Structural and functional conservation of non-lumenized lymphatic endothelial cells in the mammalian leptomeninges

轻浮 脑膜 淋巴系统 软脑膜 病理 生物 硬脑膜 淋巴管内皮 电池类型 脑脊液 细胞生物学 解剖 中枢神经系统 神经科学 细胞 医学 遗传学
作者
Shannon Shibata-Germanos,James R. Goodman,Alan Grieg,Chintan A. Trivedi,Bridget C. Benson,Sandrine C. Foti,Ana Faro,Raphael F.P. Castellan,Rosa Maria Correra,Melissa Barber,Christiana Ruhrberg,Roy O. Weller,Tammaryn Lashley,Jeffrey J. Iliff,Thomas A. Hawkins,Jason Rihel
出处
期刊:Acta Neuropathologica [Springer Science+Business Media]
卷期号:139 (2): 383-401 被引量:24
标识
DOI:10.1007/s00401-019-02091-z
摘要

The vertebrate CNS is surrounded by the meninges, a protective barrier comprised of the outer dura mater and the inner leptomeninges, which includes the arachnoid and pial layers. While the dura mater contains lymphatic vessels, no conventional lymphatics have been found within the brain or leptomeninges. However, non-lumenized cells called Brain/Mural Lymphatic Endothelial Cells or Fluorescent Granule Perithelial cells (muLECs/BLECs/FGPs) that share a developmental program and gene expression with peripheral lymphatic vessels have been described in the meninges of zebrafish. Here we identify a structurally and functionally similar cell type in the mammalian leptomeninges that we name Leptomeningeal Lymphatic Endothelial Cells (LLEC). As in zebrafish, LLECs express multiple lymphatic markers, containing very large, spherical inclusions, and develop independently from the meningeal macrophage lineage. Mouse LLECs also internalize macromolecules from the cerebrospinal fluid, including Amyloid-β, the toxic driver of Alzheimer's disease progression. Finally, we identify morphologically similar cells co-expressing LLEC markers in human post-mortem leptomeninges. Given that LLECs share molecular, morphological, and functional characteristics with both lymphatics and macrophages, we propose they represent a novel, evolutionary conserved cell type with potential roles in homeostasis and immune organization of the meninges.
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