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评估神经炎症在LRRK2模型中对神经退行性变的作用。

Evaluation of Neuroinflammatory Contribution to Neurodegeneration in LRRK2 Models.

作者信息

Nguyen Hoai Nam, Galleri Grazia, Rassu Antonio, Ciampelli Cristina, Bernardoni Roberto, Galioto Manuela, Albani Diego, Crosio Claudia, Iaccarino Ciro

机构信息

Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy.

Department Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.

出版信息

Biomedicines. 2024 Jul 12;12(7):1555. doi: 10.3390/biomedicines12071555.

Abstract

Pathological mutations in the gene are the major genetic cause of Parkinson's disease (PD). Although several animal models with either LRRK2 down- or over-expression have been developed, the physiological function of LRRK2 remains elusive. is constitutively expressed in various tissues including neurons and glial cells, but importantly, it is expressed at low levels in dopaminergic neurons, further contributing to the cryptic function of . Significant levels of LRRK2 protein and mRNA have been detected in peripheral blood mononuclear cells, lymph nodes, the spleen, and primary microglia, strongly suggesting the contribution of inflammatory cells to neuronal degeneration. In this research article, using LRRK2 models, we were able to demonstrate a significant contribution of glial cells to the LRRK2 pathological phenotype. Furthermore, in , neurodegeneration is associated with a significant and important increase in specific inflammatory peptides. Finally, levetiracetam, a compound widely used in human therapy to treat epilepsy, was able to rescue both neuronal degeneration and neuroinflammation.

摘要

该基因的病理性突变是帕金森病(PD)的主要遗传病因。尽管已经开发出几种LRRK2表达下调或上调的动物模型,但LRRK2的生理功能仍然难以捉摸。LRRK2在包括神经元和神经胶质细胞在内的各种组织中组成性表达,但重要的是,它在多巴胺能神经元中低水平表达,这进一步导致了其功能的隐秘性。在外周血单核细胞、淋巴结、脾脏和原代小胶质细胞中检测到了显著水平的LRRK2蛋白和mRNA,这强烈表明炎症细胞对神经元变性有影响。在这篇研究文章中,使用LRRK2模型,我们能够证明神经胶质细胞对LRRK2病理表型有显著影响。此外,在[具体模型名称未给出]中,神经变性与特定炎症肽的显著且重要的增加有关。最后,左乙拉西坦是一种广泛用于人类治疗癫痫的化合物,它能够挽救神经元变性和神经炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e29/11274873/389d27f73d0e/biomedicines-12-01555-g001.jpg

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