Journal
JOURNAL OF CELLULAR PHYSIOLOGY
Volume 236, Issue 7, Pages 5339-5351Publisher
WILEY
DOI: 10.1002/jcp.30240
Keywords
adiponectin; FOXO1; iron overload; metabolic syndrome; ROS; skeletal muscle
Categories
Funding
- Canadian Institutes of Health Research
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Iron overload induces adiponectin resistance in skeletal muscle cells of metabolic syndrome patients, possibly through the ROS/FOXO1/AdipoR1 axis. This cellular mechanism may contribute to the reduced adiponectin levels and signaling in response to IO.
Iron overload (IO) is a common yet underappreciated finding in metabolic syndrome (MetS) patients. With the prevalence of MetS continuing to rise, it is imperative to further elucidate cellular mechanisms leading to metabolic dysfunction. Adiponectin has many beneficial effects and is a therapeutic target for the treatment of MetS and cardiovascular diseases. IO positively correlates with reduced circulating adiponectin levels yet the impact of IO on adiponectin action is unknown. Here, we established a model of IO in L6 skeletal muscle cells and found that IO-induced adiponectin resistance. This was shown via reduced p38 mitogen-activated protein kinase phosphorylation in response to the small molecule adiponectin receptor (AdipoR) agonist, AdipoRon, in presence of IO. This correlated with reduced messenger RNA and protein levels of AdipoR1 and its facilitative signaling binding partner, APPL1. IO caused phosphorylation, nuclear extrusion, and thus inhibition of FOXO1, a known transcription factor regulating AdipoR1 expression. The antioxidant N-acetyl cystine attenuated the production of reactive oxygen species (ROS) by IO, and blunted its effect on FOXO1 phosphorylation and removal from the nucleus, as well as subsequent adiponectin resistance. In conclusion, our study identifies a ROS/FOXO1/AdipoR1 axis as a cause of skeletal muscle adiponectin resistance in response to IO. This new knowledge provides insight into a cellular mechanism with potential relevance to disease pathophysiology in MetS patients with IO.
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