dc.contributor.author
Villarroya i Terrade, Joan
dc.contributor.author
Dorado, Beatriz
dc.contributor.author
Vilà, Maya R.
dc.contributor.author
García Arumí, Elena
dc.contributor.author
Domingo, Pere (Domingo Pedrol)
dc.contributor.author
Giralt i Oms, Marta
dc.contributor.author
Hirano, Michio
dc.contributor.author
Villarroya i Gombau, Francesc
dc.date.issued
2013-05-07T11:42:37Z
dc.date.issued
2013-05-07T11:42:37Z
dc.date.issued
2013-05-07T11:42:37Z
dc.identifier
https://hdl.handle.net/2445/43178
dc.description.abstract
Mammal adipose tissues require mitochondrial activity for proper development and differentiation. The components of the mitochondrial respiratory chain/oxidative phosphorylation system (OXPHOS) are encoded by both mitochondrial and nuclear genomes. The maintenance of mitochondrial DNA (mtDNA) is a key element for a functional mitochondrial oxidative activity in mammalian cells. To ascertain the role of mtDNA levels in adipose tissue, we have analyzed the alterations in white (WAT) and brown (BAT) adipose tissues in thymidine kinase 2 (Tk2) H126N knockin mice, a model of TK2 deficiency-induced mtDNA depletion. We observed respectively severe and moderate mtDNA depletion in TK2-deficient BAT and WAT, showing both tissues moderate hypotrophy and reduced fat accumulation. Electron microscopy revealed altered mitochondrial morphology in brown but not in white adipocytes from TK2-deficient mice. Although significant reduction in mtDNA-encoded transcripts was observed both in WAT and BAT, protein levels from distinct OXPHOS complexes were significantly reduced only in TK2-deficient BAT. Accordingly, the activity of cytochrome c oxidase was significantly lowered only in BAT from TK2-deficient mice. The analysis of transcripts encoding up to fourteen components of specific adipose tissue functions revealed that, in both TK2-deficient WAT and BAT, there was a consistent reduction of thermogenesis related gene expression and a severe reduction in leptin mRNA. Reduced levels of resistin mRNA were found in BAT from TK2-deficient mice. Analysis of serum indicated a dramatic reduction in circulating levels of leptin and resistin. In summary, our present study establishes that mtDNA depletion leads to a moderate impairment in mitochondrial respiratory function, especially in BAT, causes substantial alterations in WAT and BAT development, and has a profound impact in the endocrine properties of adipose tissues.
dc.format
application/pdf
dc.format
application/pdf
dc.publisher
Public Library of Science (PLoS)
dc.relation
Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0029691
dc.relation
PLoS One, 2011, vol. 6, num. 12, p. e29691
dc.relation
http://dx.doi.org/10.1371/journal.pone.0029691
dc.rights
cc-by (c) Villarroya i Terrade, Joan et al., 2011
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Bioquímica i Biomedicina Molecular)
dc.subject
ADN mitocondrial
dc.subject
Ratolins (Animals de laboratori)
dc.subject
Mitochondrial DNA
dc.subject
Mice (Laboratory animals)
dc.subject
Adipose tissues
dc.title
Thymidine kinase 2 deficiency-induced mitochondrial DNA depletion causes abnormal development of adipose tissues and adipokine levels in mice
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion