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High-content imaging of live microglia-containing Alzheimer’s disease brain organoids
Quang D, Summers R, Dooling BR, Esquer H, Zhou Q, LaBarbera DV, Vergara MN, Chial HJ et al.. bioRxiv, 2026-10-27
Topic: Inflammation, microglia and astrocytes
Plain-language summary
This method establishes a platform for high-throughput longitudinal drug screening in immunocompetent human COs that will enable the identification of new therapeutic candidates to modulate Aβ aggregation, glial reactivity, and neurodegeneration. Highlights A platform was developed for high-resolution in vitro visualization of insoluble Aβ aggregates in live MCOs. The approach enables deep tissue imaging of Aβ pathology in intact 3D MCOs, allowing spatial mapping of Aβ aggregate distribution over time. Differences in Aβ burden and viability of neurons, neural progenitors, and astrocytes were quantified, distinguishing T21 COs from D21 control MCOs. The platform is positioned to support high-throughput longitudinal drug screening, providing a scalable tool to identify novel therapeutics targeting Aβ-mediated neurodegeneration.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Quang, D., Summers, R., Dooling, B. R., Esquer, H., Zhou, Q., LaBarbera, D. V., et al. (2026). High-content imaging of live microglia-containing Alzheimer’s disease brain organoids. bioRxiv. https://doi.org/10.64898/2026.10.26.761970
Vancouver
Quang D, Summers R, Dooling BR, Esquer H, Zhou Q, LaBarbera DV, et al. High-content imaging of live microglia-containing Alzheimer’s disease brain organoids. bioRxiv. 2026. doi:10.64898/2026.10.26.761970.
BibTeX
@article{quang2026-09848cb6,
author = {Quang, D. and Summers, R. and Dooling, B. R. and Esquer, H. and Zhou, Q. and LaBarbera, D. V. and Vergara, M. N. and Chial, H. J. and others},
title = {{High-content imaging of live microglia-containing Alzheimer’s disease brain organoids}},
journal = {bioRxiv},
year = {2026},
doi = {10.64898/2026.10.26.761970},
url = {https://doi.org/10.64898/2026.10.26.761970}
}
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Key findings
- This method establishes a platform for high-throughput longitudinal drug screening in immunocompetent human COs that will enable the identification of new therapeutic candidates to modulate Aβ aggregation, glial reactivity, and neurodegeneration.
- Highlights A platform was developed for high-resolution in vitro visualization of insoluble Aβ aggregates in live MCOs.
- The approach enables deep tissue imaging of Aβ pathology in intact 3D MCOs, allowing spatial mapping of Aβ aggregate distribution over time.
- Differences in Aβ burden and viability of neurons, neural progenitors, and astrocytes were quantified, distinguishing T21 COs from D21 control MCOs.
- The platform is positioned to support high-throughput longitudinal drug screening, providing a scalable tool to identify novel therapeutics targeting Aβ-mediated neurodegeneration.
Study details
- Study designlongitudinal study
- Evidence strengthModerate
How this study scored 16/100
Preprint — not yet peer-reviewed. It scored 35 on the same rubric, but non-peer-reviewed sources are capped at 16, so it shows as 16. Scored zero for sample size, effect reported and randomized / blinded because the record does not state it. We have no data on times cited, citations per year, impact for its field and year, cited by studies here, still being cited, senior author's track record, institution's track record and multicenter collaboration, so those were left out: it earned 22 of the 62 points we could judge it on, which is 35 out of 100.
| Component | Points | Why |
|---|---|---|
| Journal tier | 2 / 10 | Tier 4 — not a peer-reviewed journal (bioRxiv) |
| Journal's citation record | 0 / 4 | Not a journal article, so the journal's record does not count |
| Study design | 7 / 12 | A longitudinal study following the same people over time |
| Strength of evidence | 3 / 5 | Rated “moderate” in our summary |
| Peer-review validation | 4 / 10 | Preprint — not yet peer-reviewed. Hosted on a preprint server. |
| How recent | 5 / 5 | 2026 — within 1 year(s) of the newest study here |
| Sample size | 0 / 4 | Participant count not stated — scores zero (not stated in the record — scored 0) |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 0 / 3 | Laboratory or animal study (title names “organoids”) — scores zero |
| Randomized / blinded | 0 / 2 | No randomization or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | — / 7 | No citation count (not found in OpenAlex) — left out of this score |
| Citations per year | — / 5 | No citation count or no year — left out of this score |
| Impact for its field and year | — / 6 | No field-weighted citation impact (OpenAlex has none yet) — left out of this score |
| Cited by studies here | — / 6 | Not yet checked against this library's citation graph — left out of this score |
| Still being cited | — / 4 | No yearly citation counts — left out of this score |
| Senior author's track record | — / 4 | Senior author's record not available — left out of this score |
| Institution's track record | — / 3 | No institution listed in OpenAlex — left out of this score |
| Multicenter collaboration | — / 3 | Institutions not listed — left out of this score |
| Indexed in PubMed | 1 / 2 | Not in PubMed, but has a DOI |
| Free to read | 0 / 2 | Behind a paywall — scores zero |
| Points | 22 / 62 | Scored on 12 of 20 parts. We have no data for the rest, so they are left out: 22 of the 62 points we could judge it on is 35 out of 100. |
| Total | 35 / 100 | Capped to 16 because this is not a peer-reviewed article. |
What each of these 20 components measures, and what this score is not →
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