Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/176483
Title: Physiopathological bases of the disease caused by HACE1 mutations: alterations in autophagy, mitophagy and oxidative stress response
Author: Ugarteburu, Olatz
Sánchez-Vilés, Marta
Ramos, Julio
Barcos Rodríguez, Tamara
Garrabou Tornos, Glòria
García Villoria, Judit
Ribes Rubió, Maria Antònia
Tort, Frederic
Keywords: Mutació (Biologia)
Autofàgia
Mitocondris
Mutation (Biology)
Autophagy
Mitochondria
Issue Date: 26-Mar-2020
Publisher: MDPI
Abstract: Recessive HACE1 mutations are associated with a severe neurodevelopmental disorder (OMIM: 616756). However, the physiopathologycal bases of the disease are yet to be completely clarified. Whole-exome sequencing identified homozygous HACE1 mutations (c.240C>A, p.Cys80Ter) in a patient with brain atrophy, psychomotor retardation and 3-methylglutaconic aciduria, a biomarker of mitochondrial dysfunction. To elucidate the pathomechanisms underlying HACE1 deficiency, a comprehensive molecular analysis was performed in patient fibroblasts. Western Blot demonstrated the deleterious effect of the mutation, as the complete absence of HACE1 protein was observed. Immunofluorescence studies showed an increased number of LC3 puncta together with the normal initiation of the autophagic cascade, indicating a reduction in the autophagic flux. Oxidative stress response was also impaired in HACE1 fibroblasts, as shown by the reduced NQO1 and Hmox1 mRNA levels observed in H2O2-treated cells. High levels of lipid peroxidation, consistent with accumulated oxidative damage, were also detected. Although the patient phenotype could resemble a mitochondrial defect, the analysis of the mitochondrial function showed no major abnormalities. However, an important increase in mitochondrial oxidative stress markers and a strong reduction in the mitophagic flux were observed, suggesting that the recycling of damaged mitochondria might be targeted in HACE1 cells. In summary, we demonstrate for the first time that the impairment of autophagy, mitophagy and oxidative damage response might be involved in the pathogenesis of HACE1 deficiency.
Note: Reproducció del document publicat a: https://doi.org/10.3390/jcm9040913
It is part of: Journal of Clinical Medicine, 2020, vol. 9, num. 4, p. 913
URI: http://hdl.handle.net/2445/176483
Related resource: https://doi.org/10.3390/jcm9040913
ISSN: 2077-0383
Appears in Collections:Articles publicats en revistes (Medicina)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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