In vivo modulation of network activity drives the nanoscale reorganisation of axo-axonic synapses at the axon initial segment DOI Creative Commons
Benjamin Compans, Vincenzo Mastrolia,

Clara Lenherr

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Ноя. 30, 2024

Chemical synapses control their strength through the nanoscale clustering of postsynaptic receptors into sub-synaptic domains (SSDs). Despite importance in synapse function, properties and plasticity these are not well understood vivo, particularly inhibitory synapses. We used direct Stochastic Optical Resolution Microscopy (dSTORM) to show that Gephyrin, main receptor scaffold protein, is organised SSDs with distinct arrangements depending on sub-cellular location presynaptic partner. Furthermore, chronic chemogenetic increases cortical activity caused a reduction Gephyrin SSD volume specifically axo-axonic, but axo-dendritic, Functionally, this resulted weakening axo-axonic contacts. arrangement brain plastic fine-tune synaptic gain vivo.

Язык: Английский

Multi-scale spiking network model of human cerebral cortex DOI Creative Commons
Jari Pronold, Alexander van Meegen, Renan O. Shimoura

и другие.

Cerebral Cortex, Год журнала: 2024, Номер 34(10)

Опубликована: Окт. 1, 2024

Abstract Although the structure of cortical networks provides necessary substrate for their neuronal activity, alone does not suffice to understand activity. Leveraging increasing availability human data, we developed a multi-scale, spiking network model cortex investigate relationship between and dynamics. In this model, each area in one hemisphere Desikan–Killiany parcellation is represented by $1\,\mathrm{mm^{2}}$ column with layered structure. The aggregates data across multiple modalities, including electron microscopy, electrophysiology, morphological reconstructions, diffusion tensor imaging, into coherent framework. It predicts activity on all scales from single-neuron area-level functional connectivity. We compared electrophysiological resting-state magnetic resonance imaging (fMRI) data. This comparison reveals that can reproduce aspects both statistics fMRI correlations if inter-areal connections are sufficiently strong. Furthermore, study propagation single-spike perturbation macroscopic fluctuations through network. open-source serves as an integrative platform further refinements future silico studies structure, dynamics, function.

Язык: Английский

Процитировано

8

Semi-automated navigation for efficient targeting of electron tomography to regions of interest in volume correlative light and electron microscopy DOI Creative Commons

K. Konishi,

Guilherme Neves, Matthew R. G. Russell

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Ноя. 30, 2024

Electron microscopy is essential for the quantitative study of synaptic ultrastructure. At present, correlation functional and structural properties same synapse extremely challenging. We introduce a novel integrated workflow designed to simplify sample navigation across spatial scales, allowing identification individual synapses from optical mouse brain image stacks that can be targeted analysis using electron tomography imaging. developed software which has function register multimodal images segmentation-based registration algorithm as well visualize all results. Using our newly we streamline mapping high-resolution imaging onto reference maps blood vessels endogenous fiducial marks. Further demonstrate significant improvements on ultramicrotomy stage volume Correlative Light Microscopy (vCLEM) workflows, providing real time guidance trimming match previously acquired Regions Of Interest (ROIs), reliable estimates cutting depth relative ROI, based fluorescence TEM ready ultrathin sections. this workflow, successfully proximal axonal region containing Axon Initial Segment identified fluorescent light microscopy.

Язык: Английский

Процитировано

0

In vivo modulation of network activity drives the nanoscale reorganisation of axo-axonic synapses at the axon initial segment DOI Creative Commons
Benjamin Compans, Vincenzo Mastrolia,

Clara Lenherr

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Ноя. 30, 2024

Chemical synapses control their strength through the nanoscale clustering of postsynaptic receptors into sub-synaptic domains (SSDs). Despite importance in synapse function, properties and plasticity these are not well understood vivo, particularly inhibitory synapses. We used direct Stochastic Optical Resolution Microscopy (dSTORM) to show that Gephyrin, main receptor scaffold protein, is organised SSDs with distinct arrangements depending on sub-cellular location presynaptic partner. Furthermore, chronic chemogenetic increases cortical activity caused a reduction Gephyrin SSD volume specifically axo-axonic, but axo-dendritic, Functionally, this resulted weakening axo-axonic contacts. arrangement brain plastic fine-tune synaptic gain vivo.

Язык: Английский

Процитировано

0