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The common effect of these abnormalities is to disrupt a pathway that normally regulates the level of protein production in cells, allowing protein production to rise.
The researchers now are following up with studies to discover precisely why protein increases affect microglia in males so much more than in females. ASDs are found in an estimated 2.4 percent of boys and 0.5 percent of girls. The scientists found evidence that the most relevant effect of this protein overproduction occurs in brain-based immune cells called microglial cells.
Xu and his colleagues suspect that this reduction in microglial motility may be the most important factor, so that on balance the cells' synapse-pruning abilities are impaired, leading to ASD-like brain changes. They found that in young male mice, microglial cells in important brain regions, including the medial prefrontal cortex, the hippocampus and the striatum, were significantly larger and also more numerous, whereas in females these changes were much more subtle and transient.
The same behavioral abnormalities were not seen at all when the high eIF4E levels occurred in neurons or in helper cells called astrocytes, although mice whose neurons had high eIF4E levels showed more anxiety-like behaviors. The team found that when high eIF4E levels occurred in microglial cells, the mice developed ASD-like abnormalities in social behavior, as well as cognitive deficits and repetitive behaviors.

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