This work was supported in part by Grants from National Key Research and Development Program of China (2022YFA1105503), State Key Laboratory of Neuroscience (SKLN-202103), Zhejiang Natural Science Foundation of China (Y21H120019).

Animal care and use protocols were approved by the Ethics Committee of Wenzhou Medical University and followed the guidelines established by the Association for Research in Vision and Ophthalmology (ARVO). All mice were maintained in a 12-h light and 12-h dark cycle and supplied with a standard chow diet.
1. Retina dissection and fixation
<ol>
	<li>Anesthetize the mice (C57BL/6J, Male, 8-week-old, 20-25 g) by injecting 2,2,2-tribromoethanol (0.25 mg/g of body weight) intraperitoneally. Confirm the depth of anesthetization by no retraction of the back paw after pinching the toe or no blinking reflex. Then, dislocate the cervical vertebra while still under anesthesia to euthanize the animal. 
	NOTE: Tribromoethanol was chosen for its well-documented efficacy in inducing rapid and reliable anesthesia in small animal models, particularly for short-term procedures. While pharmaceutical-grade anesthetics are preferred, tribromoethanol offers specific advantages in certain protocols, making it a suitable alternative when properly prepared and administered. All precautions were taken to ensure its safe and effective use. This study adheres to ethical considerations by ensuring proper preparation, administration, and monitoring to mitigate potential risks associated with its use.</li>
	<li>Remove the eyes with curved scissors and immerse the eyes in a mixed solution containing 2% glutaraldehyde and 2% paraformaldehyde in phosphate buffer (PB, 0.1 M, pH 7.4).</li>
	<li>Remove the anterior segment and vitreous from the eyes with forceps under the dissecting microscope.</li>
	<li>Peel the sclera with the two forceps until the retina is completely isolated from the eyecup.</li>
	<li>Cut the retina rapidly into 100 - 200 &#181;m-thick strips with a razor and handle the retina strips with a Pasteur pipette into a new microcentrifuge (EP) tube containing 2% glutaraldehyde and 2% paraformaldehyde in phosphate buffer (PB, 0.1 M, pH 7.4) for 2 h at room temperature (RT) on the rotator. After completion, place the tubes to fix at 4 &#176;C for 24 h.</li>
</ol>
2. Sample embedding process
<ol>
	<li>After washing in 0.1 M sodium cacodylate buffer (pH 7.4) 5 times&#160;for 15 min each, incubate the retina strips with a solution containing 1.5% potassium ferrocyanide and 1% OsO4(in PB, pH7.4) in 0.1 M sodium cacodylate with 4 mM CaCl2 for 1.5 h in the dark on ice. 
	NOTE: Dark incubation and lack of phosphate can prevent precipitation and artifacts in the sample.</li>
	<li>Wash the retina strips 3 times&#160;in ddH2O for 10 min each, and then treat with 1% thiocarbohydrazide in ddH2O for 30 min in the dark at RT.</li>
	<li>After rinsing in ddH2O 3 times&#160;for 15 min each, incubate the retina strips in 2% OsO4 (in PB, PH 7.4) for 45 min in the dark at RT.</li>
	<li>After washing in ddH2O 3 times&#160;for 15 min each, immerse the retina strips in 1% aqueous uranyl acetate in the dark at 4 &#176;C&#160;overnight.</li>
	<li>Next day, after washing in ddH2O 3 times&#160;for 15 min each, treat the retina strips with 0.66% lead nitrate in L-aspartic acid (0.03 M, pH 5.5) for 40 min at 65 &#176;C.</li>
	<li>After washing in ddH2O 3 times&#160;for 15 min each, dehydrate the retina strips with ascending ethanol concentration of 30%, 50%, 70%, 90%, and 100% for 20 min in each solution.</li>
	<li>Treat retina strips with a mixed solution containing equal ethanol and acetone for 20 min, followed by an acetone wash 2 times&#160;for 20 min each.</li>
	<li>Infiltrate the retina strips in acetone/resin mixed in a ratio of 7:3 in the dark at RT&#160;overnight and then acetone/resin at 3:7 in the dark for 24 h at RT. 
	NOTE: The precise composition of the resin is as follows: Epon812 10.06 mL, DDSA 4 mL, MNA 5.94 mL, and DMP-30 0.2 mL.</li>
	<li>Change the tubes the next day and infiltrate the retina strips with pure resin for 24 h at 45 &#176;C. Change the resin again the next day, and embed the retina strips for 48 h at 60 &#176;C. 
	NOTE: The purpose of increasing the temperature is to improve penetration.</li>
</ol>
3. Selection of the area of interest
<ol>
	<li>Cut the resin blocks into 1 &#181;m thick sections, stain sections with 1% toluidine-blue, and observe the general structure of the retina under light microscopy to select the rough regions of interest.</li>
	<li>Coat the resin blocks with platinum using a sputter coater, followed by milling with 70 nm thick section using a focused-ion-beam scanning electron microscopy under a current of 0.23 nA and acceleration voltage of 30 kV.</li>
	<li>Pre-screen the section using FIB-SEM with 2000x magnification to identify the precise regions of interest.</li>
	<li>Collect the data using FIB-SEM with a beam current of 0.69 nA and acceleration voltage of 2 kV. The other parameters are as follows: dwell time = 2 &#181;s, voxel size = 1.8 nm x 1.8 nm x 15 nm.</li>
</ol>

Visualizing Retinal Synaptic Structures in 3D with Volume Electron Microscopy

<ol>
	<li>Masland, R. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+fundamental+plan+of+the+retina.">The fundamental plan of the retina.</a> Nat Neurosci. 4 (9), 877-886 (2001).</li><li>Harris, J. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transmission+electron+microscopy+in+molecular+structural+biology:+A+historical+survey.">Transmission electron microscopy in molecular structural biology: A historical survey.</a> Arch Biochem Biophys. 581, 3-18 (2015).</li><li>Varsano, N., Wolf, S. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Electron+microscopy+of+cellular+ultrastructure+in+three+dimensions.">Electron microscopy of cellular ultrastructure in three dimensions.</a> Curr Opin Struct Biol. 76, 102444 (2022).</li><li>Briggman, K. L., Bock, D. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Volume+electron+microscopy+for+neuronal+circuit+reconstruction.">Volume electron microscopy for neuronal circuit reconstruction.</a> Curr Opin Neurobiol. 22 (1), 154-161 (2012).</li><li>Titze, B., Genoud, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Volume+scanning+electron+microscopy+for+imaging+biological+ultrastructure.">Volume scanning electron microscopy for imaging biological ultrastructure.</a> Biol Cell. 108 (11), 307-323 (2016).</li><li>Sterling, P., Matthews, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Structure+and+function+of+ribbon+synapses.">Structure and function of ribbon synapses.</a> Trends Neurosci. 28 (1), 20-29 (2005).</li><li>Heidelberger, R., Thoreson, W. B., Witkovsky, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synaptic+transmission+at+retinal+ribbon+synapses.">Synaptic transmission at retinal ribbon synapses.</a> Prog Retin Eye Res. 24 (6), 682-720 (2005).</li><li>Thoreson, W. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transmission+at+rod+and+cone+ribbon+synapses+in+the+retina.">Transmission at rod and cone ribbon synapses in the retina.</a> Pflugers Arch. 473 (9), 1469-1491 (2021).</li><li>Moser, T., Grabner, C. P., Schmitz, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sensory+processing+at+ribbon+synapses+in+the+retina+and+the+cochlea.">Sensory processing at ribbon synapses in the retina and the cochlea.</a> Physiol Rev. 100 (1), 103-144 (2020).</li><li>Schmitz, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+making+of+synaptic+ribbons:+how+they+are+built+and+what+they+do.">The making of synaptic ribbons: how they are built and what they do.</a> Neuroscientist. 15 (6), 611-624 (2009).</li><li>Kantardzhieva, A., Peppi, M., Lane, W. S., Sewell, W. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Protein+composition+of+immunoprecipitated+synaptic+ribbons.">Protein composition of immunoprecipitated synaptic ribbons.</a> J Prot Res. 11 (2), 1163-1174 (2011).</li><li>Zampighi, G. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Conical+tomography+of+a+ribbon+synapse:+structural+evidence+for+vesicle+fusion.">Conical tomography of a ribbon synapse: structural evidence for vesicle fusion.</a> PLoS One. 6 (3), e16944 (2011).</li><li>Barnes, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Morphological+diversity+of+the+rod+spherule:+A+study+of+serially+reconstructed+electron+micrographs.">Morphological diversity of the rod spherule: A study of serially reconstructed electron micrographs.</a> Plos One. 11 (3), e0150024 (2016).</li><li>Xu, C. S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enhanced+FIB-SEM+systems+for+large-volume+3D+imaging.">Enhanced FIB-SEM systems for large-volume 3D imaging.</a> Elife. 6, e25916 (2017).</li><li>Crewe, A. V., Lin, P. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+use+of+backscattered+electrons+for+imaging+purposes+in+a+scanning+electron+microscope.">The use of backscattered electrons for imaging purposes in a scanning electron microscope.</a> Ultramicroscopy. 1 (3), 231-238 (1976).</li><li>Richards, R. G., Gwynn, I. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Backscattered+electron+imaging+of+the+undersurface+of+resin-embedded+cells+by+field-emission+scanning+electron+microscopy.">Backscattered electron imaging of the undersurface of resin-embedded cells by field-emission scanning electron microscopy.</a> J Microsc. 177, 43-52 (1995).</li><li>Wergin, W. P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Imaging+thin+and+thick+sections+of+biological+tissue+with+the+secondary+electron+detector+in+a+field-emission+scanning+electron+microscope.">Imaging thin and thick sections of biological tissue with the secondary electron detector in a field-emission scanning electron microscope.</a> Scanning. 19 (6), 386-395 (1997).</li><li>Willingham, M. C., Rutherford, A. 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H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neuronal+diversity+in+the+retina.">Neuronal diversity in the retina.</a> Curr Opin Neurobiol. 11 (4), 431-436 (2001).</li><li>Svara, F. N., Kornfeld, J., Denk, W., Bollmann, J. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Volume+EM+reconstruction+of+spinal+cord+reveals+wiring+specificity+in+speed-related+motor+circuits.">Volume EM reconstruction of spinal cord reveals wiring specificity in speed-related motor circuits.</a> Cell Rep. 23 (10), 2942-2954 (2018).</li><li>Kubota, Y., Sohn, J., Kawaguchi, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Large+volume+electron+microscopy+and+neural+microcircuit+analysis.">Large volume electron microscopy and neural microcircuit analysis.</a> Front Neural Circuits. 12, 98 (2018).</li><li>Guo, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+optimized+approach+using+cryofixation+for+high-resolution+3D+analysis+by+FIB-SEM.">An optimized approach using cryofixation for high-resolution 3D analysis by FIB-SEM.</a> J Struct Biol. 212 (1), 107600 (2020).</li><li>Seligman, A. 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The authors have no disclosures.

