| First Author | Smith BR | Year | 2014 |
| Journal | J Pathol | Volume | 232 |
| Issue | 5 | Pages | 509-21 |
| PubMed ID | 24415155 | Mgi Jnum | J:208051 |
| Mgi Id | MGI:5560840 | Doi | 10.1002/path.4328 |
| Citation | Smith BR, et al. (2014) Neuronal inclusions of alpha-synuclein contribute to the pathogenesis of Krabbe disease. J Pathol 232(5):509-21 |
| abstractText | Demyelination is a major contributor to the general decay of neural functions in children with Krabbe disease. However, recent reports have indicated a significant involvement of neurons and axons in the neuropathology of the disease. In this study, we have investigated the nature of cellular inclusions in the Krabbe brain. Brain samples from the twitcher mouse model for Krabbe disease and from patients affected with the infantile and late-onset forms of the disease were examined for the presence of neuronal inclusions. Our experiments demonstrated the presence of cytoplasmic aggregates of thioflavin-S-reactive material in both human and murine mutant brains. Most of these inclusions were associated with neurons. A few inclusions were detected to be associated with microglia and none were associated with astrocytes or oligodendrocytes. Thioflavin-S-reactive inclusions increased in abundance, paralleling the development of neurological symptoms, and distributed throughout the twitcher brain in areas of major involvement in cognition and motor functions. Electron microscopy confirmed the presence of aggregates of stereotypic beta-sheet folded proteinaceous material. Immunochemical analyses identified the presence of aggregated forms of alpha-synuclein and ubiquitin, proteins involved in the formation of Lewy bodies in Parkinson's disease and other neurodegenerative conditions. In vitro assays demonstrated that psychosine, the neurotoxic sphingolipid accumulated in Krabbe disease, accelerated the fibrillization of alpha-synuclein. This study demonstrates the occurrence of neuronal deposits of fibrillized proteins including alpha-synuclein, identifying Krabbe disease as a new alpha-synucleinopathy. |
