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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Serial Block-Face Scanning Electron Microscopy (SBEM) is applied to image and analyze dendritic spines in the murine hippocampus.

Abstract

Three-dimensional electron microscopy (3D EM) gives a possibility to analyze morphological parameters of dendritic spines with nanoscale resolution. In addition, some features of dendritic spines, such as volume of the spine and post-synaptic density (PSD) (representing post-synaptic part of the synapse), presence of presynaptic terminal, and smooth endoplasmic reticulum or atypical form of PSD (e.g., multi-innervated spines), can be observed only with 3D EM. By employing serial block-face scanning electron microscopy (SBEM) it is possible to obtain 3D EM data easier and in a more reproducible manner than when performing traditional serial sectioning. Here we show how to prepare mouse hippocampal samples for SBEM analysis and how this protocol can be combined with immunofluorescence study of dendritic spines. Mild fixation perfusion allows us to perform immunofluorescence studies with light microscopy on one half of the brain, while the other half was prepared for SBEM. This approach reduces the number of animals to be used for the study.

Introduction

Most of the excitatory synapses in the central nervous system are located on dendritic spines - small protrusions of a neuronal membrane. These protrusions form confined biochemical compartments that control intracellular signal transduction. Structural plasticity of dendritic spines and synapses is closely related to the functional changes in synaptic efficacy that underlie such important processes as learning and memory1,2. It is important to note that electron microscopy (EM) is the only technique that allows to determine if a dendritic spine has a presynaptic input. EM resolution is also needed to study ul....

Protocol

The research was performed in compliance with Nencki Institute guidelines and permission of the Local Ethical Committee. The studies were carried out in accordance with the European Communities Council Directive of 24 November 1986 (86/609/EEC), Animal Protection Act of Poland and approved by the first Local Ethics Committee in Warsaw. All efforts were made to minimize the number of animals used and their suffering.

CAUTION: All procedures described below must be carried out in a laboratory fu.......

Representative Results

Using the method described above high contrast, good resolution images of the mouse brain tissue can be obtained. A large field of view provided by the SBEM technique facilitates precise selection of the region of interest. The large image of the CA1 region of the hippocampus was taken to measure the length of stratum radiatum (SR) (Figure 2A) and to set the imaging precisely in the center (Figure 2B). Next, the stack of images was acquired and the obje.......

Discussion

There are many variations of the primary NCMIR method described by Deerinck in 201010. The basic principles remain the same but, depending on the type of material studied, slight changes are implemented. It was described previously that different resins can be used to embed specimens for SBEM and for example in the case of plants, Spurr's is the resin of choice due to its low viscosity that allows better infiltration through the cell walls22,

Acknowledgements

SBEM imaging, light microscopy imaging and electron microscopy sample preparation were performed with the use of the equipment of Laboratory of Imaging Tissue and Function which serves as an imaging core facility at the Nencki Institute of Experimental Biology.

For preparation of Figure 1, the image of a mouse (Souris_02), and a vial from the https://smart.servier.com/ was used.

This work was supported by the National Science Centre (Poland) Grant Opus (UMO-2018/31/B/NZ4/01603) awarded to KR.

....

