CoChat
Sign Up
Cited by 311Cerebrospinal fluid and hydrocephalusBarrier Structure and Function StudiesIon Transport and Channel Regulation

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

Convective influx/glymphatic system: tracers injected into the CSF enter and leave the brain along separate periarterial basement membrane pathways

Open access
Albargothy, Nazira J., Johnston, David A., MacGregor-Sharp, Matthew, Weller, Roy O., Verma, Ajay, Hawkes, Cheryl A., Carare, Roxana O.·2018·Acta Neuropathologica
DOI 10.1007/s00401-018-1862-7PMC PMC6015107
Open this paper in CoChat — free accountOpen PDF

Abstract

Tracers injected into CSF pass into the brain alongside arteries and out again. This has been recently termed the "glymphatic system" that proposes tracers enter the brain along periarterial "spaces" and leave the brain along the walls of veins. The object of the present study is to test the hypothesis that: (1) tracers from the CSF enter the cerebral cortex along pial-glial basement membranes as there are no perivascular "spaces" around cortical arteries, (2) tracers leave the brain along smooth muscle cell basement membranes that form the Intramural Peri-Arterial Drainage (IPAD) pathways for the elimination of interstitial fluid and solutes from the brain. 2 μL of 100 μM soluble, fluorescent fixable amyloid β (Aβ) were injected into the CSF of the cisterna magna of 6-10 and 24-30 month-old male mice and their brains were examined 5 and 30 min later. At 5 min, immunocytochemistry and confocal microscopy revealed Aβ on the outer aspects of cortical arteries colocalized with α-2 laminin in the pial-glial basement membranes. At 30 min, Aβ was colocalised with collagen IV in smooth muscle cell basement membranes in the walls of cortical arteries corresponding to the IPAD pathways. No evidence for drainage along the walls of veins was found. Measurements of the depth of penetration of tracer were taken from 11 regions of the brain. Maximum depths of penetration of tracer into the brain were achieved in the pons and caudoputamen. Conclusions drawn from the present study are that tracers injected into the CSF enter and leave the brain along separate periarterial basement membrane pathways. The exit route is along IPAD pathways in which Aβ accumulates in cerebral amyloid angiopathy (CAA) in Alzheimer's disease. Results from this study suggest that CSF may be a suitable route for delivery of therapies for neurological diseases, including CAA.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1007/s00401-018-1862-7

