Skip to Content
Merck
  • Muscle mitohormesis promotes cellular survival via serine/glycine pathway flux.

Muscle mitohormesis promotes cellular survival via serine/glycine pathway flux.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology (2014-12-11)
Mario Ost, Susanne Keipert, Evert M van Schothorst, Verena Donner, Inge van der Stelt, Anna P Kipp, Klaus-Jürgen Petzke, Mariona Jove, Reinald Pamplona, Manuel Portero-Otin, Jaap Keijer, Susanne Klaus
ABSTRACT

Recent studies on mouse and human skeletal muscle (SM) demonstrated the important link between mitochondrial function and the cellular metabolic adaptation. To identify key compensatory molecular mechanisms in response to chronic mitochondrial distress, we analyzed mice with ectopic SM respiratory uncoupling in uncoupling protein 1 transgenic (UCP1-TG) mice as model of muscle-specific compromised mitochondrial function. Here we describe a detailed metabolic reprogramming profile associated with mitochondrial perturbations in SM, triggering an increased protein turnover and amino acid metabolism with induced biosynthetic serine/1-carbon/glycine pathway and the longevity-promoting polyamine spermidine as well as the trans-sulfuration pathway. This is related to an induction of NADPH-generating pathways and glutathione metabolism as an adaptive mitohormetic response and defense against increased oxidative stress. Strikingly, consistent muscle retrograde signaling profiles were observed in acute stress states such as muscle cell starvation and lipid overload, muscle regeneration, and heart muscle inflammation, but not in response to exercise. We provide conclusive evidence for a key compensatory stress-signaling network that preserves cellular function, oxidative stress tolerance, and survival during conditions of increased SM mitochondrial distress, a metabolic reprogramming profile so far only demonstrated for cancer cells and heart muscle.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
L-Threonine, from non-animal source, meets EP, JP, USP testing specifications, suitable for cell culture, 99.0-101.0%
Sigma-Aldrich
L-Threonine, reagent grade, ≥98% (HPLC)
SAFC
L-Threonine
Sigma-Aldrich
L-Threonine, BioXtra, ≥99.5% (NT)
Sigma-Aldrich
DL-Methionine, 99%, FCC, FG
Sigma-Aldrich
Cystathionine, ≥90% (HPLC)
Sigma-Aldrich
DL-Leucine, ≥99% (HPLC)
Sigma-Aldrich
L-Glutathione reduced, ≥98.0%
Sigma-Aldrich
L-Glutathione reduced, BioXtra, ≥98.0%
Sigma-Aldrich
DL-Methionine, BioReagent, suitable for cell culture, suitable for insect cell culture, ≥99%
Sigma-Aldrich
DL-Methionine, ≥99%
Sigma-Aldrich
L-Glutathione reduced, suitable for cell culture, BioReagent, ≥98.0%, powder
Sigma-Aldrich
Anti-α-Tubulin antibody, Mouse monoclonal, clone B-5-1-2, purified from hybridoma cell culture