4.7 Article

Characterization of the metabolic effects of irisin on skeletal muscle in vitro

Journal

DIABETES OBESITY & METABOLISM
Volume 16, Issue 8, Pages 711-718

Publisher

WILEY
DOI: 10.1111/dom.12268

Keywords

fibronectin type III domain containing protein 5 (FNDC5); mitochondrial uncoupling protein 3 (UCP3); myokine; peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1 alpha)

Funding

  1. New Mexico Research Grant
  2. University of New Mexico Summer Office of Graduate Studies Research, Project and Travel Grant
  3. University of New Mexico
  4. Cancer Center Fluorescence Microscopy Shared Resource

Ask authors/readers for more resources

Aims: This work explored the effects of irisin on metabolism, gene expression and mitochondrial content in cultured myocytes. Methods: C2C12 myocytes were treated with various concentrations of irisin for various durations. Glycolysis and oxidative metabolism were quantified by measurement of extracellular acidification and oxygen consumption, respectively. Metabolic gene expression was measured by quantitative real-time polymerase chain reaction (qRT-PCR) and mitochondrial content was assessed by flow cytometry and confocal microscopy. Results: Cells treated with irisin exhibited significantly increased oxidative metabolism. Irisin treatment also significantly increased mitochondrial uncoupling at various doses and durations. Lastly, treatment with irisin also significantly elevated metabolic gene expression including peroxisome proliferator-activated receptor. coactivator-1 alpha (PGC-1 alpha), nuclear respiratory factor 1 (NRF1), mitochondrial transcription factor A (TFAM), irisin, glucose transporter 4 (GLUT4) and mitochondrial uncoupling protein 3 (UCP3) leading to increased mitochondrial biogenesis. Conclusions: Our observations are the first to document increased metabolism in myocytes through irisin-mediated induction of mitochondrial biogenesis and uncoupling with corresponding gene expression. These observations support the need for further investigation into the therapeutic and pharmacological effects of irisin, as well as development of irisin-based therapy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available