Cites

40 of 40 references verified0 citation errors · 0 not checkable

Statistics

Figures

Fig. 1 Anatomical entry route of Aβ into the young adult brain from the CSF at 5 and 30 min post-injection. Young 6–10-week-old mice: Entry of amyloid-β (Aβ) tracer into the brain from the CSF at 5 min (a–c). Drainage of Aβ tracer from the brain along the walls of arteries at 30 min (d–l). a 5 min: the surface of the cerebral cortex (blue line) and a cortical artery passing into the brain with Aβ tracer red in its walls. Aβ tracer colocalized with α2-laminin in the pial-glial basement membrane (yellow) indicated by the white arrow. b 5 min: a single optical section of the artery enclosed in the box in a showing α2-laminin in the astrocyte basement membrane of the glia limitans on the surface of the brain (green) and co-localisation of Aβ and α2-laminin in the pial-glial basement membrane on the outer aspect of the wall of the artery (yellow) (white arrow); c 5 min: the profile of a cortical artery with smooth muscle cells (green) in its wall shows Aβ tracer (red) colocalized (pink) with collagen IV (blue) in the pial basement membrane on the outer surface of the artery (white arrows). At 30 min after injection as shown in figures (d–l), the distribution of the Aβ in the artery walls is very different from that seen at 5 min in figures (a–c). d An artery identified by green smooth muscle actin in its wall (f, j) shows Aβ tracer (red, e, k) colocalized (pink) with collagen IV (blue, g, l) within the wall of the artery in a spiral or ladder-type distribution (arrows in d), closely resembling the pattern of deposition of Aβ in the walls of arteries as cerebral amyloid angiopathy (CAA); h a single optical section from the artery in d) showing the Aβ tracer (red) between the smooth muscle actin staining (green)
Fig. 1 Anatomical entry route of Aβ into the young adult brain from the CSF at 5 and 30 min post-injection. Young 6–10-week-old mice: Entry of amyloid-β (Aβ) tracer into the brain from the CSF at 5 min (a–c). Drainage of Aβ tracer from the brain along the walls of arteries at 30 min (d–l). a 5 min: the surface of the cerebral cortex (blue line) and a cortical artery passing into the brain with Aβ tracer red in its walls. Aβ tracer colocalized with α2-laminin in the pial-glial basement membrane (yellow) indicated by the white arrow. b 5 min: a single optical section of the artery enclosed in the box in a showing α2-laminin in the astrocyte basement membrane of the glia limitans on the surface of the brain (green) and co-localisation of Aβ and α2-laminin in the pial-glial basement membrane on the outer aspect of the wall of the artery (yellow) (white arrow); c 5 min: the profile of a cortical artery with smooth muscle cells (green) in its wall shows Aβ tracer (red) colocalized (pink) with collagen IV (blue) in the pial basement membrane on the outer surface of the artery (white arrows). At 30 min after injection as shown in figures (d–l), the distribution of the Aβ in the artery walls is very different from that seen at 5 min in figures (a–c). d An artery identified by green smooth muscle actin in its wall (f, j) shows Aβ tracer (red, e, k) colocalized (pink) with collagen IV (blue, g, l) within the wall of the artery in a spiral or ladder-type distribution (arrows in d), closely resembling the pattern of deposition of Aβ in the walls of arteries as cerebral amyloid angiopathy (CAA); h a single optical section from the artery in d) showing the Aβ tracer (red) between the smooth muscle actin staining (green)CC BY · PubMed Central
Fig. 2 Anatomical entry route of Aβ into old 24–30-month-old mouse brain from the CSF at 5 min post injection: a–c arteries showing Aβ (red) along the walls of arterioles of 10–20 µm diameter labelled with collagen IV (blue) and smooth muscle actin (green); d an artery entering the cerebral cortex (arrow) showing Aβ (red) extending into the brain; e enlargement of the artery in (d) showing laminin α-2 staining in the glia limitans on the surface of the brain (green) and co-localisation of the amyloid with laminin α-2 in the vessel wall (yellow) as indicated by the arrow; f single optical section of artery in e; g single channel image of laminin α-2 from d; h single channel image of collagen IV from d; i single channel image of Aβ from d
Fig. 2 Anatomical entry route of Aβ into old 24–30-month-old mouse brain from the CSF at 5 min post injection: a–c arteries showing Aβ (red) along the walls of arterioles of 10–20 µm diameter labelled with collagen IV (blue) and smooth muscle actin (green); d an artery entering the cerebral cortex (arrow) showing Aβ (red) extending into the brain; e enlargement of the artery in (d) showing laminin α-2 staining in the glia limitans on the surface of the brain (green) and co-localisation of the amyloid with laminin α-2 in the vessel wall (yellow) as indicated by the arrow; f single optical section of artery in e; g single channel image of laminin α-2 from d; h single channel image of collagen IV from d; i single channel image of Aβ from dCC BY · PubMed Central
Fig. 3 Anatomical route for drainage of Aβ out of the brain following entry from the CSF at 30 min post injection in old 24–30-month-old mice: a An artery and vein at the surface of the brain. The artery is identified by smooth muscle cells in its wall (green). Aβ tracer (red) is present in a ladder-like pattern in the wall of the artery. Aβ (red) in the wall of a vein is only seen at the surface suggesting that the Aβ here has entered from the CSF and not drained from the brain. Only occasional veins had Aβ in their walls. b Enlargement of the artery in a showing the ladder-like distribution of Aβ that resembles the distribution of amyloid in CAA [29]. At the surface of the brain is a branch of a leptomeningeal artery showing the ladder-like distribution of smooth muscle cells in the tunica media. The Aβ is in the intramural periarterial drainage (IPAD) pathway; c macrophages take up Aβ tracer at 30 min after injection. The arrows indicate Aβ (red) within macrophages stained for the macrophage marker CD163 (green); d astrocytes are stained for GFAP (green). Co-localisation (yellow) of Aβ and GFAP indicates uptake of Aβ tracer by perivascular astrocytes
Fig. 3 Anatomical route for drainage of Aβ out of the brain following entry from the CSF at 30 min post injection in old 24–30-month-old mice: a An artery and vein at the surface of the brain. The artery is identified by smooth muscle cells in its wall (green). Aβ tracer (red) is present in a ladder-like pattern in the wall of the artery. Aβ (red) in the wall of a vein is only seen at the surface suggesting that the Aβ here has entered from the CSF and not drained from the brain. Only occasional veins had Aβ in their walls. b Enlargement of the artery in a showing the ladder-like distribution of Aβ that resembles the distribution of amyloid in CAA [29]. At the surface of the brain is a branch of a leptomeningeal artery showing the ladder-like distribution of smooth muscle cells in the tunica media. The Aβ is in the intramural periarterial drainage (IPAD) pathway; c macrophages take up Aβ tracer at 30 min after injection. The arrows indicate Aβ (red) within macrophages stained for the macrophage marker CD163 (green); d astrocytes are stained for GFAP (green). Co-localisation (yellow) of Aβ and GFAP indicates uptake of Aβ tracer by perivascular astrocytesCC BY · PubMed Central
