| Literature DB >> 28867657 |
Daniela Weiland1, Bent Brachvogel2, Hue-Tran Hornig-Do1, Johannes F G Neuhaus1, Tatjana Holzer3, Desmond J Tobin4, Carien M Niessen5, Rudolf J Wiesner6, Olivier R Baris1.
Abstract
Accumulation of large-scale mitochondrial DNA (mtDNA) deletions and chronic, subclinical inflammation are concomitant during skin aging, thus raising the question of a causal link. To approach this, we generated mice expressing a mutant mitochondrial helicase (K320E-TWINKLE) in the epidermis to accelerate the accumulation of mtDNA deletions in this skin compartment. Mice displayed low amounts of large-scale deletions and a dramatic depletion of mtDNA in the epidermis and showed macroscopic signs of severe skin inflammation. The mtDNA alterations led to an imbalanced stoichiometry of mitochondrial respiratory chain complexes, inducing a unique combination of cytokine expression, causing a severe inflammatory phenotype, with massive immune cell infiltrates already before birth. Altogether, these data unraveled a previously unknown link between an imbalanced stoichiometry of the mitochondrial respiratory chain complexes and skin inflammation and suggest that severe respiratory chain dysfunction, as observed in few cells leading to a mosaic in aged tissues, might be involved in the development of chronic subclinical inflammation.Entities:
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Year: 2017 PMID: 28867657 DOI: 10.1016/j.jid.2017.08.019
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551