Cognitive Benefits of 'Young Blood' Linked to Brain Protein in Mice

Credit: UCSF

“At first I didn’t believe it,” Gontier said. “I did the experiment again and again to make sure that it was right. But it became clear that some circulating factor in the blood is able to change the level of Tet2 in the brain.”

Tet2 is a type of cellular enzyme known as an epigenetic regulator — responsible for making specific chemical annotations to regions of DNA that alter the activity of many different genes. Recent genetic research in humans has implicated mutations in the gene for Tet2 as a risk factor for many different diseases of aging, including cancer, cardiovascular disease, and stroke.

Gontier and colleagues found that as mice age, Tet2 levels in the hippocampus decline, as do the epigenetic tags Tet2 makes on DNA. Among the genes that lost these tags with age were those associated with neurogenesis — the ability to produce new brain cells during adulthood — a process which also declines with age in the mouse hippocampus. Looking more closely at this decline, Villeda’s team found that it closely paralleled the age-related loss of Tet2 expression.

To find out if the loss of Tet2 in aging could directly cause cognitive decline, the researchers used a technique called RNAi to block Tet2 activity in the hippocampi of young adult mice. They found that the reduction of Tet2 significantly reduced the birth of new neurons, and also caused animals to perform significantly worse — more like aged mice — on tests of learning and memory such as remembering the location of a submerged platform in a water maze.

The birth of new neurons in the mouse hippocampus starts waning in early adulthood — well before cognitive decline becomes obvious — so the researchers wondered whether boosting Tet2 levels in the adult hippocampus could restore neurogenesis and potentially prevent the onset of cognitive decline later in life.

To test this hypothesis, they used custom-designed viruses to cause over-expression of Tet2 in the hippocampi of mature adult (6-month-old) mice. Boosting Tet2 increased epigenetic DNA tagging, the researchers found, and restored neurogenesis to more youthful levels. These mice did not perform significantly differently from untreated mice in many tests of learning and memory, but did improve their memory of places where they had previously received mild electrical shocks.

“This was amazing because it’s like improving memory in a healthy, 30-year-old human,” Villeda said. “I always assumed that because there are no overt cognitive impairments in middle-aged mice, we wouldn’t be able to improve their brain function, but here we see that, no, you can improve cognition to make it better than normal.”

“This finding is exciting on many levels,” Gontier added. “I’ve spent my entire Ph.D. and now my postdoc trying to understand how the brain ages and how can we reverse it. And in this study, we find that one molecule, Tet2, is able to rescue regenerative decline and enhance some cognitive functions in the adult mouse brain.”

Credit: Steven Babuljak

It’s not yet clear exactly how Tet2 levels drive improved learning and memory in the mouse brain, or whether these improvements will translate to humans, Villeda cautions. For example, the existence of adult neurogenesis in humans is still controversial, suggesting that the same benefits seen in mice may not be possible in humans. However, Villeda says that he believes neurogenesis is just one aspect of the brain’s regenerative abilities, and probably not the only one being impacted by altering Tet2 levels.

“In our study, we found that removing Tet2 from the hippocampal stem cells that give birth to new neurons caused some cognitive impairment, but removing it from the whole hippocampus caused even more. That suggests that this is about more than just stem cells. This molecule is driving changes throughout the whole brain structure.” Villeda said. “I think of neurogenesis as a signpost of regeneration in the brain, but ultimately I think that it’s changes to the neurons themselves — preventing synapse loss, boosting plasticity — that are going to improve cognition. One of our next big steps is to catalogue exactly what’s happening, both at a genetic level and at a neural level, in mice who’ve had this treatment.”

Other authors of the paper were Manasi Iyer, Jeremy M. Shea, Gregor Bieri, Elizabeth G. Wheatley and Miguel Ramalho-Santos, all of UCSF.

The research was funded by the National Institutes of Health (F31-AG050415, F32-AG055292), the National Institute on Aging (R01 AG053382, R01 AG055797), the Irene Diamond Fund, the Glenn Foundation, and gift from Marc and Lynne Benioff.