Scientists have identified a new type of stem cell in the brain which they say has a high potential for repair following brain injury or disease.
A major goal of regenerative research is to repair the brain efficiently following injury, for example due to stroke, Alzheimer's disease or head trauma, disease or ageing. The brain is poor at repairing itself; however, it may become possible to improve repair without surgery by targeting stem cells residing in patients' brains.
Stem cells have the unique capacity to produce all of the cells in the brain but are normally kept inactive in a form of cellular 'sleep' known as quiescence. Quiescent cells do not proliferate or generate new cells. Thus, any regenerative therapy targeting stem cells must first awaken them from quiescence.
In a study published in the journal Science, researchers report the discovery in the brain of a new type of quiescent stem cell (known as 'G2 quiescent stem cell') with higher regenerative potential than quiescent stem cells identified previously. Importantly, G2 quiescent stem cells awaken to make the key types of cell in the brain - neurons and glia - much faster than known quiescent stem cells, making them attractive targets for therapeutic design.
"The brain is not good at repairing itself, but these newly-discovered stem cells suggest there may be a way to improve its ability," says the senior author. "These stem cells are in a dormant state, but once awake, they have the ability to generate key brain cells."
By studying the fruit fly (Drosophila), the authors identified a gene known as tribbles that selectively regulates G2 quiescent stem cells. The DNA of fruit flies has many similarities with that of humans, making them a useful model to understand human biology, and 60% of human genes associated with disease are also found in Drosophila.
The tribbles gene has counterparts in the mammalian genome that are expressed in stem cells in the brain. The researchers believe that drugs that target tribbles might be one route to awakening G2 quiescent stem cells.
Authors show that neural stem cells enter quiescence by promoting degradation of Cdc25String and that it subsequently maintains quiescence by inhibiting Akt activation. Insulin signaling overrides repression of Akt and silences trbl transcription, allowing NSCs to exit quiescence.
"We've found the gene that directs these cells to become quiescent," adds the lead author. "The next step is to identify potential drug-like molecules that block this gene and awaken a person's stem cells.
"We believe there may be similar quiescent stem cells in other organs, and this discovery could help improve or develop new regenerative medicines."
New sleeping brain stem cells found!
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