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Updated: Oct 3, 2025

High Content Screening in Neurodegenerative Diseases
Published on: January 6, 2012
Deficiency of Parkinson's Related Protein DJ-1 Alters Cdk5 Signalling and Induces Neuronal Death by Aberrant Cell
María José López-Grueso1, Carmen Alicia Padilla1,2, José Antonio Bárcena1,2
1Department of Biochemistry and Molecular Biology, University of Córdoba, 14071, Córdoba, Spain.
Abstract:
DJ-1 is a multifunctional protein involved in Parkinson disease (PD) that can act as antioxidant, molecular chaperone, protease, glyoxalase, and transcriptional regulator. However, the exact mechanism by which DJ-1 dysfunction contributes to development of Parkinson's disease remains elusive. Here, using a comparative proteomic analysis between wild-type cortical neurons and neurons lacking DJ-1 (data available via ProteomeXchange, identifier PXD029351), we show that this protein is involved in cell cycle checkpoints disruption. We detect increased amount of p-tau and α-synuclein proteins, altered phosphoinositide-3-kinase/protein kinase B (PI3K/AKT) and mitogen-activated protein kinase (MAPK) signalling pathways, and deregulation of cyclin-dependent kinase 5 (Cdk5). Cdk5 is normally involved in dendritic growth, axon formation, and the establishment of synapses, but can also contribute to cell cycle progression in pathological conditions. In addition, we observed a decrease in proteasomal activity, probably due to tau phosphorylation that can also lead to activation of mitogenic signalling pathways. Taken together, our findings indicate, for the first time, that aborted cell cycle re-entry could be at the onset of DJ-1-associated PD. Therefore, new approaches targeting cell cycle re-entry can be envisaged to improve current therapeutic strategies.
Insights
DJ-1 protein dysfunction disrupts cell cycle checkpoints, contributing to Parkinson disease (PD) pathogenesis. Targeting cell cycle re-entry may offer new therapeutic strategies for PD.
Area of Science:
- Neuroscience
- Cell Biology
- Biochemistry
Background:
- DJ-1 is a multifunctional protein implicated in Parkinson disease (PD).
- The precise mechanisms linking DJ-1 dysfunction to PD remain unclear.
- DJ-1's roles include antioxidant, chaperone, and transcriptional regulation.
Purpose of the Study:
- To elucidate the role of DJ-1 in the molecular mechanisms underlying Parkinson disease.
- To investigate the impact of DJ-1 deficiency on neuronal function and cell cycle regulation.
- To identify potential therapeutic targets for DJ-1-associated PD.
Main Methods:
- Comparative proteomic analysis of wild-type and DJ-1-deficient cortical neurons.
- Assessment of protein levels, including p-tau and α-synuclein.
- Analysis of key signaling pathways like PI3K/AKT and MAPK.
- Evaluation of proteasomal activity and cyclin-dependent kinase 5 (Cdk5) deregulation.
Main Results:
- DJ-1 deficiency leads to cell cycle checkpoint disruption in neurons.
- Increased levels of p-tau and α-synuclein were observed.
- Alterations in PI3K/AKT and MAPK signaling pathways were detected.
- Decreased proteasomal activity and Cdk5 deregulation were identified.
Conclusions:
- Aborted cell cycle re-entry is a potential key event in DJ-1-associated Parkinson disease.
- DJ-1's role in cell cycle regulation is critical for neuronal health.
- Targeting cell cycle re-entry presents a novel therapeutic avenue for PD.
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