Recent years have brought several promising approaches to treat different kinds of #mitochondrial dysfunction, and increasing #mtDNA amount has been proposed to be beneficial for certain defects.
In contrast, our previous findings suggested that increased #mtDNA replication is actually the culprit of the "mitochondrial" premature #aging of the mtDNA mutator mouse (carrying a mutagenic mtDNA polymerase). Check out the paper for more details! doi.org/10.1038/s42255…
So, we wondered 🤔 whether boosting #mtDNA replication (by overexpressing #Twinkle helicase) in mutators could be beneficial by increasing #mtDNA amount, or if it would instead accelerate the premature #aging phenotype...
The answer: Neither.
Surprisingly, the overactive mtDNA replisome caused instead severe #mitochondrial#cardiomyopathy and growth defect shortly after birth.
Although affected, #mtDNA integrity did not seem to be the main perpetrator. Instead, the replisome stress triggered a signaling cascade and disrupted the adaptation of cardiac #metabolism to oxidative postnatal life
This cascade included the synergistic and dose-responsive interaction between the mitochondrial integrated stress response #ISRmt and key players in the #ferroptosis pathway
Our findings indicate the need for caution when it comes to therapeutic approaches modulating #mtDNA amount, highlighting the importance of #mtDNA replication homeostasis in early #cardiac 🫀 life.
The interesting link between cardiac maturation, #mtDNA replication, and the perinatal induction of #ISRmt + #ferroptosis hopefully also brings us a little closer to understanding these severe and complex defects. biorxiv.org/content/10.110…