Epoxy Embedding Research Articles

Large-scale Scanning Transmission Electron Microscopy (Nanotomy) of Healthy and Injured Zebrafish Brain.

Large-scale 2D electron microscopy (EM), or nanotomy, is the tissue-wide application of nanoscale resolution electron microscopy. Others and we previously applied large scale EM to human skin pancreatic islets, tissue culture and whole zebrafish larvae1-7. Here we describe a universally applicable method for tissue-scale scanning EM for unbiased detection of sub-cellular and molecular features. Nanotomy was applied to investigate the healthy and a neurodegenerative zebrafish brain. Our method is based on standardized EM sample preparation protocols: Fixation with glutaraldehyde and osmium, followed by epoxy-resin embedding, ultrathin sectioning and mounting of ultrathin-sections on one-hole grids, followed by post staining with uranyl and lead. Large-scale 2D EM mosaic images are acquired using a scanning EM connected to an external large area scan generator using scanning transmission EM (STEM). Large scale EM images are typically ~ 5 - 50 G pixels in size, and best viewed using zoomable HTML files, which can be opened in any web browser, similar to online geographical HTML maps. This method can be applied to (human) tissue, cross sections of whole animals as well as tissue culture1-5. Here, zebrafish brains were analyzed in a non-invasive neuronal ablation model. We visualize within a single dataset tissue, cellular and subcellular changes which can be quantified in various cell types including neurons and microglia, the brain's macrophages. In addition, nanotomy facilitates the correlation of EM with light microscopy (CLEM)8 on the same tissue, as large surface areas previously imaged using fluorescent microscopy, can subsequently be subjected to large area EM, resulting in the nano-anatomy (nanotomy) of tissues. In all, nanotomy allows unbiased detection of features at EM level in a tissue-wide quantifiable manner.

Grinding and polishing instead of sectioning for the tissue samples with a graft: Implications for light and electron microscopy

A broad use of the graft replacement requires a detailed investigation of the host-graft interaction, including both histological examination and electron microscopy. A high quality sectioning of the host tissue with a graft seems to be complicated; in addition, it is difficult to examine the same tissue area by both of the mentioned microscopy techniques. To solve these problems, we developed a new technique of epoxy resin embedding with the further grinding, polishing, and staining. Graft-containing tissues prepared by grinding and polishing preserved their structure; however, sectioning frequently required the explantation of the graft and led to tissue disintegration. Moreover, stained samples prepared by grinding and polishing may then be assessed by both light microscopy and backscattered scanning electron microscopy. Therefore, grinding and polishing outperform sectioning when applied to the tissues with a graft.

Insertion trauma of a cochlear implant electrode array with Nitinol inlay

The integration of a shape memory actuator is a potential mechanism to achieve a consistent perimodiolar position after electrode insertion during cochlear implant surgery. After warming up, and therefore activation of the shape memory effect, the electrode array will change from a straight configuration into a spiral shaped one leading to a final position close to the modiolus. The aim of this study was to investigate whether the integration of an additional thin wire (referred to as an "inlay") made of Nitinol, a well-established shape memory alloy, in a conventional hearing preservation electrode array will affect the insertion behaviour in terms of increased risk of insertion trauma. Six conventional Hybrid-L electrode arrays (Cochlear Ltd., Sydney, Australia) were modified to incorporate a wire inlay made of Nitinol. The diameter of the wires was 100µm with a tapered tip region. Electrodes were inserted into human temporal bone specimens using a standard surgical approach. After insertion and embedding in epoxy resin, histological sections were prepared to evaluate insertion trauma. Insertion was straightforward and no difficulties were observed. The addition of a shape memory wire, thin but also strong enough to curl the electrode array, does not result in histologically detectable insertion trauma. Atraumatic insertion seems possible.

Morphofunctional Merits of an In Vivo Cryotechnique for Living Animal Organs: Challenges of Clinical Applications from Basic Medical Research.

