ABSTRACT
Oligodendrocyte and myelin deficits have been reported in mental/psychiatric diseases. The p21-activated kinase 3 (PAK3), a serine/threonine kinase, whose activity is stimulated by the binding of active Rac and Cdc42 GTPases is affected in these pathologies. Indeed, many mutations of Pak3 gene have been described in non-syndromic intellectual disability diseases. Pak3 is expressed mainly in the brain where its role has been investigated in neurons but not in glial cells. Here, we showed that PAK3 is highly expressed in oligodendrocyte precursors (OPCs) and its expression decreases in mature oligodendrocytes. In the developing white matter of the Pak3 knockout mice, we found defects of oligodendrocyte differentiation in the corpus callosum and to a lesser extent in the anterior commissure, which were compensated at the adult stage. In vitro experiments in OPC cultures, derived from Pak3 knockout and wild type brains, support a developmental and cell-autonomous role for PAK3 in regulating OPC differentiation into mature oligodendrocytes. Moreover, we did not detect any obvious alterations of the proliferation or migration of Pak3 null OPCs compared to wild type. Overall, our data highlight PAK3 as a new regulator of OPC differentiation.
Subject(s)
Cell Differentiation/physiology , Neural Stem Cells/metabolism , Oligodendroglia/metabolism , p21-Activated Kinases/metabolism , Animals , Anterior Commissure, Brain/cytology , Anterior Commissure, Brain/growth & development , Anterior Commissure, Brain/metabolism , Cell Movement/physiology , Cells, Cultured , Corpus Callosum/cytology , Corpus Callosum/growth & development , Corpus Callosum/metabolism , Male , Mice, Knockout , Neural Stem Cells/cytology , Oligodendroglia/cytology , White Matter/cytology , White Matter/growth & development , White Matter/metabolism , p21-Activated Kinases/geneticsABSTRACT
The two cortical hemispheres of the mammalian forebrain are interconnected by major white matter tracts, including the corpus callosum (CC) and the posterior branch of the anterior commissure (ACp), that bridge the telencephalic midline. We show here that the intracellular signaling domains of the EphB1 and EphB2 receptors are critical for formation of both the ACp and CC. We observe partial and complete agenesis of the corpus callosum, as well as highly penetrant ACp misprojection phenotypes in truncated EphB1/2 mice that lack intracellular signaling domains. Consistent with the roles for these receptors in formation of the CC and ACp, we detect expression of these receptors in multiple brain regions associated with the formation of these forebrain structures. Taken together, our findings suggest that a combination of forward and reverse EphB1/2 receptor-mediated signaling contribute to ACp and CC axon guidance.
Subject(s)
Anterior Commissure, Brain/embryology , Anterior Commissure, Brain/metabolism , Corpus Callosum/embryology , Corpus Callosum/metabolism , Receptor, EphB1/metabolism , Receptor, EphB2/metabolism , Animals , Anterior Commissure, Brain/cytology , Axons/metabolism , Cell Movement/physiology , Corpus Callosum/cytology , Gene Knock-In Techniques , Gene Knockout Techniques , Immunohistochemistry , Intracellular Space , Mice, Transgenic , Neuroanatomical Tract-Tracing Techniques , Protein Domains , Receptor, EphB1/genetics , Receptor, EphB2/genetics , Signal TransductionABSTRACT
Guidepost cells present at and surrounding the midline provide guidance cues that orient the growing axons through commissures. Here we show that the transcription factor Nkx2.1 known to control the specification of GABAergic interneurons also regulates the differentiation of astroglia and polydendrocytes within the mouse anterior commissure (AC). Nkx2.1-positive glia were found to originate from three germinal regions of the ventral telencephalon. Nkx2.1-derived glia were observed in and around the AC region by E14.5. Thereafter, a selective cell ablation strategy showed a synergistic role of Nkx2.1-derived cells, both GABAergic interneurons and astroglia, towards the proper formation of the AC. Finally, our results reveal that the Nkx2.1-regulated cells mediate AC axon guidance through the expression of the repellent cue, Slit2. These results bring forth interesting insights about the spatial and temporal origin of midline telencephalic glia, and highlight the importance of neurons and astroglia towards the formation of midline commissures.