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Alpha-Synuclein produces a long-lasting increase in neurotransmitter release.


ABSTRACT: Wild-type alpha-synuclein, a protein of unknown function, has received much attention because of its involvement in a series of diseases that are known as synucleinopathies. We find that long-lasting potentiation of synaptic transmission between cultured hippocampal neurons is accompanied by an increase in the number of alpha-synuclein clusters. Conversely, suppression of alpha-synuclein expression through antisense nucleotide and knockout techniques blocks the potentiation, as well as the glutamate-induced increase in presynaptic functional bouton number. Consistent with these findings, alpha-synuclein introduction into the presynaptic neuron of a pair of monosynaptically connected cells causes a rapid and long-lasting enhancement of synaptic transmission, and rescues the block of potentiation in alpha-synuclein null mouse cultures. Also, we report that the application of nitric oxide (NO) increases the number of alpha-synuclein clusters, and inhibitors of NO-synthase block this increase, supporting the hypothesis that NO is involved in the enhancement of the number of alpha-synuclein clusters. Thus, alpha-synuclein is involved in synaptic plasticity by augmenting transmitter release from the presynaptic terminal.

SUBMITTER: Liu S 

PROVIDER: S-EPMC526467 | biostudies-literature | 2004 Nov

REPOSITORIES: biostudies-literature

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alpha-Synuclein produces a long-lasting increase in neurotransmitter release.

Liu Shumin S   Ninan Ipe I   Antonova Irina I   Battaglia Fortunato F   Trinchese Fabrizio F   Narasanna Archana A   Kolodilov Nikolai N   Dauer William W   Hawkins Robert D RD   Arancio Ottavio O  

The EMBO journal 20041028 22


Wild-type alpha-synuclein, a protein of unknown function, has received much attention because of its involvement in a series of diseases that are known as synucleinopathies. We find that long-lasting potentiation of synaptic transmission between cultured hippocampal neurons is accompanied by an increase in the number of alpha-synuclein clusters. Conversely, suppression of alpha-synuclein expression through antisense nucleotide and knockout techniques blocks the potentiation, as well as the gluta  ...[more]

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