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Cell Death & Differentiation 22, 1957-1969 (December 2015) | doi:10.1038/cdd.2015.43
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M J Son
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! v8 Z5 v4 o6 g% J1 `$ \Mitofusins deficiency elicits mitochondrial metabolic reprogramming to pluripotency
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  T2 t% Q, v. x( E. l! VM J Son, Y Kwon, M-Y Son, B Seol, H-S Choi, S-W Ryu, C Choi and Y S Cho. k9 U( `9 ?) P6 m0 t
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Abstract
/ h( H" r, d# t+ N2 F' ACell reprogramming technology has allowed the in vitro control of cell fate transition, thus allowing for the generation of highly desired cell types to recapitulate in vivo developmental processes and architectures. However, the precise molecular mechanisms underlying the reprogramming process remain to be defined. Here, we show that depleting p53 and p21, which are barriers to reprogramming, yields a high reprogramming efficiency. Deletion of these factors results in a distinct mitochondrial background with low expression of oxidative phosphorylation subunits and mitochondrial fusion proteins, including mitofusin 1 and 2 (Mfn1/2). Importantly, Mfn1/2 depletion reciprocally inhibits the p53-p21 pathway and promotes both the conversion of somatic cells to a pluripotent state and the maintenance of pluripotency. Mfn1/2 depletion facilitates the glycolytic metabolic transition through the activation of the Ras-Raf and hypoxia-inducible factor 1α (HIF1α) signaling at an early stage of reprogramming. HIF1α is required for increased glycolysis and reprogramming by Mfn1/2 depletion. Taken together, these results demonstrate that Mfn1/2 constitutes a new barrier to reprogramming, and that Mfn1/2 ablation facilitates the induction of pluripotency through the restructuring of mitochondrial dynamics and bioenergetics.

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cartoonyang

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