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Synaptic plasticity in human thalamocortical assembloids
Patton, M. H., Thomas, K. T., Bayazitov, I. T., Newman, K. D., Kurtz, N. B., Robinson, C. G., Ramirez, C. A., Trevisan, A. J., Bikoff, J. B., Peters, S. T., Pruett-Miller, S. M., Jiang, Y., Schild, A. B., Nityanandam, A., Zakharenko, S. S.
biorxiv · 2024
Abstract
Synaptic plasticities, such as long-term potentiation (LTP) and depression (LTD), tune synaptic efficacy and are essential for learning and memory. Current studies of synaptic plasticity in humans are limited by a lack of adequate human models. Here, we modeled the thalamocortical system by fusing human induced pluripotent stem cell-derived thalamic and cortical organoids. Single-nucleus RNA-sequencing revealed that most cells in mature thalamic organoids were glutamatergic neurons. When fused to form thalamocortical assembloids, thalamic and cortical organoids formed reciprocal long-range axonal projections and reciprocal synapses detectable by light and electron microscopy, respectively. Using whole-cell patch-clamp electrophysiology and two-photon imaging, we characterized glutamatergic synaptic transmission. Thalamocortical and corticothalamic synapses displayed short-term plasticity analogous to that in animal models. LTP and LTD were reliably induced at both synapses; however, their mechanisms differed from those previously described in rodents. Thus, thalamocortical assembloids provide a model system for exploring synaptic plasticity in human circuits.
HighlightsO_LIHuman thalamic organoids consist of mostly glutamatergic projection neurons.
C_LIO_LIThalamocortical assembloids form reciprocal glutamatergic synapses.
C_LIO_LISynapses are functional and undergo short-term plasticity resembling animal models.
C_LIO_LILong-term potentiation and depression reveal mechanisms distinct from rodents.
C_LI
eTOCHuman organoids are often used to model diseases with synaptic pathology; however, few studies have examined synaptic function via single-cell or single-synapse recordings. Patton et al. fused human thalamic and cortical organoids into assembloids to examine synaptic transmission and short- and long-term synaptic plasticity in human thalamocortical and corticothalamic circuits.
GRAPHICAL ABSTRACT
O_FIG O_LINKSMALLFIG WIDTH=199 HEIGHT=200 SRC="FIGDIR/small/578421v2_ufig1.gif" ALT="Figure 1">
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Provenance
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- bioRxiv
- DOI
- 10.1101/2024.02.01.578421
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- 2026-10-12 MST
Cite this
APA
H., P.M., T., T.K., T., B.I., D., N.K., B., K.N., G., R.C., A., R.C., J., T.A., B., B.J., T., P.S., M., P.S., Y., J., B., S.A., A., N., & S., Z.S. (2024). Synaptic plasticity in human thalamocortical assembloids. <em>biorxiv</em>. https://doi.org/10.1101/2024.02.01.578421
Vancouver
H. PM, T. TK, T. BI, D. NK, B. KN, G. RC, et al. Synaptic plasticity in human thalamocortical assembloids. biorxiv. 2024. doi:10.1101/2024.02.01.578421.
BibTeX
@unpublished{patton2024Synapt,
title = {Synaptic plasticity in human thalamocortical assembloids},
author = {Patton, M. H. and Thomas, K. T. and Bayazitov, I. T. and Newman, K. D. and Kurtz, N. B. and Robinson, C. G. and Ramirez, C. A. and Trevisan, A. J. and Bikoff, J. B. and Peters, S. T. and Pruett-Miller, S. M. and Jiang, Y. and Schild, A. B. and Nityanandam, A. and Zakharenko, S. S.},
journal = {biorxiv},
year = {2024},
doi = {10.1101/2024.02.01.578421},
}
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