Abstract

The mature neocortex contains many different classes of GABAergic inhibitory interneurons, distributed, with some degree of selectivity, through six layers, and through many different regions. Some of the events in the early lives of these neurones that may determine their ultimate destination, their maturation and their selective innervation of targets appropriate for each subtype, are discussed. Both time and place of birth influence the class of interneuron that an early post-mitotic interneuronal precursor will become, driven by the selective expression of different combinations of transcription factors in different regions of their birth places in the ganglionic eminence and ventricular zone. The long distance migration of these precursors along tangential routes in marginal, subventricular, and intermediate zones and their final radial movement, into the developing cortex, is regulated by chemical cues, both attractant and repellent. Once they arrive at their final destination, they must integrate into the developing circuitry. As they mature within the cortex, their axons grow and branch in highly specific patterns that may be partially determined by the genetic blueprint for each interneuronal class and partly by the environment in which they find themselves. Finally, as each interneuron class begins to form synapses with only certain postsynaptic targets, cell–cell recognition, most probably via protein–protein interactions across the synaptic cleft, facilitate the formation of appropriate synapses.

Highlights

  • The mature neocortex contains many different classes of GABAergic inhibitory interneurons, distributed, with some degree of selectivity, through six layers, and through many different regions

  • WHAT CAN MATURE NEURONAL STRUCTURE SUGGEST ABOUT DEVELOPMENT? Anyone who has spent hours at the microscope, reconstructing cortical axons at high power, will be aware of the immense complexity of these axonal arbors and their huge diversity

  • That pyramidal cell axons, run almost straight through the neuropil, deviating significantly only as they encounter large obstacles, like blood vessels. They may have a gross structure that is peculiar to just one particular class of pyramidal cell, innervating only certain layers for example, but whatever the pattern of their branches, they run more or less straight through the cortex

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Summary

Development of cortical GABAergic innervation

Reviewed by: Graziella DiCristo, University of Montreal, Canada Laura Cancedda, Istituto Italiano di Tecnologia, Italy. That pyramidal cell axons (with the exception of the drum stick like branches of layer 6 cortico-thalamic pyramidal axons in layer 4, Zhang and Deschênes, 1997), run almost straight through the neuropil, deviating significantly only as they encounter large obstacles, like blood vessels They may have a gross structure that is peculiar to just one particular class of pyramidal cell, innervating only certain layers for example, but whatever the pattern of their branches, they run more or less straight through the cortex. They do not give the impression of axons in search of a target. The following section explores the possibility that these differences result in part from the order in which different types of neurones arrive in the neocortex; spiny excitatory cells typically arriving before the GABAergic inhibitory interneurons that are assigned, at their birth, to the same layer (Miller, 1986a,b; Rymar and Sadikot, 2007)

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