Elongated nanoporous Au networks improve somatic cell direct conversion into induced dopaminergic neurons for Parkinson's disease therapy

Authors
Sungwoo LeeHyun Soo ShimHyeok Ju ParkYujung ChangYoung-Eun HanOh, Soo JinWonwoong LeeHyeonjoo ImSeol YunHeeRyu, HoonHoon KangYong Kyu LeeSungho ParkJunsang Yoo
Issue Date
2022-10
Publisher
Elsevier BV
Citation
Acta Biomaterialia, v.151, pp.561 - 575
Abstract
The efficient production of dopaminergic neurons via the direct conversion of other cell types is of inter-est as a potential therapeutic approach for Parkinson's disease. This study aimed to investigate the use of elongated porous gold nanorods (AuNpRs) as an enhancer of cell fate conversion. We observed that AuNpRs promoted the direct conversion of fibroblasts into dopaminergic neurons in vivo and in vitro. The extent of conversion of fibroblasts into dopaminergic neurons depended on the porosity of AuNpRs, as determined by their aspect ratio. The mechanism underlying these results involves specific AuNpR-induced transcriptional changes that altered the expression of antioxidant-related molecules. The gener-ation of dopaminergic neurons via the direct conversion method will open a new avenue for developing a therapeutic platform for Parkinson's disease treatment.Statement of significance In this study, we applied modified gold nanoporous materials (AuNpRs) to the direct lineage reprogram-ming of dopaminergic neurons. The cell reprogramming process is energy-intensive, resulting in an ex-cess of oxidative stress. AuNpRs facilitated the direct conversion of dopaminergic neurons by ameliorat-ing oxidative stress during the reprogramming process. We have found this mechanistic clue from high throughput studies in this research work.(c) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
Keywords
GOLD NANOPARTICLES; FUNCTIONAL-NEURONS; HUMAN FIBROBLASTS; CLINICAL-TRIALS; STEM-CELLS; IN-VIVO; DELIVERY; Porous gold nanoparticles; Parkinson?s disease; Direct lineage reprogramming; Induced dopaminergic neurons; Antioxidant-related molecule
ISSN
1742-7061
URI
https://pubs.kist.re.kr/handle/201004/75993
DOI
10.1016/j.actbio.2022.07.058
Appears in Collections:
KIST Article > 2022
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