# Expansive spatial pattern of Aβ deposition in patients with cerebral amyloid angiopathy: A three-dimensional surface-to-depth analysis

**Authors:** Hideki Hayashi, Rie Saito, Akinori Miyashita, Takeshi Ikeuchi, Mari Tada, Kohei Akazawa, Osamu Onodera, Kazuki Tainaka, Akiyoshi Kakita

PMC · DOI: 10.1126/sciadv.aea7539 · Science Advances · 2026-02-06

## TL;DR

This study uses 3D imaging to show how amyloid-beta builds up in brain blood vessels, starting from the surface and moving deeper.

## Contribution

The study introduces a 3D imaging method to visualize Aβ progression in CAA, revealing a surface-to-depth pattern.

## Key findings

- Aβ deposition and SMA loss were prominent in leptomeningeal and superficial cortical segments.
- Aβ-positive segments were anatomically connected, showing a surface-to-depth progression pattern.
- Perivascular plaque density was lower around Aβ-positive vessels.

## Abstract

Cerebral amyloid angiopathy (CAA) is a neurodegenerative condition characterized by amyloid-β (Aβ) deposition in small vessel walls, often coexisting with Alzheimer’s disease due to impaired Aβ clearance. However, the spatial distribution of Aβ within the human brain remains unclear as the vascular network’s complexity and scale hinder visualization by conventional thin-slice analysis. To address this, we performed three-dimensional (3D) volumetric imaging of the cerebrovascular network and Aβ deposition in autopsied brains with CAA using advanced tissue clearing and light-sheet fluorescence microscopy, labeling for smooth muscle actin (SMA) and Aβ. We found prominent Aβ deposition and SMA loss in leptomeningeal and superficial cortical segments, which were anatomically contiguous with deeper Aβ-positive segments, indicating a surface-to-deep progression pattern of Aβ extension. The perivascular plaque density was significantly lower around Aβ-positive vessels. This technology may provide further insights into CAA pathology and is recommended for research on the 3D pathology of neurological disorders.

3D imaging of CAA autopsy brains showed that vascular Aβ deposition can progress from the brain surface to peripheral vessels.

## Linked entities

- **Proteins:** ab (abrupt)
- **Diseases:** Cerebral amyloid angiopathy (MONDO:0005620), Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, DDX41 (DEAD-box helicase 41) [NCBI Gene 51428] {aka ABS, MPLPF}, SEPHS1 (selenophosphate synthetase 1) [NCBI Gene 22929] {aka SELD, SPS, SPS1, VERBRAS2}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}, TSHZ1 (teashirt zinc finger homeobox 1) [NCBI Gene 10194] {aka CAA, NY-CO-33, SDCCAG33, TSH1}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** vascular edema (MESH:D004487), AD (MESH:D000544), neurological disorders (MESH:D009461), atherosclerosis (MESH:D050197), amyloid (MESH:C000718787), inflammatory (MESH:D007249), necrosis (MESH:D009336), cerebral microbleeds (MESH:D002547), Down syndrome (MESH:D004314), CAA (MESH:D016657), fibrinoid necrosis (MESH:D038261), hemorrhage (MESH:D006470), cerebral hemorrhage (MESH:D002543), DLB (MESH:D020961), white matter (MESH:D056784), ARIA (MESH:C564543), arteriolosclerosis (MESH:D050379)
- **Chemicals:** acid (MESH:D000143), Triton X-100 (MESH:D017830), NaN3 (MESH:D019810), benzyl benzoate (MESH:C006723), water (MESH:D014867), H2O2 (MESH:D006861), benzyl alcohol (MESH:D019905), 1,2-hexanediol (MESH:C119102), PBS (MESH:D007854), paraffin (MESH:D010232), methanol (MESH:D000432), lipid (MESH:D008055), formalin (MESH:D005557), Alexa Fluor 647 (MESH:C569686), BABB (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12880530/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12880530/full.md

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Source: https://tomesphere.com/paper/PMC12880530