Neural substrates within primary visual cortex for interactions between parallel visual pathways.
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Biomedical subjects
Edward M Callaway
Publications and source records attributed to Edward M Callaway.
Targeted gene delivery to telencephalic inhibitory neurons by directional in utero electroporation.
Telencephalic inhibitory neurons originate in the ganglionic eminences and migrate to the cerebral cortex following a tangential trajectory, before they differentiate and integrate within the local circuitry. Current studies of interneuron development and function benefit from the use of knock-out and transgenic mice, whereas none take advantage of the versatility of in utero electroporation. Here, we show how in utero electroporation can be directed to the ganglionic eminences to specifically target gene expression to interneurons. Electroporation of GFP-encoding plasmids into the ganglionic eminences results in selective labeling of migrating interneurons during development. In the adult brain of electroporated animals, a wide variety of cortical, hippocampal and olfactory bulb interneurons are labeled. We also show that GFP-expressing interneurons can be visualized in living slices of adult cerebral cortex, where they display normal electrophysiological properties. Photostimulation studies using acute slices show that cortical GFP+ interneurons receive normal, layer-specific synaptic input, indicating that these neurons integrate within the local cortical circuitry. Ganglionic eminence-directed in utero electroporation is therefore an effective, rapid, and versatile method of selectively transfecting telencephalic interneurons, optimal for both developmental studies and adult functional studies.
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Laminar patterns of local excitatory input to layer 5 neurons in macaque primary visual cortex.
Layer 5 neurons in primary visual cortex make putative reciprocal feedback connections to the superficial layers. To test this hypothesis, we employed scanning laser photostimulation combined with intracellular dye injection to examine local functional excitatory inputs to and axonal projections from individual layer 5 neurons in brain slices from monkey V1. In contrast with previous studies of other V1 neurons, layer 5 neurons received significant input from nearly all of the cortical layers, suggesting individual layer 5 cells integrate information from a broad range of input sources. Nevertheless relative strengths of laminar inputs varied across neurons. Cluster analysis of relative strength of laminar inputs to individual layer 5 neurons revealed four discrete clusters representing recurring input patterns; each cluster included both excitatory and inhibitory neurons. Twenty-five of 40 layer 5 neurons fell into two clusters, both characterized by very strong input from superficial layers. These input patterns are consistent with layer 5 neurons providing feedback to superficial layers. The remaining 15 neurons received stronger input from deep layers. Differences in input from layer 4Calpha versus 4Cbeta also suggest specific associations of the magnocellular and parvocellular visual pathways, with populations receiving stronger input from deep versus superficial cortical layers.
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Close encounters: how cortical neurons find and connect to their correct synaptic partners depends on the cell type.
In this issue of Neuron, Stepanyants et al. embark on quantitative analyses of the axonal and dendritic arbors of cortical neurons. They test whether the paths taken by axons actually bring them closer to their true synaptic partners than they would have gotten by chance encounters based on the same axon trajectories. The results depend on the type of presynaptic neuron. Inhibitory cells take paths that explicitly link them to their actual partners while excitatory axons are as likely to have close encounters with actual partners as with other neurons. These results suggest that the mechanisms for selectivity depend on the type of presynaptic neuron.
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Topographic specificity of functional connections from hippocampal CA3 to CA1.
The hippocampus is a cortical region thought to play an important role in learning and memory. Most of our knowledge about the detailed organization of hippocampal circuitry responsible for these functions is derived from anatomical studies. These studies present an incomplete picture, however, because the functional character and importance of connections are often not revealed by anatomy. Here, we used a physiological method (photostimulation with caged glutamate) to probe the fine pattern of functional connectivity between the CA3 and CA1 subfields in the mouse hippocampal slice preparation. We recorded intracellularly from CA1 and CA3 pyramidal neurons while scanning with photostimulation across the entire CA3 subfield with high spatial resolution. Our results show that, at a given septotemporal level, nearby CA1 neurons receive synaptic inputs from neighboring CA3 neurons. Thus, the CA3 to CA1 mapping preserves neighbor relations.
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Antisense inhibition of reward learning.
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Parallel colour-opponent pathways to primary visual cortex.
The trichromatic primate retina parses the colour content of a visual scene into 'red/green' and 'blue/yellow' representations. Cortical circuits must combine the information encoded in these colour-opponent signals to reconstruct the full range of perceived colours. Red/green and blue/yellow inputs are relayed by the lateral geniculate nucleus (LGN) of thalamus to primary visual cortex (V1), so understanding how cortical circuits transform these signals requires understanding how LGN inputs to V1 are organized. Here we report direct recordings from LGN afferent axons in muscimol-inactivated V1. We found that blue/yellow afferents terminated exclusively in superficial cortical layers 3B and 4A, whereas red/green afferents were encountered only in deeper cortex, in lower layer 4C. We also describe a distinct cortical target for 'blue-OFF' cells, whose afferents terminated in layer 4A and seemed patchy in organization. The more common 'blue-ON' afferents were found in 4A as well as lower layer 2/3. Chromatic information is thus conveyed to V1 by parallel, anatomically segregated colour-opponent systems, to be combined at a later stage of the colour circuit.
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Orientation tuning--a crooked path to the straight and narrow.
Neurons in visual cortex are selective for the orientation of a visual stimulus, while the receptive fields of their thalamic input are circular. Cortical orientation selectivity arises from the organization of both thalamic input and local cortical circuits. In this issue of Neuron, Schummers and colleagues provide evidence that the local circuit mechanisms contributing to orientation selectivity differ depending on the local organization of the orientation map.
