Kawalec 2015 PLoS One

From Bioblast
Publications in the MiPMap
Kawalec M, BoratyΕ„ska-JasiΕ„ska A, BerΔ™sewicz M, Dymkowska D, ZabΕ‚ocki K, ZabΕ‚ocka B (2015) Mitofusin 2 deficiency affects energy metabolism and mitochondrial biogenesis in MEF cells. PLoS One 10:e0134162.

Β» PMID: 26230519 Open Access

Kawalec M, Boratynska-Jasinska A, Beresewicz M, Dymkowska D, Zablocki K, Zablocka B (2015) PLoS One

Abstract: Mitofusin 2 (Mfn2), mitochondrial outer membrane protein which is involved in rearrangement of these organelles, was first described in pathology of hypertension and diabetes, and more recently much attention is paid to its functions in Charcot-Marie-Tooth type 2A neuropathy (CMT2A). Here, cellular energy metabolism was investigated in mouse embryonic fibroblasts (MEF) differing in the presence of the Mfn2 gene; control (MEFwt) and with Mfn2 gene depleted MEFMfn2-/-. These two cell lines were compared in terms of various parameters characterizing mitochondrial bioenergetics. Here, we have shown that relative rate of proliferation of MEFMfn2-/- cells versus control fibroblasts depend on serum supplementation of the growth media. Moreover, MEFMfn2-/- cells exhibited significantly increased respiration rate in comparison to MEFwt, regardless of serum supplementation of the medium. This effect was correlated with increased level of mitochondrial markers (TOM20 and NAO) as well as mitochondrial transcription factor A (TFAM) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1Ξ±) protein levels and unchanged total ATP content. Interestingly, mitochondrial DNA content in MEFMfn2-/- cells was not reduced. Fundamentally, these results are in contrast to a commonly accepted belief that mitofusin 2 deficiency inevitably results in debilitation of mitochondrial energy metabolism. However, we suggest a balance between negative metabolic consequences of mitofusin 2 deficiency and adaptive processes exemplified by increased level of PGC-1Ξ± and TFAM transcription factor which prevent an excessive depletion of mtDNA and severe impairment of cell metabolism. β€’ Keywords: Mouse embryonic fibroblast

β€’ O2k-Network Lab: PL Warsaw Zablocki K

Labels: MiParea: Respiration, mt-Structure;fission;fusion, mt-Membrane, mtDNA;mt-genetics, Genetic knockout;overexpression, Comparative MiP;environmental MiP 

Organism: Mouse  Tissue;cell: Fibroblast  Preparation: Permeabilized cells 

Coupling state: LEAK, ROUTINE, ET 

HRR: Oxygraph-2k 

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