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SIRT2 inhibition exacerbates p53-mediated ferroptosis in mice following experimental traumatic brain injury.
Neuroreport ( IF 1.7 ) Pub Date : 2021-06-07 , DOI: 10.1097/wnr.0000000000001679
Jinpeng Gao 1 , Yunfeng Li 2 , Ran Song 3
Affiliation  

Ferroptosis plays an important role in traumatic brain injury (TBI). The p53 protein is a major mediator of ferroptosis. However, the role of p53-mediated ferroptosis in TBI has not been studied. Sirtuin 2 (SIRT2) exerts a protective effects role in TBI, although the underlying mechanism of this protection remains unclear. In the present study, we tested the hypothesis that that SIRT2 mitigates TBI by regulating p53-mediated ferroptosis.

中文翻译:

在实验性创伤性脑损伤后,SIRT2 抑制加剧了 p53 介导的小鼠铁死亡。

铁死亡在创伤性脑损伤(TBI)中起重要作用。p53 蛋白是铁死亡的主要介质。然而,尚未研究 p53 介导的铁死亡在 TBI 中的作用。Sirtuin 2 (SIRT2) 在 TBI 中发挥保护作用,尽管这种保护的潜在机制仍不清楚。在本研究中,我们检验了 SIRT2 通过调节 p53 介导的铁死亡来减轻 TBI 的假设。
更新日期:2021-06-10
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