾电流(GIRK-I)激活介导的自抑制来预防的。膜片钳研究发现,慢性约束应激(RS)小鼠LC神经元中na诱导的GIRK-I减少,而重复刺激也逐渐引起类似的减少。慢性RS引起LC神经元细胞膜表达α2A-ARs内化,膜组分α2A-ARs/GIRKs蛋白/mRNA水平降低。随后,慢性RS增加了MAO-A、dopegal诱导的天冬酰胺内肽酶(AEP)和tau N368的蛋白水平。这些结果表明,由于α2A-ARs/GIRK内化引起的慢性rs诱导的过度兴奋伴随着[Ca2+]i的增加,随后增加Ca2+依赖性MAO-A活性和NA自分泌。因此,α2A-AR的内化很可能通过促进自分泌释放的NA的再摄取而增加细胞质内NA,这反映在AEP的增加上。抑制α2A-AR内化可能在焦虑/AD治疗中具有翻译潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic stress impairs autoinhibition in neurons of the locus coeruleus to increase asparagine endopeptidase activity.

Impairments of locus coeruleus (LC) are implicated in anxiety/depression and Alzheimer's disease (AD). Increases in cytosolic noradrenaline (NA) concentration and monoamine oxidase A (MAO-A) activity initiate the LC impairment through production of NA metabolite, 3,4-dihydroxyphenyl-glycolaldehyde (DOPEGAL), by MAO-A. However, how NA accumulates in soma/dendritic cytosol of LC neurons has never been addressed despite the fact that NA is virtually absent in cytosol while NA is produced exclusively in cytoplasmic vesicles from dopamine by dopamine-β-hydroxylase. Since reuptake of autocrine-released NA following spike activity is the major source of NA accumulation, we investigated whether and how chronic stress can increase the spike activity accompanied by NA autocrine. Overexcitation of LC neurons is normally prevented by the autoinhibition mediated by activation of α2A-adrenergic receptor (AR)-coupled inwardly rectifying potassium-current (GIRK-I) with autocrine-released NA. Patch-clamp study revealed that NA-induced GIRK-I in LC neurons was decreased in chronic restraint stress (RS) mice, while a similar decrease was gradually caused by repeated excitation. Chronic RS caused internalization of α2A-ARs expressed in cell membrane in LC neurons and decreased protein/mRNA levels of α2A-ARs/GIRKs in membrane fraction. Subsequently, chronic RS increased the protein levels of MAO-A, DOPEGAL-induced asparagine endopeptidase (AEP), and tau N368. These results suggest that chronic RS-induced overexcitation due to the internalization of α2A-ARs/GIRK is accompanied by [Ca2+]i increases, subsequently increasing Ca2+-dependent MAO-A activity and NA autocrine. Thus, it is likely that internalization of α2A-AR increased cytosolic NA, as reflected in AEP increases, by facilitating reuptake of autocrine-released NA. The suppression of α2A-AR internalization may have a translational potential for anxiety/AD treatment.

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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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