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Dendritic spines are post-synaptic compartments of most excitatory synapses. Alterations to dendritic spine morphology occur during neurodevelopment, aging, learning, and many neurological and psychiatric disorders, underscoring the importance of reliable dendritic spine analysis. This protocol describes quantifying dendritic spine morphology accurately and reproducibly using automatic three-dimensional neuron reconstruction software.
Synaptic connections allow for the exchange and processing of information between neurons. The post-synaptic site of excitatory synapses is often formed on dendritic spines. Dendritic spines are structures of great interest in research centered around synaptic plasticity, neurodevelopment, and neurological and psychiatric disorders. Dendritic spines undergo structural modifications during their lifespan, with properties such as total spine number, dendritic spine size, and morphologically defined subtype altering in response to different processes. Delineating the molecular mechanisms regulating these structural alterations of dendritic spines relies on morphological measurement. This mandates accurate and reproducible dendritic spine analysis to provide experimental evidence. The present study outlines a detailed protocol for dendritic spine quantification and classification using Neurolucida 360 (automatic three-dimensional neuron reconstruction software). This protocol allows for the determination of key dendritic spine properties such as total spine density, spine head volume, and classification into spine subtypes thus enabling effective analysis of dendritic spine structural phenotypes.
Dendritic spines are protrusions of dendrites often comprising the post-synaptic site of glutamatergic synapses1,2. Dendritic spines are of particular interest in the field of synaptic plasticity. Spines are often altered when synaptic strength changes, becoming larger and stronger in long-term synaptic potentiation or smaller and weaker in long-term synaptic depression3,4,5,6,7. Beyond synaptic plasticity, the profile of dendritic spines changes th....
All animal procedures followed the US National Institutes of Health Guidelines Using Animals in Intramural Research and were approved by the National Institute of Mental Health Animal Care and Use Committee.
1. Preparation of fixed hippocampal slices
Effectively utilizing this analysis method begins with the selection of dendritic segments for tracing. As described in Figure 1, the ideal dendrites for tracing are not in close proximity to other dendrites. Dendrites running in parallel can result in improperly identifying spines from a neighboring dendrite. Dendrites directly intersecting or running perpendicular in a different z-plane add significant difficulty to accurate dendritic tracing as well. It is also important to note the diffe.......
This protocol details the specific steps of sample preparation, imaging, and the process of dendritic spine quantification and classification using three-dimensional reconstruction software. This software is a powerful tool capable of producing robust structural data that contributes to a diverse array of investigations. Throughout the process, there are some critical steps that make this protocol less of a methodological burden and enhance the overall output of the data. The method for labeling dendritic spines is one o.......
We would like to acknowledge Carolyn Smith, Sarah Williams Avram, Ted Usdin, and the NIMH SNIR for technical assistance. We would additionally like to acknowledge the Colgate University Bethesda Biomedical Research Study Group. This work is supported by the NIMH Intramural Program (1ZIAMH002881 to Z.L.).
....Name | Company | Catalog Number | Comments |
518F Immersion Oil | Zeiss | 444960-0000-000 | |
Cryostat | Leica | CM3050S | For slice preparation |
Fine Forceps | FST | 11150-10 | |
Hemostat Forceps | FST | 13020-12 | |
Large Surgical Scissors | FST | 14002-16 | |
LSM 880 Confocal Microscope | Zeiss | LSM 880 | |
Microscope Cover Glass | Fisherbrand | 12-541-035 | |
Mini-Peristaltic Pump II | Harvard Apparatus | 70-2027 | For perfusions |
Neurolucida 360 | MBF Bioscience | v2022.1.1 | Spine Analysis Software |
Neurolucida Explorer | MBF Bioscience | v2022.1.1 | Spine Analysis Software |
OCT Compound | Sakura Finetek | 4583 | For cryostat sectioning |
Paraformaldehyde (37%) | Fisherbrand | F79-1 | |
Plan-Apochromat 63x/1.40 Oil DIC | Zeiss | 440762-9904-000 | |
Scalpel Blade | FST | 10022-00 | |
Small Surgical Scissors | FST | 14060-09 | |
Spatula | FST | 10091-12 | |
Sucrose | FIsherbrand | S5-500 | |
Superfrost Plus Microslides | Diagger | ES4951+ | |
Vectashield HardSet Mounting Medium | Vector Laboratories | H-1400-10 |
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