The biological causes underlying obesity have been under intense scrutiny with studies suggesting a link between the nervous and the immune systems. Now, in a breakthrough study to be published in Nature Medicine, a research team discovered an unforeseen population of immune cells associated with neurons that play a direct role in obesity.

These immune cells are macrophages, a type of white blood cells responsible for inflammatory responses in the body. Previous studies had alluded to a role for macrophages in the adipose tissue inflammation that occurs in obesity, but the mechanism of action linking these cells to neurons and fat breakdown was unclear. Now, the team showed that specialized macrophages are in direct contact with neurons and affect neuronal activation that is critical for fat mass reduction.

The team had previously discovered that adipose tissue is innervated by a set of sympathetic neurons that release norepinephrine, a neurotransmitter that induces fat breakdown. Now, they show that these sympathetic neurons are in intimate contact with a particular type of macrophage that they coined SAMs (sympathetic neuron-associated macrophages). The researchers found that SAMs clear out norepinephrine and that obese mice had many more of these cells attached to neurons than lean mice. This means that SAMs contribute to obesity by decreasing norepinephrine content in fat, thus preventing subsequent fat reduction.

By conducting genetic studies in mice, the research team was able to pinpoint the molecular mechanism underlying SAM-mediated destruction of norepinephrine. The import mechanism of this neurotransmitter involves the transporter for norepinephrine (the protein Slc6a2) that is present in SAMs but not in other immune cells. Furthermore, they showed that blocking the import mechanism of norepinephrine by SAMs boosts fat breakdown, energy dissipation, and weight loss.

They further confirmed that SAMs and the associated molecular machinery for norepinephrine clearing also exist in humans, through analysis of human nervous system samples. "The role of norepinephrine transporter in SAMs offers a targeted approach that may overcome the noxious off-target effects of several known drugs that block this molecular target", says the senior author. These results set the stage for the development of new anti-obesity therapies.

http://www.igc.gulbenkian.pt/pages/pressReleases.php/year=2017

https://www.nature.com/nm/journal/vaop/ncurrent/full/nm.4422.html