Characterization of dural sinus-associated lymphatic vasculature in human Alzheimer’s dementia subjects

•Dural sinus-associated lymphatic vessels were observed in 19/21 human post mortem samples.•No differences in vessel number or diameter were observed between control and Alzheimer’s subjects.•Amyloid β deposition was not observed along lymphatic vessels in control or Alzheimer’s disease subjects. Re...

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Published inBrain, behavior, and immunity Vol. 73; pp. 34 - 40
Main Authors Goodman, James R., Adham, Zachariah O., Woltjer, Randall L., Lund, Amanda W., Iliff, Jeffrey J.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Inc 01.10.2018
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Summary:•Dural sinus-associated lymphatic vessels were observed in 19/21 human post mortem samples.•No differences in vessel number or diameter were observed between control and Alzheimer’s subjects.•Amyloid β deposition was not observed along lymphatic vessels in control or Alzheimer’s disease subjects. Recent reports describing lymphatic vasculature in the meninges have challenged the traditional understanding of interstitial solute clearance from the central nervous system, although the significance of this finding in human neurological disease remains unclear. To begin to define the role of meningeal lymphatic function in the clearance of interstitial amyloid beta (Aβ), and the contribution that its failure may make to the development of Alzheimer’s disease (AD), we examined meningeal tissue from a case series including AD and control subjects by confocal microscopy. Our findings confirm the presence of lymphatic vasculature in the human meninges and indicate that, unlike perivascular efflux pathways in the brain parenchyma in subjects with AD, Aβ is not deposited in or around meningeal lymphatic vessels associated with dural sinuses. Our findings demonstrate that while the meningeal lymphatic vasculature may serve as an efflux route for Aβ from the brain and cerebrospinal fluid, Aβ does not deposit in the walls of meningeal lymphatic vessels in the setting of AD.
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JRG, ZOA, AWL, and JJI wrote the manuscript. JRG and ZOA performed immunofluorescence, acquisition, and post-image processing. Data analysis was performed by JRG, ZOA, AWL, RLW, and JJI. Study design was planned by JRG, RLW, and JJI.
Author Contributions
ISSN:0889-1591
1090-2139
1090-2139
DOI:10.1016/j.bbi.2018.07.020