摘要
Leucine-rich repeat kinase 2 (LRRK2), a gene linked to autosomal- dominantly inherited and sporadic Parkinson’s disease (PD) as a risk factor, encodes a large and complex protein with a dual enzymatic activity. LRRK2 contains several domains involved in protein-protein interactions, however, the presence of both a kinase and GTPase domain points to intracellular signaling functions (Marin, 2006). While LRRK2 has been linked to several molecular pathways important for neuronal activity (Martin et al., 2014), the observation that its expression is high in microglia has attracted the attention of different groups to understand whether LRRK2 dysfunctions in these cells may impact neuronal activity as secondary event.
基金
supported by Michael J Fox Foundation,InCure(EU Joint Programme–Neurogenerative Disease Research,JPND)
by the University of Padova(STARS Grants,LRRKing-Role of the Parkinson’s disease kinase LRRK2 in shaping neurites and synapses)
by the Intramural Research program of the NIH and Umberto Veronesi post-doctoral fellowship year 2015 and 2017 Award(693 and 1395)