Explains Zhang, This experiment confirmed that TLX specifically induces the genetic program necessary for maintaining neural stem cells in their stem-like state, handing the Salk researchers the perfect tool to track the contribution of newborn neurons to normal brain function a question Gage is particularly interested in.
In the past, methods to knock out neurogenesis, such as radiation and mitotic inhibitors that block all cell division have been rather crude, he says. So, maybe not surprisingly the literature is riddled with contradictory results.
Adult neural stem cells continually generate new brain cells or neurons in two small areas of mammalian brains: the olfactory bulb, which processes odors, and the central part of the hippocampus, which is involved in the formation of memories and learning. Some of these newborn cells die shortly after they are born but many of them become functionally integrated into the surrounding brain tissue. Whether they live or die is regulated by the animals experience.
Combining mouse genetics and gene transfer techniques, Zhang genetically engineered mice that allowed him to specifically delete TLX in the brains of adult mice and thus shut down neurogenesis. He then put the mice through a battery of standard behavioral tests.
The mice passed with flying colors in all but one test: the Morris water maze, a common behavioral test in which mice have to rely on visual cues on the surrounding walls to find and remember the location of a subme
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| Contact: Gina Kirchweger kirchweger@salk.edu 858-453-4100 x1340 Salk Institute Source:Eurekalert |