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A second development was the discovery that adult brains continue to produce new cells, overturning conventional wisdom that brain cells are not replenished.
In overweight people leptin either is not getting to their brains, or their brain cells are not responding to leptin's message.
However, mouse brain cells are not susceptible to HIV infection, so in their current form the models cannot be used to study viral evolution in the brain.
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The chemical prolactin, which may promote new brain cells, is not only found in high levels in pregnant women, but also increases during sex.
The extent to which this differentiation depends on paracrine signaling from other brain cells is not clear.
Thus, the majority of the normal brain cells were not expected to survive the stress of the culture conditions.
Taken together, these data support strong evidence that rA75/17red non-cytolytic cell-to-cell spread in primary canine brain cells is not mediated by viral free particle formation but rather through direct contact with neighboring cells associated with transfer of viral nucleocapsids.
In the brain, the nerve cells are not the same.
In several brain regions, such as in the cerebellum, cells are not scattered randomly in the 3D space but are laid out in manifolds.
Isotype control cells are not detectable in mouse brains.
Histological assessment of the brain structure revealed some minor pathological changes, but the number of brain cortex cells was not affected.
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