TNFAIP3通过影响HMOX1蛋白和ACSL3的去泛素化和泛素化途径影响外伤性脑损伤后铁凋亡。

IF 7.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Free Radical Biology and Medicine Pub Date : 2024-12-30 DOI:10.1016/j.freeradbiomed.2024.12.048
Lin Zhou, Lei Li, Jinghao Yang, Maierdan Mansuer, Xianyu Deng, Yida Wang, Hui Ren, Daming Cui, Yang Jiang, Liang Gao
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引用次数: 0

摘要

外伤性脑损伤的发生和发展是一个复杂的过程。神经元损伤引发的病理生理机制包括各种形式的程序性细胞死亡,包括铁下垂。我们观察到创伤性脑损伤后小鼠TNFAIP3表达上调。过表达TNFAIP3通过铁下垂抑制HT-22增殖和细胞活力。机制上,TNFAIP3与HMOX1蛋白相互作用,并通过去泛素化途径促进其稳定性。此外,TNFAIP3可以通过nedd4介导的泛素化促进ACSL3降解,从而增强脂质过氧化、线粒体损伤和神经元细胞死亡。注射AAV-shTNFAIP3的小鼠表现出皮层撞击损伤后神经元变性减少,运动和认知功能改善。综上所述,我们的研究结果表明,TNFAIP3缺乏抑制神经元细胞铁凋亡,改善创伤性脑损伤引起的认知功能障碍,并证明其在创伤性脑损伤治疗中的潜在适用性。
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TNFAIP3 affects ferroptosis after traumatic brain injury by affecting the deubiquitination and ubiquitination pathways of the HMOX1 protein and ACSL3.

The occurrence and progression of traumatic brain injury involve a complex process. The pathophysiological mechanisms triggered by neuronal damage include various forms of programmed cell death, including ferroptosis. We observed upregulation of TNFAIP3 in mice after traumatic brain injury. Overexpression of TNFAIP3 inhibits HT-22 proliferation and cell viability through ferroptosis. Mechanistically, TNFAIP3 interacts with the HMOX1 protein and promotes its stability through the deubiquitination pathway. Additionally, TNFAIP3 can enhance lipoperoxidation, mitochondrial damage, and neuronal cell death by promoting ACSL3 degradation via NEDD4-mediated ubiquitination. Mice injected with AAV-shTNFAIP3 exhibited reduced neuronal degeneration and improved motor and cognitive function following cortical impact injury. In conclusion, our findings demonstrate that TNFAIP3 deficiency inhibits neuronal cell ferroptosis and ameliorates cognitive impairment caused by traumatic brain injury and demonstrate its potential applicability in the treatment of traumatic brain injury.

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来源期刊
Free Radical Biology and Medicine
Free Radical Biology and Medicine 医学-内分泌学与代谢
CiteScore
14.00
自引率
4.10%
发文量
850
审稿时长
22 days
期刊介绍: Free Radical Biology and Medicine is a leading journal in the field of redox biology, which is the study of the role of reactive oxygen species (ROS) and other oxidizing agents in biological systems. The journal serves as a premier forum for publishing innovative and groundbreaking research that explores the redox biology of health and disease, covering a wide range of topics and disciplines. Free Radical Biology and Medicine also commissions Special Issues that highlight recent advances in both basic and clinical research, with a particular emphasis on the mechanisms underlying altered metabolism and redox signaling. These Special Issues aim to provide a focused platform for the latest research in the field, fostering collaboration and knowledge exchange among researchers and clinicians.
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