Facial reconstruction

Search LJMU Research Online

Browse Repository | Browse E-Theses

'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich's ataxia'

Abeti, R, Parkinson, MH, Hargreaves, IP, Angelova, PR, Sandi, C, Pook, MA, Giunti, P and Abramov, AY (2016) 'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich's ataxia'. Cell Death and Disease, 7. ISSN 2041-4889

Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreichs ataxia.pdf - Published Version
Available under License Creative Commons Attribution.

Download (1MB) | Preview


Friedreich’s ataxia (FRDA) is an inherited neurodegenerative disease. The mutation consists of a GAA repeat expansion within the FXN gene, which downregulates frataxin, leading to abnormal mitochondrial iron accumulation, which may in turn cause changes in mitochondrial function. Although, many studies of FRDA patients and mouse models have been conducted in the past two decades, the role of frataxin in mitochondrial pathophysiology remains elusive. Are the mitochondrial abnormalities only a side effect of the increased accumulation of reactive iron, generating oxidative stress? Or does the progressive lack of iron-sulphur clusters (ISCs), induced by reduced frataxin, cause an inhibition of the electron transport chain complexes (CI, II and III) leading to reactive oxygen species escaping from oxidative phosphorylation reactions? To answer these crucial questions, we have characterised the mitochondrial pathophysiology of a group of disease-relevant and readily accessible neurons, cerebellar granule cells, from a validated FRDA mouse model. By using live cell imaging and biochemical techniques we were able to demonstrate that mitochondria are deregulated in neurons from the YG8R FRDA mouse model, causing a decrease in mitochondrial membrane potential (▵Ψm) due to an inhibition of Complex I, which is partially compensated by an overactivation of Complex II. This complex activity imbalance leads to ROS generation in both mitochondrial matrix and cytosol, which results in glutathione depletion and increased lipid peroxidation. Preventing this increase in lipid peroxidation, in neurons, protects against in cell death. This work describes the pathophysiological properties of the mitochondria in neurons from a FRDA mouse model and shows that lipid peroxidation could be an important target for novel therapeutic strategies in FRDA, which still lacks a cure.

Item Type: Article
Uncontrolled Keywords: 0601 Biochemistry and Cell Biology, 1112 Oncology and Carcinogenesis
Subjects: Q Science > QH Natural history > QH301 Biology
Q Science > QH Natural history > QH426 Genetics
R Medicine > RM Therapeutics. Pharmacology
Divisions: Pharmacy & Biomolecular Sciences
Publisher: Springer (part of Springer Nature)
Related URLs:
Date Deposited: 22 Sep 2020 12:03
Last Modified: 04 Sep 2021 06:38
DOI or ID number: 10.1038/cddis.2016.111
URI: https://researchonline.ljmu.ac.uk/id/eprint/13697
View Item View Item