Cel Huntington’s disease (HD) is a neurodegenerative disorder caused by expansion of a CAG repeat, within the gene encoding huntingtin (Htt) and characterized by the progressive neurodegeneration and associated motor, cognitive and behavioral disturbances. Mutant Htt exerts adverse effects in neurons and non-neuronal cells. Animal studies describe white matter segmentation and myelin breakdown in HD. These evidences recapitulate the brain white matter volume loss described in pre-symptomatic and symptomatic subjects suggesting that white matter dysfunctions may represent a critical determinant in HD pathogenesis and may be identified as an early event of the disease.Recently, the applicant indentified a new dysfunctional pathway in HD, the dysregulation of ganglioside metabolism. High levels of gangliosides, in particular GM1, have been found to localize also in the myelin sheaths of oligodendrocytes where they play a crucial role in the maintenance of myelin integrity and in the regulation of axon–glia interactions. The applicant demonstrated that levels of GM1 are decreased in HD models and in fibroblasts from HD patients, contributing to heighten HD cells susceptibility to apoptosis. Importantly, administration of GM1 restored ganglioside levels and induced protective effects in HD models suggesting a therapeutic potential of GM1 in CNS. Our hypothesis is that decreased levels of GM1 may also affect white matter homeostasis. Interestingly, no studies correlating the dysregulation in gangliosides metabolism with white matter defects in HD have been conducted, so far. Thus, the main goal of this study is to look for white matter abnormalities and to determine the relationship with the degree of ganglioside dysfunctions and the severity of clinical status in HD. This will represent a new and interesting line of investigation in the field of HD and will provide more clear and deep understanding of the molecular mechanisms underlying the pathogenesis of the disease. Dziedzina nauki natural sciencesbiological sciencesneurobiologymedical and health sciencesbasic medicinephysiologyhomeostasis Program(-y) FP7-PEOPLE - Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) Temat(-y) FP7-PEOPLE-2011-IIF - Marie Curie Action: "International Incoming Fellowships" Zaproszenie do składania wniosków FP7-PEOPLE-2011-IIF Zobacz inne projekty w ramach tego zaproszenia System finansowania MC-IIF - International Incoming Fellowships (IIF) Koordynator INSTITUTO NEUROLOGICO MEDITERRANEO NEUROMED SOCIETA PER AZIONI Wkład UE € 249 911,60 Adres VIA ATINENSE 18 86077 Pozzilli Is Włochy Zobacz na mapie Region Sud Molise Isernia Rodzaj działalności Private for-profit entities (excluding Higher or Secondary Education Establishments) Kontakt administracyjny Ferdinando Squitieri (Dr.) Linki Kontakt z organizacją Opens in new window Strona internetowa Opens in new window Koszt całkowity Brak danych
