Mitochondria are a substrate of cellular memory

Cellular memory underlies cellular identity, and thus constitutes a unifying mechanism of genetic disposition, environmental influences, and cellular adaptation. Here, we demonstrate that enduring physicochemical changes of mitochondrial networks invoked by transient stress, a phenomenon we term ‘mi...

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Veröffentlicht in:Free radical biology & medicine 2019-01, Vol.130, p.528-541
Hauptverfasser: Cheikhi, Amin, Wallace, Callen, St Croix, Claudette, Cohen, Charles, Tang, Wan-Yee, Wipf, Peter, Benos, Panagiotis V., Ambrosio, Fabrisia, Barchowsky, Aaron
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Sprache:eng
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Zusammenfassung:Cellular memory underlies cellular identity, and thus constitutes a unifying mechanism of genetic disposition, environmental influences, and cellular adaptation. Here, we demonstrate that enduring physicochemical changes of mitochondrial networks invoked by transient stress, a phenomenon we term ‘mitoengrams’, underlie the transgenerational persistence of epigenetically scripted cellular behavior. Using C2C12 myogenic stem-like cells, we show that stress memory elicited by transient, low-level arsenite exposure is stored within a self-renewing subpopulation of progeny cells in a mitochondrial-dependent fashion. Importantly, we demonstrate that erasure of mitoengrams by administration of mitochondria-targeted electron scavenger was sufficient to reset key epigenetic marks of cellular memory and redirect the identity of the mitoengram-harboring progeny cells to a non-stress-like state. Together, our findings indicate that mnemonic information emanating from mitochondria support the balance between the persistence and transience of cellular memory. [Display omitted] •Memory storage within self-renewing stem cell progeny is dependent on mitochondria.•Mitochondrial memory requires specific architectural network structure.•Inherited mitochondrial networks underlie transgenerational epigenetic change.•Mitochondrial memory within the population obeys precise statistical distribution.
ISSN:0891-5849
1873-4596
DOI:10.1016/j.freeradbiomed.2018.11.028