doctoralThesis
Roles of ZBTB20 in the specification of upper layer neurons and astrocytes in the neocortex
Fecha
2019-12-17Registro en:
ARAÚJO, Jéssica Alves de Medeiros. Roles of ZBTB20 in the specification of upper layer neurons and astrocytes in the neocortex. 2019. 146f. Tese (Doutorado em Neurociências) - Instituto do Cérebro, Universidade Federal do Rio Grande do Norte, Natal, 2019.
Autor
Araújo, Jéssica Alves de Medeiros
Resumen
Organization of neocortical circuits is critical for sensory perception, learning and
multisensory integration. In the primary somatosensory area (S1) layer IV neurons
receive thalamic inputs and synapse onto layer II/III neurons. These superficial neurons
may connect other neurons within S1 and within other areas in the ipsi- or contralateral
hemisphere, thus cooperating to select an interpretation consistent with their various
cortical and subcortical inputs. Here we show that expression of the transcription factor
Zinc Finger and BTB Domain-Containing Protein 20 (Zbtb20) in neocortical progenitors is
necessary and sufficient to regulate the generation and wiring patterns of upper layer
neurons. Conditional deletion of the Zbtb20 gene in progenitors leads to an increase in
the number and radial occupancy of RORβ+/layer IV neurons at the expense of
BRN2+/layers II/III neurons. This change in the laminar organization of the neocortex is
accompanied by an expansion of thalamic axonal arborization and barrel area in S1.
Furthermore, upper layer neurons increase their intra-hemispheric axonal projections,
while reducing contralateral innervation in the absence of Zbtb20 expression. These
alterations are also observed, albeit at a lesser extent, after Zbtb20 deletion in post-mitotic
neurons, indicating that Zbtb20 act at sequential stages of the lineage progression of
neocortical progenitors, fine-tuning neuronal fates in upper cortical layers and contributing
to the proper wiring of callosal projecting neurons (CPNs). Besides these effects in CPN
fate specification, we also show that ZBTB20 regulates astrogliogenesis in a time-specific
fashion. ZBTB20 overexpression at E14, but not at E16, increases neocortical
astrogliogenesis, whereas expression of a dominant-negative (DN) ZBTB20 at E16, but
not E14, reduces astrogliogenesis. Altogether, our results indicate that ZBTB20 is an
important regulator of cell type/subtype specification in the developing neocortex.