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Serial Block-Face Scanning Electron Microscopy (SBEM) is applied to image and analyze dendritic spines in the murine hippocampus.
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.
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....
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.......
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.......
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,
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.
....Name | Company | Catalog Number | Comments |
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, USA | G5882 | Grade I, 25% in H2O, specially purified for use as an electron microscopy fixative |
Hydrochloric acid (HCl) | POCH, Gliwice, Poland | 575283115 | pure p.a. |
Paraformaldehyde (PFA) | Sigma-Aldrich,St. Louis, MI, USA | 441244 | prilled, 95% |
Phosphate buffered saline (PBS), pH 7.4 | Sigma-Aldrich,St. Louis, MI, USA | P4417-50TAB | tablets |
Sodium hydroxide (NaOH) | Sigma-Aldrich,St. Louis, MI, USA | S5881 | reagent grade, 98%, pellets (anhydrous) |
Sodium phosphate dibasic (Na2HPO4) | Sigma-Aldrich,St. Louis, MI, USA | S3264 | |
Sodium phosphate monobasic (NaH2PO4) | Sigma-Aldrich,St. Louis, MI, USA | S3139 | |
Perfusion: | |||
Large blunt/blunt curved scissors (~14.5 cm) | Fine Science Tools, Foster City, CA, USA | 14519-14 | |
Micro-spatula (double 2" flat ends, one rounded, one tapered to 1/8") | Fine Science Tools, Foster City, CA, USA | 10091-12 | |
Needle tip, 15 GA, blunt (perfusion needle) | KD Medical GmbH Hospital Products, Berlin, Germany | KD-FINE 900413 | 1.80 x 40 mm |
Pair of fine (Graefe) tweezers | Fine Science Tools, Foster City, CA, USA | 11050-10 | |
Perfusion pump | Lead Fluid | BQ80S | |
Plastic vials | Profilab, Warsaw, Poland | 534.02 | plastic vials with blue cap for tissue storage, 20 ml, 31 x 48 mm |
Straight iris scissors (~9 cm) | Fine Science Tools, Foster City, CA, USA | 14058-11 | |
Brain slices preparation for EM: | |||
12-well plate | NEST, Rahway, NJ, USA | 712001 | |
Cyanoacrylic glue | Fenedur, Montevideo, Uruguay | ||
Glass vials | Electron Microscopy Sciences, Hatfield, PA, USA | 72632 | 20 ml Scintillation Vial, a pack of 100 |
Pasteur pipette | VWR, Radnor, PA, USA | 612-4545 | LDPE, disposable, 7.5 ml |
Razor blade | Wilkinson Sword, London, UK | Classic double edge safety razor blades | |
Scalpel blade | Swann-Morton, Sheffield, UK | No. 20 | |
Vibratome | Leica Microsystems, Vienna, Austria | Leica VT1000 S | |
Brain slices preparation for IF: | |||
96-well plate | NEST, Rahway, NJ, USA | 701101 | |
Criostat | Leica Microsystems, Vienna, Austria | Leica CM 1950 | |
Ethylene glycol | Bioshop, Burlington, Canada | ETH001 | |
Low-profile disposable blade 819 | Leica Biosystems Inc., USA | 14035838925 | |
Scalpel blade | Swann-Morton, Sheffield, UK | No. 20 | |
Sodium azide (NaN3) | POCH, Gliwice, Poland | 792770426 | |
Sucrose | POCH, Gliwice, Poland | 772090110 | |
Tissue freezing medium for cryosectioning, OCT-Compound | Leica Biosystems, Switzerland | 14020108926 | |
Immunostaining: | |||
24-well plate | NEST, Rahway, NJ, USA | 702001 | |
Anti-Post Synaptic Density Protein 95 Antibody | Merck-Millipore, Burlington, MA, USA | MAB1598 | |
Confocal microscope | Zeiss, Göttingen, Germany | Zeiss Spinning Disc microscope (63 × oil objective, NA 1.4, pixel size 0.13 µm × 0.13 µm) | |
Cover slide | Menzel Glaser, Braunschweig, Germany | B-1231 | 24 x 60 mm |
Donkey anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 555 | Invitrogen, Carlsbad, CA, USA | A31570 | |
Fluoromount-G Mounting Medium, with DAPI | Invitrogen, Carlsbad, CA, USA | 00-4959-52 | |
