CoChat
Sign Up
Cited by 131Retinal Diseases and TreatmentsRetinal Imaging and AnalysisAlzheimer's disease research and treatments

The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.

Viewing Ageing Eyes: Diverse Sites of Amyloid Beta Accumulation in the Ageing Mouse Retina and the Up-Regulation of Macrophages

Open access
Hoh Kam, Jaimie, Lenassi, Eva, Jeffery, Glen·2010·PLoS ONE
DOI 10.1371/journal.pone.0013127PMC PMC2948519
Open this paper in CoChat — free accountOpen PDF

Abstract

BACKGROUND: Amyloid beta (Aβ) accumulates in the ageing central nervous system and is associated with a number of age-related diseases, including age-related macular degeneration (AMD) in the eye. AMD is characterised by accumulation of extracellular deposits called drusen in which Aβ is a key constituent. Aβ activates the complement cascade and its deposition is associated with activated macrophages. So far, little is known about the quantitative measurements of Aβ accumulation and definitions of its relative sites of ocular deposition in the normal ageing mouse. METHODOLOGY/PRINCIPAL FINDINGS: We have traced Aβ accumulation quantitatively in the ageing mouse retina using immunohistochemistry and Western blot analysis. We reveal that it is not only deposited at Bruch's membrane and along blood vessels, but unexpectedly, it also coats photoreceptor outer segments. While Aβ is present at all sites of deposition from 3 months of age, it increases markedly from 6 months onward. Progressive accumulation of deposits on outer segments was confirmed with scanning electron microscopy, revealing age-related changes in their morphology. Such progress of accumulation of Aβ on photoreceptor outer segments with age was also confirmed in human retinae using immunohistochemistry. We also chart the macrophage response to increases in Aβ showing up-regulation in their numbers using both confocal laser imaging of the eye in vivo followed by in vitro immunostaining. With age macrophages become bloated with cellular debris including Aβ, however, their increasing numbers fail to stop Aβ accumulation. CONCLUSIONS: Increasing Aβ deposition in blood vessels and Bruch's membrane will impact upon retinal perfusion and clearance of cellular waste products from the outer retina, a region of very high metabolic activity. This accumulation of Aβ may contribute to the 30% reduction of photoreceptors found throughout life and the shortening of those that remain. The coating of Aβ on outer segments may also have an impact upon visual function with age.

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 · 10.1371/journal.pone.0013127

