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Whole-brain microscopy reveals distinct temporal and spatial efficacy of anti-A beta therapies
Univ Zurich, Switzerland.
Stanford Univ, CA 94305 USA.
Univ Zurich, Switzerland.
Univ Zurich, Switzerland; Univ Zurich, Switzerland; Swiss Fed Inst Technol, Switzerland.
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2023 (English)In: EMBO Molecular Medicine, ISSN 1757-4676, E-ISSN 1757-4684, Vol. 15, article id e16789Article in journal (Refereed) Published
Abstract [en]

Many efforts targeting amyloid-beta (A beta) plaques for the treatment of Alzheimers Disease thus far have resulted in failures during clinical trials. Regional and temporal heterogeneity of efficacy and dependence on plaque maturity may have contributed to these disappointing outcomes. In this study, we mapped the regional and temporal specificity of various anti-A beta treatments through high-resolution light-sheet imaging of electrophoretically cleared brains. We assessed the effect on amyloid plaque formation and growth in Thy1-APP/PS1 mice subjected to beta-secretase inhibitors, polythiophenes, or anti-A beta antibodies. Each treatment showed unique spatiotemporal A beta clearance, with polythiophenes emerging as a potent anti-A beta compound. Furthermore, aligning with a spatial-transcriptomic atlas revealed transcripts that correlate with the efficacy of each A beta therapy. As observed in this study, there is a striking dependence of specific treatments on the location and maturity of A beta plaques. This may also contribute to the clinical trial failures of A beta-therapies, suggesting that combinatorial regimens may be significantly more effective in clearing amyloid deposition.

Place, publisher, year, edition, pages
WILEY , 2023. Vol. 15, article id e16789
Keywords [en]
Alzheimers disease; amyloid-beta; brain; light-sheet microscopy; tissue clearing
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:liu:diva-190335DOI: 10.15252/emmm.202216789ISI: 000884202900001PubMedID: 36382364OAI: oai:DiVA.org:liu-190335DiVA, id: diva2:1716307
Note

Funding Agencies|Swiss National Research Foundation [179040, 207872, 183563]; Gelu Foundation; Nomis Foundation; Swiss Personalized Health Network (SPHN) [2017DRI17]; USZ Foundation; Swedish Research Council [2016-00748]; European Research Council (BRAINCOMPATH) [670757]; NIH/NINDS [R01NS087159, R01NS091461]; NIH/NIA [RF1AG047666]; NIH/NIMH [RF1MH114227]

Available from: 2022-12-05 Created: 2022-12-05 Last updated: 2023-06-09

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