RANKL/RANK/OPG信号通路对双硫死亡影响的机制研究
Mechanism study of the effect of RANKL/RANK/OPG signaling pathway on disulfidptosis
  
DOI:10.3969/j.issn.1006-7108.2025.04.024
中文关键词:  双硫死亡  RANKL/RANK/OPG信号通路  SLC7A11  NFATc1  机制研究
英文关键词:disulfidptosis  RANKL/RANK/OPG signaling  pathway  SLC7A11  NFATc1  mechanism research
基金项目:国家自然科学基金(82160915、81860859);兰州市科技局项目(2022-3-23)
作者单位
马小成1 曹林忠1,2* 拦玉鑫1 刘德孙1 胡康一1 1.甘肃中医药大学,甘肃 兰州 730030 2.甘肃中医药大学附属医院,甘肃 兰州 730030 
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中文摘要:
      双硫死亡是二硫键应激引发的一种由于二硫键细胞内积累导致肌动蛋白细胞骨架崩溃,导致细胞死亡的新型细胞死亡形式。研究发现双硫死亡与RANKL/RANK/OPG信号通路密切相关,但其具体机制尚未明确。本文以RANKL/RANK/OPG信号通路对双硫死亡的发生机制的影响进行阐述,对其关系进行总结,为防治骨代谢相关疾病提供新途径。
英文摘要:
      Disulfidptosis is a novel form of cell death caused by intracellular accumulation of disulfide bonds due to disulfide bond stress, leading to collapse of the actin cytoskeleton and cell death. Studies have found that double sulfide death is closely related to the RANKL/RANK/OPG signaling pathway. However, the specific mechanism is not clear. This article discusses the influence of the RANKL/RANK/OPG signaling pathway in the occurrence of double sulfide death, summarizes the relationship between them, and provides a new approach for the prevention and treatment of bone metabolism-related diseases.
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