| Literature DB >> 34264082 |
Ching-Hsiang Fan, Kuo-Chen Wei1,2, Nai-Hua Chiu, En-Chi Liao, Hsien-Chu Wang, Ruo-Yu Wu3, Yi-Ju Ho, Hong-Lin Chan, Tsung-Shing Andrew Wang3, Ying-Zu Huang, Tsung-Hsun Hsieh, Chin-Hsien Lin4, Yu-Chun Lin, Chih-Kuang Yeh.
Abstract
Sonogenetics is a promising strategy allowing the noninvasive and selective activation of targeted neurons in deep brain regions; nevertheless, its therapeutic outcome for neurodegeneration diseases that need long-term treatment remains to be verified. We previously enhanced the ultrasound (US) sensitivity of targeted cells by genetic modification with an engineered auditory-sensing protein, mPrestin (N7T, N308S). In this study, we expressed mPrestin in the dopaminergic neurons of the substantia nigra in Parkinson's disease (PD) mice and used 0.5 MHz US for repeated and localized brain stimulation. The mPrestin expression in dopaminergic neurons persisted for at least 56 days after a single shot of adeno-associated virus, suggesting that the period of expression was long enough for US treatment in mice. Compared to untreated mice, US stimulation ameliorated the dopaminergic neurodegeneration 10-fold and mitigated the PD symptoms of the mice 4-fold, suggesting that this sonogenetic strategy has the clinical potential to treat neurodegenerative diseases.Entities:
Keywords: Parkinson’s disease; dopaminergic neuron; sonogenetics; ultrasound; ultrasound-sensing protein
Year: 2021 PMID: 34264082 DOI: 10.1021/acs.nanolett.1c00886
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189