Microscope slide | Thermo Scientific, Waltham, MA, USA | AGAA00008 | SuperFrost |
Normal donkey serum (NDS) | Jackson ImmunoResearch Laboratories, West Grove, PA, USA | 017-000-121 | |
Shaker | JWElectronic, Warsaw, Poland | KL-942 | |
TritonT X-100 Reagent Grade | Bioshop, Burlington, Canada | TRX506 | |
Electron microsocpy sample preparation | |||
Potassium hexacyanoferrate(II) trihydrate | POCH, Gliwice, Poland | 746980113 | |
Aclar 33C Film | Electron Microscopy Sciences, Hatfield, PA, USA | 50425 | Fluoropolymer Film embedding sheet |
DMP-30, 2,4,6-Tris(dimethylaminomethyl)phenol | Sigma-Aldrich,St. Louis, MI, USA | T58203 | Epoxy embedding medium accelerator |
Durcupan ACM single component A, M | Sigma-Aldrich,St. Louis, MI, USA | 44611 | Durcupan ACM single component A, M epoxy resin |
Durcupan ACM single component B | Sigma-Aldrich,St. Louis, MI, USA | 44612 | Durcupan ACM single component B, hardener 964 |
Durcupan ACM single component D | Sigma-Aldrich,St. Louis, MI, USA | 44614 | Durcupan ACM single component D , plasticizer |
Ethyl alcohol absolute | POCH, Gliwice, Poland | 64-17-5 | Ethyl alcohol absolute 99.8 % pure P.A.-BASIC |
Genlab laboratory oven | Wolflabs, York, UK | Mino/18/SS | Oven 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 acid | Sigma-Aldrich,St. Louis, MI, USA | A-9256 | reagent grade, 98% (HPLC) |
Lead (II) nitrate | Sigma-Aldrich,St. Louis, MI, USA | 467790 | 99.95% trace metals basis |
Osmium tetroxide | Sigma-Aldrich,St. Louis, MI, USA | 75632 | for electron microscopy, 4% in H2O |
pH meter | Elmetron, Zabrze, Poland | CP-5-5 | |
Rotator | BioSan, Józefów, Poland | Multi Bio RS-24 | rotator Multi Bio RS-24 |
Sodium hydroxide (NaOH) | Sigma-Aldrich,St. Louis, MI, USA | S5881 | reagent grade, 98%, pellets (anhydrous) |
Sunflower mini shaker | Grant bio, Shepreth,UK | PD-3D | |
Syringe filter | Millipore, Burlington, MA, USA | SLGP033NB | 0,22 µm pore size |
Thiocarbohydrazide | Sigma-Aldrich,St. Louis, MI, USA | 88535 | purum p.a., for electron microscopy, 99.0% (N) |
Uranyl acetate | Serva, Heidelberg, Germany | 77870 | Uranyl acetate·2H2O, research grade |
Water bath | WSL, Swietochlowice, Poland | LWT | |
Specimen mounting for SBEM | |||
96-well culture plate | VWR, Radnor, PA, USA | 734-2782 | 96-well plates, round bottom, non treated |
AM Gatan 3View stub handling tweezers | Micro to Nano, Haarlem, Netherlands Netherlands | 50-001521 | |
Binocular | OPTA-TECH, Warsaw, Poland | X2000 | |
Conductive glue | Chemtronics, Georgia, USA | CW2400 | conductive eopxy |
Gatan 3View sample pin stubs | Micro to Nano, Haarlem, Netherlands Netherlands | 10-006003 | |
Parafilm | Sigma-Aldrich,St. Louis, MI, USA | P7793 | roll size 20 in. × 50 ft |
Pelco conductive silver paint | Ted Pella, Redding, CA, USA | 16062-15 | PELCO® Conductive Silver Paint, 15g |
Razor blades double edge | Electron Microscopy Sciences, Hatfield, PA, USA | 72000 | Stainless Steel "PTFE" coated. PERSONNA brand .004" thick, wrapped individually, 250 blades in a box. |
Scanning Electron Microscope | Zeiss, Oberkochen, Germany | Sigma 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 knife | Diatome Ltd., Nidau, Switzerland | DTB90 | |
Ultramicrotome | Leica Microsystems, Vienna, Austria | Leica ultracutR | |
Software | webpage | tutorials | |
FijiJ | https://fiji.sc/ | ||
Microscopy Image Browser | http://mib.helsinki.fi/ | http://mib.helsinki.fi/tutorials.html | |
Reconstruct | https://synapseweb.clm.utexas.edu/software-0 | https://synapseweb.clm.utexas.edu/software-0) | |
Animals | |||
Mice | Adult 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. |
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