ADCK2 haploinsuciency reduces mitochondrial lipid oxidation and causes myopathy associated with CoQ deficiency
dc.contributor.author | Matté, Cristiane | pt_BR |
dc.contributor.author | Vázquez-Fonseca, Luis | pt_BR |
dc.contributor.author | Navas, Plácido | pt_BR |
dc.date.accessioned | 2020-11-20T04:15:33Z | pt_BR |
dc.date.issued | 2019 | pt_BR |
dc.identifier.issn | 2077-0383 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/10183/215302 | pt_BR |
dc.description.abstract | Fatty acids and glucose are the main bioenergetic substrates in mammals. Impairment of mitochondrial fatty acid oxidation causes mitochondrial myopathy leading to decreased physical performance. Here, we report that haploinsu ciency of ADCK2, a member of the aarF domain-containing mitochondrial protein kinase family, in human is associated with liver dysfunction and severe mitochondrial myopathy with lipid droplets in skeletal muscle. In order to better understand the etiology of this rare disorder, we generated a heterozygous Adck2 knockout mouse model to perform in vivo and cellular studies using integrated analysis of physiological and omics data (transcriptomics–metabolomics). The data showed that Adck2+/ mice exhibited impaired fatty acid oxidation, liver dysfunction, and mitochondrial myopathy in skeletal muscle resulting in lower physical performance. Significant decrease in Coenzyme Q (CoQ) biosynthesis was observed and supplementation with CoQ partially rescued the phenotype both in the human subject and mouse model. These results indicate that ADCK2 is involved in organismal fatty acid metabolism and in CoQ biosynthesis in skeletal muscle. We propose that patients with isolated myopathies and myopathies involving lipid accumulation be tested for possible ADCK2 defect as they are likely to be responsive to CoQ supplementation. | en |
dc.format.mimetype | application/pdf | pt_BR |
dc.language.iso | eng | pt_BR |
dc.relation.ispartof | Journal of clinical medicine. Basel. Vol. 8, no. 9 (Sep. 2019), 1374, 22 p. | pt_BR |
dc.rights | Open Access | en |
dc.subject | Ácidos graxos | pt_BR |
dc.subject | Coenzyme Q deficiency | en |
dc.subject | Mitochondrial disease | en |
dc.subject | Glucose | pt_BR |
dc.subject | Ubiquinona | pt_BR |
dc.subject | Respiratory chain | en |
dc.subject | Fatty acids | en |
dc.subject | Miopatias mitocondriais | pt_BR |
dc.subject | Proteínas mitocondriais | pt_BR |
dc.subject | Myopathy | en |
dc.subject | aarF domain-containing mitochondrial protein kinase 2(ADCK2) | en |
dc.title | ADCK2 haploinsuciency reduces mitochondrial lipid oxidation and causes myopathy associated with CoQ deficiency | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dc.identifier.nrb | 001116275 | pt_BR |
dc.type.origin | Estrangeiro | pt_BR |
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