We implemented the OTO&#39;s Volume EM sample preparation protocol to analyze the photoreceptors&#39; terminal structure in retinal tissue. The focus was on detailing the entire procedure, starting from the detachment and fixation of the retina to showcasing the results of 3D reconstruction of photoreceptor axon terminals.
The distinctive feature of retinal tissue, unlike brain tissue, lies in its lack of regional differences. Comprising three layers of neuronal cell bodies and two layers of s...

The retina is densely packed with intertwining neuronal axons and dendrites that form synapses between them1. Microscopy is an indispensable tool for studying retinal anatomy as it has fine, intricate, and small structures. Although electron microscopy (EM) provides unparalleled power to investigate the ultrastructure of subcellular organelles and the accurate localization of specific proteins at the nanometer level2, it produces images limited to the two-dimensional (2D) plane, leading to potential loss of key information.
The development of emerging high-resolution volume electron microscopy (Volume EM) techniques supports the provision of more comprehensive and larger-scale three-dimensional (3D) structural information. Some 3D EM methods have been recently reviewed by others3,4,5. 3D EM allows for the reconstruction of neuronal shape and connectivity details, enabling precise quantitative analysis of structures of interest. This demonstrates that the data obtained by volume EM are more systematic, complete, and accurate.
Retinal photoreceptors, constituting the initial neurons in visual signaling6,7, establish synapses with dendrites of second-order bipolar and horizontal cells in the photoreceptor&#39;s terminal to facilitate excitatory signals8,9. These terminals, referred to as cone pedicles and rod spherules, encompass three crucial components: mitochondria, synaptic ribbons, and synaptic vesicles. While previous studies have predominantly concentrated on the general structure of ribbon synapses, there has been a notable absence of investigation into the fine structure of major components, including mitochondria, ribbon, vesicle pools, and their spatial organization in terminals10,11,12,13. A precise and systematic analysis of each component, along with an understanding of their inter-association within photoreceptor terminals, is vital for unraveling spatial organization and comprehensively grasping visual processing functions. In photoreceptors, mitochondria are mainly present in the inner segment, cell body, and terminal. We focused here on the mitochondria in the terminal photoreceptors. Focused ion beam scanning electron microscopy (FIB-SEM), a type of volume EM boasting high resolution (x, y, and z resolution &#60; 5 nm) and a relatively large volume flux4,14, stands as a potent tool for accurately visualizing the 3D structure of photoreceptor terminals.
