Feng Qian, Li Ying, Wen Xiangru, Li Hui, Qi Chengyu, Wang Nan, Zhu Guang, Fu Yanyan, Liu Changdong, Liu Dan, Zhang Zhen, Yang Fan, Zhou Zhongyuan, Song Jinjin, Liang Jia, Chen Yuling, Zhou Xiaoyan, Liu Yan, Song Yuanjian
Jiangsu Engineering Center for Precision Diagnosis and Treatment Research of Polygenic Diseases, Jiangsu Key Laboratory of Brain Disease and Bioinformation, Research Center for Biochemistry and Molecular Biology, Xuzhou Engineering Center for Precision Diagnosis and Treatment Research of Polygenic Diseases, Xuzhou Key Laboratory of Clinical and Experimental Pathology, Key Laboratory of Genetic Foundation and Clinical Application, Department of Genetics, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China.
Clinical Laboratory, Xuzhou Medical University Affiliated Hospital, Xuzhou, Jiangsu, 221002, China.
Mol Neurobiol. 2025 May 3. doi: 10.1007/s12035-025-04926-1.
Cerebral ischemia/reperfusion (I/R) injury manifests as progressive motor and cognitive dysfunction, primarily attributed to neuronal apoptosis. However, there is a lack of neuroprotective drugs targeting neuronal apoptosis in ischemic stroke. In this study, utilizing bioinformatics analysis, we hypothesized that TRPV1 could serve as a novel molecular target implicated in neuronal apoptosis during cerebral ischemia/reperfusion (I/R) injury. To validate our hypothesis in vivo, we employed mouse models of I/R injury induced by transient middle cerebral artery occlusion (tMCAO). Importantly, pre-injecting capsazepine (CPZ), a TRPV1 antagonist, significantly suppressed apoptotic pathway activity in neurons. Additionally, we investigated the regulatory role of CDK5, a well-known neuronal-specific kinase, in modulating the internalization and functionality of TRPV1 ion channels. Our findings revealed an augmented interaction between TRPV1 and CDK5 during cerebral ischemia/reperfusion (I/R) injury. The administration of the TAT-T407 interference peptide, derived from the phosphorylation site of TRPV1 for CDK5, resulted in a reduction of neuronal apoptosis within ischemic regions following cerebral ischemia/reperfusion (I/R) injury. This intervention significantly diminished cerebral infarct volume and improved neurological function. In summary, disrupting the TRPV1/CDK5 interaction through TAT-T407 peptides provides protection against neuronal apoptosis and cognitive decline, suggesting an innovative therapeutic strategy for ischemic stroke treatment.
脑缺血/再灌注(I/R)损伤表现为进行性运动和认知功能障碍,主要归因于神经元凋亡。然而,在缺血性卒中中,缺乏针对神经元凋亡的神经保护药物。在本研究中,利用生物信息学分析,我们假设TRPV1可能是脑缺血/再灌注(I/R)损伤期间与神经元凋亡相关的新型分子靶点。为了在体内验证我们的假设,我们采用了短暂大脑中动脉闭塞(tMCAO)诱导的I/R损伤小鼠模型。重要的是,预先注射TRPV1拮抗剂辣椒素(CPZ)可显著抑制神经元中的凋亡途径活性。此外,我们研究了著名的神经元特异性激酶CDK5在调节TRPV1离子通道的内化和功能方面的调节作用。我们的研究结果显示,在脑缺血/再灌注(I/R)损伤期间,TRPV1与CDK5之间的相互作用增强。给予源自TRPV1 CDK5磷酸化位点的TAT-T407干扰肽,可减少脑缺血/再灌注(I/R)损伤后缺血区域内的神经元凋亡。这种干预显著减小了脑梗死体积并改善了神经功能。总之,通过TAT-T407肽破坏TRPV1/CDK5相互作用可提供针对神经元凋亡和认知衰退的保护作用,提示了一种用于缺血性卒中治疗的创新策略。