焦亡在帕金森神经病理学中的潜在作用和NLRP3炎性体靶向治疗的新见解以及基于纳米颗粒的miRNA治疗的最新进展。

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-07-01 Epub Date: 2025-03-18 DOI:10.1007/s12035-025-04818-4
Hebatallah M Saad, Esraa Atef, Abeer E Elsayed
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引用次数: 0

摘要

帕金森病(PD)是一种广泛存在的神经退行性疾病,其特征是黑质致密部(SNc)多巴胺能神经元的逐渐退化。本文综述了NLRP3炎性小体介导的焦亡病理生理机制在PD进展中的最新进展,以及针对NLRP3炎症途径和miRNA的抗焦亡药物的研究进展。PD的病理生理主要与α-突触核蛋白的聚集、活性氧(ROS)的过量产生以及小胶质细胞激活引起的神经炎症的发生有关。先前的研究表明,在PD患者和1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)小鼠模型中,大量的小胶质细胞被激活,引发神经炎症并导致细胞级联死亡。小胶质细胞具有一种复杂的炎症途径,称为核苷酸结合寡聚化结构域,富含亮氨酸的重复序列和含pyrin结构域3 (NLRP3)炎症小体。NLRP-3炎性小体的激活导致先天细胞因子成熟,包括IL-18和IL-1β,其启动神经炎症信号并诱导一种称为焦亡的炎症细胞死亡。在神经元损伤时,细胞内损伤相关分子模式(DAMPs)水平,包括活性氧(ROS)将会建立。DAMPs诱导不受调节的细胞死亡,随后释放氧化中间体和促炎细胞因子,导致PD的进展。因此,通过阻断NLRP3和阻断IL-1β信号传导和释放,可以有效地利用抗焦性药物靶向神经炎症。此外,许多研究表明,mirna已被鉴定为NLRP3炎性体和Nrf2信号的调节因子,从而调节PD中的NLRP3-Nrf2轴。纳米技术有望推动基于mirna的治疗。需要创建确保miRNA稳定性、穿越血脑屏障(BBB)和分布miRNA靶向区域的纳米颗粒。综上所述,通过NLRP3或miRNA靶向焦亡通路可能是未来PD的前瞻性治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Insights on the Potential Role of Pyroptosis in Parkinson's Neuropathology and Therapeutic Targeting of NLRP3 Inflammasome with Recent Advances in Nanoparticle-Based miRNA Therapeutics.

Parkinson's disease (PD) is a widespread neurodegenerative disorder characterized by the gradual degeneration of dopaminergic neurons in the substantia nigra pars compacta (SNc). This review aims to summarize the recent advancements in the pathophysiological mechanisms of pyroptosis, mediated by NLRP3 inflammasome, in advancing PD and the anti-pyroptotic agents that target NLRP3 inflammatory pathways and miRNA. PD pathophysiology is primarily linked to the aggregation of α-synuclein, the overproduction of reactive oxygen species (ROS), and the development of neuroinflammation due to microglial activation. Prior research indicated that a significant quantity of microglia is activated in both PD patients and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mouse models, triggering neuroinflammation and resulting in a cascade of cellular death. Microglia possess an inflammatory complex pathway termed the nucleotide-binding oligomerization domain-, leucine-rich repeat, and pyrin domain-containing 3 (NLRP3) inflammasome. Activation of the NLRP-3 inflammasome results in innate cytokines maturation, including IL-18 and IL-1β, which initiates the neuroinflammatory signal and induces a type of inflammatory cell death known as pyroptosis. Upon neuronal damage, intracellular levels of damage-associated molecular patterns (DAMPs), including reactive oxygen species (ROS), would build. DAMPs induce unregulated cell death and subsequent release of oxidative intermediates and pro-inflammatory cytokines, leading to the progression of PD. Thus, targeting of neuroinflammation using antipyroptotic medications can be efficiently achieved by blocking NLRP3 and obstructing IL-1β signaling and release. Furthermore, many research studies showed that miRNAs have been identified as regulators of the NLRP3 inflammasome and Nrf2 signal, which subsequently modulate the NLRP3-Nrf2 axis in PD. Nanotechnology promises potential for the advancement of miRNA-based therapies. Nanoparticles that ensure miRNA stability, traverse the blood-brain barrier (BBB) and distribute miRNA targeting regions needed to be created. In conclusion, targeting the pyroptosis pathway via NLRP3 or miRNA may serve as a prospective therapeutic strategy for PD in the future.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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