An explanation for why our brains produce fewer and fewer neurons with age, a phenomenon thought to underlie age-related cognitive decline is offered in a new study from Cold Spring Harbor Laboratory (CSHL). The study, published as the cover story in the May 6 issue of Cell Stem Cell, suggests that this drop in production is due to the shrinking cache of adult stem cells in our brains.
"It's only recently that scientists have found hard evidence for the importance of new neuron production in the adult brain's hippocampus, a region critical for memory and cognitive function," explains Associate Professor Grigori Enikolopov, Ph.D., who led the CSHL team. The new neurons are critical for some facets of memory—for instance, when similar events need to be memorized as separate episodes—and for the response to anti-depressant therapies and repair after brain injury.
"That the production of new neurons declines with age has been well established, but why this happens has been a matter of debate," Enikolopov says. One prevalent idea has been that the population of adult stem cells—which differentiate into a cascade of progenitor cells that ultimately give rise to mature neurons—remains stable, but the stem cells gradually lose their ability to produce neurons. Working with a genetic and molecular "toolbox" that they developed, Enikolopov's group now proposes a different reason for the production drop-off.
In the team's toolbox are genetically engineered lines of mice in which different classes of neural cells such as stem and progenitor cells can be visually identified and counted, because they are tagged with different fluorescent colors. Postdoctoral researcher Juan Encinas, Ph.D., and the rest of Enikolopov's team could thus "quantitatively assess how the various populations of cells in the brain changed with age."
Between one month and two years of age—a mouse's normal life span—the scientists observed a 100-fold decrease in the number of brain stem cells. The rate of this decrease slowed with age, but the output per cell—measured as the number of progeny each cell gives rise to—increased, which Enikolopov says might be a strategy to cope with the loss of stem cells.
While the scientists in Enikolopov's lab used genetic and molecular labeling methods to track division of the adult stem cells and trace the lineage of their progeny, computational biologist and CSHL Associate Professor Alexei Koulakov generated a mathematical model based on data produced by the team's experiments. These various approaches all converged to focus on a single conclusion: a unique mode of stem cell regulation in the brain that differs from the conventional model.
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"This implies that each adult brain stem cell is used only once and hence is disposable, as opposed to stem cells in the blood or gut that self-renew many times during the lifespan," explains Enikolopov. Whether the stem cells that have converted into astrocytes in the aging brain can be enticed to revert to their former identity and be recruited back into the stem cell pool is a question that his team is pursuing.
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The answer depends on how the production of new neurons has been induced, according to Enikolopov. Whereas Parkinson's disease and traumatic brain injury, which activate stem cells directly, may result in a depletion of the stem cell pool, therapeutic deep brain stimulation of certain brain areas, Prozac, and exercise stimulate the downstream progeny of stem cells and increase production of new neurons while keeping the stem cell pool itself safe and intact. Enikolopov and his colleagues plan to use these findings and their mouse toolbox to find drugs that can spur neuronal growth without harming the adult stem cell cache.
Source-Eurekalert