Receptor proteins that respond to nicotine may help fat cells burn energy, researchers find

The same proteins that moderate nicotine dependence in the brain may be involved in regulating metabolism by acting directly on certain types of fat cells, new research from the University of Michigan Life Sciences Institute shows.

Previous research by LSI research assistant professor Jun Wu, Ph.D., and others identified a new type of fat cells in mice and humans, in addition to the white fat cells that store energy as lipids. These thermogenic, or “beige” fat cells can be activated to burn energy through a process called thermogenesis.

To better understand what makes beige fat unique, Wu and her colleagues analyzed activated beige fat and uncovered a molecule directly linked to thermogenesis in these cells: CHRNA2 (for cholinergic receptor nicotinic alpha 2), a type of receptor that is best known for regulating nicotine dependence in brain cells.

Their findings, published May 21 in Nature Medicine, reveal that CHRNA2 functions in mouse and human beige fat cells, but not in energy-storing white fat cells — indicating that this protein plays a role in energy metabolism.

This doesn’t mean that smoking is good for you, cautions Wu, but the findings may help further explain some of the weight gain that is associated with smoking cessation. Research has shown that nicotine can suppress appetite. But by identifying how nicotine affects metabolism directly, this new study may open the door to more novel approaches to combatting the weight gain that often occurs when individuals stop smoking.

Relevance for metabolic and human health research

In research conducted in human and mouse cells and in genetically modified mice, Wu and her colleagues determined that CHRNA2 receptor protein can be activated both by nicotine and by acetylcholine molecules produced by nearby immune cells. When the CHRNA2 protein receives the acetylcholine or nicotine, it stimulates the beige fat cells to start burning energy.

 “It is really cool to discover a selective pathway for beige fat, a new cell type — and even more exciting that this is conserved in humans,” explains Wu, the study’s senior author and an assistant professor of molecular and integrative physiology at the U-M Medical School.

To further test the role of CHRNA2 in metabolism, the researchers analyzed mice that lacked the gene needed to make this protein. “And the mice definitely are metabolically worse off, compared to the control group,” Wu says.

Mice without the Chrna2 gene showed no differences from the control group when they were fed a regular diet; but when they were switched to a high-fat diet, the mice lacking the gene exhibited greater weight gain, higher body fat content, and higher levels of blood glucose and insulin — indicators of diabetes.

“Beige fat is very important in regulating whole-body metabolic health,” Wu explains. “Our results in mice show that if you lose even one aspect of this regulation — not the whole cell function, but just one part of its function — you will have a compromised response to metabolic challenges.”

Wu believes that understanding the specific CHRNA2 signaling pathway in beige fat also opens a new avenue for identifying druggable targets to treat obesity and metabolic syndrome.

“This pathway is important from a basic research standpoint, but it also has relevance for metabolic and human health research,” she says. “The more we can narrow down a precise pathway for activating beige fat, the more likely we are to find an effective therapy for metabolic health that does not carry harmful side effects.”

share this
Top Image: Illustration of thermogenesis in mice beige fat cells in response to acetylcholine stimulation.

Disclosure & Authorship

This research was supported by the Human Frontier Science Program, the Edward Mallinckrodt Jr. Foundation, the American Diabetes Association, the American Heart Association and the National Institutes of Health.

 Study authors were: Heejin Jun, Hui Yu, Eric Perkey, Dong-il Kim, Margo P. Emont, Alexander G. Zestos, Jung-Sun Cho Robert T. Kennedy, Ivan Maillard, X.Z. Shawn Xu and Jun Wu, all of U-M; Jianke Gong of U-M and Huazhong University of Science and Technology, China; Juan Jiang of U-M and Central South University, China; Xiaona Qiao of U-M and Fudan University, China; and Jiangfeng Liu of Huazhong University of Science and Technology, China.

Go to Article