Researchers at the Max Planck Florida Institute for Neuroscience have developed a new combination of technologies that allows them to identify the functional properties of individual synapses that link the two hemispheres and determine how they are arranged within a neuron’s dendritic field.
Each of the 20 billion neurons in the cerebral cortex receives thousands of synaptic connections from other neurons, forming complex neural networks that make sensation, perception, movement, and higher cognitive functions possible. Ultimately the function of these networks depends on events that occur within a neuron’s dendrite— extensions from the neuron’s cell body that resemble branches of a tree and receive synaptic connections from the axons of other neurons, A critical piece of the puzzle of cortical networks that continues to challenge neuroscientists is understanding the functional organization of synapses within a neuron’s dendritic field. This requires determining the functional properties of the synaptic inputs a neuron receives (what they are communicating), the source of the inputs (where they are coming from), and how they are arranged within the dendrite. In a new article in Neuron, MPFI researchers detail how they recently devised new methods to answer these questions, revealing a functional order to the arrangement of distant and local synaptic inputs within a neuron’s dendritic field that may play an important role in coordinating network activity.
Graduate student Kuo-Sheng Lee, along with other members of the Fitzpatrick lab, explored this question in the mouse visual cortex by mapping the synaptic inputs that link the two cortical hemispheres via a fiber bundle called the corpus callosum. This pathway is thought to play a critical role in coordinating the activity of the two cerebral hemispheres, and, for the visual system, unifying our binocular view of the world. They developed an approach that would permit them to visualize the individual dendritic spines of a neuron (small dendritic specializations that receive excitatory synaptic inputs), characterize their functional properties, and determine whether they receive callosal inputs.
To visualize the activity of individual dendritic spines, Lee et al., used an advanced imaging technique that relies on calcium signals that are detected as changes in fluorescence. By watching the dendritic spines ‘light up’ with activity in the living brain, they could present different visual stimuli to the animal and determine which was most effective. The dendritic spines, like most of the cells in visual cortex, respond selectively to the orientation of edges in the visual scene, so this was the functional property they chose to define for each spine. Then to determine whether a spine received synaptic input from the callosum, Lee et al. used direct stimulation of the other hemisphere and looked to see which of the dendritic spines would light up. Having found that a small percentage of spines were reliably and consistently activated by stimulating callosal inputs, then they were ready to address how are they were arranged within the dendritic field.
One interesting possibility was that the callosal inputs with similar orientation preference might be clustered together within the dendritic field. Previous results had provided evidence for clustering of synaptic inputs by functional properties and suggested that coactivation of clustered inputs could amplify their impact on the neuron’s response. But, when they performed the analysis, they found that close pairs of spines receiving callosal input were no more likely to have similar orientation preference than a random distribution of the spines within the dendritic field. Then they considered another possibility. Perhaps the callosal spines were clustered with non-callosal spines with the same orientation preference, bringing spines with distant and local inputs that have similar orientation preference into close proximity on the dendrite. When they took pairs of close spines, one a callosal recipient and the other non-callosal recipient, and examined the orientation preference of the pairs, they were excited to find that they were they more similar to each other than would be expected by chance.
Lee et al. recognized that their conclusions would be strengthened if they could confirm the functional evidence for orderly local and callosal connectivity with another experimental approach: defining the synaptic connections anatomically. To accomplish this, they used a novel technique called expansion microscopy to anatomically visualize the nanoscale synaptic contacts with conventional light microscopy. The results were consistent with the functional stimulation results, demonstrating that callosal inputs and local inputs (derived from the region right around the targeted neuron) that exhibit similar or¬ientation preference are clustered within the dendritic field.
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