Intracellular crowding by age-dependent neuromelanin accumulation disrupts neuronal proteostasis and triggers Parkinson disease pathology
Vila Bover, Miquel (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular)
Laguna, Ariadna (Hospital Universitari Vall d'Hebron)
Carballo-Carbajal, Iria (Hospital Universitari Vall d'Hebron)
Universitat Autònoma de Barcelona

Fecha:	2019
Resumen:	In Parkinson disease (PD), there is a preferential degeneration of neurons that contain the dark-brown cytoplasmic pigment neuromelanin, in particular dopaminergic neurons of the substantia nigra (SN), the loss of which leads to the typical motor symptoms of the disease and constitutes the cardinal pathological diagnostic criterion for PD. Neuromelanin is generally considered a byproduct of dopamine oxidative metabolism and, in humans, it is first detected in early childhood and accumulates progressively with age until occupying most of the neuronal cytoplasm, as neurons apparently lack the means to degrade or eliminate this pigment. Aging is the main risk factor for developing PD, but the molecular substrate underlying this link remains unknown. Despite the close and long-established association between neuromelanin and PD, the potential contribution of neuromelanin to PD pathogenesis has remained elusive because, in contrast to humans, common laboratory animal species, such as rodents, lack neuromelanin. To overcome this major limitation, we have recently generated the first experimental in vivo rodent model exhibiting age-dependent production and accumulation of human-like neuromelanin within PD-vulnerable dopaminergic nigral neurons, at levels up to those reached in elderly humans.
Ayudas:	Ministerio de Economía y Competitividad SAF2015-73997-JIN Agencia Estatal de Investigación SAF2016-77541-R
Derechos:	Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.
Lengua:	Anglès
Documento:	Article ; recerca ; Versió publicada
Materia:	Alpha-synuclein ; Autophagy ; Cellular trafficking ; Dopamine ; Lewy bodies ; Neurodegeneration ; Neuromelanin ; Parkinson's disease
Publicado en:	Autophagy, Vol. 15 (september 2019) , p. 2028-2030, ISSN 1554-8635

DOI: 10.1080/15548627.2019.1659621
PMID: 31480882

4 p, 1.5 MB

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