Inhibition of vesicular monoamine transporter-2 activity in α-synuclein stably transfected SH-SY5Y cells

JT Guo, AQ Chen, QI Kong, H Zhu, CM Ma… - Cellular and molecular …, 2008 - Springer
JT Guo, AQ Chen, QI Kong, H Zhu, CM Ma, C Qin
Cellular and molecular neurobiology, 2008Springer
Abstract α-Synuclein plays a key role in the pathological neurodegeneration in Parkinson's
disease. Although its contribution to normal physiology remains elusive, the selective
degeneration of α-synuclein-containing dopaminergic neurons in Parkinson's disease may
be linked to abnormal α-synuclein induced toxicity. In the present study, a complex of α-
synuclein and vesicular monoamine transporter-2 was identified by GST-Pull Down
experiment. In wild-type α-synuclein stably transfected SH-SY5Y cell lines, the activity of …
Abstract
α-Synuclein plays a key role in the pathological neurodegeneration in Parkinson’s disease. Although its contribution to normal physiology remains elusive, the selective degeneration of α-synuclein-containing dopaminergic neurons in Parkinson’s disease may be linked to abnormal α-synuclein induced toxicity. In the present study, a complex of α-synuclein and vesicular monoamine transporter-2 was identified by GST-Pull Down experiment. In wild-type α-synuclein stably transfected SH-SY5Y cell lines, the activity of vesicular monoamine transporter-2 decreased by 31% as determined by [3H] dopamine uptake, and its expression also decreased in both protein and mRNA levels using western and northern blot analysis. Overexpression of wild-type α-synuclein did not induce cell death or apoptosis, but significantly enhanced the intracellular reactive oxygen species level as assayed by flow cytometry. These data suggest that Up-regulated α-synuclein expression inhibits the activity of vesicular monoamine transporter-2, thereby interrupting dopamine homeostasis and resulting in dopaminergic neuron injury in Parkinson’s disease.
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