Human induced pluripotent stem cell-derived dopaminergic neurons release alpha-synuclein through neuronal activity

Lewy body diseases, including Parkinson's disease (PD), are characterized by the spread of alpha-synuclein (αSyn) between neurons across synapses, a process crucial for understanding their pathophysiology and developing effective treatments. In this study, we aimed to investigate the role of neuronal activity in releasing αSyn from human induced pluripotent stem cell-derived dopaminergic neurons. We examined human induced pluripotent stem cell-derived dopaminergic neurons, both healthy and those with the αSyn gene mutation associated with PD. We employed pharmacological agents and optogenetic techniques and demonstrated that increased neuronal activity, induced by bicuculline or optogenetic stimulation, significantly enhances αSyn release. However, suppression of neuronal activity with cyanquixaline reduces αSyn secretion. These findings underscore the pivotal role of neuronal activity in αSyn transmission between neurons, showing its potential impact on the spread of Lewy pathology in patients with neurodegenerative diseases like PD. Therefore, this study advances our understanding of PD and opens new avenues for therapeutic strategies to mitigate Lewy body disease progression.

Authors

Institutions

Publication Details

Journal
Neuroscience Research
Published
2024-11-29
DOI
https://doi.org/10.1016/j.neures.2024.11.007
Citations
1
Primary Topic
Neuroscience and Neural Engineering
Type
article
Field-Weighted Citation Impact
0.27
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Human induced pluripotent stem cell-derived dopaminergic neurons release alpha-synuclein through neuronal activity

Taiji Tsunemi, Risa Nonaka, Ryota Nakamura, Nobutaka Hattori et al.
1 citations
Neuroscience Research
Neuroscience and Neural Engineering
0.27
article

Human induced pluripotent stem cell-derived dopaminergic neurons release alpha-synuclein through neuronal activity

Taiji Tsunemi, Risa Nonaka, Ryota Nakamura, Nobutaka Hattori, Takayuki Jo, Genko Oyama, Kei‐ichi Ishikawa, Maierdanjiang Nuermaimaiti, Wado Akamatsu, Takahiro Shiga, Rejko Krüger
article en
1 citations

Abstract

Lewy body diseases, including Parkinson's disease (PD), are characterized by the spread of alpha-synuclein (αSyn) between neurons across synapses, a process crucial for understanding their pathophysiology and developing effective treatments. In this study, we aimed to investigate the role of neuronal activity in releasing αSyn from human induced pluripotent stem cell-derived dopaminergic neurons. We examined human induced pluripotent stem cell-derived dopaminergic neurons, both healthy and those with the αSyn gene mutation associated with PD. We employed pharmacological agents and optogenetic techniques and demonstrated that increased neuronal activity, induced by bicuculline or optogenetic stimulation, significantly enhances αSyn release. However, suppression of neuronal activity with cyanquixaline reduces αSyn secretion. These findings underscore the pivotal role of neuronal activity in αSyn transmission between neurons, showing its potential impact on the spread of Lewy pathology in patients with neurodegenerative diseases like PD. Therefore, this study advances our understanding of PD and opens new avenues for therapeutic strategies to mitigate Lewy body disease progression.

Neuroscience ResearchVol. 212
Centre Hospitalier de Luxembourg (LU), University of Luxembourg (LU), Juntendo University (JP), Luxembourg Institute of Health (LU)
Zero hunger
Openalex Percentile: Top 42%
Neuroscience and Neural Engineering
0.27
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.