Recent advances in molecular and genetic techniques have led to establishment of new biomedical fields; however, morphological techniques are still required for a more precise understanding of functioning cells and tissues. Conventional preparation procedures involve a series of chemical fixation, alcohol dehydration, paraffin or epoxy resin embedding, sectioning, and staining steps. In these steps, technical artifacts modify original morphologies of the cells being examined. Furthermore, difficulties are associated with capturing dynamic images in vivo using conventional chemical fixation. Therefore, a quick-freezing (QF) method was introduced for biological specimens in the 20th century. However, specimens have to be resected from living animal organs with blood supply, and their dynamical morphologies have not been investigated in detail using the QF method. In order to overcome these issues, the tissue resection step of organs had to be avoided and samples needed to be frozen under blood circulation. Our in vivo cryotechnique (IVCT) was an original technique to cryofix samples without resecting their tissues. The most significant merit of IVCT is that blood circulation into organs is preserved at the exact moment of freezing, which has been useful for arresting transient physiological processes of cells and tissues and maintaining their components in situ.

Recurrent laryngeal nerve alterations in developing spontaneously hypertensive rats.

It is well known that the recurrent laryngeal nerve not only innervates the larynx but also contains baroreceptor fibers, as demonstrated by physiological studies. Because hypertension has a negative impact on both peripheral nerve morphology and the baroreflex, we investigated the recurrent laryngeal nerve morphological alterations related to the development of hypertension. We compared morphological and morphometric aspects of different segments of the recurrent laryngeal nerve in male and female spontaneously hypertensive rats in different ages: 5, 8, and 20 weeks (n = 6 per group). Blood pressure and heart rate were recorded in anesthetized animals, followed by removal of the right and left recurrent laryngeal nerves for epoxy resin embedding and light microscopy analysis. Computer software was used for morphometric analysis. The blood pressure was significantly higher in 20-week-old animals compared to those at 5 weeks. Body weight increased significantly with age, as did the nerve fascicles. For the myelinated fibers and respective axons, there was a reduction of fiber size, more evident on the axon, associated with a reduction of the small myelinated fibers percentage in animals with high blood pressure. Also, 20-week-old animals showed a significant reduction of the blood vessel percentage of occupancy compared to younger ages. No differences were observed between genders. Hypertension development impaired axon growth, affecting mainly the small myelinated fibers. Males and females were affected equally. The alterations of the endoneural blood vessels probably played an important role on the small fibers alterations.

Pathology of Internal Limiting Membrane Specimens Following Intravitreal Injection of Ocriplasmin

To describe ultrastructure and immunocytochemistry of internal limiting membrane peelings after unsuccessful treatment with ocriplasmin, to compare with untreated eyes, and to correlate with clinical imaging data. Interventional comparative case series. Internal limiting membrane specimens were removed from 10 eyes with small macular holes and vitreomacular traction during vitrectomy after intravitreal ocriplasmin injection without release of traction or closure of macular holes during follow-up. Based on optical coherence tomography analysis, specimens from 10 other eyes without ocriplasmin treatment served as controls. All specimens were processed as flat mounts for phase-contrast microscopy followed by immunolabeling for fluorescence microscopy and embedding in epoxy resin with serial sectioning for transmission electron microscopy. Despite the absence of contractive epiretinal membranes on optical coherence tomography, we found epiretinal cells and vitreous collagen fibrils on the internal limiting membrane in specimens removed from eyes with and without previous pharmacologic vitreolysis. Immunolabeling revealed glial cells and hyalocytes in macular holes, whereas myofibroblasts were predominant in vitreomacular traction. There was no apparent damage of the vitreoretinal interface after unsuccessful pharmacologic vitreolysis compared to untreated controls. Epiretinal cell proliferation and vitreous collagen fibrils with close adhesions to the internal limiting membrane are not always detectable by optical coherence tomography or may not have been recognized. Since they are associated with unsuccessful ocriplasmin treatment, presence and topography of epiretinal cells and vitreous collagen remnants on the internal limiting membrane should be further elucidated in order to refine criteria and indications for case selection in pharmacologic vitreolysis.

