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RESEARCH PAPER / 2026-07-22

CSF clearance through arachnoid fenestrations to olfactory meningeal lymphatics.

Seon Pyo Hong, Cheolhwa Jin, Myung Jin Yang, Hokyung Jin, Jin-Hui Yoon, Du Ri Choi, Junho Jung, Chae Min Yuk, Salli Antila, Su Jin Seo, Leul A Admasu, Jincheol Seo, Kyung Seob Lim, Won-Suk Chung, Kari Alitalo, Donald M McDonald, Gou Young Koh

Center for Vascular Research, Institute for Basic Science, Daejeon 34141, Republic of Korea. Electronic address: [email protected]. · pubmed

Abstract

Meningeal (dural) lymphatics are essential for cerebrospinal fluid (CSF) clearance to cervical lymph nodes, yet the precise pathway is incompletely understood. Using a multifaceted approach in mice, we examined tracer dynamics and the CSF outflow pathway from the subarachnoid space (SAS) to the nasal mucosa and identified a discrete arachnoid region surrounding the olfactory bulbs with abundant fenestrations. Similar arachnoid fenestrations were found in cynomolgus monkeys. Fluorescent tracers in the SAS passed through arachnoid fenestrations into dural lymphatics, which traversed the cribriform plate foramina, joined the nasal lymphatics, and drained to the cervical lymph nodes. In aged mice, the known reduction in CSF outflow was accompanied by lymphatic atrophy in the olfactory dura and nasal mucosa and by fewer arachnoid fenestrations and smaller cribriform plate foramina. Importantly, the lymphatics and CSF clearance were restored to normal by intranasal delivery of vascular endothelial growth factor-C (VEGF-C), thereby documenting the reversibility of the aging-related impairment in CSF clearance.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The study identifies arachnoid fenestrations as a critical pathway for CSF clearance and demonstrates that aging-related impairment in this pathway can be reversed by intranasal VEGF-C delivery. This is relevant to longevity research as it addresses the glymphatic system's role in clearing neurotoxic waste, a root cause of neurodegeneration, and offers a potential therapeutic intervention to restore youthful clearance mechanisms.

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