Author(s):
Almeida, Filipa ; Ferreira, Ildete L. ; Naia, Luana ; Marinho, Daniela ; Vilaça-Ferreira, Ana Catarina ; Costa, Marta D. ; Duarte-Silva, Sara ; Maciel, Patrícia ; Rego, A. Cristina
Date: 2023
Persistent ID: https://hdl.handle.net/10316/111824
Origin: Estudo Geral - Universidade de Coimbra
Subject(s): Machado–Joseph disease; oxygen consumption; calciumhandling; mitochondrial membrane potential; mitochondrial transcription; Mice; Animals; Cytochromes c; Nerve Tissue Proteins; Repressor Proteins; Mice, Transgenic; Mitochondria; Disease Models, Animal; Machado-Joseph Disease
Description
Mitochondrial dysfunction has been described in many neurodegenerative disorders; however, there is less information regarding mitochondrial deficits in Machado-Joseph disease (MJD), a polyglutamine (polyQ) disorder caused by CAG repeat expansion in the ATXN3 gene. In the present study, we characterized the changes in mitochondrial function and biogenesis markers in two MJD models, CMVMJD135 (MJD135) transgenic mice at a fully established phenotype stage and tetracycline-regulated PC6-3 Q108 cell line expressing mutant ataxin-3 (mATXN3). We detected mATXN3 in the mitochondrial fractions of PC6-3 Q108 cells, suggesting the interaction of expanded ATXN3 with the organelle. Interestingly, in both the cerebella of the MJD135 mouse model and in PC6-3 Q108 cells, we found decreased mitochondrial respiration, ATP production and mitochondrial membrane potential, strongly suggesting mitochondrial dysfunction in MJD. Also, in PC6-3 Q108 cells, an additional enhanced glycolytic flux was observed. Supporting the functional deficits observed in MJD mitochondria, MJD135 mouse cerebellum and PC6-3 Q108 cells showed reduced cytochrome c mRNA and protein levels. Overall, our findings show compromised mitochondrial function associated with decreased cytochrome c levels in both cell and animal models of MJD.
