摘要：SummaryThe neuropathological feature of multiple system atrophy (MSA), a fatal adult-onset disorder without effective therapy, is the accumulation of pathological α-synuclein (α-Syn) in the central nervous system (CNS). Here we show that pathological α-Syn exists in nerve terminals in detrusor and external urethral sphincter (EUS) of patients with MSA. Furthermore, α-Syn-preformed fibrils (PFFs) injected in the EUS or detrusor in TgM83+/−mice initiated the transmission of pathological α-Syn from the urogenital tract to brain via micturition reflex pathways, and these mice developed widespread phosphorylated α-Syn inclusion pathology together with phenotypes. In addition, urinary dysfunction and denervation-reinnervation of external anal sphincter were detected earlier in the mouse models with α-Syn PFFs inoculation before the behavioral manifestations. These results suggest that pathological α-Syn spreading through the micturition reflex pathways retrogradely from the urogenital tract to CNS may lead to urinary dysfunction in patients with MSA, which is different from the etiology of idiopathic Parkinson disease.Graphical AbstractDisplay OmittedHighlights•Pathological α-Syn exhibits in nerve terminals in DET and EUS of patients with MSA•Propagation of pathological α-Syn from urinary tract to CNS causes MSA-like syndrome•The mouse models show urinary dysfunction and abnormal EAS EMG before motor deficits•Lower urinary tract injection of α-Syn PFFs induces autonomic and motor dysfunctionsBiological Sciences; Neuroscience; Behavioral Neuroscience
