A team of researchers affiliated with several institutions in the U.S. reports that newly generated nerve cells in the brain’s dentate gyrus impact older nerve cells in two ways. In their paper published in the journal Science, the group describes their study of neurogenesis in mouse models and what they learned from it. María Llorens-Martín, with Centro de Biología Molecular Severo Ochoa has published a Perspectives piece on the study in the same journal issue.
Neuroscientists have only recently found proof of neurogenesis in adult mammals, but are now forging ahead with studies designed to learn more about it. In this new effort, the researchers sought to learn more about the role of neurogenesis in memory and mood. To that end, they conducted multiple studies using transgenic mouse models via optogenetics and electrophysical recordings on different parts of the hippocampus. In so doing, they found that the behavior of mature neurons in the dentate gyrus is impacted by the behavior of newly generated neurons in the same vicinity. They also found that the behavior of the newly born neurons was seemingly controlled by signals from the entorhinal cortex (located in the medial temporal lobe).
More specifically, the researchers found that newly generated neurons, which they refer to as adult-born granule cells (abGCs), behave in different ways depending on what signals they receive from one of two parts of the entorhinal cortex. If they receive a signal from the lateral entorhinal cortex, the researchers explain, then abGCs inhibit activity by the more mature neural cells in their vicinity. But if they receive signals from the medial entorhinal cortex, they do the opposite, exciting the older cells.
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