Small clusters of brown fat cells in our bodies begin to burn up energy when exposed to sufficient cold or exercise. This form of fat can be active in adults, which can turn up the heat from cells to treat obesity, diabetes, and other metabolic conditions.
Immature fat cells can produce heat without gathering fat may open opportunities to treat obesity and diabetes, reports a new study. The findings of the study are published in the journal Nature Communications.// Researchers in the lab of Joslin's Yu-Hua Tseng, Ph.D., a Senior Investigator in the Section on Integrative Physiology and Metabolism, now have discovered an unexpected biological pathway by which brown fat cells can translate energy into heat.
‘Brown adipose tissue plays a vital role in adaptive thermogenesis, a physiological process in which energy is dissipated in response to environmental changes such as cold and diet.
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Studies in mice showed that activating this pathway in precursors of brown or white fat cells boosts the heat-generating capacity of these cells without pushing the cells to accumulate fat, says Farnaz Shamsi, a postdoctoral associate in the Tseng lab and lead author on a paper.
Previously, researchers have found that certain biological signals that boost the production of brown fat cells are also likely to create unhelpful white fat cells, thus posing one of the research challenges in enhancing brown fat activity. The finding, however, suggests that the pathway the Joslin team uncovered might offer a solution to that challenge.
The research began with a protein called UCP1 that is located on mitochondria, the cell's powerhouses. UCP1 is known to be a crucial component in activating brown fat cells, explains Tseng, who is also an Associate Professor of Medicine at Harvard Medical School.
Her team screened more than 5,000 mammalian proteins to identify factors that heightened UCP1 production in brown fat precursor cells. The screen identified two proteins called FGF6 and FGF9, members of the "fibroblast growth factor" family of proteins that can help to regulate diverse biological processes including cell development and growth.
Next, the investigators tried increasing the levels of the two proteins and thus increasing UCP1 production in immature mouse brown fat cells. The scientists expected that these cells would start to accumulate fats and other lipids, and to develop into mature brown fat cells--but surprisingly, that didn't happen.
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Shamsi, Tseng, and their colleagues saw that the two FGF proteins provide similar effects on the production of UCP1 but are driven by different exposures in mice. FGF9 is stimulated by cold, while FGF6 is stimulated by exercise.
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"This suggests that if we can activate this pathway, we potentially can benefit people with obesity, diabetes and related metabolic diseases," Tseng says.
Her team is working with collaborators to synthesize a version of the FGF protein that is optimized for greater efficacy and easier delivery, she says. Since her group has traced the mechanisms at work in this pathway, it also may eventually be possible to develop drugs that build up UCP1 production by targeting specific molecular steps in the pathway.
"As obesity becomes epidemic, we hope that our research in brown fat can help," Tseng says. "With a collective effort from many labs around the globe, we are getting closer to that goal."
Source-Eurekalert