Monoamine oxidase-A promotes protective autophagy in human SH-SY5Y neuroblastoma cells through Bcl-2 phosphorylation

Ugun-Klusek, A. ORCID: 0000-0002-0199-0275, Theodosi, T.S., Fitzgerald, J.C., Burté, F., Ufer, C., Boocock, D.J. ORCID: 0000-0002-7333-3549, Yu-Wai-Man, P., Bedford, L. and Billett, E.E. ORCID: 0000-0001-8245-6519, 2019. Monoamine oxidase-A promotes protective autophagy in human SH-SY5Y neuroblastoma cells through Bcl-2 phosphorylation. Redox Biology, 20, pp. 167-181. ISSN 2213-2317

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Abstract

Monoamine oxidases (MAOs) are located on the outer mitochondrial membrane and are drug targets for the treatment of neurological disorders. MAOs control the levels of neurotransmitters in the brain via oxidative deamination and contribute to reactive oxygen species (ROS) generation through their catalytic by-product H2O2. Increased ROS levels may modulate mitochondrial function and mitochondrial dysfunction is implicated in a vast array of disorders. However, the downstream effects of MAO-A mediated ROS production in a neuronal model has not been previously investigated.

In this study, using MAO-A overexpressing neuroblastoma cells, we demonstrate that higher levels of MAO-A protein/activity results in increased basal ROS levels with associated increase in protein oxidation. Increased MAO-A levels result in increased Lysine-63 linked ubiquitination of mitochondrial proteins and promotes autophagy through Bcl-2 phosphorylation. Furthermore, ROS generated locally on the mitochondrial outer membrane by MAO-A promotes phosphorylation of dynamin-1-like protein, leading to mitochondrial fragmentation and clearance without complete loss of mitochondrial membrane potential. Cellular ATP levels are maintained following MAO-A overexpression and complex IV activity/protein levels increased, revealing a close relationship between MAO-A levels and mitochondrial function. Finally, the downstream effects of increased MAO-A levels are dependent on the availability of amine substrates and in the presence of exogenous substrate, cell viability is dramatically reduced.

This study shows for the first time that MAO-A generated ROS is involved in quality control signalling, and increase in MAO-A protein levels leads to a protective cellular response in order to mediate removal of damaged macromolecules/organelles, but substrate availability may ultimately determine cell fate. The latter is particularly important in conditions such as Parkinson's disease, where a dopamine precursor is used to treat disease symptoms and highlights that the fate of MAO-A containing dopaminergic neurons may depend on both MAO-A levels and catecholamine substrate availability.

Item Type: Journal article
Publication Title: Redox Biology
Creators: Ugun-Klusek, A., Theodosi, T.S., Fitzgerald, J.C., Burté, F., Ufer, C., Boocock, D.J., Yu-Wai-Man, P., Bedford, L. and Billett, E.E.
Publisher: Elsevier
Date: January 2019
Volume: 20
ISSN: 2213-2317
Identifiers:
NumberType
10.1016/j.redox.2018.10.003DOI
S2213231718307341Publisher Item Identifier
Divisions: Schools > School of Science and Technology
Depositing User: Linda Sullivan
Date Added: 17 Oct 2018 09:38
Last Modified: 18 Oct 2018 08:13
URI: http://irep.ntu.ac.uk/id/eprint/34683

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