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Advanced glycation end products induce in vitro cross-linking of α-synuclein and accelerate the process of intracellular inclusion body formation

✍ Scribed by Shamim Shaikh; Louise F.B. Nicholson


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
923 KB
Volume
86
Category
Article
ISSN
0360-4012

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✦ Synopsis


Abstract

Cross‐linking of α‐synuclein and Lewy body formation have been implicated in the dopaminergic neuronal cell death observed in Parkinson's disease (PD); the mechanisms responsible, however, are not clear. Reactive oxygen species and advanced glycation end products (AGEs) have been found in the intracellular, α‐synuclein‐positive Lewy bodies in the brains of both PD as well as incidental Lewy body disease patients, suggesting a role for AGEs in α‐synuclein cross‐linking and Lewy body formation. The aims of the present study were to determine 1) whether AGEs can induce cross‐linking of α‐synuclein peptides, 2) the progressive and time‐dependent intracellular accumulation of AGEs and inclusion body formation, and 3) the effects of extracellular or exogenous AGEs on intracellular inclusion formation. We first investigated the time‐dependent cross‐linking of recombinant human α‐synuclein in the presence of AGEs in vitro, then used a cell culture model based on chronic rotenone treatment of human dopaminergic neuroblastoma cells (SH‐SY5Y) over a period of 1–4 weeks, in the presence of different doses of AGEs. Cells (grown on coverslips) and cell lysates, collected at the end of every week, were analyzed for the presence of intracellular reactive oxygen species, AGEs, α‐synuclein proteins, and intracellular α‐synuclein‐ and AGE‐positive inclusion bodies by using immunocytochemical, biochemical, and Western blot techniques. Our results show that AGEs promote in vitro cross‐linking of α‐synuclein, that intracellular accumulation of AGEs precedes α‐synuclein‐positive inclusion body formation, and that extracellular AGEs accelerate the process of intracellular α‐synuclein‐positive inclusion body formation. © 2008 Wiley‐Liss, Inc.