Materials

NameCompanyCatalog NumberComments
Anesthetic:
Ketamine/xylazine mixture (Ketamina/Sedazin)Biowet Pulawy, Pulawy, Poland
Sodium pentobarbital (Morbital)Biowet Pulawy, Pulawy, Poland
Fixatives:
Glutaraldehyde (GA)Sigma-Aldrich,St. Louis, MI, USAG5882Grade I, 25% in H2O, specially purified for use as an electron microscopy fixative
Hydrochloric acid (HCl)POCH, Gliwice, Poland575283115pure p.a.
Paraformaldehyde (PFA)Sigma-Aldrich,St. Louis, MI, USA441244prilled, 95%
Phosphate buffered saline (PBS), pH 7.4Sigma-Aldrich,St. Louis, MI, USAP4417-50TABtablets
Sodium hydroxide (NaOH)Sigma-Aldrich,St. Louis, MI, USAS5881reagent grade, figure-materials-132598%, pellets (anhydrous)
Sodium phosphate dibasic (Na2HPO4)Sigma-Aldrich,St. Louis, MI, USAS3264
Sodium phosphate monobasic (NaH2PO4)Sigma-Aldrich,St. Louis, MI, USAS3139
Perfusion:
Large blunt/blunt curved scissors (~14.5 cm)Fine Science Tools, Foster City, CA, USA14519-14
Micro-spatula (double 2" flat ends, one rounded, one tapered to 1/8")Fine Science Tools, Foster City, CA, USA10091-12
Needle tip, 15 GA, blunt (perfusion needle)KD Medical GmbH Hospital Products, Berlin, GermanyKD-FINE 9004131.80 x 40 mm
Pair of fine (Graefe) tweezersFine Science Tools, Foster City, CA, USA11050-10
Perfusion pumpLead FluidBQ80S
Plastic vialsProfilab, Warsaw, Poland534.02plastic vials with blue cap for tissue storage, 20 ml, 31 x 48 mm
Straight iris scissors (~9 cm)Fine Science Tools, Foster City, CA, USA14058-11
Brain slices preparation for EM:
12-well plateNEST, Rahway, NJ, USA712001
Cyanoacrylic glueFenedur, Montevideo, Uruguay
Glass vialsElectron Microscopy Sciences, Hatfield, PA, USA7263220 ml Scintillation Vial, a pack of 100
Pasteur pipetteVWR, Radnor, PA, USA612-4545LDPE, disposable, 7.5 ml
Razor bladeWilkinson Sword, London, UKClassic double edge safety razor blades
Scalpel bladeSwann-Morton, Sheffield, UKNo. 20
VibratomeLeica Microsystems, Vienna, AustriaLeica VT1000 S
Brain slices preparation for IF:
96-well plateNEST, Rahway, NJ, USA701101
CriostatLeica Microsystems, Vienna, AustriaLeica CM 1950
Ethylene glycolBioshop, Burlington, CanadaETH001
Low-profile disposable blade 819Leica Biosystems Inc., USA14035838925
Scalpel bladeSwann-Morton, Sheffield, UKNo. 20
Sodium azide (NaN3)POCH, Gliwice, Poland792770426
SucrosePOCH, Gliwice, Poland772090110
Tissue freezing medium for cryosectioning, OCT-CompoundLeica Biosystems, Switzerland14020108926
Immunostaining:
24-well plateNEST, Rahway, NJ, USA702001
Anti-Post Synaptic Density Protein 95 AntibodyMerck-Millipore, Burlington, MA, USAMAB1598
Confocal microscopeZeiss, Göttingen, GermanyZeiss Spinning Disc microscope (63 × oil objective, NA 1.4, pixel size 0.13 µm × 0.13 µm)
Cover slideMenzel Glaser, Braunschweig, GermanyB-123124 x 60 mm
Donkey anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 555Invitrogen, Carlsbad, CA, USAA31570
Fluoromount-G Mounting Medium, with DAPIInvitrogen, Carlsbad, CA, USA00-4959-52
Microscope slideThermo Scientific, Waltham, MA, USAAGAA00008SuperFrost
Normal donkey serum (NDS)Jackson ImmunoResearch Laboratories, West Grove, PA, USA017-000-121
ShakerJWElectronic, Warsaw, PolandKL-942
TritonT X-100 Reagent GradeBioshop, Burlington, CanadaTRX506
Electron microsocpy sample preparation
Potassium hexacyanoferrate(II) trihydratePOCH, Gliwice, Poland746980113
Aclar 33C FilmElectron Microscopy Sciences, Hatfield, PA, USA50425Fluoropolymer Film embedding sheet
DMP-30, 2,4,6-Tris(dimethylaminomethyl)phenolSigma-Aldrich,St. Louis, MI, USAT58203Epoxy embedding medium accelerator
