Mei Yingxue, She Fei, Zhang Ling, Kim Gamin, Li Ruomeng, Zheng Xiuzhi, Wang Zonghai, Chen Renxuan, Wang Long, Chen Dongmei, Kim Jungho, Zhang Tao, Lee Tae Ho
Fujian Key Laboratory of Translational Research in Cancer and Neurodegenerative Diseases, Institute of Basic Medicine, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, China.
Laboratory of Molecular and Cellular Biology, Department of Life Science, Sogang University, Seoul, Korea.
Cell Death Dis. 2025 Mar 4;16(1):151. doi: 10.1038/s41419-025-07474-7.
Neuronal cell death is a causative process in traumatic brain injury (TBI)-induced structural and functional impairment of the central nervous system. However, the upstream trigger of TBI-induced neuronal loss and the underlying molecular pathways remain unclear. Zipper-interacting protein kinase (ZIPK) has been shown to be upregulated in Alzheimer's disease and ischemic stroke and to play a role in cellular apoptosis, while its pathological significance in TBI has not been reported. Herein, we discovered for the first time that ZIPK expression was markedly elevated in neurons after TBI and that ZIPK caused massive neuronal apoptosis in peri-contusional brain regions. Zipk haploinsufficiency antagonized neuronal cell death and reversed several typical neuropathological changes induced by TBI. Mechanistically, we found that ZIPK affected neuronal viability by modulating death effector domain-containing DNA binding protein (DEDD) and caspase-3 pathway. Specifically, ZIPK could bind to and phosphorylate DEDD at the S9 residue, thus enhancing the stability of DEDD, and leading to the activation of caspase-3-mediated apoptotic cascade in neurons. The rescue of neuronal loss by ZIPK downregulation effectively alleviated TBI-induced behavioral deficits by preserving motor and cognitive abilities in vivo, supporting the decisive role of ZIPK dysregulation in TBI-associated neuronal dysfunctions by modulating neuronal survival. Furthermore, pharmacological suppression of ZIPK activity by a specific inhibitor prior to TBI protected neurons from brain injury-induced cell death and neuronal degeneration in vitro and in vivo by preventing DEDD upregulation and caspase-3 activation. In conclusion, our data reveal the essential contribution of ZIPK to TBI-induced neuronal cell death through the DEDD/caspase-3 cascade, and suggest the potential of targeting ZIPK as an effective strategy for treating TBI-related neuropathologies.
神经元细胞死亡是创伤性脑损伤(TBI)诱导的中枢神经系统结构和功能损害的一个致病过程。然而,TBI诱导的神经元丢失的上游触发因素及其潜在的分子途径仍不清楚。拉链相互作用蛋白激酶(ZIPK)已被证明在阿尔茨海默病和缺血性中风中上调,并在细胞凋亡中起作用,而其在TBI中的病理意义尚未见报道。在此,我们首次发现TBI后神经元中ZIPK表达显著升高,且ZIPK在挫伤周围脑区导致大量神经元凋亡。Zipk单倍体不足拮抗神经元细胞死亡,并逆转了TBI诱导的几种典型神经病理变化。机制上,我们发现ZIPK通过调节含死亡效应结构域的DNA结合蛋白(DEDD)和半胱天冬酶-3途径影响神经元活力。具体而言,ZIPK可与DEDD结合并在S9残基处使其磷酸化,从而增强DEDD的稳定性,并导致神经元中半胱天冬酶-3介导的凋亡级联反应的激活。通过下调ZIPK来挽救神经元丢失,通过在体内保留运动和认知能力,有效减轻了TBI诱导的行为缺陷,支持了ZIPK失调通过调节神经元存活在TBI相关神经元功能障碍中的决定性作用。此外,在TBI之前用特异性抑制剂对ZIPK活性进行药理学抑制,通过防止DEDD上调和半胱天冬酶-3激活,在体外和体内保护神经元免受脑损伤诱导的细胞死亡和神经元变性。总之,我们的数据揭示了ZIPK通过DEDD/半胱天冬酶-3级联反应对TBI诱导的神经元细胞死亡的重要贡献,并表明靶向ZIPK作为治疗TBI相关神经病理学的有效策略的潜力。