دورية أكاديمية

Mutant α-synuclein propagates via the lymphatic system of the brain in the monomeric state.

التفاصيل البيبلوغرافية
العنوان: Mutant α-synuclein propagates via the lymphatic system of the brain in the monomeric state.
المؤلفون: Fujita, Kyota, Homma, Hidenori, Jin, Meihua, Yoshioka, Yuki, Jin, Xiaocen, Saito, Yuko, Tanaka, Hikari, Okazawa, Hitoshi
المصدر: Cell Reports; Aug2023, Vol. 42 Issue 8, pN.PAG-N.PAG, 1p
مستخلص: Prion-like protein propagation is considered a common pathogenic mechanism in neurodegenerative diseases. Here we investigate the in vivo propagation pattern and aggregation state of mutant α-synuclein by injecting adeno-associated viral (AAV)-α-synuclein-A53T-EGFP into the mouse olfactory cortex. Comparison of aggregation states in various brain regions at multiple time points after injection using western blot analyses shows that the monomeric state of the mutant/misfolded protein propagates to remote brain regions by 2 weeks and that the propagated proteins aggregate in situ after being incorporated into neurons. Moreover, injection of Alexa 488-labeled α-synuclein-A53T confirms the monomeric propagation at 2 weeks. Super-resolution microscopy shows that both α-synuclein-A53T proteins propagate via the lymphatic system, penetrate perineuronal nets, and reach the surface of neurons. Electron microscopy shows that the propagated mutant/misfolded monomer forms fibrils characteristic of Parkinson's disease after its incorporation into neurons. These findings suggest a mode of propagation different from that of aggregate-dependent propagation. [Display omitted] • Prionoid protein propagation is a common mechanism of neurodegenerative diseases • Neuron-to-neuron propagation of aggregated disease proteins has been assumed • We reveal propagation of the monomer disease protein via brain lymphatic system • The brain lymphatic propagation of monomer is a target of future therapeutics In neurodegenerative disease, prion-like infection of disease protein is suspected. As a route of propagation, neuron-to-neuron propagation of aggregated disease proteins has been assumed thus far. In this study, Fujita et al. describe a pathway for rapidly propagating the monomer state of disease protein via the brain lymphatic system. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:26391856
DOI:10.1016/j.celrep.2023.112962