Anti-Human alpha-Synuclein N-Terminal Peptide Antibody Protects against Dopaminergic Cell Death and Ameliorates Behavioral Deficits in an AAV-alpha-Synuclein Rat Model of Parkinson's Disease

作者：Shahaduzzaman Md; Nash Kevin; Hudson Charles; Sharif Masroor; Grimmig Bethany; Lin Xiaoyang; Bai Ge; Liu Hui; Ugen Kenneth E; Cao Chuanhai^*; Bickford Paula C

来源：PLos One, 2015, 10(2): e0116841.

DOI：10.1371/journal.pone.0116841

The protein alpha-synuclein (alpha-Syn) has a central role in the pathogenesis of Parkinson's disease (PD) and immunotherapeutic approaches targeting this molecule have shown promising results. In this study, novel antibodies were generated against specific peptides from full length human alpha-Syn and evaluated for effectiveness in ameliorating alpha-Syn-induced cell death and behavioral deficits in an AAV-alpha-Syn expressing rat model of PD. Fisher 344 rats were injected with rAAV vector into the right substantia nigra (SN), while control rats received an AAV vector expressing green fluorescent protein (GFP). Beginning one week after injection of the AAV-alpha-Syn vectors, rats were treated intraperitoneally with either control IgG or antibodies against the N-terminal (AB1), or central region (AB2) of alpha-Syn. An unbiased stereological estimation of TH+, NeuN+, and OX6 (MHC-II) immunostaining revealed that the alpha-Syn peptide antibodies (AB1 and AB2) significantly inhibited alpha-Syn-induced dopaminergic cell (DA) and NeuN+ cell loss (one-way ANOVA (F (3, 30) = 5.8, p = 0.002 and (F (3, 29) = 7.92, p = 0.002 respectively), as well as decreasing the number of activated microglia in the ipsilateral SN (one-way ANOVA F = 14.09; p = 0.0003). Antibody treated animals also had lower levels of alpha-Syn in the ipsilateral SN (one-way ANOVA F (7, 37) = 9.786; p = 0.0001) and demonstrated a partial intermediate improvement of the behavioral deficits. Our data suggest that, in particular, an alpha-Syn peptide antibody against the N-terminal region of the protein can protect against DA neuron loss and, to some extent behavioral deficits. As such, these results may be a potential therapeutic strategy for halting the progression of PD.

• 出版日期2015-2-6