Abstract
Studying neocortex and hippocampus in parallel, we are struck by the similarities. All three to four layered allocortices and the six layered mammalian neocortex arise in the pallium. All receive and integrate multiple cortical and subcortical inputs, provide multiple outputs and include an array of neuronal classes. During development, each cell positions itself to sample appropriate local and distant inputs and to innervate appropriate targets. Simpler cortices had already solved the need to transform multiple coincident inputs into serviceable outputs before neocortex appeared in mammals. Why then do phylogenetically more recent cortices need multiple pyramidal cell layers? A simple answer is that more neurones can compute more complex functions. The dentate gyrus and hippocampal CA regions—which might be seen as hippocampal antecedents of neocortical layers—lie side by side, albeit around a tight bend. Were the millions of cells of rat neocortex arranged in like fashion, the surface area of the CA pyramidal cell layers would be some 40 times larger. Even if evolution had managed to fold this immense sheet into the space available, the distances between neurones that needed to be synaptically connected would be huge and to maintain the speed of information transfer, massive, myelinated fiber tracts would be needed. How much more practical to stack the “cells that fire and wire together” into narrow columns, while retaining the mechanisms underlying the extraordinary precision with which circuits form. This demonstrably efficient arrangement presents us with challenges, however, not the least being to categorize the baffling array of neuronal subtypes in each of five “pyramidal layers.” If we imagine the puzzle posed by this bewildering jumble of apical dendrites, basal dendrites and axons, from many different pyramidal and interneuronal classes, that is encountered by a late-arriving interneurone insinuating itself into a functional circuit, we can perhaps begin to understand why definitive classification, covering every aspect of each neurone's structure and function, is such a challenge. Here, we summarize and compare the development of these two cortices, the properties of their neurones, the circuits they form and the ordered, unidirectional flow of information from one hippocampal region, or one neocortical layer, to another.
Highlights
If we imagine the puzzle posed by this bewildering jumble of apical dendrites, basal dendrites and axons, from many different pyramidal and interneuronal classes, that is encountered by a late-arriving interneurone insinuating itself into a functional circuit, we can perhaps begin to understand why definitive classification, covering every aspect of each neurone’s structure and function, is such a challenge
Development of an additional germinal layer, the subventricular zone (SVZ) coincides with the appearance of L2-4 and emergence of the mammalian six layered neocortex (Noctor et al, 2004; Wu et al, 2005); the layers of phylogenetically older, three layered cortices being considered equivalent to L1, L5, and L6
If we look at broad classes of GABAergic neurones, those, for example that express the same markers, we find a similar picture in hippocampus and neocortex
Summary
One subclass of these upright cells, with apical dendritic tufts in L4, send narrow, ascending axonal arbors to L4 (and sometimes lower L3) where it terminates with characteristic short, drumstick-like side branches. Despite their frequent innervation of parvalbumin (PV) interneurones (which receive depressing inputs from all other pyramidal classes), L6 corticothalamic pyramids elicited facilitating EPSPs (excitatory postsynaptic potentials) in all cell types studied, including ventroposterior, posterior medial thalamic and nRT neurones.
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