LOS ANGELES (EMBARGOED UNTIL 5:00 A.M. EST ON FEB. 20, 2019) -- A new study has found that transplanting the bone marrow of young laboratory mice into old mice prevented cognitive decline in the old mice, preserving their memory and learning abilities. The findings support an emerging model that attributes cognitive decline, in part, to aging of blood cells, which are produced in bone marrow.
"While prior studies have shown that introducing blood from young mice can reverse cognitive decline in old mice, it is not well understood how this happens," said Helen Goodridge, PhD, associate professor of Medicine and Biomedical Sciences at Cedars-Sinai and co-senior author of the study. "Our research suggests one answer lies in specific properties of youthful blood cells."
If further research confirms similar processes in people, the findings could provide a pathway for designing therapies to slow progression of neurodegenerative diseases, including Alzheimer's, that affect millions of Americans, Goodridge said.
In the study, published in the journal Communications Biology, 18-month-old laboratory mice received bone marrow transplants from either 4-month-old mice or mice their own age. Six months later, both transplanted groups underwent standard laboratory tests of activity level and learning, plus spatial and working memory. Mice that received young bone marrow outperformed mice that received old bone marrow. They also outperformed a control group of old mice that did not get transplants.
The research team then examined the hippocampus, a region associated with memory, in the mice brains. Recipients of young bone marrow retained more connections, known as synapses, between neurons in the hippocampus than did recipients of old bone marrow, even though they had about the same number of neurons. Synapses are critical to brain performance.
Further tests showed a possible reason for the missing synapses. The blood cells made by the young bone marrow reduced the activation of microglia, a type of immune cell in the brain. Microglia support neuron health but can become overactive and participate in disconnection of the synapses. With fewer overactive microglia, neurons would remain healthy and more synapses would survive.
"We are entering an era in which there will be more elderly people in the population, along with an increased incidence of Alzheimer's disease, putting a huge burden on the health system," said Clive Svendsen, PhD, director of the Cedars-Sinai Board of Governors Regenerative Medicine Institute, professor of Biomedical Sciences and Medicine and co-senior author of the new study. "Our work indicates that cognitive decline in mice can be significantly reduced by simply providing young blood cells, which act on the brain to reduce the loss of synapses related to aging."
Translating the findings, if confirmed in human samples, into potential treatments may be challenging, given that bone marrow transplants are not currently feasible for this use. But for future studies in people, Svendsen is working on creating "personalized" young blood stem cells for an individual through stem cell technology. These cells possibly could be used to help replace the individual's own aging blood stem cells and help prevent cognitive decline and perhaps neurodegenerative diseases such as Alzheimer's as well.