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Brain-wide pathway for waste clearance captured by contrast-enhanced MRI
Jeffrey J. Iliff, Hedok Lee, Mei Yu, Tian Feng, Jean Logan, Maiken Nedergaard, Helene Benveniste
Jeffrey J. Iliff, Hedok Lee, Mei Yu, Tian Feng, Jean Logan, Maiken Nedergaard, Helene Benveniste
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Technical Advance

Brain-wide pathway for waste clearance captured by contrast-enhanced MRI

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Abstract

The glymphatic system is a recently defined brain-wide paravascular pathway for cerebrospinal fluid (CSF) and interstitial fluid (ISF) exchange that facilitates efficient clearance of solutes and waste from the brain. CSF enters the brain along para-arterial channels to exchange with ISF, which is in turn cleared from the brain along para-venous pathways. Because soluble amyloid β clearance depends on glymphatic pathway function, we proposed that failure of this clearance system contributes to amyloid plaque deposition and Alzheimer’s disease progression. Here we provide proof of concept that glymphatic pathway function can be measured using a clinically relevant imaging technique. Dynamic contrast-enhanced MRI was used to visualize CSF-ISF exchange across the rat brain following intrathecal paramagnetic contrast agent administration. Key features of glymphatic pathway function were confirmed, including visualization of para-arterial CSF influx and molecular size-dependent CSF-ISF exchange. Whole-brain imaging allowed the identification of two key influx nodes at the pituitary and pineal gland recesses, while dynamic MRI permitted the definition of simple kinetic parameters to characterize glymphatic CSF-ISF exchange and solute clearance from the brain. We propose that this MRI approach may provide the basis for a wholly new strategy to evaluate Alzheimer’s disease susceptibility and progression in the live human brain.

Authors

Jeffrey J. Iliff, Hedok Lee, Mei Yu, Tian Feng, Jean Logan, Maiken Nedergaard, Helene Benveniste

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Figure 4

Fluorescence-based imaging of paravascular CSF-ISF exchange.

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Fluorescence-based imaging of paravascular CSF-ISF exchange.
Small (TR-d...
Small (TR-d3; MW 3 kDa) and large (FITC-d500; MW 500 kDa) molecular weight fluorescent tracers were injected intrathecally and imaged ex vivo by conventional and laser scanning confocal fluorescence microscopy. (A, B, F, and H) Whole-slice montages were generated, showing paravascular (arrowheads) CSF tracer influx into the brain at (A and B) 30 minutes, (F) 60 minutes, and (H) 180 minutes after injection. (B) Coronal slice counter labeled with vascular endothelial marker isolectin B4 (IB4) 30 minutes after injection. (C and D) High-power confocal imaging shows that CSF tracer enters the brain along penetrating arteries (arrowheads) (E) but not along draining veins. Large molecular weight FITC-d500 remains confined to the paravascular spaces, while small molecular weight TR-d3 moves readily into and through the surrounding interstitium. (F) 60 minutes after injection, small molecular weight TR-d3 is localized diffusely throughout the brain interstitium, (G) while large molecular weight FITC-d500 is apparent along terminal capillary bed. The inset depicts z-projection of image stack, demonstrating the extent of capillary labeling with FITC-d500. (H) At 180 minutes after injection, parenchymal tracer levels are reduced compared with 30 and 60 minutes after injection, (I) while intrathecal tracer persists along para-venous clearance pathways. Original magnification (scale bar measurements are shown parenthetically): ×40 (A, B, F, and H); ×200 (100 μm) (C); ×400 (50 μm) (D, E, G, and I and insets in D, E, and G); ×40 (inset, I).

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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