Thermal Property Imaging of Aluminum Nitride Composites

Frequency domain thermoreflectance (FDTR) imaging is used to create quantitative thermal conductivity maps of porous Aluminum Nitride (AlN) particles embedded in epoxy. The AlN-epoxy composite is polished and coated with a metal layer. A piezo stage is used to move the sample for imaging with our FDTR system. For each pixel, a periodically modulated continuous-wave laser (the red pump beam) is focused to a Gaussian spot, less than 2 um in diameter, to locally heat the sample, while a second beam (the green probe beam) monitors the surface temperature through a proportional change in the metals' reflectivity. The pump beam is modulated simultaneously at six frequencies and the thermal properties of the AlN composite are extracted by minimizing the error between the measured probe phase lag at each frequency and an analytical solution to the heat diffusion equation in a multilayer stack of materials. A schematic of the AlN sample in our measurement system and an optical image of the polished surface of the AlN-epoxy composite before coating with metal is shown in a. Two scanning electron microscope images of the porous AlN particles prior to embedding in epoxy are shown in b. One of the six simultaneously collected phase images of the probe laser is shown in c. The dark blue regions in the phase image are pits on the sample surface. We fit the six phase images to our thermal model and obtain thermal conductivity maps. The conductivity maps of four particles are shown in d. A log color bar is used to highlight the contrast of thermal conductivity in a single particle. The thermal conductivity of the AlN particles ranges from 80W/mK in the dense regions to 5W/mK in the porous regions.

Tandem high-pressure freezing and quick freeze substitution of plant tissues for transmission electron microscopy.

Since the 1940s transmission electron microscopy (TEM) has been providing biologists with ultra-high resolution images of biological materials. Yet, because of laborious and time-consuming protocols that also demand experience in preparation of artifact-free samples, TEM is not considered a user-friendly technique. Traditional sample preparation for TEM used chemical fixatives to preserve cellular structures. High-pressure freezing is the cryofixation of biological samples under high pressures to produce very fast cooling rates, thereby restricting ice formation, which is detrimental to the integrity of cellular ultrastructure. High-pressure freezing and freeze substitution are currently the methods of choice for producing the highest quality morphology in resin sections for TEM. These methods minimize the artifacts normally associated with conventional processing for TEM of thin sections. After cryofixation the frozen water in the sample is replaced with liquid organic solvent at low temperatures, a process called freeze substitution. Freeze substitution is typically carried out over several days in dedicated, costly equipment. A recent innovation allows the process to be completed in three hours, instead of the usual two days. This is typically followed by several more days of sample preparation that includes infiltration and embedding in epoxy resins before sectioning. Here we present a protocol combining high-pressure freezing and quick freeze substitution that enables plant sample fixation to be accomplished within hours. The protocol can readily be adapted for working with other tissues or organisms. Plant tissues are of special concern because of the presence of aerated spaces and water-filled vacuoles that impede ice-free freezing of water. In addition, the process of chemical fixation is especially long in plants due to cell walls impeding the penetration of the chemicals to deep within the tissues. Plant tissues are therefore particularly challenging, but this protocol is reliable and produces samples of the highest quality.

Tandem High-pressure Freezing and Quick Freeze Substitution of Plant Tissues for Transmission Electron Microscopy

Since the 1940s transmission electron microscopy (TEM) has been providing biologists with ultra-high resolution images of biological materials. Yet, because of laborious and time-consuming protocols that also demand experience in preparation of artifact-free samples, TEM is not considered a user-friendly technique. Traditional sample preparation for TEM used chemical fixatives to preserve cellular structures. High-pressure freezing is the cryofixation of biological samples under high pressures to produce very fast cooling rates, thereby restricting ice formation, which is detrimental to the integrity of cellular ultrastructure. High-pressure freezing and freeze substitution are currently the methods of choice for producing the highest quality morphology in resin sections for TEM. These methods minimize the artifacts normally associated with conventional processing for TEM of thin sections. After cryofixation the frozen water in the sample is replaced with liquid organic solvent at low temperatures, a process called freeze substitution. Freeze substitution is typically carried out over several days in dedicated, costly equipment. A recent innovation allows the process to be completed in three hours, instead of the usual two days. This is typically followed by several more days of sample preparation that includes infiltration and embedding in epoxy resins before sectioning. Here we present a protocol combining high-pressure freezing and quick freeze substitution that enables plant sample fixation to be accomplished within hours. The protocol can readily be adapted for working with other tissues or organisms. Plant tissues are of special concern because of the presence of aerated spaces and water-filled vacuoles that impede ice-free freezing of water. In addition, the process of chemical fixation is especially long in plants due to cell walls impeding the penetration of the chemicals to deep within the tissues. Plant tissues are therefore particularly challenging, but this protocol is reliable and produces samples of the highest quality.

