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- Title
Non-Newly Generated, "Immature" Neurons in the Sheep Brain Are Not Restricted to Cerebral Cortex.
- Authors
Piumatti, Matteo; Palazzo, Ottavia; Crociara, Paola; Parolisi, Roberta; La Rosa, Chiara; Bonfanti, Luca; Luzzati, Federico; Lévy, Frederic
- Abstract
A newly proposed form of brain structural plasticity consists of non-newly generated, "immature" neurons of the adult cerebral cortex. Similar to newly generated neurons, these cells express the cytoskeletal protein Doublecortin (DCX), yet they are generated prenatally and then remain in a state of immaturity for long periods. In rodents, the immature neurons are restricted to the paleocortex, whereas in other mammals, they are also found in neocortex. Here, we analyzed the DCX-expressing cells in the whole sheep brain of both sexes to search for an indicator of structural plasticity at a cellular level in a relatively large-brained, long-living mammal. Brains from adult and newborn sheep (injected with BrdU and analyzed at different survival times) were processed for DCX, cell proliferation markers (Ki-67, BrdU), pallial/subpallial developmental origin (Tbrl, SpH), and neuronal/glial antigens for phenotype characterization. We found immature-like neurons in the whole sheep cortex and in large populations of DCX-expressing cells within the external capsule and the surrounding gray matter (claustrum and amygdala). BrdU and Ki-67 detection at neonatal and adult ages showed that all of these DCX+ cells were generated during embryogenesis, not after birth. These results show that the adult sheep, unlike rodents, is largely endowed with non-newly generated neurons retaining immature features, suggesting that such plasticity might be particularly important in largebrained, long-living mammals.
- Subjects
CYTOSKELETAL proteins; CEREBRAL cortex; NEURONS; NEUROPLASTICITY; POSTNATAL development in animals; DEVELOPMENTAL neurobiology; SHEEP; PHENOTYPES
- Publication
Journal of Neuroscience, 2018, Vol 38, Issue 4, p826
- ISSN
0270-6474
- Publication type
Article
- DOI
10.1523/JNEUROSCI.1781-17.2017