Researchers have identified the location, genetic expression and function of human brown adipose tissue (BAT), or brown fat, and have also generated new BAT cells. These findings, reported in the April 2013 issue of Nature Medicine, may contribute to further study of BAT’s role in human metabolism and developing treatments that use BAT to promote weight loss. (Watch video describing research.)
Two types of adipose (fat) tissue—brown and white—are found in mammals. Unlike the more predominant white adipose tissue (WAT) which stores fat, BAT burns fat to produce heat when the body is exposed to cold and also plays a role in energy metabolism. Human studies have shown that greater quantities of BAT are associated with lower body weight. BAT has been a major focus of study among scientists and pharmaceutical companies based on its potential as a treatment to combat obesity, a major risk factor for type 2 diabetes.
Studies in mice have identified two types of BAT: constitutive or “classical” BAT which is present at birth and persists throughout life and recruitable or “beige” BAT which can be produced from within white fat in response to metabolic conditions. These two types of BAT may also be present in humans.
Previous studies have identified the human neck as a primary location for BAT deposits. To determine the precise locations of these deposits, Joslin scientists obtained fat samples from five neck regions of patients undergoing neck surgery. Analysis of the samples showed that BAT was most abundant in deep regions of the neck, near the carotid sheath and longus colli muscles. These samples expressed the BAT marker gene, uncoupling protein 1 (UCP1), which is involved in heat generation.
“BAT is most abundant in the deep locations of the neck, close to the sympathetic chain and the carotid arteries, where it likely helps to warm blood and raise body temperature. Now that we know where brown fat is, we can easily collect more cells for further study,” says Aaron Cypess, senior author and HMS assistant professor of medicine at Joslin Diabetes Center.
In analyzing genetic expression in superficial and deep human neck fat tissue, the fat from deep locations was found to most closely resemble cells from constitutive mouse BAT, the kind already known to consume large quantities of glucose and fat.
The scientists compared the oxygen consumption rate (OCR), which demonstrates the capacity to burn calories, of human BAT cells to mouse constitutive BAT cells and human WAT. This is the first study to directly measure brown fat cells’ OCR at baseline. The OCR of the human BAT cells from the deep location next to the longus colli was nearly 50 percent of the mouse BAT cells; in contrast, the OCR of human WAT was only one-hundredth of the OCR found in the most active human BAT from the longus colli depot.
“We show that at baseline, brown fat cells have a great capacity to burn fat,” said Cypess.
The scientists were able to grow new functional brown fat cells (adipocytes) by differentiating precursor cells (preadipocytes) derived from both superficial and deep human neck fat tissue. When stimulated, the cells expressed the same genes as naturally occurring brown fat cells. This is the first report of the production of brown fat cells (adipogenesis) that can respond to pharmacological stimulation.
The researchers are following up on this study to learn more about the functions of BAT, including how it affects energy balance and uses glucose. Having the ability to produce brown fat cells outside the body will make it possible to develop drugs and other potential treatments that increase BAT activity to combat obesity.
“Our research has significant practical applications. If we stimulate the growth of brown fat in people, it may burn their white fat and help them lose weight, which lessens insulin resistance and improves diabetes,” said Cypess.
This study was funded by grants from the National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health (grants DK087317, DK081604, DK046200, DK077097, P30 DK036836 and KL2 RR025757), Harvard University and its affiliated academic health care centers, the Harvard Stem Cell Institute, and Eli Lilly Foundation.
Adapted from Joslin Diabetes Center news release.
Related research papers:
Brown-fat paucity due to impaired BMP signalling induces compensatory browning of white fat, Nature, March 21, 2013
Turning on brown fat and muscle metabolism: hedging your bets, Cell, Oct 12, 2012
Cold but not sympathomimetics activates human brown adipose tissue in vivo, Proc. Natl. Acad. Sci. U.S.A.. Jun 19, 2012