| Literature DB >> 29046994 |
Giorgia Puorro1, Angela Marsili1, Francesca Sapone1, Chiara Pane1, Anna De Rosa1, Silvio Peluso1, Giuseppe De Michele1, Alessandro Filla1, Francesco Saccà2.
Abstract
Polyglutamine disorders are neurodegenerative diseases that share a CAG repeat expansion in the coding region, resulting in aggregated proteins that can be only degraded through aggrephagy. We measured the expression of autophagy genes in peripheral blood mononuclear cells of 20 patients with Huntington's disease (HD), 20 with spinocerebellar ataxia type 2 (SCA2), and 20 healthy individuals. HD patients showed increased expression of MAP1LC3B (+ 43%; p = 0.048), SQSTM1 (+ 49%; p = 0.002), and WDFY3 (+ 89%; p < 0.001). SCA2 patients had increased expression of WDFY3 (+ 69%; p < 0.001). We show that peripheral markers of autophagy are elevated in polyQ diseases, and this is particularly evident in HD.Entities:
Keywords: Autophagy; Huntington’s disease; MAP1LC3B; SCA2; SQSTM1; Spinocerebellar ataxia type 2; WDFY3
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Year: 2017 PMID: 29046994 DOI: 10.1007/s10072-017-3156-6
Source DB: PubMed Journal: Neurol Sci ISSN: 1590-1874 Impact factor: 3.307