Blockade of VEGFR3 signaling leads to functional impairment of dural lymphatic vessels without affecting autoimmune neuroinflammation

• Published in: Science immunology 2023-04, Vol.8 (82), p.eabq0375
• Main Authors: Li, Zhilin, Antila, Salli, Nurmi, Harri, Chilov, Dmitri, Korhonen, Emilia A, Fang, Shentong, Karaman, Sinem, Engelhardt, Britta, Alitalo, Kari
• Format: Article
• Language: English
• Subjects: Animals; Endothelial Cells - metabolism; Lymphangiogenesis; Lymphatic Vessels; Mice; Neuroinflammatory Diseases; Signal Transduction; Vascular Endothelial Growth Factor C - metabolism; Vascular Endothelial Growth Factor C - pharmacology; Vascular Endothelial Growth Factor Receptor-3 - metabolism
• ISSN: 2470-9468; 2470-9468
• DOI: 10.1126/sciimmunol.abq0375

The recent discovery of lymphatic vessels (LVs) in the dura mater, the outermost layer of meninges around the central nervous system (CNS), has opened a possibility for the development of alternative therapeutics for CNS disorders. The vascular endothelial growth factor C (VEGF-C)/VEGF receptor 3 (VEGFR3) signaling pathway is essential for the development and maintenance of dural LVs. However, its significance in mediating dural lymphatic function in CNS autoimmunity is unclear. We show that inhibition of the VEGF-C/VEGFR3 signaling pathway using a monoclonal VEGFR3-blocking antibody, a soluble VEGF-C/D trap, or deletion of the gene in adult lymphatic endothelium causes notable regression and functional impairment of dural LVs but has no effect on the development of CNS autoimmunity in mice. During autoimmune neuroinflammation, the dura mater was only minimally affected, and neuroinflammation-induced helper T (T ) cell recruitment, activation, and polarization were significantly less pronounced in the dura mater than in the CNS. In support of this notion, during autoimmune neuroinflammation, blood vascular endothelial cells in the cranial and spinal dura expressed lower levels of cell adhesion molecules and chemokines, and antigen-presenting cells (i.e., macrophages and dendritic cells) had lower expression of chemokines, MHC class II-associated molecules, and costimulatory molecules than their counterparts in the brain and spinal cord, respectively. The significantly weaker T cell responses in the dura mater may explain why dural LVs do not contribute directly to CNS autoimmunity.