Target cell-specific synaptic dynamics of excitatory to inhibitory neuron connections in supragranular layers of human neocortex
Author:
Kim Mean-Hwan1ORCID, Radaelli Cristina1, Thomsen Elliot R1, Monet Deja1, Chartrand Thomas1ORCID, Jorstad Nikolas L1, Mahoney Joseph T1ORCID, Taormina Michael J1, Long Brian1, Baker Katherine1, Bakken Trygve E1ORCID, Campagnola Luke1, Casper Tamara1, Clark Michael1, Dee Nick1, D'Orazi Florence1, Gamlin Clare1, Kalmbach Brian E12, Kebede Sara1, Lee Brian R1ORCID, Ng Lindsay1, Trinh Jessica1, Cobbs Charles3, Gwinn Ryder P3, Keene C Dirk4ORCID, Ko Andrew L5, Ojemann Jeffrey G5, Silbergeld Daniel L5, Sorensen Staci A1, Berg Jim1, Smith Kimberly A1, Nicovich Philip R1, Jarsky Tim1ORCID, Zeng Hongkui1ORCID, Ting Jonathan T12, Levi Boaz P1, Lein Ed145
Affiliation:
1. Allen Institute for Brain Science 2. Department of Physiology & Biophysics, School of Medicine, University of Washington 3. Swedish Neuroscience Institute 4. Department of Laboratory Medicine & Pathology, School of Medicine, University of Washington 5. Department of Neurological Surgery, School of Medicine, University of Washington
Abstract
Rodent studies have demonstrated that synaptic dynamics from excitatory to inhibitory neuron types are often dependent on the target cell type. However, these target cell-specific properties have not been well investigated in human cortex, where there are major technical challenges in reliably obtaining healthy tissue, conducting multiple patch-clamp recordings on inhibitory cell types, and identifying those cell types. Here, we take advantage of newly developed methods for human neurosurgical tissue analysis with multiple patch-clamp recordings, post-hoc fluorescent in situ hybridization (FISH), machine learning-based cell type classification and prospective GABAergic AAV-based labeling to investigate synaptic properties between pyramidal neurons and PVALB- vs. SST-positive interneurons. We find that there are robust molecular differences in synapse-associated genes between these neuron types, and that individual presynaptic pyramidal neurons evoke postsynaptic responses with heterogeneous synaptic dynamics in different postsynaptic cell types. Using molecular identification with FISH and classifiers based on transcriptomically identified PVALB neurons analyzed by Patch-seq, we find that PVALB neurons typically show depressing synaptic characteristics, whereas other interneuron types including SST-positive neurons show facilitating characteristics. Together, these data support the existence of target cell-specific synaptic properties in human cortex that are similar to rodent, thereby indicating evolutionary conservation of local circuit connectivity motifs from excitatory to inhibitory neurons and their synaptic dynamics.
Funder
National Institutes of Health
Publisher
eLife Sciences Publications, Ltd
Subject
General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience
Cited by
15 articles.
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