Fig. 4 Periarterial penetration of Aβ is of greater distance after 30 min than after 5 min in cortical, subcortical and posterior brain regions of young mice. Bar charts of periarterial Aβ distance against time after injection into cisternal CSF (5 and 30 min) in the olfactory bulbs (a), somatomotor area (b), somatosensory area and caudoputamen (c), thalamus and hypothalamus (d), superior colliculus, pontine reticular nucleus, entorhinal and visual areas (e) and cerebellar molecular layer (f). Values are presented as mean ± SEM of untransformed data, with p values indicated for log10-transformed data (one-way ANOVA with Sidak’s post hoc)
Fig. 4 Periarterial penetration of Aβ is of greater distance after 30 min than after 5 min in cortical, subcortical and posterior brain regions of young mice. Bar charts of periarterial Aβ distance against time after injection into cisternal CSF (5 and 30 min) in the olfactory bulbs (a), somatomotor area (b), somatosensory area and caudoputamen (c), thalamus and hypothalamus (d), superior colliculus, pontine reticular nucleus, entorhinal and visual areas (e) and cerebellar molecular layer (f). Values are presented as mean ± SEM of untransformed data, with p values indicated for log10-transformed data (one-way ANOVA with Sidak’s post hoc)CC BY · PubMed Central
Fig. 5 Regional differences in periarterial distance of penetration of Aβ at 5- and 30-min post-injection in old mice. a Schematic showing a sagittal mouse brain section with five brain levels (I–V) from which distance measurements were taken in six brain regions at 5 min after injection of Aβ into cisterna magna. (Allen Institute for Brain Science. Allen Mouse Brain Atlas. Available from: http://mouse.brain-map.org/static/atlas.) b Bar charts of periarterial Aβ distance against time after injection into cisternal CSF (5 and 30 min) in the olfactory bulbs (teal), somatomotor area (green), caudoputamen (blue), thalamus (salmon), superior colliculus (pink) and pontine reticular nucleus (orange). Values are presented as mean ± SEM of untransformed data, with p values indicated for log10-transformed data (one-way ANOVA with Sidak’s post hoc)
Fig. 5 Regional differences in periarterial distance of penetration of Aβ at 5- and 30-min post-injection in old mice. a Schematic showing a sagittal mouse brain section with five brain levels (I–V) from which distance measurements were taken in six brain regions at 5 min after injection of Aβ into cisterna magna. (Allen Institute for Brain Science. Allen Mouse Brain Atlas. Available from: http://mouse.brain-map.org/static/atlas.) b Bar charts of periarterial Aβ distance against time after injection into cisternal CSF (5 and 30 min) in the olfactory bulbs (teal), somatomotor area (green), caudoputamen (blue), thalamus (salmon), superior colliculus (pink) and pontine reticular nucleus (orange). Values are presented as mean ± SEM of untransformed data, with p values indicated for log10-transformed data (one-way ANOVA with Sidak’s post hoc)CC BY · PubMed Central
Fig. 6 Pathways for influx of CSF into the brain and drainage of CSF/ISF out of the brain along capillary and periarterial basement membranes. (1) Entry of tracers from the CSF into the brain along pial-glial basement membranes on the outer aspects of artery walls. The sites of entry of tracer into the brain extracellular compartment are unclear and could be multiple. (2) CSF enters the brain parenchyma and (3) mixes with interstitial fluid (ISF). (4) The mixture of CSF/ISF diffuses through the narrow extracellular spaces of the brain to enter (5) basement membranes in the walls of capillaries to drain out of the brain along (6) basement membranes of smooth muscle cells in the tunica media in the walls of arterioles and arteries (IPAD pathway). Key to the microanatomy of the capillary and artery walls: BM1 endothelial basement membrane. BM2 smooth muscle cell basement membrane identified in this study by the presence of collagen IV. BM3 basement membrane between pia mater (pink) and smooth muscle cell. BM4 pia-glial basement membrane between the pia mater and the astrocytes of the glia limitans. In this study, BM4 is identified by the presence of α2-laminin [9, 13]. Proposed route of IPAD tracer is located in the capillary endothelial basement membrane (5) apparently entering from the brain parenchyma. In the artery wall, tracer is observed in the basement membranes between smooth muscle cells (light purple) but not in the basement membranes on the outer aspect of the artery wall or in the endothelial basement membrane of the artery wall (both dull blue) [4, 27]. The light green arrow indicates the proposed intramural peri-arterial drainage (IPAD) pathway for fluid and solutes out of the brain
Fig. 6 Pathways for influx of CSF into the brain and drainage of CSF/ISF out of the brain along capillary and periarterial basement membranes. (1) Entry of tracers from the CSF into the brain along pial-glial basement membranes on the outer aspects of artery walls. The sites of entry of tracer into the brain extracellular compartment are unclear and could be multiple. (2) CSF enters the brain parenchyma and (3) mixes with interstitial fluid (ISF). (4) The mixture of CSF/ISF diffuses through the narrow extracellular spaces of the brain to enter (5) basement membranes in the walls of capillaries to drain out of the brain along (6) basement membranes of smooth muscle cells in the tunica media in the walls of arterioles and arteries (IPAD pathway). Key to the microanatomy of the capillary and artery walls: BM1 endothelial basement membrane. BM2 smooth muscle cell basement membrane identified in this study by the presence of collagen IV. BM3 basement membrane between pia mater (pink) and smooth muscle cell. BM4 pia-glial basement membrane between the pia mater and the astrocytes of the glia limitans. In this study, BM4 is identified by the presence of α2-laminin [9, 13]. Proposed route of IPAD tracer is located in the capillary endothelial basement membrane (5) apparently entering from the brain parenchyma. In the artery wall, tracer is observed in the basement membranes between smooth muscle cells (light purple) but not in the basement membranes on the outer aspect of the artery wall or in the endothelial basement membrane of the artery wall (both dull blue) [4, 27]. The light green arrow indicates the proposed intramural peri-arterial drainage (IPAD) pathway for fluid and solutes out of the brainCC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 40 references

