iPSC model of human specific neuroinflammation in Alzheimer’s disease

We found dual effect of CHRFAM7A on Aβ<sub>1-42</sub> associated pathology in AD: it provides protection against toxic concentration of Aβ<sub>1-42</sub> by decreased uptake through the humanized α7/CHRFAM7A nAChR and increases the innate immune response by switching the α7nAChR from an anti-inflammatory to pro-inflammatory transducer. Our iPSC model presents an opportunity to elucidate the molecular mechanism of these processes and establish high throughput screens.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70861_108756
Primary Topic
Nicotinic Acetylcholine Receptors Study
Type
article
Field-Weighted Citation Impact
0.00
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article

iPSC model of human specific neuroinflammation in Alzheimer’s disease

Ruea‐Yea Huang, Ryu Dorn, Ivanna Ihnatovych, Kinga Szigeti et al.
Alzheimer s & Dementia
Nicotinic Acetylcholine Receptors Study
article

iPSC model of human specific neuroinflammation in Alzheimer’s disease

Ruea‐Yea Huang, Ryu Dorn, Ivanna Ihnatovych, Kinga Szigeti, Robin Schwartz
article en

Abstract

We found dual effect of CHRFAM7A on Aβ<sub>1-42</sub> associated pathology in AD: it provides protection against toxic concentration of Aβ<sub>1-42</sub> by decreased uptake through the humanized α7/CHRFAM7A nAChR and increases the innate immune response by switching the α7nAChR from an anti-inflammatory to pro-inflammatory transducer. Our iPSC model presents an opportunity to elucidate the molecular mechanism of these processes and establish high throughput screens.

Alzheimer s & DementiaVol. 21(S7)
University at Buffalo, State University of New York (US)
Openalex Percentile: Top 37%
Nicotinic Acetylcholine Receptors Study
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