Inducing aggresome and stable tau aggregation in Neuro2a cells with an optogenetic tool Article Swipe
Shigeo Sakuragi
,
Tomoya Uchida
,
Naoki Kato
,
Boxiao Zhao
,
Toshiki Takahashi
,
A Hattori
,
Yoshihiro Sakata
,
Yoshiyuki Soeda
,
Akihiko Takashima
,
Hideaki� Yoshimura
,
Gen Matsumoto
,
Hiroko Bannai
·
YOU?
·
· 2024
· Open Access
·
· DOI: https://doi.org/10.1101/2024.05.07.592868
YOU?
·
· 2024
· Open Access
·
· DOI: https://doi.org/10.1101/2024.05.07.592868
Tauopathy is a spectrum of diseases characterized by fibrillary tau aggregate formation in neurons and glial cells in the brain. Tau aggregation originates in the brainstem and entorhinal cortex and then spreads throughout the brain in Alzheimer’s disease (AD), which is the most prevalent type of tauopathy. Understanding the mechanism by which locally developed tau pathology propagates throughout the brain is crucial for comprehending AD pathogenesis. Therefore, a novel model of tau pathology that artificially induces tau aggregation in targeted cells at specific times is essential. This study describes a novel optogenetic module, OptoTau, which is a human tau with the P301L mutation fused with a photosensitive protein CRY2olig, inducing various forms of tau according to the temporal pattern of blue light illumination pattern. Continuous blue light illumination for 12 h to Neuro2a cells that stably express OptoTau (OptoTauKI cells) formed clusters along microtubules, many of which eventually accumulated in aggresomes. Conversely, methanol-resistant tau aggregation was formed when alternating light exposure and darkness in 30-min cycles for 8 sets per day were repeated over 8 days. Methanol-resistant tau was induced more rapidly by repeating 5-min illumination followed by 25-min darkness over 24 h. These results indicate that OptoTau induced various tau aggregation stages based on the temporal pattern of blue light exposure. Thus, this technique exhibits potential as a novel approach to developing specific tau aggregation in targeted cells at desired time points. Significance This study developed an approach to manipulate tau aggregation in a blue light-dependent manner using cells that stably express OptoTau, which is an optogenetic tool based on the CRY2olig module. Tau accumulation in aggresomes or stable tau aggregation were selectively induced by blue light illumination conditions. These results are crucial as they provide a new technological basis for establishing a singular point of tau aggregation in specific targeted cells at a particular time.
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Metadata
- Type
- preprint
- Language
- en
- Landing Page
- https://doi.org/10.1101/2024.05.07.592868
- https://www.biorxiv.org/content/biorxiv/early/2024/05/16/2024.05.07.592868.full.pdf
- OA Status
- green
- References
- 41
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4396732947
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4396732947Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1101/2024.05.07.592868Digital Object Identifier
- Title
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Inducing aggresome and stable tau aggregation in Neuro2a cells with an optogenetic toolWork title
- Type
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preprintOpenAlex work type
- Language
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enPrimary language
- Publication year
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2024Year of publication
- Publication date
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2024-05-08Full publication date if available
- Authors
-
Shigeo Sakuragi, Tomoya Uchida, Naoki Kato, Boxiao Zhao, Toshiki Takahashi, A Hattori, Yoshihiro Sakata, Yoshiyuki Soeda, Akihiko Takashima, Hideaki� Yoshimura, Gen Matsumoto, Hiroko BannaiList of authors in order
- Landing page
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https://doi.org/10.1101/2024.05.07.592868Publisher landing page
- PDF URL
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https://www.biorxiv.org/content/biorxiv/early/2024/05/16/2024.05.07.592868.full.pdfDirect link to full text PDF
- Open access
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YesWhether a free full text is available
- OA status
-
greenOpen access status per OpenAlex
- OA URL
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https://www.biorxiv.org/content/biorxiv/early/2024/05/16/2024.05.07.592868.full.pdfDirect OA link when available
- Concepts
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Aggresome, Optogenetics, Chemistry, Neuroscience, Nanotechnology, Psychology, Materials science, Biochemistry, Autophagy, ApoptosisTop concepts (fields/topics) attached by OpenAlex
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0Total citation count in OpenAlex
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41Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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