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尼拉替丁作为坏死性凋亡和铁死亡调控细胞死亡的双重抑制剂。

Nigratine as dual inhibitor of necroptosis and ferroptosis regulated cell death.

机构信息

SeaBeLife Biotech, Place Georges Teissier, 29680, Roscoff, France.

Sorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models Laboratory (LBI2M), Station Biologique de Roscoff, 29680, Roscoff, France.

出版信息

Sci Rep. 2022 Mar 24;12(1):5118. doi: 10.1038/s41598-022-09019-w.

Abstract

Nigratine (also known as 6E11), a flavanone derivative of a plant natural product, was characterized as highly specific non-ATP competitive inhibitor of RIPK1 kinase, one of the key components of necroptotic cell death signaling. We show here that nigratine inhibited both necroptosis (induced by Tumor Necrosis Factor-α) and ferroptosis (induced by the small molecules glutamate, erastin, RSL3 or cumene hydroperoxide) with EC in the µM range. Taken together, our data showed that nigratine is a dual inhibitor of necroptosis and ferroptosis cell death pathways. These findings open potential new therapeutic avenues for treating complex necrosis-related diseases.

摘要

尼格拉丁(也称为 6E11)是一种植物天然产物的黄烷酮衍生物,被鉴定为 RIPK1 激酶的高度特异性非 ATP 竞争性抑制剂,RIPK1 激酶是细胞坏死性死亡信号转导的关键组成部分之一。我们在这里表明,尼格拉丁以 µM 范围的 EC 抑制了由肿瘤坏死因子-α诱导的坏死性细胞死亡和由小分子谷氨酸、恩替诺特、RSL3 或 cumene 氢过氧化物诱导的铁死亡。总之,我们的数据表明,尼格拉丁是坏死性细胞死亡和铁死亡细胞死亡途径的双重抑制剂。这些发现为治疗复杂的坏死相关疾病开辟了新的潜在治疗途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e8f/8948175/3797207fd5df/41598_2022_9019_Fig1_HTML.jpg

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