Brown fat cells can burn fat to generate heat. University of Bonn researchers have discovered a new method to measure the activity of brown fat cells in humans and mice. The researchers showed that microRNA-92a can be used as an indirect measure for the activity of energy consuming brown fat cells. They showed that a small blood sample was sufficient. Results were published in Nature Communications, a well-known scientific journal.
People who want to lose weight often encounter boundaries: No matter what diet they try, the pounds won’t drop. Being overweight and obese can have severe health consequences, and has shown to increase a person’s chance of developing type-2-diabetes or cardiovascular diseases.
Prof. Dr. Alexander Pfeifer, head of the Institute of Pharmacology and Toxicology of the University Bonn, has been investigating brown fat in mice for years. He has been trying to understand how to turn unfavored white fat cells into energy-consuming brown ones. Brown fat cells can “burn” excessive energy by producing heat instead of storing fat. Prof. Pfeifer´s team has discovered multiple signaling cascades and possible drug targets in rodents that are responsible for the conversion from white-energy-storing to brown-energy-consuming fat cells. However, for these basic research findings to become human treatment, clinical trials are needed to discover which drug is most efficient in activating brown fat and has few or no side effects. These clinical trials are hampered because so far no method is on the market to measure the brown fat activity without health risk and expensive equipment.
Brown fat cells release miR-92a into the circulation
In collaboration with the University Maastricht (Netherlands), Turku (Finland) and the University Hospital Hamburg-Eppendorf, researchers in Prof. Pfeifer’s group found an easy way to display brown fat activity: miR-92a. miRNAs are known to be responsible for the regulation of genes. The researchers showed for the first time that brown fat cells deliver these microRNAs into the blood by packaging into so-called exosomes, which “can be seen as little packages that are delivered by the brown fat cells through the circulation.” However, Prof. Pfeiffer said, “to whom the packages are delivered is yet unknown.”
Many miRNAs were investigated during the investigation. miR-92a is present in human and mice and importantly, this microRNA is related to brown fat activity. Whenever miR-92a is low in circulation, people can burn a lot of energy with brown fat. To prove the connection in humans, scientists tested 41 participants from Finland and the Netherlands. “We found a significant relation between brown fat activity and miR-92a that needs to be proven in larger cohorts,” said co-first author Joschka Johannes Buyel, a PhD student in Prof. Pfeifer´s lab. Measuring miR-92a would allow for a much more accurate measure of the brown fat activity.
Biomarker might enable for efficacy testing of new pharmaceuticals
“miR-92a seems to be a promising biomarker to test new drugs in the field of weight reduction or transition from white-to-brown fat in humans; this promising biomarker should be tested in larger cohorts” said Prof. Pfeifer. This new method might enable advances in obesity research and related fields.
Exosomal microRNA miR-92a concentration in serum reflects human brown fat activity.Yong Chen, Joschka J. Buyel, Mark J. W. Hanssen, Franziska Siegel, Ruping Pan, Jennifer Naumann, Michael Schell, Anouk van der Lans, Christian Schlein, Holger Froehlich, Joerg Heeren, Kirsi A. Virtanen, Wouter van Marken Lichtenbelt & Alexander Pfeifer. Nature Communications. DOI:10.1038/ncomms11420. Published online 27 April 2016.