A new discovery by researchers at the Albert Einstein College of Medicine has shown that stem cells found in the brain’s hypothalamus affect how fast our body’s age. The discovery which was made in mice, could possibly lead to new strategies for defending against age related diseases and even extending lifespan.
The hypothalamus regulates critical processes including development, growth, metabolism and reproduction. Einstein researchers made the surprising discovery that it also regulates aging throughout the entire body. Now, they have pinpointed the exact cells in the hypothalamus that control the process of aging. These cells are a tiny population of adult neural stem cells which are known to be responsible for the formation of new brain neurons.
The research has shown that the number of hypothalamic neural stem cells will naturally decline throughout the life of an animal. This decline will accelerate with aging. The team also discovered that the effects of this stem cell loss are not irreversible. Through replenishing these stem cell or the molecules they produce, it is possible to slow down and even reverse a variety of the aspects associated with aging within the body.
To study whether stem cells found in the hypothalamus hold the key to aging, the team first looked at the fate of the stem cells as healthy mice aged. The number of these stem cells did begin to decline when the mice reached almost 10 months of age which is quit a few months before the normal signs of aging start to appear. By old age which is about two years in mice, most of these stem cells were gone.
The team then wanted to learn whether the progressive loss of these stem cells was actually causing the aging and was not only associated with it. They observed what happened after they selectively disrupted these stem cells in the hypothalamus in middle aged mice. The disruption greatly accelerated the aging compared with control mice. The mice with the disrupted stem cells also died earlier than what would be normal.
The question became, could adding stem cells to the hypothalamus actually counteract aging? The team sought to answer that question by injecting hypothalamic stem cells in the brains of the middle aged mice whose stem cells were destroyed along with injecting the brains of the normal older mice. In both groups of mice the treatment either slowed or reserved a variety of measures of aging.
The team found that the hypothalamic stem cells appeared to exert their anti aging effects by the release of molecules called microRNAs. Rather than being involved in the synthesis of protein, they instead played key roles in regulating gene expression. MicroRNAs are contained inside tiny particles known as exosomes which stem cells in the hypothalamus release into the cerebrospinal fluid of mice.
The team then extracted microRNA containing exosomes from the hypothalamic stem cells and injected them into the cerebrospinal fluid of two different groups of mice…middle aged mice whose hypothalamic stem cells were destroyed and the normal middle aged mice. The treatment showed significant slowing of aging in both groups of mice through a measure of tissue analysis and also behavioral testing which involved assessing any changes in the mice’s coordination, muscle endurance, cognitive ability and social behavior.
They are now working at identifying the particular populations of the microRNAs and even other factors secreted by these stem cells which are responsible for the anti aging effects. This is potentially a first step to possibly slowing down the aging process and also treating a variety of age related diseases.
To view the original scientific study click belowHypothalamic stem cells control ageing speed partly through exosomal miRNAs