Search

Investigators over the years have noted many striking similarities in the structural organization and function of neural circuits in higher invertebrates and vertebrates. In more recent years, the discovery of similarities in the cellular and molecular mechanisms that guide development of these circuits has driven a revolution in our understanding of neural development. Cellular mechanisms discovered to underlie axon pathfinding in grasshoppers have guided productive studies in mammals. Genes discovered to play key roles in the patterning of the fruitfly's central nervous system have subsequently been found to play key roles in mice. The diversity of invertebrate species offers to investigators numerous opportunities to conduct experiments that are harder or impossible to do in vertebrate species, but that are likely to shed light on mechanisms at play in developing vertebrate nervous systems. These experiments elucidate the broad suite of cellular and molecular interactions that have the potential to influence neural circuit formation across species. Here we focus on what is known about roles for glial cells in some of the important steps in neural circuit formation in experimentally advantageous insect species. These steps include axon pathfinding and matching to targets, dendritic patterning, and the sculpting of synaptic neuropils. A consistent theme is that glial cells interact with neurons in two-way, reciprocal interactions. We emphasize the impact of studies performed in insects and explore how insect nervous systems might best be exploited next as scientists seek to understand in yet deeper detail the full repertory of functions of glia in development., (Copyright © 2010 Wiley-Liss, Inc.)

In the olfactory (antennal) lobe of the moth Manduca sexta, olfactory receptor axons strongly influence the distribution and morphology of glial cells. In the present study, we asked whether the development of the electrophysiological properties of the glial cells is influenced by the receptor axons. Whole-cell currents were measured in antennal lobe glial cells in acute brain slices prepared from animals at different stages of metamorphic development (stages 3, 6, and 12). Outward currents were induced by depolarizing voltage steps from a holding potential of -70 mV. At all developmental stages investigated, the outward currents were partly blocked by bath application of the potassium channel blocker 4-aminopyridine (4AP, 10 mM) or by including tetraethylammonium (TEA, 30 mM) in the pipette solution. The relative contribution of the 4AP-sensitive current to the outward current increased from 18% at stages 3 and 6 to 42% at stage 12, while the TEA-sensitive current increased from 18% at stage 3 to 81% at stage 6, and then declined again to 40% at stage 12. In contrast, in the absence of receptor axons, these changes in the contribution of the TEA- and 4AP-sensitive currents to the total outward current did not occur; rather, the current profile remained in the most immature state (stage 3). The results suggest that olfactory receptor axons are essential for development of the mature pattern of glial potassium currents., (Copyright 2001 Wiley-Liss, Inc.)

Partitioning of the first-order olfactory neuropil into glomeruli in the developing brain of the moth Manduca sexta occurs only in the presence of olfactory sensory axons and appears to be mediated by changes in glial cells (Oland et al.: J. Neurosci., 8:353-367, 1988). The arrival of sensory axons in the brain triggers changes in glial shape and position that lead to the formation of a glial scaffolding for the developing glomeruli. The presence of mitotic figures in glial cells at stages before glomeruli emerge (Oland and Tolbert: J. Comp. Neurol., 255:196-207, 1987) suggested that glial proliferation might also contribute to the formation of the glomerular envelopes. To determine whether glial proliferation is induced by olfactory axons, we have used 3H-thymidine to label dividing cells before, during, and after the formation of glomeruli and have compared the patterns of proliferation in normal and chronically unafferented olfactory neuropils. We found significant differences in mitotic indices only after glomerular walls had been established, indicating that the sensory axons induce the formation of glomerular envelopes primarily via the changes in glial morphology and distribution, not by stimulating glial proliferation.