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Doron, M.

Publications and source records attributed to Doron, M..

2 recordsLinked to original sources

Whole-neuron synaptic mapping reveals local balance between excitatory and inhibitory synapse organization

The balance between excitatory and inhibitory (E and I) synaptic inputs is thought to be critical for information processing in neural circuits. However, little is known about the principles of spatial organization of E and I synapses across the entire dendritic tree of mammalian neurons. We developed a new, open-source, reconstruction platform for mapping the size and spatial distribution of E and I synapses received by individual, genetically-labeled, layer 2/3 cortical pyramidal neurons (PNs) in vivo. We mapped over 90,000 E and I synapses across twelve L2/3 PNs and uncovered structured organization of E and I synapses across dendritic domains as well as within individual dendritic segments in these cells. Despite significant, domain-specific, variations in the absolute density of E and I synapses, their ratio is strikingly balanced locally across dendritic segments. Computational modeling indicates that this spatially-precise E/I balance dampens dendritic voltage fluctuations and strongly impacts neuronal firing output.

neuroscience

Shaping dendritic NMDA spikes by timed synaptic inhibition: Implications for the I/O properties of cortical neurons

The pronounced, long lasting, regenerative NMDA-spike is initiated in individual dendritic branches of different types of neurons and is known to play a key role in dendritic computations and plasticity. Combining dynamic system theory and computational approaches, we systematically analyzed how timed synaptic inhibition activated during the NMDA-spike time-course, sculpts this spike and its associated current influx. When impinging on its early phase, individual GABAergic synapse activation transiently, but strongly, dampened the NMDA-spike; later inhibition prematurely terminated it. This inhibition reduced the NMDA-mediated Ca2+ current by up to 60%. NMDA-spikes in distal dendritic branches/spines are longer lasting and more resilient to inhibition, and thus enhance synaptic plasticity at these branches. Examination of this sensitivity of the NMDA-spike to well-timed synaptic inhibition suggests that NMDA-spikes are highly modifiable signals which enable sparse weak distal dendritic inhibition to finely tune both the neuron's output spikes as well as the branch's/spine's Ca2+ current associated with the local NMDA spike.

neuroscience