Extracellular vesicles from hiPSC-derived NSCs protect human neurons against Aβ-42 oligomers induced neurodegeneration, mitochondrial dysfunction and tau phosphorylation

An optimal dose of hiPSC-NSC-EVs could significantly decrease the degeneration of human neurons induced by Aβ-42o. The results support further research into the effectiveness of hiPSC-NSC-EVs in AD, particularly their proficiency in preserving neurons and slowing disease progression.

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Publication Details

Journal
Stem Cell Research & Therapy
Published
2025-04-18
DOI
https://doi.org/10.1186/s13287-025-04324-3
Citations
9
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
10.48

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article

Extracellular vesicles from hiPSC-derived NSCs protect human neurons against Aβ-42 oligomers induced neurodegeneration, mitochondrial dysfunction and tau phosphorylation

Roshni Sara Babu, Goutham Shankar, James J. Cai, Ashok K. Shetty et al.
9 citations
Stem Cell Research & Therapy
Alzheimer's disease research and treatments
10.48
article

Extracellular vesicles from hiPSC-derived NSCs protect human neurons against Aβ-42 oligomers induced neurodegeneration, mitochondrial dysfunction and tau phosphorylation

Roshni Sara Babu, Goutham Shankar, James J. Cai, Ashok K. Shetty, Shama Rao, Esha Narvekar, Raghavendra Upadhya, Leelavathi N. Madhu, Sanya Kotian, Advaidhaa Nagarajan
article en
9 citations

Abstract

An optimal dose of hiPSC-NSC-EVs could significantly decrease the degeneration of human neurons induced by Aβ-42o. The results support further research into the effectiveness of hiPSC-NSC-EVs in AD, particularly their proficiency in preserving neurons and slowing disease progression.

Stem Cell Research & TherapyVol. 16(1)
Texas A&M Health Science Center (US), Texas A&M University (US)
National Science Council, National Institute on Aging
Zero hunger
Openalex Percentile: Top 2%
Alzheimer's disease research and treatments
10.48
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