Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Tianjin Neurological Institute, Key Laboratory of Post -Neuroinjury Neuro -repair and Regeneration in Central Nervous System, Ministry of Education and Tianjin, Tianjin, 300052, China.
Acta Neuropathol Commun. 2020 Feb 14;8(1):16. doi: 10.1186/s40478-020-0888-y.
Subdural haematomas (SDHs) are characterized by rapidly or gradually accumulated haematomas between the arachnoid and dura mater. The mechanism of haematoma clearance has not been clearly elucidated until now. The meningeal lymphatic vessel (mLV) drainage pathway is a novel system that takes part in the clearance of waste products in the central nervous system (CNS). This study aimed to explore the roles of the mLV drainage pathway in SDH clearance and its impacting factors. We injected FITC-500D, A488-fibrinogen and autologous blood into the subdural space of mice/rats and found that these substances drained into deep cervical lymph nodes (dCLNs). FITC-500D was also observed in the lymphatic vessels (LYVE+) of the meninges and the dCLNs in mice. The SDH clearance rate in SDH rats that received deep cervical lymph vessel (dCLV) ligation surgery was significantly lower than that in the control group, as evaluated by haemoglobin quantification and MRI scanning. The drainage rate of mLVs was significantly slower after the SDH model was established, and the expression of lymphangiogenesis-related proteins, including LYVE1, FOXC2 and VEGF-C, in meninges was downregulated. In summary, our findings proved that SDH was absorbed through the mLV drainage pathway and that haematomas could inhibit the function of mLVs.
硬脑膜下血肿(SDH)的特征是蛛网膜和硬脑膜之间迅速或逐渐积聚的血肿。到目前为止,血肿清除的机制尚未明确。脑膜淋巴管(mLV)引流途径是一种新的系统,参与中枢神经系统(CNS)中废物的清除。本研究旨在探讨 mLV 引流途径在 SDH 清除中的作用及其影响因素。我们将 FITC-500D、A488-纤维蛋白原和自体血液注入小鼠/大鼠的硬脑膜下腔,发现这些物质排入深部颈淋巴结(dCLNs)。在小鼠的脑膜和 dCLNs 中也观察到 FITC-500D 在淋巴管(LYVE+)中。通过血红蛋白定量和 MRI 扫描评估,接受深部颈淋巴管(dCLV)结扎手术的 SDH 大鼠的 SDH 清除率明显低于对照组。SDH 模型建立后,mLV 的引流速度明显减慢,脑膜中淋巴管生成相关蛋白(包括 LYVE1、FOXC2 和 VEGF-C)的表达下调。综上所述,我们的研究结果证明 SDH 通过 mLV 引流途径吸收,血肿可抑制 mLV 功能。