Zou Wenyan, Pu Tinglin, Feng Weixi, Lu Ming, Zheng Ying, Du Renhong, Xiao Ming, Hu Gang
1Department of Pharmacology, School of Medicine and Life Sciences, Nanjing University of Chinese Medicine, 138 Xianlin Avenue, Nanjing, 210023 Jiangsu China.
2Jiangsu Key Laboratory of Neurodegeneratiion, Department of Pharmacology, Nanjing Medical University, 101 Longmian Avenue, Nanjing, 211166 Jiangsu China.
Transl Neurodegener. 2019 Mar 1;8:7. doi: 10.1186/s40035-019-0147-y. eCollection 2019.
Abnormal aggregation of brain α-synuclein is a central step in the pathogenesis of Parkinson's disease (PD), thus, it is reliable to promote the clearance of α-synuclein to prevent and treat PD. Recent studies have revealed an essential role of glymphatic system and meningeal lymphatic vessels in the clearance of brain macromolecules, however, their pathophysiological aspects remain elusive.
Meningeal lymphatic drainage of 18-week-old A53T mice was blocked via ligating the deep cervical lymph nodes. Six weeks later, glymphatic functions and PD-like phenotypes were systemically analyzed.
Glymphatic influx of cerebrospinal fluid tracer was reduced in A53T mice, accompanied with perivascular aggregation of α-synuclein and impaired polarization of aquaporin 4 expression in substantia nigra. Cervical lymphatic ligation aggravated glymphatic dysfunction of A53T mice, causing more severe accumulation of α-synuclein, glial activation, inflammation, dopaminergic neuronal loss and motor deficits.
The results suggest that brain lymphatic clearance dysfunction may be an aggravating factor in PD pathology.
脑α-突触核蛋白的异常聚集是帕金森病(PD)发病机制的核心步骤,因此,促进α-突触核蛋白的清除对预防和治疗PD是可靠的。最近的研究揭示了类淋巴系统和脑膜淋巴管在脑大分子清除中的重要作用,然而,它们的病理生理学方面仍不清楚。
通过结扎颈深淋巴结来阻断18周龄A53T小鼠的脑膜淋巴引流。六周后,系统分析类淋巴功能和PD样表型。
A53T小鼠脑脊液示踪剂的类淋巴流入减少,伴有α-突触核蛋白的血管周围聚集和黑质中 aquaporin 4表达的极化受损。颈淋巴结扎加重了A53T小鼠的类淋巴功能障碍,导致α-突触核蛋白更严重的积累、胶质细胞活化、炎症、多巴胺能神经元丢失和运动缺陷。
结果表明脑淋巴清除功能障碍可能是PD病理中的一个加重因素。