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Yakoubi, R.

Publications and source records attributed to Yakoubi, R..

2 recordsLinked to original sources

Area-specific synapse structure in branched axons reveals a subcellular level of complexity in thalamocortical networks

Thalamocortical Posterior nucleus (Po) axons innervating the somatosensory (S1) and motor (MC) vibrissal cortices are key links in the brain neuronal network that allows rodents to explore the environment whisking with their motile vibrissae. Here, using high-end 3D electron microscopy, we demonstrate massive differences between MC vs. S1 Po synapses in a) bouton and active zone size; b) neurotransmitter vesicle pool size; c) mitochondria distribution near synapses; and d) proportion of non-spinous dendrite contacts. These differences are as large, or bigger, than those between Po and ventroposterior thalamic nucleus synapses in S1. Moreover, using single-axon transfection labeling, we show that the structure of boutons in the MC vs. S1 branches of individual Po axons is different. These structural differences parallel striking, recently-discovered divergences in functional efficacy and plasticity between S1 and MC Po synapses, and overall reveal a new, subcellular level of thalamocortical circuit complexity, unaccounted for in current models.

neuroscience↗

Ultrastructural heterogeneity of human layer 4 excitatory synaptic boutons in the adult temporal lobe neocortex

Synapses are fundamental building blocks that control and modulate the behavior of brain networks. How their structural composition, most notably their quantitative morphology underlies their computational properties remains rather unclear, particularly in humans. Here, excitatory synaptic boutons (SBs) in layer 4 (L4) of the temporal lobe neocortex (TLN) were quantitatively investigated.\n\nBiopsies from epilepsy surgery were used for fine-scale and tomographic electron microscopy to generate 3D-reconstructions of SBs. Particularly, the size of active zones (AZs) and of the three functionally defined pools of synaptic vesicles (SVs) were quantified.\n\nSBs were comparably small ([~]2.50 m2), with a single AZ ([~]0.13 {micro}m2) and preferentially established on spines. SBs had a total pool of [~]1800SVs with strikingly large readily releasable ([~] 20), recycling ([~] 80) and resting pools ([~]850).\n\nThus, human L4 SBs may act as amplifiers of signals from the sensory periphery and integrate, synchronize and modulate intra- and extra-cortical synaptic activity.

neuroscience↗