淋巴系统
神经炎症
淋巴管新生
淋巴管
病理
小胶质细胞
淋巴管内皮
薄壁组织
CCL21型
生物
中枢神经系统
神经科学
趋化因子
医学
炎症
免疫学
趋化因子受体
转移
内科学
癌症
作者
Qian Li,Yan Chen,Weixi Feng,Jiachen Cai,Junying Gao,Feifei Ge,Tiantian Zhou,Ze Wang,Fengfei Ding,Ting Wu,Chengyu Sheng,Yongjie Zhang,Mingkuan Sun,Jingping Shi,Ming Xiao
标识
DOI:10.1016/j.bbi.2022.04.005
摘要
Recent progress on the central lymphatic system has greatly increased our understanding of how the brain maintains its own waste homeostasis. Here, we showed that perivascular spaces and meningeal lymphatic vessels form a functional route for clearance of senescent astrocytes from the aging brain. Blocking meningeal lymphatic drainage by ligation of the deep cervical lymph nodes impaired clearance of senescent astrocytes from brain parenchyma, subsequently increasing neuroinflammation in aged mice. By contrast, enhancing meningeal lymphatic vessel diameter by a recombinant adeno-associated virus encoding mouse vascular endothelial growth factor-C (VEGF-C) improved clearance of senescent astrocytes and mitigated neuroinflammation. Mechanistically, VEGF-C was highly expressed in senescent astrocytes, contributing themselves to migrate across lymphatic vessels along C–C motif chemokine ligand 21 (CCL21) gradient by interacting with VEGF receptor 3. Moreover, intra-cisternal injection of antibody against CCL21 hampered senescent astrocytes into the lymphatic vessels and exacerbated short memory defects of aged mice. Together, these findings reveal a new perspective for the meningeal lymphatics in the removal of senescent astrocytes, thus offering a valuable target for therapeutic intervention.
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