Here’s why belly fat increases as we age
In a bid to find a new treatment for improving metabolic health,
researchers have discovered why belly fat surrounding organs increases
as people age.
Led by Dr. Vishwa Deep Dixit, the Waldemar Von Zedtwitz Professor of Comparative Medicine and of Immunobiology, the study was published in 'Cell Metabolism'.
Previous work found that as people age, their body's ability to generate energy by burning the belly fat is reduced. Consequently, the fat that surrounds the internal organs increases in the elderly.
Dixit's lab had found that the immune cells necessary to the fat-burning process, called macrophages, were still active but their overall numbers declined as belly fat increased with aging.
This latest study found that something else is happening as well. Adipose B cells in belly fat unexpectedly proliferated as animals aged, contributing to increased inflammation and metabolic decline.
"These adipose B cells are a unique source of inflammation," Dixit said, "Normally the B cells produce antibodies, and defend against infection. But with aging, the increased adipose B cells become dysfunctional, contributing to metabolic disease."
When they are working correctly, Dixit said, some B cells expand as needed to protect the body from infection, and then contract to baseline. But with aging, they don't contract in belly fat.
"This predisposes an animal to diabetes and metabolic dysfunction like inability to burn fat," he said.
Dixit theorises that this ongoing expansion may be due to increased human life expectancy - a pushing of the body's cells beyond their evolutionary limits. "Several mechanisms in the body are not selected for longevity," he said.
Researchers discovered that adipose B cells expand by receiving signals from nearby macrophages. Relatedly, they found that by reducing the macrophage signal and by removing adipose B cells, they could reverse the expansion process, and protect against an age-induced decline in metabolic health.
This could lead to exciting possibilities for repurposing drugs to target these dysfunctional adipose B cells for improved health outcomes and to protect against metabolic disease, Dixit said. One drug, called cytokine IL-1B, reduces one of the small proteins driving this process and is currently used to protect against heart disease.
"It's important to study whether reducing this cytokine in the elderly can lower B cell expansion in belly fat," Dixit said.
He added that there are also immunotherapy drugs that neutralise B cells that are used in certain cancers. These, too, could be tested for their effectiveness in reducing metabolic disease in elderly people, Dixit added.
Led by Dr. Vishwa Deep Dixit, the Waldemar Von Zedtwitz Professor of Comparative Medicine and of Immunobiology, the study was published in 'Cell Metabolism'.
Previous work found that as people age, their body's ability to generate energy by burning the belly fat is reduced. Consequently, the fat that surrounds the internal organs increases in the elderly.
Dixit's lab had found that the immune cells necessary to the fat-burning process, called macrophages, were still active but their overall numbers declined as belly fat increased with aging.
This latest study found that something else is happening as well. Adipose B cells in belly fat unexpectedly proliferated as animals aged, contributing to increased inflammation and metabolic decline.
"These adipose B cells are a unique source of inflammation," Dixit said, "Normally the B cells produce antibodies, and defend against infection. But with aging, the increased adipose B cells become dysfunctional, contributing to metabolic disease."
When they are working correctly, Dixit said, some B cells expand as needed to protect the body from infection, and then contract to baseline. But with aging, they don't contract in belly fat.
"This predisposes an animal to diabetes and metabolic dysfunction like inability to burn fat," he said.
Dixit theorises that this ongoing expansion may be due to increased human life expectancy - a pushing of the body's cells beyond their evolutionary limits. "Several mechanisms in the body are not selected for longevity," he said.
Researchers discovered that adipose B cells expand by receiving signals from nearby macrophages. Relatedly, they found that by reducing the macrophage signal and by removing adipose B cells, they could reverse the expansion process, and protect against an age-induced decline in metabolic health.
This could lead to exciting possibilities for repurposing drugs to target these dysfunctional adipose B cells for improved health outcomes and to protect against metabolic disease, Dixit said. One drug, called cytokine IL-1B, reduces one of the small proteins driving this process and is currently used to protect against heart disease.
"It's important to study whether reducing this cytokine in the elderly can lower B cell expansion in belly fat," Dixit said.
He added that there are also immunotherapy drugs that neutralise B cells that are used in certain cancers. These, too, could be tested for their effectiveness in reducing metabolic disease in elderly people, Dixit added.