Expansion Behavior of Octadecylammonium-Exchanged Low- to High-Charge Reference Smectite-Group Minerals as Revealed by High-Resolution Transmission Electron Microscopy on Ultrathin Sections

AbstractUltrathin sections of reference 2:1 layer silicates treated with octadecylammonium cations were examined using high-resolution transmission electron microscopy (HRTEM) to establish the layer structure. Hitherto, few HRTEM ultrathin-section data existed on the expansion behavior of smectite-group minerals with different interlayer-charge values. Without such information, the expansion behavior of both low-charge and high-charge smectite minerals cannot be characterized and the structures observed in HRTEM images of clay-mineral mixtures cannot be interpreted reliably. Reference smectite-group minerals (Upton, Wyoming low-charge montmorillonite; Otay, California high-charge montmorillonite; a synthetic fluorohectorite; and a Jeanne d’Arc Basin offshore Newfoundland clay sample) with a range of layer charge values were examined. To prevent possible intrusion of epoxy resin into interlayers during embedding, the clay samples were first embedded in epoxy, sectioned with an ultra microtome, and then treated with octadecylammonium cations before examination using HRTEM. Lattice-fringe images showed that lower-charge (<0.38 eq/O10(OH)2) 2:1 layers had 13–14 Å spacings, whereas higher-charge (>0.38 eq/O10(OH)2) 2:1 layers had 21 and 45 Å spacings. These differently expanded silicate layers can occur within the same crystal and an alternation of these layer types can generate rectorite-like structures. For comparison, clay samples were also treated with octadecylammonium before epoxy embedding and sectioning and then examined with HRTEM. These samples mostly had highly expanded interlayers due to epoxy intrusion in the interlayer space. The reference clay minerals embedded in epoxy resin, sectioned, and treated with octadecylammonium cations were used to characterize smectite-group minerals in a natural clay sample from the Jeanne d’Arc Basin, Eastern Canada. Smectite-group minerals in this sample revealed similar structures in lattice-fringe images to those observed in the pure reference clay samples. Rectorite-like structures observed in lattice-fringe images were in fact smectite crystals with short, alternating sequences of low-charge and high-charge smectite layers rather than illite-smectite (I-S) phases with expanded smectite layers and non-expanded 10 Å illite layers.

Cellular composition and ultrastructure of periapical granulation tissue in primary and secondary chronic periodontitis.

Background. There are no complete data on the occurrence of bacteria in the outbreak of chronic inflammation a consequence of their high virulence, or the result of a defect of local mechanisms of immune protection. To answer these questions, as well as to evaluate the nature, severity changes periapical tissues of the tooth and the activity of the inflammatory process in the apex of the tooth root is possible only during the morphological study of biopsy material. Objective. The aim of this work was to study the cellular composition and ultrastructural features of the granulation tissue formed during the current the primary and secondary apical periodontitis. Methods. There were included in the histological examination of the teeth 78, who underwent resection of the apex, followed by a fence of histological material. For ultrastructural studies of granuloma periodontal tissue samples were fixed with 2.5% glutaraldehyde solution, material embedded in Epon-812 («SPI-Pon ™ 812 Epoxy Embedding Kit», USA). The study was conducted using a transmission electron microscopy. Results. In the development of destructive periodontal inflammation are actively involved both specific and non-specific mechanisms of immunity. Conclusion. In primary periodontitis granulation tissue contains a moderate amount of white blood cells of various types, as well as single macrophages and plasma cells with reduced functional activity. In secondary periodontitis granuloma contains numerous mononuclear macrophages, plasma cells and giant multinucleated cells with increased activity, which corresponds to the morphological picture of the formation of immune granulomas.

