短暂受体电位香草蛋白4阻断可减轻匹罗卡品诱导的癫痫持续状态小鼠海马的焦凋亡。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Lihan Liu, Yue Wang, Xiaolin Wang, Guowen Zhang, Sha Sha, Rong Zhou, Yimei Du, Chunfeng Wu, Lei Chen
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引用次数: 0

摘要

焦亡有助于癫痫期间发生的神经元损伤。钙活化的中性蛋白酶(calpain)将半胱氨酸天冬氨酸特异性蛋白酶-1 (caspase-1, cas1)从细胞骨架上解离,激活的cas1负责产生气凝胶蛋白D (N-GSDMD)的n端,这是焦亡的最终执行者。阻断瞬时受体电位香草样蛋白4 (TRPV4)可减轻颞叶癫痫(TLE)模型小鼠的神经元损伤。本研究探讨了TRPV4在TLE中焦亡的作用。在匹罗卡品诱导的癫痫持续状态(PISE)小鼠海马中,失活的calpain1蛋白水平与总蛋白水平之比(失活/总calpain1)显著降低,而失活的calpain2蛋白水平与总蛋白水平之比保持不变。PISE小鼠海马NLRP3、cleaved cas-1 (c-cas-1)、白细胞介素(IL)-1β和N-GSDMD蛋白水平升高,GSDMD免疫荧光阳性(GSDMD+)细胞增多,存活锥体神经元减少。除了NLRP3水平升高外,MDL-28170抑制Calpain逆转了这些变化。靶向NLRP3 (MCC950)和cas-1 (Ac-YVAD-cmk)的抑制剂可阻断PISE小鼠海马中c-cas-1、IL-1β和N-GSDMD水平的升高。通过HC-067047抑制TRPV4增加了PISE小鼠的失活/总calpain1比值,降低了NLRP3、c- cas1、IL-1β和N-GSDMD蛋白水平,减少了GSDMD+细胞数量,提高了PISE小鼠海马锥体神经元的存活率。相反,用GSK1016790A激活TRPV4可降低失活钙蛋白酶1 /总钙蛋白酶1比值,升高NLRP3、c-cas-1、IL-1β和N-GSDMD水平,增加海马中GSDMD+细胞数量。注射gsk1016790a的小鼠海马中,MDL-28170增加了失活/总calpain 1比值,MDL-28170、MCC950和Ac-YVAD-cmk分别显著降低了c-cas-1、IL-1β和N-GSDMD蛋白水平。综上所述,TRPV4抑制通过下调calpain 1-NLRP3/cas-1-GSDMD通路减轻PISE小鼠焦亡,最终减轻神经元损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transient receptor potential vanilloid 4 blockage attenuates pyroptosis in hippocampus of mice following pilocarpine‑induced status epilepticus.

Pyroptosis contributes to the neuronal damage that occurs during epilepsy. Calcium-activated neutral protease (calpain) dissociates cysteinyl aspartate specific proteinase-1 (caspase-1, cas-1) from the cytoskeleton, and the activated cas-1 is responsible for the production of N-terminus of gasdermin D (N-GSDMD), the final executor of pyroptosis. Blocking transient receptor potential vanilloid 4 (TRPV4) can reduce neuronal injury in temporal lobe epilepsy (TLE) model mice. This study investigated the role of TRPV4 in pyroptosis during TLE. In the hippocampus of pilocarpine-induced status epilepticus (PISE) mice, the ratio of inactive calpain 1 protein level to its total protein level (inactive/total calpain 1) significantly decreased, while the ratio of inactive calpain 2 protein level to its total protein level remained unchanged. The protein levels of NLRP3, cleaved cas-1 (c-cas-1), interleukin (IL)-1β, and N-GSDMD increased, with more GSDMD-immunofluorescence-positive (GSDMD+) cells and fewer surviving pyramidal neurons observed in the hippocampus of PISE mice. Calpain inhibition with MDL-28170 reversed these changes, except for the elevated NLRP3 levels. Inhibitors targeting NLRP3 (MCC950) and cas-1 (Ac-YVAD-cmk) blocked the increase in c-cas-1, IL-1β, and N-GSDMD levels in the hippocampus of PISE mice. TRPV4 inhibition via HC-067047 increased the inactive/total calpain 1 ratio, decreased NLRP3, c-cas-1, IL-1β, and N-GSDMD protein levels, reduced GSDMD+ cells number, and improved pyramidal neuron survival in the hippocampus of PISE mice. Conversely, TRPV4 activation with GSK1016790A decreased the inactive/total calpain 1 ratio, elevated NLRP3, c-cas-1, IL-1β, and N-GSDMD levels, and increased GSDMD+ cells number in the hippocampus. In the hippocampus of GSK1016790A-injected mice, the inactive/total calpain 1 ratio was increased by MDL-28170, and c-cas-1, IL-1β, and N-GSDMD protein levels were markedly attenuated by MDL-28170, MCC950, and Ac-YVAD-cmk, respectively. In conclusion, TRPV4 inhibition mitigates pyroptosis in PISE mice by downregulating the calpain 1-NLRP3/cas-1-GSDMD pathway, ultimately reducing neuronal damage.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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