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Pathogenic neuropsychiatric effect of stress-induced microglial interleukin 12/23 axis in systemic lupus erythematosus

https://repo.qst.go.jp/records/2000372
https://repo.qst.go.jp/records/2000372
117fbb8f-0e06-44ce-adae-fd5fa16bf89c
アイテムタイプ 学術雑誌論文 / Journal Article(1)
公開日 2024-01-25
タイトル
タイトル Pathogenic neuropsychiatric effect of stress-induced microglial interleukin 12/23 axis in systemic lupus erythematosus
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Nobuya Abe

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Nobuya Abe

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Masato Tarumi

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Masato Tarumi

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Yuichiro Fujieda

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Yuichiro Fujieda

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Nobuhiko Takahashi

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Nobuhiko Takahashi

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Kohei Karino

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Kohei Karino

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Mona Uchida

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Mona Uchida

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Michihito Kono

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Michihito Kono

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Yuki Tanaka

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Yuki Tanaka

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Rie Hasebe

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Rie Hasebe

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Masaru Kato

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Masaru Kato

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Olga Amengual

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Olga Amengual

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Yoshiyuki Arinuma

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Yoshiyuki Arinuma

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Kenji Oku

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Kenji Oku

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Wakiro Sato

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Wakiro Sato

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Khin Khin Tha

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Khin Khin Tha

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Miwako Yamasaki

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Miwako Yamasaki

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Masahiko Watanabe

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Masahiko Watanabe

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Tatsuya Atsumi

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Tatsuya Atsumi

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Masaaki Murakami

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Masaaki Murakami

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抄録
内容記述タイプ Abstract
内容記述 Objectives: The central nervous system disorder in systemic lupus erythematosus (SLE), called neuropsychiatric lupus (NPSLE), is one of the most severe phenotypes with various clinical symptoms, including mood disorder, psychosis and delirium as diffuse neuropsychological manifestations (dNPSLE). Although stress is one of the aggravating factors for neuropsychiatric symptoms, its role in the pathogenesis of dNPSLE remains to be elucidated. We aimed to investigate stress effects on the neuropsychiatric pathophysiology in SLE using lupus-prone mice and patients' data.

Methods: Sleep disturbance stress (SDS) for 2 weeks was placed on 6-8-week-old female MRL/lpr and control mice. Behavioural phenotyping, histopathological analyses and gene and protein expression analyses were performed to assess SDS-induced neuroimmunological alterations. We also evaluated cytokines of the cerebrospinal fluid and brain regional volumes in patients with dNPSLE and patients with non-dNPSLE.

Results: SDS-subjected MRL/lpr mice exhibited less anxiety-like behaviour, whereas stressed control mice showed increased anxiety. Furthermore, stress strongly activated the medial prefrontal cortex (mPFC) in SDS-subjected MRL/lpr. A transcriptome analysis of the PFC revealed the upregulation of microglial activation-related genes, including Il12b. We confirmed that stress-induced microglial activation and the upregulation of interleukin (IL) 12/23p40 proteins and increased dendritic spines in the mPFC of stressed MRL/lpr mice. IL-12/23p40 neutralisation and tyrosine kinase 2 inhibition mitigated the stress-induced neuropsychiatric phenotypes of MRL/lpr mice. We also found a higher level of cerebrospinal fluid IL-12/23p40 and more atrophy in the mPFC of patients with dNPSLE than those with non-dNPSLE.

Conclusions: The microglial IL-12/23 axis in the mPFC might be associated with the pathogenesis and a promising therapeutic target for dNPSLE.

Keywords: Magnetic Resonance Imaging; cytokines; inflammation; lupus erythematosus, systemic; psychology.
書誌情報 Annals of the Rheumatic Diseases

巻 81, 号 11, p. 1564-1575, 発行日 2022-07
出版者
出版者 BMJ
ISSN
収録物識別子タイプ ISSN
収録物識別子 0003-4967
DOI
識別子タイプ DOI
関連識別子 10.1136/ard-2022-222566
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