Structural, morphologic and morphometric study of the phrenic nerve: association between experimental diabetes and arterial hypertension (728.24)

Although the association between hypertension and diabetes is common in clinical practice, it is not well known the contribution of each of these diseases in the development of diabetic neuropathy in patients with hypertension. We investigated the presence of peripheral neuropathy, through morphology and morphometry analysis of the phrenic nerve in normotensive rats (Wistar) and spontaneously hypertensive rats (SHR) with experimentally induced chronic diabetes. Diabetic animals received a single injection of streptozotocin (STZ) intravenously while controls received vehicle on the same date. Twelve weeks after injection, arterial pressure and heart rate were recorded and the right and left phrenic nerves were removed and prepared for embedding in epoxy resin and computer morphometry. The phrenic nerves of SHR and diabetic SHR (SHR + STZ) showed reduced number and density of myelinated fibers and Schwann cell nuclei, compared to Wistar. The SHR and SHR+STZ rats showed myelinated fiber size distributions skewed to the right, with an important reduction of the small myelinated fibers. This finding was more pronounced on diabetic SHR when compared to normotensive diabetic animals. We suggest that hypertension causes a reduction of small myelinated fibers and the association of the hypertension and diabetes did not interfere with the small fiber neuropathy present in the hypertensive animals.Grant Funding Source: CAPES, FAPESP, CNPq and FAEPA

A method of mesa trimming with glass knives for obtaining large series of ultrathin sections

Ultrastructural analysis of tissue based on 3D reconstruction from serial ultrathin sections is one of the most adequate methods in studies of spatial organization of bio-objects. The sample preparation technique for 3D reconstruction includes the two most technically difficult procedures: an obtaining of stable ribbon of serial sections and mounting of this ribbon onto a slot grid coated with a support film. To mount the ribbon, special approaches and technical tools have been proposed and well evaluated. Much attention has also been paid to obtaining a large and stable ribbon, but this attention deals mainly with the choice of epoxy embedding media. The critical condition of obtaining the straight and stable ribbon is the precise parallelism of trailing and leading edges of mesa falling onto the knife cutting edge. The mesa trimming with dry diamond knife for cryoultratomy allows this condition to be maintained. In the present communication, the way of obtaining parallel sides of the mesa has been proposed with the aid of two forms of glass knives.

Histological and ultrastructural findings of corneal tissue after failed descemet membrane endothelial keratoplasty

To investigate in a retrospective review the histological and ultrastructural findings after failed primary and early Descemet membrane endothelial keratoplasty (DMEK), propose possible pathomechanisms of graft failure and give clinical implications. The explanted grafts underwent light- and electromicroscopical investigations in eight failed DMEK cases. Haematoxylin - Eosin, periodic acid Schiff and Alcian blue stainings were performed. Special note was given to any residual stromal remnants, absence of endothelial cells, lamellar structure and 'activation' of keratocytes. Of the eight cases, six were re-DMEKs and two penetrating keratoplasties. Partial graft separation was seen in six and no graft separation in two of the cases. The average time-interval to the re-DMEK or penetrating keratoplasty was 4.6 months. Light and electron microscopy of the two explanted stromal specimens showed varying degrees of keratocyte activation. Endothelial cell loss was observed in essentially all explants with varying degrees and positive correlation with intraoperative difficulty. Assumed upside-down situations showed large areas of intact endothelial cells. In addition, a new layer, situated between the endothelial cell layer and the posterior nonbanded layer, was observed with loose intercellular structure. A loss of the endothelial cell layer of varying degrees and positive correlation with intraoperative difficulty are the prominent feature of primary and early DMEK graft failure. Of note is the upside-down situation, in which in some cases, the endothelial cell layer not only remains intact but also demonstrates metabolical activity in forming a novel cellular layer.

Structural modifications of dentinal microcracks with human aging

Several studies have reported the mechanism of crack propagation with aging. Although structural modifications of dentinal microcracks with aging have been evaluated by observing the cracked surface using scanning electron microscope (SEM), very few attempts have been made at sectional observation of the microcracks inside dentine using transmission electron microscopy (TEM). The objectives of this study were to: (1) examine the process of dentinal microcrack formation using TEM and (2) to morphologically evaluate the relation between dentinal microcrack propagation and human aging. Molars from 'young' (16-28 years) and 'aged' (62-76 years) subjects were evaluated. Dentine blocks were cracked with an indenter and sectioned using a diamond knife and ultramicrotome after embedding in epoxy resin. Microcracks were observed by TEM and ultra-high-voltage electron microscope tomography to determine the characteristics of crack propagation in the young and aged teeth. The results show that, in young teeth, crack propagation tended to pass through the dentinal tubules, while in aged teeth, it tended to deflect to the outer side of peritubular dentine (PTD), especially in coronal dentine. The advantage of this method is that it allows visualization and evaluation of the ultrastructural propagation of microcracks in dentine. The differences in crack propagation between young and aged dentine could be explained by differences in PTD thickness.

