Ectopic localization of FOXO3a protein in Lewy bodies in Lewy body dementia and Parkinson's diseaseAuthor(s): Su Bo | Liu Haihua | Wang Xinglong | Chen Shu | Siedlak Sandra | Kondo Eisaku | Choi Raymond | Takeda Atsushi | Castellani Rudy | Perry George | Smith Mark | Zhu Xiongwei | Lee Hyoung-gon
Journal: Molecular Neurodegeneration ISSN 1750-1326
Volume: 4; Issue: 1; Start page: 32; Date: 2009;
Abstract Lewy bodies and Lewy neurites constitute the cardinal neuropathological features of both Parkinson's disease (PD) and Lewy body dementia (LBD). Whereas α-synuclein has been found to be the major component of the Lewy body, the mechanisms by which neurons degenerate, as well as basic mechanisms involved in the formation of α-synuclein-related inclusions, remain obscure. We have suggested previously that potential mechanisms are likely to leave a "molecular signature" or protein adduct within the Lewy body, and have found examples of such signatures in previous studies. In this study, we demonstrate increased FOXO3 in association with Lewy bodies and Lewy neurites in LBD and PD brain tissue. Since FOXO proteins are involved in several pathways responsible for the regulation of cell death, cell proliferation, and cell metabolism, the ectopic localization of FOXO3 to Lewy bodies provides evidence that aberrations in basic cellular biochemistry may contribute to inclusion formation, which is likely more complex than a simple "gain of function" toxicity as is commonly opined. In light of the known interaction of FOXO3 and 14-3-3, basic protein-protein interaction between these proteins and α-synuclein may be key.