Cites

65 of 65 references verified0 citation errors · 0 not checkable

Statistics

Figures

Figure 1 Retinal imaging and macrophage histology. A. Scanning laser ophthalmoscope images of the retinae of mice taken at 3, 6, 12 and 24 months of age. With time there is an accumulation of fluorescent point sources. B. The images are overlaid with the eyecups of a 12 months old mouse once they have been stained for Iba-1 to reveal macrophages and Aβ. This shows that many of the point sources are macrophages containing Aβ (indicated with arrows). These are arranged in a grid like pattern. C. A higher power image of Aβ containing macrophages of a 12 months old mouse. D. The number of macrophages present in the whole mounts at progressive ages. There are significant increases at 12 and 24 months (see text for statistics).
Figure 1 Retinal imaging and macrophage histology. A. Scanning laser ophthalmoscope images of the retinae of mice taken at 3, 6, 12 and 24 months of age. With time there is an accumulation of fluorescent point sources. B. The images are overlaid with the eyecups of a 12 months old mouse once they have been stained for Iba-1 to reveal macrophages and Aβ. This shows that many of the point sources are macrophages containing Aβ (indicated with arrows). These are arranged in a grid like pattern. C. A higher power image of Aβ containing macrophages of a 12 months old mouse. D. The number of macrophages present in the whole mounts at progressive ages. There are significant increases at 12 and 24 months (see text for statistics).CC BY · PubMed Central
Figure 2 Graphs showing the distance between macrophages and measurement of the dendritic processes. A. Graph showing the distance between macrophages in a cluster of seven cells for the 12 months and six cells for the 24 months old mouse. B. Graph showing the length of the dendritic processes of these seven cells of the 12 months and six cells of the 24 months old mouse (P<0.01). C. Graph showing the length of the dendritic processes of eight individual macrophage cells for the 12 months and four individual cells for the 24 months old mouse.
Figure 2 Graphs showing the distance between macrophages and measurement of the dendritic processes. A. Graph showing the distance between macrophages in a cluster of seven cells for the 12 months and six cells for the 24 months old mouse. B. Graph showing the length of the dendritic processes of these seven cells of the 12 months and six cells of the 24 months old mouse (P<0.01). C. Graph showing the length of the dendritic processes of eight individual macrophage cells for the 12 months and four individual cells for the 24 months old mouse.CC BY · PubMed Central
Figure 3 Aβ is deposited at the Bruch's membrane (BM)/RPE interface and among photoreceptor outer segments. A. The accumulation of amyloid beta in sections showing BM/RPE interface and the regions of the outer segments (OS) in mice of 3, 6 and 12 months age. Here Aβ label is red and the outer nuclear layer (ONL) is blue. This progressive accumulation was quantified with two independent methods at the two sites. First, the integrated density of label from immunostained sections was measured. The results of this are shown graphically in B and C. There are significant increases at both sites, particularly at 12 months (see text for levels of significance). Second, Western blots were run for Aβ at each site shown in D and E. F and G show the measurements at the same three time points as in B and C. The amount of Aβ increases significantly over time (see text for levels of significance). Differences between B and C and F and G are probably due to the different amounts of tissue sampled as F and G will also include measures derived from inner and outer retinal blood vessels.
Figure 3 Aβ is deposited at the Bruch's membrane (BM)/RPE interface and among photoreceptor outer segments. A. The accumulation of amyloid beta in sections showing BM/RPE interface and the regions of the outer segments (OS) in mice of 3, 6 and 12 months age. Here Aβ label is red and the outer nuclear layer (ONL) is blue. This progressive accumulation was quantified with two independent methods at the two sites. First, the integrated density of label from immunostained sections was measured. The results of this are shown graphically in B and C. There are significant increases at both sites, particularly at 12 months (see text for levels of significance). Second, Western blots were run for Aβ at each site shown in D and E. F and G show the measurements at the same three time points as in B and C. The amount of Aβ increases significantly over time (see text for levels of significance). Differences between B and C and F and G are probably due to the different amounts of tissue sampled as F and G will also include measures derived from inner and outer retinal blood vessels.CC BY · PubMed Central
Figure 4 Retinal blood vessels stained for Aβ. A. Inner retinal vessels stained for Aβ (red), Iba-1 (green) and neuronal cell bodies (blue) at 24 months. The amyloid deposits can be seen to be at focal points along the vessel rather than being continuous. B. Choroidal vessels also accumulated Aβ, however, the accumulation of this material appeared to be specific to a sub-group of vessels with other showing no sign of Aβ accumulation. This is taken from a 12 months old animal. C. Immunostaining of retinal section of a 12 months old animal using the colorimetric method (3,3-diaminobenzidine) to confirm the presence of Aβ in the outer segment of the photoreceptor and in the blood vessels. D. Negative control of the colorimetric staining showing the absence of staining.
Figure 4 Retinal blood vessels stained for Aβ. A. Inner retinal vessels stained for Aβ (red), Iba-1 (green) and neuronal cell bodies (blue) at 24 months. The amyloid deposits can be seen to be at focal points along the vessel rather than being continuous. B. Choroidal vessels also accumulated Aβ, however, the accumulation of this material appeared to be specific to a sub-group of vessels with other showing no sign of Aβ accumulation. This is taken from a 12 months old animal. C. Immunostaining of retinal section of a 12 months old animal using the colorimetric method (3,3-diaminobenzidine) to confirm the presence of Aβ in the outer segment of the photoreceptor and in the blood vessels. D. Negative control of the colorimetric staining showing the absence of staining.CC BY · PubMed Central
Figure 5 Aβ staining in human outer retina from individuals aged 31, 47, 80 and 90 years. This was undertaken on retinae separated from the RPE. Aβ is red and the outer nuclear layer (ONL) is blue. The outer segments (OS) are positive for Aβ but the intensity of the staining increases with age. In spite of this, the overall progression of Aβ accumulation here mirrors that found in mice.
Figure 5 Aβ staining in human outer retina from individuals aged 31, 47, 80 and 90 years. This was undertaken on retinae separated from the RPE. Aβ is red and the outer nuclear layer (ONL) is blue. The outer segments (OS) are positive for Aβ but the intensity of the staining increases with age. In spite of this, the overall progression of Aβ accumulation here mirrors that found in mice.CC BY · PubMed Central
Figure 6 Scanning electron micrographs of photoreceptor outer segments taken from animals at 3, 6, 12 and 24 months of age. In each case the right hand panel is a higher magnification of that on the left and the orientation is such that the RPE would be to the top and the outer nuclear layer to the bottom. Even at 3 months of age deposits can be found on outer segments, however they are more common towards the tip of the outer segment than the base. They are largely spherical in morphology or have rounded edges. By 6 months, their coating has increased and the deposits are present along the length of the outer segment. At 12 months the deposits have thickened, but also appear to have changed qualitatively (See Figure 7). At 24 months while thick deposits remain the tips of many outer segments have enlarged and those that remain are shorter making direct comparison with earlier stages difficult.
Figure 6 Scanning electron micrographs of photoreceptor outer segments taken from animals at 3, 6, 12 and 24 months of age. In each case the right hand panel is a higher magnification of that on the left and the orientation is such that the RPE would be to the top and the outer nuclear layer to the bottom. Even at 3 months of age deposits can be found on outer segments, however they are more common towards the tip of the outer segment than the base. They are largely spherical in morphology or have rounded edges. By 6 months, their coating has increased and the deposits are present along the length of the outer segment. At 12 months the deposits have thickened, but also appear to have changed qualitatively (See Figure 7). At 24 months while thick deposits remain the tips of many outer segments have enlarged and those that remain are shorter making direct comparison with earlier stages difficult.CC BY · PubMed Central
Figure 7 There appeared to be a qualitative change in the morphology of deposits found on outer segments at 12 months of age. The two panels show higher magnification scanning electron micrographs of debris on outer segments at 3 and 12 months. At the earlier stage the deposits are largely spherical with thin processes connecting them to the wall of the outer segment. At 12 months very different picture is present. Here the deposits appear as ruptured hemispheres that have partially collapsed leaving rough edges.
Figure 7 There appeared to be a qualitative change in the morphology of deposits found on outer segments at 12 months of age. The two panels show higher magnification scanning electron micrographs of debris on outer segments at 3 and 12 months. At the earlier stage the deposits are largely spherical with thin processes connecting them to the wall of the outer segment. At 12 months very different picture is present. Here the deposits appear as ruptured hemispheres that have partially collapsed leaving rough edges.CC 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

