論文

査読有り
2017年12月

Indirubin derivatives protect against endoplasmic reticulum stress-induced cytotoxicity and down-regulate CHOP levels in HT22 cells

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  • Yasuhiro Kosuge
  • ,
  • Hiroaki Saito
  • ,
  • Tatsuki Haraguchi
  • ,
  • Yoshimi Ichimaru
  • ,
  • Sachiyo Ohashi
  • ,
  • Hiroko Miyagishi
  • ,
  • Shunsuke Kobayashi
  • ,
  • Kumiko Ishige
  • ,
  • Shinichi Miyairi
  • ,
  • Yoshihisa Ito

27
23
開始ページ
5122
終了ページ
5125
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bmcl.2017.10.069
出版者・発行元
PERGAMON-ELSEVIER SCIENCE LTD

Indirubin and its derivatives have been reported to exhibit anti-cancer and anti-inflammatory activities. Recently, some of its derived analogs have been shown to have neuroprotective potential. Endoplasmic reticulum (ER) stress has been demonstrated to contribute to the pathogenesis of various neurodegenerative diseases, whereas the effects of indirubin derivatives on ER stress-induced cell death have not been addressed. In the present study, a series of 44 derivatives of indirubin was prepared to search for a novel class of neuroprotective agents against ER stress-induced neuronal death. The MTT reduction assay indicated that tunicamycin (TM), an inducer of ER stress, significantly decreased the viability of hippocampal neuronal HT22 cells. Among the compounds tested, eight showed significant inhibitory activity against TM-induced cell death. Western blot analysis showed that application of these analogs to the cells simultaneously with TM reduced the TM-induced expression of CHOP, an established mediator of ER stress. Our results suggest that the preventive effect of these indirubin derivatives against ER stress-induced neuronal death may be due, at least in part, to attenuation of the CHOP-dependent signaling system. (C) 2017 Elsevier Ltd. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.bmcl.2017.10.069
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000415643400007&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.bmcl.2017.10.069
  • ISSN : 0960-894X
  • eISSN : 1464-3405
  • Web of Science ID : WOS:000415643400007

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