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論文
タイトル
タイトル(英)
Sustaining microglial reparative function enhances stroke recovery
参照URL
https://researchmap.jp/junt/published_papers/46504429
著者
著者(英)
Jun Tsuyama,Seiichiro Sakai,Kumiko Kurabayashi,Ryuki Koyama,Yuichiro Hara,Ito Kawakami,Hideya Kawaji,Takashi Shichita
担当区分
概要
概要(英)
Abstract Neurological symptoms after brain injury can remain as lifelong detrimental sequelae since most spontaneous brain recovery disappears within a few months after brain injury. Microglia play an essential role in recovery processes after brain injury; however, cellular and molecular mechanisms that diminish spontaneous brain functional recovery remain unknown. We discovered by cellular fate analysis that reparative myeloid cells remained in the post-stroke brain even after losing their reparative function. ZFP384 was identified as a pivotal transcriptional regulator that diminished recovery phase–associated gene expression in reparative myeloid cells, turning them into ruined cells which lost reparative functions. ZFP384 diminished the YY1-mediated chromatin interaction necessary for expressing recovery phase–associated genes. Antisense oligonucleotide againstZfp384sustained the broad range of neural repair effects of myeloid cells and enhanced stroke recovery, even in the chronic phase of ischemic stroke recovery. Thus, therapeutics preventing the myeloid reparative immunity from reaching a ruined state sustains brain functional recovery.
出版者・発行元
出版者・発行元(英)
Cold Spring Harbor Laboratory
誌名
誌名(英)
開始ページ
終了ページ
出版年月
2024年4月13日
査読の有無
招待の有無
掲載種別
ISSN
DOI URL
https://doi.org/10.1101/2024.04.10.588813
共同研究・競争的資金等の研究課題
研究者
七田 崇 (シチタ タカシ) , 酒井 誠一郎 (サカイ セイイチロウ) , 川路 英哉 ( ) , 津山 淳 (ツヤマ ジュン) , 原 雄一郎 ( )