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S cone contributions to the magnocellular visual pathway in macaque monkey.
The magnocellular visual pathway is believed to receive input from long (L) and middle (M), but not short (S), wavelength-sensitive cones. Recording from neurons in magnocellular layers of lateral geniculate nucleus (LGN) in macaque monkeys, we found that magnocellular neurons were unequivocally responsive to S cone-isolating stimuli. A quantitative analysis suggests that S cones provided about 10% of the input to these cells, on average, while L:M ratios were far more variable. S cone signals influenced responses with the same sign as L and M cone inputs (i.e., no color opponency). Magnocellular afferent recordings following inactivation of primary visual cortex demonstrated that S cone signals were feedforward in nature and did not arise from cortical feedback to LGN
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Reorganization of exuberant axonal arbors contributes to the development of laminar specificity in ferret visual cortex.
Layer-specific cortical axons are believed to develop precisely from the outset without making exuberant branches in incorrect cortical layers. We tested this hypothesis by following the development of axonal arbors of layer 2/3 pyramidal neurons in ferret visual cortex, which in the adult have dense axonal arbors in layers 2/3 and 5 and not in layer 4. We began our studies at earlier ages and sampled at closer intervals than in previous studies. Our studies reveal that between postnatal day (P) 14 and P18 the initial growth of axonal arbors lacks specificity for layers 2/3 and 5 and involves the formation of a small number of branches incorrectly in layer 4. After P18 the number of incorrect axonal branches in layer 4 decreased, whereas there was extensive axonal growth specifically in layers 2/3 and 5. To further study the mechanisms involved in directing the layer-specific growth and elimination of axonal branches, we studied the development of layer 2/3 neurons in slices kept in culture for 5 d. In these studies the initial imprecise growth at P14-18 followed by precise growth after P18 was mimicked in vitro, but the elimination of incorrect axons from layer 4 did not occur. These studies reveal that most axonal arbors grow precisely in the correct layers, but the initial growth involves the formation of a small number of incorrect axonal branches that are later eliminated. Therefore the mechanisms that regulate axonal growth are not as precise initially as later, and mechanisms must exist to allow selective elimination of axon collaterals from incorrect layers.
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A genetic method for selective and quickly reversible silencing of Mammalian neurons.
Genetic methods for neuronal silencing have great promise for allowing selective inactivation of specific cell types within complex neural systems. Present methods, however, are limited in their reversibility by the slow time scale (days) of transcriptional regulation. We report the rapid and reversible inactivation of mammalian cortical neurons expressing the insect G-protein-coupled receptor AlstR (Drosophila allatostatin receptor) [corrected] after application of its peptide ligand allatostatin (AL). The onset and reversal of inactivation could be achieved rapidly, within minutes. Moreover, the effects of AL were selective for AlstR-transfected neurons. The AlstR/AL system is therefore a promising genetic method for selective and quickly reversible silencing of neuronal activity.
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Stimulating neurons with light.
Recent technological advances have enabled the use of different optical methods to activate neurons, including 'caged' glutamate, photoactivation of genetically engineered cascades, and direct two-photon excitation. The ability to use light as a stimulation tool provides, in principle, a non-invasive method for the temporally and spatially precise activation of any neuron or any part of a neuron. When combined with two-photon excitation, excellent spatial control can be achieved even in complex and highly scattering preparations, such as living nervous tissue. Different methods that have been developed in the last several decades have been used to probe neuronal sensitivity, mimic synaptic input, and elucidate patterns of neural connectivity.
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Feedforward, feedback and inhibitory connections in primate visual cortex.
Visual cortical circuits are organized at multiple levels of complexity including cortical areas, layers and columns, and specific cell types within these modules. Making sense of the functions of these circuits from anatomical observations requires linking these circuits to function at each of these levels of complexity. Observations of these relationships have become increasingly sophisticated over the last several decades, beginning with correlations between the connectivities and functions of various visual cortical areas and progressing toward cell type-specificity. These studies have informed current views about the functional interactions between cortical areas and modules and the mechanisms by which fine scale microcircuits influence interactions at more coarse levels of organization.
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Cell type specificity of local cortical connections.
The function of the cerebral cortex is dependent on the precise organization of the circuits formed by its component neurons. The connections between neurons are not random, but are specific at multiple levels of organization. For example, each cortical area connects to only a selected subset of other areas and within any given area the axonal and dendritic arbors of individual neurons arborize in precise, layer-specific patterns (for review see Felleman & Van Essen, 1991; Callaway, 1998). In each layer there are dendrites from multiple cell types including cells with somata both within and outside that layer. Anatomical studies have shown that axons arborizing in a particular cortical layer can connect selectively onto dendrites of some cell types in the layer, while avoiding the dendrites of other cell types (e.g. Freund & Gulyas, 1991; Hornung & Celio, 1992; Staiger et al., 1996). These cell type specific connections are, however, difficult to elucidate with anatomical methods, so the frequency of such specificity has remained elusive. Recent experimental methods combining intracellular recording of single neurons with focal neuronal stimulation by uncaging glutamate with light ("photostimulation") have made the analysis of cell type specific cortical connections more tractable. These studies show that cell type specificity of connections is prevalent in cortex. Here I review photostimulation-based studies investigating the laminar sources of cortical input to distinct cell types in the visual and somatosensory cortices of rats and the primary visual cortex of monkeys.
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