Floor plate

Embryonic structure

The floor plate is a structure integral to the developing nervous system of vertebrate organisms. Located on the ventral midline of the embryonic neural tube, the floor plate is a specialized glial structure that spans the anteroposterior axis from the midbrain to the tail regions. It has been shown that the floor plate is conserved among vertebrates, such as zebrafish and mice, with homologous structures in invertebrates such as the fruit fly Drosophila and the nematode C. elegans. Functionally, the structure serves as an organizer to ventralize tissues in the embryo as well as to guide neuronal positioning and differentiation along the dorsoventral axis of the neural tube.

Induction of the floor plate during embryogenesis of vertebrate embryos has been studied extensively in chick and zebrafish and occurs as a result of a complex signaling network among tissues, the details of which have yet to be fully refined. Currently there are several competing lines of thought. First, floor plate differentiation may be mediated by inductive signaling from the underlying notochord, an axial mesoderm derived signaling structure. This is supported experimentally in chick, in which floor plate induction, as well as associative ventral nervous tissue differentiation, is mediated by the secreted signaling molecule sonic hedgehog (Shh). Shh is expressed in a gradient with highest concentration localized in the notochord and floor plate. In vitro tissue grafting experiments show that removal of this molecule prevents differentiation of the floor plate, whereas its ectopic expression induces differentiation of floor plate cells. An alternative view proposes that neural tube floor plate cells stem from precursor cells which migrate directly from axial mesoderm. Through chick – quail hybrid experiments as well as genetic interaction experiments in zebrafish, it appears that notochord and floor plate cells originate from a common precursor. Furthermore, in zebrafish, Nodal signaling is required for differentiation of medial floor plate cells whereas Shh is expendable. These data may indicate that the floor plate induction mechanism in amniotes and anamniotes differs. To reconcile these differences, a dual mode induction model has been proposed in chick. In this model, exclusively ectodermal cells are induced to become medial floor plate during gastrulation by prechordal mesoderm, possibly through Nodal signaling. Later in development during neurulation, extended contact and interaction between notochord and fated floor plate cells causes differentiation, suggesting a cooperative effect between Nodal and Shh signaling.

In the development of the central nervous system, the decision of a neuron to cross or not cross the midline is critical. In vertebrates, this choice is mediated by the floor plate, and enables the embryo to develop successful left and right body halves with respect to nervous tissue. For example, while ipsilateral neurons do not cross the midline, commissural neurons cross the midline forming a single commissure. These particular neurons develop in the dorsal region of the neural tube and travel ventrally toward the floor plate. Upon reaching the floor plate, commissural neurons cross through the structure to emerge on the opposite side of the neural tube, whereupon they project anteriorly or posteriorly within the tube. Netrins: Netrins are proteins expressed and secreted by cells of the floor plate. Experiments using floor plate extracts and commissural neurons embedded in a collagen matrix show attraction of neurons towards the floor plate in vitro. Moreover, Isolation and transfection of Netrin 1 and Netrin 2, two secreted proteins, into Cos cells has similar effects. Further research confirmed that Netrins act as attractant proteins in addition to Shh to guide commissural axons toward the floor plate. Netrins are secreted by the floor plate cells and function to bind the axon receptor DCC in a chemotactic manner. Recent studies have challenged this model and showed that floor plate derived Netrin 1 is dispensable for midline crossing and that Netrin 1 primarily derives from ventricular zone progenitors. Slit: Slit is a secreted ligand expressed in the floor plate and functions to inhibit axonal crossing of the neural tube. While netrins attract commissural neurons toward the midline, slit proteins repel and expel neurons from the midline. As axons not destined to cross the midline project through the neural tube they are repelled by the ligand slit which is expressed in the cells of the floor plate. Slit acts through its receptors Roundabout (Robo) 1 and 2. This interaction inhibits the chemotaxis provided by the Netrin/DCC pathway. However, Robo 3 (Rig 1) is upregulated during growth of commissural axons during migration toward the floor plate, which sequesters Robo 1/2 inside the cell within vesicles. Consequently, the Netrin/DCC attraction pathway dominates over the Slit/Robo repulsion pathway and the axon can grow toward the midline and enter the floor plate. Upon entering, through a mechanism not yet fully understood, Robo 3 becomes downregulated and this liberates and upregulates Robo 1/2, effectively repelling the neuron from the floor plate midline. Through this complex cross talk of Slit, Robo 1/2, and Robo 3, commissural axons are guided toward the midline to cross the neural tube and prevented from crossing back. The signaling molecules guiding the growth and projections of commissural neurons have well studied homologs in invertebrates. In the Netrin/DCC chemoattraction pathway the C. elegans homologs are Unc 6/Unc 40 and Unc 5 while the Drosophila homologs are Netrin A and Netrin B/Frazzled and Dunc5. In the Slit/Robo chemoreppelant pathway the C. elegans homologs are Slt 1/Sax 3 whereas the Drosophila homologs are also known as Slit/Robo(1 3). The floor plate (FP) region of the spinal cord individually contributes to gliogenesis, or the formation of glial cells. Traditionally, progenitor cells are driven from their progenitor expansion phase, to the neurogenic phase, and ultimately to the gliogenic phase. From the gliogenic phase, the former progenitor cells can then become astrocytes, oligodendrocytes, or other more specialized glial cell types. Recently, there have been efforts to use conditional mutagenesis to selectively inactivate the Shh pathway specifically in the FP region to identify different roles of molecules involved in oligodendrocyte cell fate. Oligodendrocytes are the cells responsible for myelinating axons in the CNS. Shh regulates Gli processing through two proteins, Ptch1 and Smo. When Shh is not active, Ptch1 is responsible for suppressing the pathway through the inhibition of Smo. Smo is crucial to the overall transduction of signal of the Shh pathway. If Smo is inhibited, the Shh pathway is also inactive, which ultimately represses gliogenesis. Specific factors such as Gli3 are required for oligodendrocyte cell fate. Since Shh regulates Gli processing, if Smo is compromised or inhibited by Ptch1, this inactivates the Shh pathway and prevents Gli processing which disrupts glial cell fate mapping. Shh signaling in the FP region is very important because it needs to be active in order for gliogenesis to occur. If Shh is inactivated within the FP region and activated in other regions of the spinal cord such as the Dbx or pMN domains, gliogenesis is compromised. But, when Shh is active in the FP region, gliogenesis is activated and glial cells begin migrating to their targeted destinations to function.

The floor plate region aids in axon guidance, glial fate mapping, and embryogenesis. If this area of the spinal cord becomes injured, there could be serious complications to all contributing functions of this region, namely limited proliferation and production of the glial cells responsible for myelination and phagocytosis in the CNS. Spinal cord injury (SCI) also most often results in axon denudation or severance. Wnt signaling is a common signaling pathway involved in injury cases. Wnt signaling regulates regeneration after spinal cord injury. Immediately following injury, Wnt expression dramatically increases. Axon guidance is driven by Netrin 1 Injury compromises Akhirin expression and regulation and the cells of the FP region cannot properly be restored by the ependymal stem cell populations.