Parkinson's Disorder Research Laboratory, Iowa Center for Advanced Neurotoxicology, Department of Biomedical Sciences, Iowa State University, Ames, IA 50011, USA.
Parkinson's Disorder Research Laboratory, Iowa Center for Advanced Neurotoxicology, Department of Biomedical Sciences, Iowa State University, Ames, IA 50011, USA.
Pharmacol Ther. 2019 May;197:61-82. doi: 10.1016/j.pharmthera.2019.01.001. Epub 2019 Jan 22.
With the increased incidence of neurodegenerative diseases worldwide, Parkinson's disease (PD) represents the second-most common neurodegenerative disease. PD is a progressive multisystem neurodegenerative disorder characterized by a marked loss of nigrostriatal dopaminergic neurons and the formation of Lewy pathology in diverse brain regions. Although the mechanisms underlying dopaminergic neurodegeneration remain poorly characterized, data from animal models and postmortem studies have revealed that heightened inflammatory responses mediated via microglial and astroglial activation and the resultant release of proinflammatory factors may act as silent drivers of neurodegeneration. In recent years, numerous studies have demonstrated a positive association between the exposure to environmental neurotoxicants and the etiology of PD. Although it is unclear whether neuroinflammation drives pesticide-induced neurodegeneration, emerging evidence suggests that the failure to dampen neuroinflammatory mechanisms may account for the increased vulnerability to pesticide neurotoxicity. Furthermore, recent studies provide additional evidence that shifts the focus from a neuron-centric view to glial-associated neurodegeneration following pesticide exposure. In this review, we propose to summarize briefly the possible factors that regulate neuroinflammatory processes during environmental neurotoxicant exposure with a focus on the potential roles of mitochondria-driven redox mechanisms. In this context, a critical discussion of the data obtained from experimental research and possible epidemiological studies is included. Finally, we hope to provide insights on the pivotal role of exosome-mediated intercellular transmission of aggregated proteins in microglial activation response and the resultant dopaminergic neurodegeneration after exposure to pesticides. Collectively, an improved understanding of glia-mediated neuroinflammatory signaling might provide novel insights into the mechanisms that contribute to neurodegeneration induced by environmental neurotoxicant exposure.
随着世界各地神经退行性疾病发病率的增加,帕金森病(PD)是第二常见的神经退行性疾病。PD 是一种进行性多系统神经退行性疾病,其特征是黑质纹状体多巴胺能神经元明显丧失和不同脑区路易体病理形成。尽管多巴胺能神经退行性变的机制仍未得到很好的描述,但来自动物模型和尸检研究的数据表明,通过小胶质细胞和星形胶质细胞激活介导的炎症反应增强以及由此产生的促炎因子的释放可能是神经退行性变的无声驱动因素。近年来,许多研究表明,环境神经毒素暴露与 PD 的病因之间存在正相关。尽管尚不清楚神经炎症是否驱动农药诱导的神经退行性变,但新出现的证据表明,未能抑制神经炎症机制可能是导致对农药神经毒性易感性增加的原因。此外,最近的研究提供了额外的证据,表明关注点从农药暴露后神经元中心的观点转变为与神经胶质相关的神经退行性变。在这篇综述中,我们拟简要总结环境神经毒素暴露期间调节神经炎症过程的可能因素,重点关注线粒体驱动的氧化还原机制的潜在作用。在这方面,包括对实验研究和可能的流行病学研究获得的数据的批判性讨论。最后,我们希望深入了解外泌体介导的聚集蛋白细胞间传递在接触农药后小胶质细胞激活反应和由此产生的多巴胺能神经退行性变中的关键作用。总之,对神经胶质细胞介导的神经炎症信号的更好理解可能为环境神经毒素暴露引起的神经退行性变的机制提供新的见解。