Both FIB-SEM and Serial Block Face Scanning Electron Microscope (SBF-SEM) are Volume EM based on SEM for obtaining the image of tissues by scanning the surface of the sample. The ultrastructural features of a specimen&#39;s surface are revealed through the contrast created by the intensity of secondary or backscattered electrons (BSE) when the electron beam scans the sample15. Essentially, detecting BSE or secondary electrons from the cross-section surface of a resin-embedded tissue sample in SEM allows for obtaining images of the embedded sample16,17. When BSE or secondary electrons are less generated, information on the sample surface can only be obtained. Achieving consistent contrast and high-quality serial images necessitates sufficient deposition of heavy metals in the sample. Therefore, specific sample preparation protocols are crucial for subsequent segmentation, 3D reconstruction, and analysis when utilizing SEM for serial imaging. The osmium-thiocarbohydrazide-osmium (OTO) method is a typical sample preparation scheme for 3D electron microscopy of biological samples, preserving the structure of lipid-containing membranes and maintaining good contrast18,19.
Here, we developed the OTO method for the preparation of retinal samples for the use of Volume EM. This process particularly focuses on dissecting the retina, determining the optimal fixation time for retinal tissue, and detailing the specific procedures and precautions in 3D sample preparation. Additionally, segmentation and 3D reconstruction of the target structure are integral steps in this extended application. The retina, being a small and challenging structure to obtain materials from, requires swift and precise operations for EM, with fixed times and fresh reagents prepared for immediate use.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>2,2,2-Tribromoethanol</td>
			<td>Sigma-Aldrich</td>
			<td>T48402</td>
			<td></td>
		</tr>
		<tr>
			<td>Acetone</td>
			<td>Electron Microscopy Science</td>
			<td>10000</td>
			<td></td>
		</tr>
		<tr>
			<td>Amira 6.8</td>
			<td>Thermo Fisher Scientific</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>CaCl2</td>
			<td>Sigma</td>
			<td>C-2661</td>
			<td></td>
		</tr>
		<tr>
			<td>Embedding mold</td>
			<td>Beijing Zhongjingkeyi Technology</td>
			<td>GP10590</td>
			<td></td>
		</tr>
		<tr>
			<td>Epon resin</td>
			<td>Electron Microscopy Science</td>
			<td>14900</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethanol</td>
			<td>Sigma</td>
			<td>64-17-5</td>
			<td></td>
		</tr>
		<tr>
			<td>Glutaraldehyde</td>
			<td>Electron Microscopy Science</td>
			<td>16020</td>
			<td></td>
		</tr>
		<tr>
			<td>Helios NanoLab 600i dual-beam SEM</td>
			<td>FEI</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>L-aspartic acid</td>
			<td>Sigma</td>
			<td>56-84-8</td>
			<td></td>
		</tr>
		<tr>
			<td>Lead nitrate</td>
			<td>Sigma</td>
			<td>10099-74-8</td>
			<td></td>
		</tr>
		<tr>
			<td>Na2HPO4.12H2O</td>
			<td>Sigma</td>
			<td>71650</td>
			<td>A component of phosphate buffer</td>
		</tr>
		<tr>
			<td>NaH2PO4.H2O</td>
			<td>Sigma</td>
			<td>71507</td>
			<td>A component of phosphate buffer</td>
		</tr>
		<tr>
			<td>OsO4</td>
			<td>TED PELLA</td>
			<td>4008-160501</td>
			<td></td>
		</tr>
		<tr>
			<td>Paraformaldehyde</td>
			<td>Electron Microscopy Science</td>
			<td>157-8</td>
			<td></td>
		</tr>
		<tr>
			<td>Potassium ferrocyanide</td>
			<td>Sigma</td>
			<td>14459-95-1</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium cacodylate</td>
			<td>Sigma</td>
			<td>6131-99-3</td>
			<td></td>
		</tr>
		<tr>
			<td>Sputter coater</td>
			<td>Leica</td>
			<td>ACE200</td>
			<td></td>
		</tr>
		<tr>
			<td>Thiocarbohydrazide</td>
			<td>Sigma</td>
			<td>2231-57-4</td>
			<td></td>
		</tr>
		<tr>
			<td>Uranyl acetate</td>
			<td>TED PELLA</td>
			<td>CA96049</td>
			<td></td>
		</tr>
	</tbody>
</table>

