Researchers conducting the study were surprised to see that the injected cells even acted like “missionaries,” converting existing belly fat cells into so-called thermogenic cells, which use fat to generate heat.
Over time, the mice gained back some weight. But they resisted any dramatic weight gain on a high-fat diet and burned away more than a fifth of the cells that make up their visceral fat, which surrounds the organs and is linked to higher risk for Type 2 diabetes, cancer and heart disease.
The scientists took advantage of the heat-generating properties of a so-called good fat in the body, brown fat, to cut back on the white fat cells that compose the visceral fat that tends to accumulate in the belly.
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The scientists combined those brown fat thermogenic cells with genetically modified cells missing an enzyme that leads to visceral fat growth. The engineered cells were placed inside a gel-like capsule that allowed for release of its contents without triggering an immune response.
“With a very small number of cells, the effect of the injection of this capsule was more pronounced at the beginning, when the mice dramatically lost about 10 percent of their weight. They gained some weight back after that. But then we started to look at how much visceral fat was present, and we saw about a 20 percent reduction in those lipids. Importantly, other nontreated peripheral or subcutaneous fat, which has some beneficial health effects, remained the same. That’s what we want,” said Ouliana Ziouzenkova, assistant professor of human nutrition at Ohio State University and lead author of the study.
“We observed the mice for 80 days after injection and the capsule didn’t break or cause any scarring or inflammation. This suggests it’s a clean, safe potential therapy for obesity,” added Ziouzenkova, also an investigator in Ohio State’s Comprehensive Cancer Center and the Center for Clinical and Translational Science. Studies in larger animals would be needed before trials in humans could begin, she said.
If this were someday approved for humans, Ziouzenkova said such a therapy would be best suited to patients who develop visceral fat with aging, aren’t able to exercise and shouldn’t dramatically reduce their calories because that can cause the loss of beneficial subcutaneous fat. She also noted that anti-obesity drugs for humans currently on the market can reduce body weight by about 10 to 15 percent, but also have side effects.
The research is published in a recent issue of the journal Biomaterials.
A year ago, Ziouzenkova’s lab identified an enzyme in mice that relates to fat accumulation after consumption of a high-fat diet, and she recently published a paper indicating that mice lacking that enzyme could stay lean even while eating excess fat. She applied those findings in this work by using the genetically modified cells that are missing that enzyme to potentially help boost the ability of brown fat cells to burn up visceral fat.
For this study, she collaborated with Ohio State chemists to create the capsules. They are composed of alginate-poly-L-lysine, a compound that creates enough of a barrier to encapsulate cells without signaling the immune system that it should react to a foreign object in the body, while also enabling nutrient supply to the encapsulated cells for their long-term survival.
The researchers used three groups of normal mice for the study, feeding them all a high-fat diet for 90 days. After that, five mice received no treatment, five were treated with empty capsules and five received an injection of active capsules containing genetically engineered cells. The capsules were injected into two areas of visceral fat in their abdomens.
The mice continued to eat a high-fat diet for another 80 days. The mice receiving no treatment continued to gain weight in those 80 days, while the mice receiving thermogenic cells lost weight for 23 days and then began to gain it back, eventually maintaining a steady weight even after continuing to eat excessive saturated fat. Mice receiving empty capsules also lost some weight, but the researchers determined in a separate pilot study that the sham injections did not reduce visceral fat.
The researchers examined visceral fat pads from the mice and determined that overall, lipid content was at least 20 percent lower in mice treated with active capsules compared to the placebo injection group of mice.
A closer look at exactly what was going on in the animals’ cells showed that the injected cells produced high levels of a protein called Ucp1, which burns fat, suggesting that this protein assisted in the visceral fat reduction.
By tagging the injected cells with a fluorescent protein, the scientists could use imaging technology to track the cells in the body; this not only benefited the research, but also provides a way to safely remove these capsules if needed, Ziouzenkova noted.
“The injected cells were perfectly inversely correlated with lipids – so the more injected cells we have capable of burning fat, the more fat gets burned,” she said. “These injected cells worked almost like missionaries, starting to convert host cells and turning them into thermogenic cells.”
“The injected cells were perfectly inversely correlated with lipids – so the more injected cells we have capable of burning fat, the more fat gets burned.”
Because that creation of heat could be uncomfortable inside a human body, the researchers analyzed the treated mice further to see if the thermogenesis in the belly would produce effects similar to hot flashes.
“Heat production was higher in injected animals, but it was not dramatically higher. So there is some kind of response, but it seems not to be at a magnitude impairing a patient’s well-being,” Ziouzenkova said. “The animals were also moving less than noninjected animals, but in spite of that, they were still able to lose visceral fat. Their glucose tolerance improved, as well, which is probably related to reduced visceral fat.”
Ziouzenkova said she hopes to design additional capsules to target a variety of diseases beyond obesity.
This work was supported by the American Heart Association Great Rivers Affiliate, the National Institutes of Health, a pilot industry partnership grant at the Center for Clinical and Translational Science (funded by the National Center for Advancing Translational Sciences), the Ohio State College of Education and Human Ecology (EHE), a Food Innovation Center Seed grant and an EHE dissertation fellowship.
Ziouzenkova collaborated with several Ohio State scientists on this research, including L. James Lee, director of the NSF Nanoscale Science and Engineering Center for Affordable Nanoengineering of Polymeric Biomedical Devices (NSEC); and Sanjay Rajagopalan, Chandan Sen and Sashwati Roy of the Davis Heart and Lung Research Institute (DHLRI). Additional co-authors include Fangping Yang and David DiSilvestro of the Department of Human Nutrition; Xulang Zhang of the NSEC; Andrei Maiseyeu of the DHLRI; Georgeta Mihai, Santosh Maurya and Muthu Periasamy of the Department of Physiology & Cell Biology; and Rumana Yasmeen and Valerie Bergdall of University Laboratory Animal Resources, all at Ohio State; and Gregg Duester of the Sanford-Burnham Medical Research Institute in La Jolla, Calif.
Contact: Ouliana Ziouzenkova, (614) 292-5034; Ziouzenkova.firstname.lastname@example.org
Written by Emily Caldwell, (614) 292-8310; Caldwell.email@example.com