Ultrastructure of the sciatic nerve in diabetic rats.

Animal models of diabetes have been widely used in experimental studies because they offer promise of new insights into human diabetes. Streptozotocin (STZ)–treated rats are an animal model of insulin‐dependent diabetes mellitus commonly used to study peripheral nervous system alterations even though the changes do not fully match the alterations observed in clinical conditions. Nevertheless, animal studies can be informative as to the changes that develop in the early stages of human diabetes. Male Wistar rats (n = 12) at 42 days of age were used. Induced diabetic animals (n=6) were fasted for 12 hours prior to being injected intraperitoneally with STZ (60mg/kg) in a single dose. Control animals (n=6) received vehicle. Ten weeks after STZ injection the animals were perfused intracardially with Karnovsky solution. Right and left sciatic nerves were dissected and processed for epoxy resin embedding. Samples were imaged with a transmission electron microscope. Large myelinated fibers with morphological signs of axonal atrophy in the sciatic nerves were readily observed. We also showed smaller myelinated fibers with sighs of demyelination. These results suggest that chronic STZ‐induced diabetes in rats caused alterations in the myelinated fibers as well as in the Schwann cells, compatible to the classic diabetes signs and symptoms reported in humans.Support: PNPD/CAPES; FAPESP; CNPq

Morphological and morphometric parameters of sural nerves of Wistar rats are not gender during development.

It is known that gender influences the re‐myelination, pain sensibilization, neural regulation of the vascular function, in vitro axonal growth and the conduction velocity of nerves. However, little is known about the influence of gender on peripheral nerves development. Previous studies from our laboratory described the development of the sural nerves in female rats [1] and concluded that at 180‐days of life the sural nerves are fully developed. We compared the morphological and morphometric aspects of different segments of the sural nerves in male (N=6) and female (N=6) adult (180 days of life) Wistar rats. The animals were anesthetized, perfused and the right and left sural nerves were removed and prepared for epoxy resin embedding and light microscopy. Morphometric analysis was performed with the aid of computer software, and took into consideration the fascicle area and diameter, as well as myelinated fiber number, density, area and diameter. Comparisons between segments and sides were performed and significant differences were considered when p<0.05. The results showed that adult males are larger and heavier than the females. Nevertheless, there were no significant differences between genders, when the sural nerve fascicular parameters were compared. Thus, the morphological and morphometric parameters of sural nerve are not gender related.

Description of the microscopic anatomy of sural nerves in newborn rats.

The morphology of the sural nerve is widely study, however, little is known about the morphometry of this nerve in newborns. We describe the morphological and morphometric aspects of different segments of the sural nerve in female Wistar rats (N=6) with 15 days of life. The animals were anesthetized, perfused and the right and left sural nerves were removed and prepared for epoxy resin embedding and light microscopy. Morphometric analysis was performed with the aid of computer software, and took into consideration the fascicle area and diameter, as well as myelinated fiber number, density, area and diameter. Comparisons between segments and sides were performed and significant differences were considered when p<0.05. There were no differences on the morphology and morphometry between the segments and sides of sural nerve in female Wistar rats with 15 days of life. Comparing the present results with previous data from our laboratory [1], we conclude that the newborns have similar fascicular parameters to those of 30 days‐old animals leading to the conclusion that the sural nerve is fully developed at birth and will grow following the animals’ body weight increase with age.