Durcupan ACM single component A, MSigma-Aldrich,St. Louis, MI, USA44611Durcupan ACM single component A, M epoxy resin
Durcupan ACM single component BSigma-Aldrich,St. Louis, MI, USA44612Durcupan ACM single component B, hardener 964
Durcupan ACM single component DSigma-Aldrich,St. Louis, MI, USA44614Durcupan ACM single component D , plasticizer
Ethyl alcohol absolutePOCH, Gliwice, Poland64-17-5Ethyl alcohol absolute 99.8 % pure P.A.-BASIC
Genlab laboratory ovenWolflabs, York, UKMino/18/SSOven Genlab MINO/18/SS 18l volume, no fan circulation, no digital display, standard temperature gradient, standard recovery rate, no timer, 250°C maximum temperature, 240V electrical supply
L-Aspartic acidSigma-Aldrich,St. Louis, MI, USAA-9256reagent grade, figure-materials-838698% (HPLC)
Lead (II) nitrateSigma-Aldrich,St. Louis, MI, USA467790figure-materials-858699.95% trace metals basis
Osmium tetroxideSigma-Aldrich,St. Louis, MI, USA75632for electron microscopy, 4% in H2O
pH meterElmetron, Zabrze, PolandCP-5-5
RotatorBioSan, Józefów, PolandMulti Bio RS-24rotator Multi Bio RS-24
Sodium hydroxide (NaOH)Sigma-Aldrich,St. Louis, MI, USAS5881reagent grade, figure-materials-923698%, pellets (anhydrous)
Sunflower mini shakerGrant bio, Shepreth,UKPD-3D
Syringe filterMillipore, Burlington, MA, USASLGP033NB0,22 µm pore size
ThiocarbohydrazideSigma-Aldrich,St. Louis, MI, USA88535purum p.a., for electron microscopy, figure-materials-974499.0% (N)
Uranyl acetateServa, Heidelberg, Germany77870Uranyl acetate·2H2O, research grade
Water bathWSL, Swietochlowice, PolandLWT
Specimen mounting for SBEM
96-well culture plateVWR, Radnor, PA, USA734-278296-well plates, round bottom, non treated
AM Gatan 3View stub handling tweezersMicro to Nano, Haarlem, Netherlands
Netherlands
50-001521
BinocularOPTA-TECH, Warsaw, PolandX2000
Conductive glueChemtronics, Georgia, USACW2400conductive eopxy
Gatan 3View sample pin stubsMicro to Nano, Haarlem, Netherlands
Netherlands
10-006003
ParafilmSigma-Aldrich,St. Louis, MI, USAP7793roll size 20 in. × 50 ft
Pelco conductive silver paintTed Pella, Redding, CA, USA16062-15PELCO® Conductive Silver Paint, 15g
Razor blades double edgeElectron Microscopy Sciences, Hatfield, PA, USA72000Stainless Steel "PTFE" coated. PERSONNA brand .004" thick, wrapped individually, 250 blades in a box.
Scanning Electron MicroscopeZeiss, Oberkochen, GermanySigma VP with Gatan 3View2 chamber, acceleration voltage 2.5 kV, variable pressure 5 Pa, aperture 20 µm, dwell time 6 µs, slice thickness 60 nm, magnification 15 000 x, image resolution 2048 x 2048 pixels, pixel size 7.3 nm
trim 90° diamond knifeDiatome Ltd., Nidau, SwitzerlandDTB90
UltramicrotomeLeica Microsystems, Vienna, AustriaLeica ultracutR
Softwarewebpagetutorials
FijiJhttps://fiji.sc/
Microscopy Image Browserhttp://mib.helsinki.fi/http://mib.helsinki.fi/tutorials.html
Reconstructhttps://synapseweb.clm.utexas.edu/software-0https://synapseweb.clm.utexas.edu/software-0)
Animals
MiceAdult 3-month old and 20±1 month old female Thy1-GFP(M) mice (Thy1-GFP +/-) (Feng et al.,2000) which express GFP in a sparsely distributed population of glutamatergic neurons. Animals were bred as heterozygotes with the C57BL/6J background in the Animal House of the Nencki Institute of Experimental Biology.

References

  1. Bosch, M., Hayashi, Y. Structural plasticity dendritic spines. Current Opinion in Neurobiology. 22 (3), 383-388 (2012).
  2. Borczyk, M., Radwanska, K., Giese, K. P. The importance of ultrastructural analysis of memory. Brain Resea....

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