preparation of retinal samples for volume electron microscopy

Volume electron microscopy (Volume EM) has emerged as a powerful tool for visualizing the 3D structure of cells and tissues with nanometer-level precision. Within the retina, various types of neurons establish synaptic connections in the inner and outer plexiform layers. While conventional EM techniques have yielded valuable insights into retinal subcellular organelles, their limitation lies in providing 2D image data, which can hinder accurate measurements. For instance, quantifying the size of three distinct synaptic vesicle pools, crucial for synaptic transmission, is challenging in 2D. Volume EM offers a solution by providing large-scale, high-resolution 3D data. It is worth noting that sample preparation is a critical step in Volume EM, significantly impacting image clarity and contrast. In this context, we outline a sample preparation protocol for the 3D reconstruction of photoreceptor axon terminals in the retina. This protocol includes three key steps: retina dissection and fixation, sample embedding processes, and selection of the area of interest.

Author Spotlight: Retinal Neuroscience Studies with Volume Electron Microscopy

Preparation of Retinal Samples for Volume Electron Microscopy

We focus on examining the nanoscale 3D structural features of photoreceptor terminals in the mouse retina. Our primary goal is to design 3D EM sample preparation method suitable for small volume of biological samples, and we have reconstructed the terminal structure of retina photoreceptors using FIB-SEM. Using the retinal 3D EM samples with the OTO method, we segmented and reconstructed the 3D structure of four types of photoreceptor terminals and subsequently analyze the relationship between their components.Our retinal sample variation protocol is user friendly, requires no auditory equipment and reduce sensor processing time. However, there may be some in the details of the cell membrane, which we will In the future, we hope to further explore the function of each component within the retinal terminal and its role(indistinct)

Figure 1A shows the image of retinal photoreceptor terminals prepared using the traditional chemical double fixation method, and Figure 1B shows the image of retinal photoreceptor terminals prepared using the OTO method. Both were sampled by FIB-SEM. It can be clearly seen that the cell membrane structure can be retained as much as possible by using the OTO method, and even the outline of vesicles can be clearly seen. In addition, the contrast of images obtained...

This protocol describes the detailed steps for preparing retinal samples for volume electron microscopy, focusing on the structural features of retinal photoreceptor terminals.

Volume electron microscopy (Volume EM) has emerged as a powerful tool for visualizing the 3D structure of cells and tissues with nanometer-level ...

preparation-of-retinal-samples-for-volume-electron-microscopy

Research

JoVE Journal

Neuroscience

Retina Dissection and Fixation for High-Resolution 3D Volume Electron Microscopy

To begin, place the euthanized mouse on the operating table. Using curved scissors, excise the eyes under dim red light and immediately place them in the fixation solution. After removing the anterior segment and vitreous from the eye, isolate the retina completely.Under a dissection microscope, quickly slice the retina into 100 to 200 micrometer thick strips and transfer them into a new micro centrifuge tube containing fixation solution. Incubate the tube in a rotator for two hours at room temperature and then place it at four degrees Celsius for 24 hours.

Embedding Retina Samples to Study Photoreceptor-Synapses Using Volume Electron Microscopy

To begin, obtain the retinal strips from mice and wash them five times in 0.1 molar sodium cacodylate buffer for 15 minutes. Then incubate the strips with potassium ferrocyanide and osmium tetroxide solution in the dark on ice for 1.5 hours. Wash the strips three times in double distilled water and incubate them with 1%thio-carbo-hydrazide.After rinsing with double distilled water, sequentially treat the retina strips with osmium tetroxide, uranyl acetate, and lead nitrate. Dehydrate the retina strips with increasing concentrations of ethanol. Then, treat retina strips with a solution containing equal ethanol and acetone for 20 minutes, followed by two acetone washes for 20 minutes each.Sequentially incubate the retina strips in acetone resin mixtures in the dark at room temperature. Infiltrate the retina strips with pure resin for 24 hours at 45 degrees Celsius, followed by fresh resin for 48 hours at 60 degrees Celsius. The focused ion beam scanning electron microscopy of retinal photoreceptor terminals using this method preserves cell membrane structure and vesicle outlines more clearly than the traditional double fixation method.

313 Views.  Wenzhou Medical University.  This protocol describes the detailed steps for preparing retinal samples for volume electron microscopy, focusing on the structural features of retinal photoreceptor terminals.

Visualizing Retinal Synaptic Structures in 3D with Volume Electron Microscopy

Summary