A correlative approach for combining microCT, light and transmission electron microscopy in a single 3D scenario

BackgroundIn biomedical research, a huge variety of different techniques is currently available for the structural examination of small specimens, including conventional light microscopy (LM), transmission electron microscopy (TEM), confocal laser scanning microscopy (CLSM), microscopic X-ray computed tomography (microCT), and many others. Since every imaging method is physically limited by certain parameters, a correlative use of complementary methods often yields a significant broader range of information. Here we demonstrate the advantages of the correlative use of microCT, light microscopy, and transmission electron microscopy for the analysis of small biological samples.ResultsWe used a small juvenile bivalve mollusc (Mytilus galloprovincialis, approximately 0.8 mm length) to demonstrate the workflow of a correlative examination by microCT, LM serial section analysis, and TEM-re-sectioning. Initially these three datasets were analyzed separately, and subsequently they were fused in one 3D scene. This workflow is very straightforward. The specimen was processed as usual for transmission electron microscopy including post-fixation in osmium tetroxide and embedding in epoxy resin. Subsequently it was imaged with microCT. Post-fixation in osmium tetroxide yielded sufficient X-ray contrast for microCT imaging, since the X-ray absorption of epoxy resin is low. Thereafter, the same specimen was serially sectioned for LM investigation. The serial section images were aligned and specific organ systems were reconstructed based on manual segmentation and surface rendering. According to the region of interest (ROI), specific LM sections were detached from the slides, re-mounted on resin blocks and re-sectioned (ultrathin) for TEM. For analysis, image data from the three different modalities was co-registered into a single 3D scene using the software AMIRA®. We were able to register both the LM section series volume and TEM slices neatly to the microCT dataset, with small geometric deviations occurring only in the peripheral areas of the specimen. Based on co-registered datasets the excretory organs, which were chosen as ROI for this study, could be investigated regarding both their ultrastructure as well as their position in the organism and their spatial relationship to adjacent tissues. We found structures typical for mollusc excretory systems, including ultrafiltration sites at the pericardial wall, and ducts leading from the pericardium towards the kidneys, which exhibit a typical basal infolding system.ConclusionsThe presented approach allows a comprehensive analysis and presentation of small objects regarding both the overall organization as well as cellular and subcellular details. Although our protocol involves a variety of different equipment and procedures, we maintain that it offers savings in both effort and cost. Co-registration of datasets from different imaging modalities can be accomplished with high-end desktop computers and offers new opportunities for understanding and communicating structural relationships within organisms and tissues. In general, the correlative use of different microscopic imaging techniques will continue to become more widespread in morphological and structural research in zoology. Classical TEM serial section investigations are extremely time consuming, and modern methods for 3D analysis of ultrastructure such as SBF-SEM and FIB-SEM are limited to very small volumes for examination. Thus the re-sectioning of LM sections is suitable for speeding up TEM examination substantially, while microCT could become a key-method for complementing ultrastructural examinations.

Cellular Changes that Accompany Shedding of Human Corneocytes

Corneocyte desquamation has been ascribed to either: 1) proteolytic degradation of corneodesmosomes (CD); 2) disorganization of extracellular lamellar bilayers; and/or 3) ‘swell-shrinkage-slough’ (SSS) from hydration/dehydration. To address the cellular basis for normal exfoliation, we compared changes in lamellar bilayer architecture and CD structure in DSquame® strips from the 1st vs. 5th stripping (‘outer’ vs. ‘mid’-stratum corneum [SC], respectively) from 9 normal adult forearms. Strippings were either processed for standard EM or for ruthenium (Ru-V)- or osmium-tetroxide (Os-V) vapor fixation, followed by immediate epoxy embedment, an artifact-free protocol that to our knowledge is previously unreported. CDs are largely intact in the mid-SC, but replaced by electron-dense (hydrophilic) clefts (lacunae) that expand laterally, splitting lamellar arrays in the outer SC. Some undegraded DSG1/DSC1 redistribute uniformly into corneocyte envelopes (CEs) in the outer SC (shown by proteomics, Z-stack confocal imaging and immunoEM). CEs then thicken, likely facilitating exfoliation by increasing corneocyte rigidity. In vapor-fixed images, hydration only altered the volume of the extracellular compartment, expanding lacunae further separating membrane arrays. During dehydration, air replaced water, maintaining the expanded extracellular compartment. Hydration also provoked degradation of membranes by activating contiguous acidic ceramidase activity. Together, these studies identify several parallel mechanisms that orchestrate exfoliation from the surface of normal human skin.