1 retracted

Show all 65 references

Research works printed but not linked: 1

  1. [58]Graymore CN 1969 General aspects of the metabolism of the retina. Davson H In the Eye. 2nd ed New York Academic Press 601 645

Cited by

Sorted by citations

Related

See all

Metadata

Authors
Hoh Kam, J., Lenassi, E., & Jeffery, G.
Affiliations
  • Ljubljana University Medical Centre (SI)
  • University College London (GB)
Corresponding author
Jeffery, Glen
ORCID
Jeffery, Glen
Venue
PLoS ONE
Publisher
Public Library of Science (PLoS)
Published
2010-10-01
Volume
5
Issue
10
Pages
e13127
ISSN
1932-6203 (ISSN-L)
DOI
10.1371/journal.pone.0013127
PMC
PMC2948519
OpenAlex
W1982572468
Cited by
131
References
65
Citations by year
2026: 6 · 2025: 6 · 2024: 5 · 2023: 7 · 2022: 6 · 2021: 8 · 2020: 12 · 2019: 9 · 2018: 7 · 2017: 7 · 2016: 14 · 2015: 10 · 2014: 8 · 2013: 11 · 2012: 12
FWCI
9.07
Type
journal article
Language
en
Open access
Licence
Locations
  • PLoS ONE (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • UCL Discovery (University College London) (submittedVersion)
Funders
Rosetrees Trust
Topics
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Retinal Imaging and Analysis
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
Keywords
amyloid-beta, retinal aging, age-related macular degeneration, drusen, photoreceptor outer segments, Bruch's membrane, retinal macrophages, complement activation, mouse retina, photoreceptor degeneration, retinal blood flow
MeSH terms
Aging, Animals, Humans, Immunohistochemistry, Macrophage Activation, Macrophages, Macular Degeneration, Retina, Blotting, Western, Up-Regulation, Amyloid beta-Peptides, 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