Scientific Understanding of Consciousness
Embryonic Development of Cortical Columns
Nature 486, 41–42 (07 June 2012)
Sibling neurons bond to share sensations
Thomas D. Mrsic-Flogel & Tobias Bonhoeffer
Thomas D. Mrsic-Flogel is in the Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6DE, UK.
Tobias Bonhoeffer is at the Max-Planck Institute of Neurobiology, 82152 München-Martinsried, Germany.
Even though cortical columns have long been considered to be exemplars of basic computational units of cortical organization, the precise relationship between their anatomy and function has been difficult to define and remains the subject of debate. This is particularly true in rodents, in which the cortex seems to lack functional columns almost entirely. What is common to rodents and other mammals, however, is a highly specific organization of cortical connections that link neurons across layers in the cortex to relay and process related sensory information. Researchers have reported some of the developmental events that could give rise to such precisely arranged functional circuits.
It has long been known that, during embryonic development of the cortex, neuronal progenitor cells give birth to daughter cells that migrate towards the brain surface to form strings of 'sibling' neurons that span the cortical layers. These radially aligned clones, referred to as radial units or ontogenetic columns, have been proposed to constitute the basis of the functional columns in the mature brain. However, a direct link between cellular lineage, microcircuit development and the sensory preference of neurons had not been demonstrated.
Researchers used viruses to label sibling neurons in the developing cortex of mouse embryos with a fluorescent protein, and then recorded the cells' electrical activity in brain slices prepared shortly after birth. The authors showed that gap junctions — small pores that couple adjacent cells electrically by bridging their membranes — formed transiently between sibling neurons in the same radial unit, very early in development. Gap junctions had previously been observed between clusters of excitatory neurons in the developing cortex and had been proposed to contribute to the establishment of neuronal assemblies, but the ancestry and significance of such cell clusters were unknown. Moreover, other work had revealed that, later in development, neurons in radial clones mostly connect to one another through chemical synapses mediated by neurotransmitter molecules showed that gap-junction inactivation abolished the formation of such synapses, and report that transient electrical coupling is thus essential for the establishment of chemical synapses between sibling neurons.
Researchers used the same method to label radial clones, and then used a microscopy technique known as two-photon calcium imaging to monitor the activity of sibling neurons in the cortex of live mice in response to visual stimuli. The authors observed that clonally related neurons, when compared with a random subset of neighbouring cells, were more likely to respond to stimuli of the same orientation in the animals' visual field. Moreover, the blockade of gap junctions eliminated the shared preference for stimulus orientation, which further supports the idea that electrical coupling between sibling neurons plays a part in influencing the functional organization of the cortex.
Research results lend support to the involvement of genetic lineage in the assembly of precise columnar circuits in the cortex. An extreme interpretation of the results is that ontogenetic columns constitute an elementary unit of functional organization in the cortex; that is, a basic, repeating circuit comprising excitatory neurons that process related sensory information. However, the relevance of ontogenetic columns for sensory processing is still unclear; an excitatory neuron in the mammalian cortex receives inputs from at least 1,000 others, but only a handful of these connections are with sibling neurons. It will be important to assess how much the connections between siblings actually contribute to shaping their sensory responses.
The small size of mouse ontogenetic columns, might explain why functional columns have not previously been described in the visual cortex of rodents, in which neurons with different sensory preferences seem to be locally intermixed.
The research findings also raise the question of whether there is any relationship between ontogenetic columns and the much larger functional columns in the cortices of other mammals such as cats or primates. Large functional columns could form as aggregates of multiple ontogenetic mini-columns, or from larger radial clones containing many more neurons than those of rodents, or by a different mechanism altogether.
Regardless, the two studies demonstrate that at least some of the connection specificity in cortical microcircuits is established intrinsically by clonal lineage. The studies also show that cellular lineage could influence neurons' development of a similar sensory preference during early postnatal life. Results suggest a close interplay between clonal lineage and early neuronal activity. Electrical coupling is likely to influence the formation and/or stabilization of chemical synapses between neurons that share gap junctions, because it is known that synapses can grow stronger or weaker if the cells' electrical activities are correlated or uncorrelated, respectively — a process known as synaptic plasticity. It is tempting to speculate that the sensory preference of these sub-networks might then be developed by similar mechanisms: electrically coupled neurons could select and stabilize a common set of sensory inputs, which would endow these cells with a shared preference for certain sensory features. Future experiments are required to determine the developmental events that define how non-sibling neurons with similar stimulus preferences become connected to each other in the cortical circuit.
Other important questions remain unanswered. To what extent is the electrical coupling between cortical neurons necessary for the establishment of stimulus selectivity? In other words, did the early blockade of gap junctions between sibling neurons result in a fundamentally altered visual cortex? Results indicate that gap-junction blockade does not prevent the emergence of orientation preference, but more subtle features — such as the range of orientations that a neuron detects — could depend on gap-junction connectivity.
Another issue relates to the fact that, during embryonic development, clonally related neurons not only migrate radially towards the cortical surface — some are also distributed tangentially. The connectivity and functional fate of these displaced sibling neurons remains undetermined. Do they also establish functional sub-networks with their siblings, or do they form local connections with non-sibling neighbours? How does the interplay between sensory input and synapse plasticity link up neurons from different ontogenetic columns with similar sensory preferences to form larger functional assemblies? And do displaced sibling neurons have a role in this process? Whatever the answers to these questions, the two studies reveal the fascinating way in which neurons emerging from the same progenitor cell are destined to share functional properties, and thus show how the earliest developmental events influence the elaborate functional circuitry of the brain.
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