在蛋白质毒性Charcot-Marie-Tooth型1B模型中,XBP1s的激活减轻了疾病的严重程度
Thierry Touvier1, Francesca A Veneri1, Anke Claessens1
1Division of Genetics and Cell Biology, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
bioRxiv : the preprint server for biology
|February 14, 2024
概括
IRE1α/XBP1通路对于在Charcot-Marie-Tooth类型1B (CMT1B) 神经病变中管理内质网膜 (ER) 压力至关重要. 激活这种途径有助于防止施万细胞中有毒蛋白质的积累,为CMT1B.提供了潜在的治疗点.
科学领域:
- 神经科学是一个神经科学.
- 细胞生物学 细胞生物学
- 遗传学 是一个遗传学.
背景情况:
- 查尔科-玛丽-牙1B型 (CMT1B) 是一种由髓蛋白零 (MPZ) 突变引起的脱髓化神经病变.
- MPZ突变导致蛋白质错误折叠,细胞内膜网膜 (ER) 应激,并激活 Schwann 细胞中的未折叠蛋白质反应 (UPR).
- 虽然PERK通路的作用已知,但UPR的IRE1α/XBP1信号臂在CMT1B病原发生中的贡献尚不清楚.
结论:
- 在蛋白质毒性CMT1B神经病变中,XBP1起着重要的适应作用.
- IRE1α/XBP1通路是CMT1B中 Schwann细胞对ER应激反应的关键调节者.
- 针对 IRE1α/XBP1 途径是CMT1B和其他可能与UPR相关的神经病变的有前途的治疗策略.
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