Selective autophagy as a potential therapeutic target for neurodegenerative disorders

A Scrivo, M Bourdenx, O Pampliega… - The Lancet …, 2018 - thelancet.com
Cells rely on surveillance systems such as autophagy to handle protein alterations and
organelle damage. Dysfunctional autophagy, an evolutionarily conserved cellular …

Parkinson disease from mendelian forms to genetic susceptibility: new molecular insights into the neurodegeneration process

A Karimi-Moghadam, S Charsouei, B Bell… - Cellular and molecular …, 2018 - Springer
Parkinson disease (PD) is known as a common progressive neurodegenerative disease
which is clinically diagnosed by the manifestation of numerous motor and nonmotor …

Alternative mitochondrial quality control mediated by extracellular release

CJ Choong, T Okuno, K Ikenaka, K Baba… - Autophagy, 2021 - Taylor & Francis
Mitochondrial quality control, which is crucial for maintaining cellular homeostasis, has been
considered to be achieved exclusively through mitophagy. Here we report an alternative …

P arkin deficiency modulates NLRP 3 inflammasome activation by attenuating an A 20‐dependent negative feedback loop

F Mouton‐Liger, T Rosazza, J Sepulveda‐Diaz… - Glia, 2018 - Wiley Online Library
Neuroinflammation and mitochondrial dysfunction, key mechanisms in the pathogenesis of
Parkinson's disease (PD), are usually explored independently. Loss‐of‐function mutations …

PARIS induced defects in mitochondrial biogenesis drive dopamine neuron loss under conditions of parkin or PINK1 deficiency

SK Pirooznia, C Yuan, MR Khan… - Molecular …, 2020 - Springer
Background Mutations in PINK1 and parkin cause autosomal recessive Parkinson's disease
(PD). Evidence placing PINK1 and parkin in common pathways regulating multiple aspects …

The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations

CA Gautier, Z Erpapazoglou… - Human molecular …, 2016 - academic.oup.com
Mutations in PARK2, encoding the E3 ubiquitin protein ligase Parkin, are a common cause
of autosomal recessive Parkinson's disease (PD). Loss of PARK2 function compromises …

Defects in mitochondrial biogenesis drive mitochondrial alterations in PARKIN-deficient human dopamine neurons

M Kumar, J Acevedo-Cintrón, A Jhaldiyal, H Wang… - Stem Cell Reports, 2020 - cell.com
Mutations and loss of activity in PARKIN, an E3 ubiquitin ligase, play a role in the
pathogenesis of Parkinson's disease (PD). PARKIN regulates many aspects of mitochondrial …

ER lipid defects in neuropeptidergic neurons impair sleep patterns in Parkinson's disease

JS Valadas, G Esposito, D Vandekerkhove… - Neuron, 2018 - cell.com
Parkinson's disease patients report disturbed sleep patterns long before motor dysfunction.
Here, in parkin and pink1 models, we identify circadian rhythm and sleep pattern defects …

Age-associated insolubility of parkin in human midbrain is linked to redox balance and sequestration of reactive dopamine metabolites

JM Tokarew, DN El-Kodsi, NA Lengacher, TK Fehr… - Acta …, 2021 - Springer
The mechanisms by which parkin protects the adult human brain from Parkinson disease
remain incompletely understood. We hypothesized that parkin cysteines participate in redox …

Autophagy, its mechanisms and regulation: implications in neurodegenerative diseases

M Moloudizargari, MH Asghari, E Ghobadi… - Ageing research …, 2017 - Elsevier
Autophagy is a major regulatory cellular mechanism which gives the cell an ability to cope
with some of the destructive events that normally occur within a metabolically living cell. This …