Literature DB >> 32464088

Rapid 3D Enhanced Resolution Microscopy Reveals Diversity in Dendritic Spinule Dynamics, Regulation, and Function.

Colleen R Zaccard1, Lauren Shapiro1, Maria D Martin-de-Saavedra1, Christopher Pratt1, Kristoffer Myczek1, Amy Song1, Marc P Forrest1, Peter Penzes2.   

Abstract

Dendritic spinules are thin protrusions, formed by neuronal spines, not adequately resolved by diffraction-limited light microscopy, which has limited our understanding of their behavior. Here we performed rapid structured illumination microscopy and enhanced resolution confocal microscopy to study spatiotemporal spinule dynamics in cortical pyramidal neurons. Spinules recurred at the same locations on mushroom spine heads. Most were short-lived, dynamic, exploratory, and originated near simple PSDs, whereas a subset was long-lived, elongated, and associated with complex PSDs. These subtypes were differentially regulated by Ca2+ transients. Furthermore, the postsynaptic Rac1-GEF kalirin-7 regulated spinule formation, elongation, and recurrence. Long-lived spinules often contained PSD fragments, contacted distal presynaptic terminals, and formed secondary synapses. NMDAR activation increased spinule number, length, and contact with distal presynaptic elements. Spinule subsets, dynamics, and recurrence were validated in cortical neurons of acute brain slices. Thus, we identified unique properties, regulatory mechanisms, and functions of spinule subtypes, supporting roles in neuronal connectivity.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  calcium transients; dendritic spine dynamics; intrabodies; kalirin-7; live imaging; multi-synaptic spines; postsynaptic density; structured illumination microscopy; synaptic plasticity; synaptic spinules

Mesh:

Substances:

Year:  2020        PMID: 32464088      PMCID: PMC7879711          DOI: 10.1016/j.neuron.2020.04.025

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  53 in total

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