Cited by

Sorted by citations

Items 201–300 of 310

Related

See all

Metadata

Authors
Albargothy, N. J., Johnston, D. A., MacGregor-Sharp, M., Weller, R. O., Verma, A., Hawkes, C. A., & Carare, R. O.
Affiliations
  • University of Southampton (GB)
  • Biogen (United States) (US)
  • The Open University (GB)
Corresponding author
Carare, Roxana O.
ORCID
Venue
Acta Neuropathologica
Publisher
Springer Science and Business Media LLC
Published
2018-05-12
Volume
136
Issue
1
Pages
139-152
ISSN
  • 0001-6322 (ISSN-L)
  • 1432-0533
DOI
10.1007/s00401-018-1862-7
PMC
PMC6015107
OpenAlex
W2801110912
Cited by
311
References
40
Citations by year
2026: 23 · 2025: 40 · 2024: 35 · 2023: 36 · 2022: 46 · 2021: 41 · 2020: 47 · 2019: 32 · 2018: 10
FWCI
14.81
Type
journal article
Language
en
Open access
Licence
Locations
  • Acta Neuropathologica (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Open Research Online - ORO (The Open University) (acceptedVersion)
  • ePrints Soton (University of Southampton) (submittedVersion)
  • Lancaster EPrints (Lancaster University) (submittedVersion)
Funders
Biogen (FE-13227)
Topics
  • Health Sciences › Medicine › Clinical Neurology › Cerebrospinal fluid and hydrocephalus
  • Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
Keywords
glymphatic system, cerebrospinal fluid, amyloid-beta, cortical arteries, laminin alpha 2, type IV collagen, cerebral amyloid angiopathy, Alzheimer's disease, interstitial fluid drainage
MeSH terms
Parenchymal Tissue, Glymphatic System, CD163 Antigen, Actins, Age Factors, Animals, Basement Membrane, Blood Vessels, Brain, Cerebrospinal Fluid, Glial Fibrillary Acidic Protein, Male, Mice, Inbred C57BL, Receptors, Cell Surface, Time Factors, Antigens, Differentiation, Myelomonocytic, Antigens, CD, Amyloid beta-Peptides, Fluorescein-5-isothiocyanate, Collagen Type IV, Extracellular Fluid, Mice

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review