Inactivation of ERK1/2 signaling mediates dysfunction of basal meningeal lymphatic vessels in experimental subdural hematoma

被引:4
|
作者
Yuan, Jiangyuan [1 ,2 ]
Liu, Xuanhui [1 ,2 ]
Nie, Meng [1 ,2 ]
Chen, Yupeng [1 ,2 ]
Liu, Mingqi [1 ,2 ]
Huang, Jinhao [1 ,2 ]
Jiang, Weiwei [1 ,2 ]
Gao, Chuang [1 ,2 ]
Quan, Wei [1 ,2 ]
Gong, Zhitao [3 ]
Xiang, Tangtang [1 ,2 ]
Zhang, Xinjie [1 ,2 ]
Sha, Zhuang [1 ,2 ]
Wu, Chenrui [1 ,2 ]
Wang, Dong [1 ,2 ]
Li, Shenghui [1 ,2 ]
Zhang, Jianning [1 ,2 ]
Jiang, Rongcai [1 ,2 ,4 ]
机构
[1] Tianjin Med Univ, Gen Hosp, Dept Neurosurg, Tianjin 300052, Peoples R China
[2] Minist Educ & Tianjin, Tianjin Neurol Inst, Key Lab Post Neuroinjury Neurorepair & Regenerat C, Tianjin, Peoples R China
[3] Anhui Med Univ, Affiliated Hosp 2, Dept Rehabil Med, Hefei 230601, Peoples R China
[4] Tianjin Med Univ, Gen Hosp, State Key Lab Expt Hematol, Tianjin 300052, Peoples R China
来源
THERANOSTICS | 2024年 / 14卷 / 01期
基金
中国国家自然科学基金;
关键词
subdural hematoma; meningeal lymphatic vessels; meningeal lymphatic drainage; ERK1/2; atorvastatin; T-CELLS; ATORVASTATIN; DRAINAGE; SYSTEM; MAINTENANCE; FOXC2; FLUID; EGFR;
D O I
10.7150/thno.87633
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rationale: Meningeal lymphatic vessels (MLVs) are essential for the clearance of subdural hematoma (SDH). However, SDH impairs their drainage function, and the pathogenesis remains unclear. Herein, we aimed to understand the pathological mechanisms of MLV dysfunction following SDH and to test whether atorvastatin, an effective drug for SDH clearance, improves meningeal lymphatic drainage (MLD).Methods: We induced SDH models in rats by injecting autologous blood into the subdural space and evaluated MLD using Gadopentetate D, Evans blue, and CFSE-labeled erythrocytes. Whole-mount immunofluorescence and transmission electron microscopy were utilized to detect the morphology of MLVs. Phosphoproteomics, western blot, flow cytometry, and in vitro experiments were performed to investigate the molecular mechanisms underlying dysfunctional MLVs.Results: The basal MLVs were detected to have abundant valves and play an important role in draining subdural substances. Following SDH, these basal MLVs exhibited disrupted endothelial junctions and dilated lumen, leading to impaired MLD. Subsequent proteomics analysis of the meninges detected numerous dephosphorylated proteins, primarily enriched in the adherens junction, including significant dephosphorylation of ERK1/2 within the meningeal lymphatic endothelial cells (LECs). Subdural injection of the ERK1/2 kinase inhibitor PD98059 resulted in dilated basal MLVs and impaired MLD, resembling the dysfunctional MLVs observed in SDH. Moreover, inhibiting ERK1/2 signaling severely disrupted intercellular junctions between cultured LECs. Finally, atorvastatin was revealed to protect the structure of basal MLVs and accelerate MLD following SDH. However, these beneficial effects of atorvastatin were abolished when combined with PD98059.Conclusion: Our findings demonstrate that SDH induces ERK1/2 dephosphorylation in meningeal LECs, leading to disrupted basal MLVs and impaired MLD. Additionally, we reveal a beneficial effect of atorvastatin in improving MLD.
引用
收藏
页码:304 / 323
页数:20
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