Mitochondria facilitate neuronal differentiation by metabolising nuclear-encoded RNA

Autor: Filip Vujovic, Mary Simonian, William E. Hughes, Claire E. Shepherd, Neil Hunter, Ramin M. Farahani
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: Cell Communication and Signaling, Vol 22, Iss 1, Pp 1-19 (2024)
Druh dokumentu: article
ISSN: 1478-811X
DOI: 10.1186/s12964-024-01825-1
Popis: Abstract Mitochondrial activity directs neuronal differentiation dynamics during brain development. In this context, the long-established metabolic coupling of mitochondria and the eukaryotic host falls short of a satisfactory mechanistic explanation, hinting at an undisclosed facet of mitochondrial function. Here, we reveal an RNA-based inter-organellar communication mode that complements metabolic coupling of host-mitochondria and underpins neuronal differentiation. We show that within minutes of exposure to differentiation cues and activation of the electron transport chain, the mitochondrial outer membrane transiently fuses with the nuclear membrane of neural progenitors, leading to efflux of nuclear-encoded RNAs (neRNA) into the positively charged mitochondrial intermembrane space. Subsequent degradation of mitochondrial neRNAs by Polynucleotide phosphorylase 1 (PNPase) located in the intermembrane space curbs the transcriptomic memory of progenitor cells. Further, acquisition of neRNA by mitochondria leads to a collapse of proton motive force, suppression of ATP production, and a resultant amplification of autophagic flux that attenuates proteomic memory. Collectively, these events force the progenitor cells towards a “tipping point” characterised by emergence of a competing neuronal differentiation program. It appears that neuronal differentiation is a consequence of reprogrammed coupling of metabolomic and transcriptomic landscapes of progenitor cells, with mitochondria emerging as key “reprogrammers” that operate by acquiring and metabolising neRNAs. However, the documented role of mitochondria as “reprogrammers” of differentiation remains to be validated in other neuronal lineages and in vivo.
Databáze: Directory of Open Access Journals
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