Correlative light-electron microscopy (CLEM) is a developing technique for combined analysis of immunostaining for various biological molecules coupled with investigations of ultrastructural features of individual cells within a large field of view. This study first introduces a method of CLEM imaging of the same endocrine cells of compact and diffuse Langerhans islets from human pancreatic tissue specimens. The method utilises serial sections obtained from Epon-embedded specimens fixed with glutaraldehyde and osmium tetroxide. Next, serial block-face imaging using scanning electron microscopy (SBF-SEM) is advanced to enable rapid and efficient acquisition of three-dimensional (3D) ultrastructural information from Langerhans islets of mouse pancreas corresponding to the CLEM images. Samples for SBF-SEM observations were postfixed with osmium and stained en bloc and embedded in conductive resins with ketjenblack significantly reduced the charging of samples during SBF-SEM imaging.
- correlative light-electron microscopy (CLEM)
- serial block face SEM (SBF-SEM)
- compact and diffuse Langerhans islets
- conductive resin
Correlative light-electron microscopy (CLEM) is a developing technique for combined analysis of immunostaining for various biological molecules coupled with investigations of ultrastructural features of individual cells within a large field of view. Combined analysis of immunostaining for various biological molecules coupled with investigations of ultrastructural features of individual cells is a powerful approach for studies of cellular functions in normal and pathological conditions of human Langerhans islets.
Next, serial block-face imaging using scanning electron microscopy (SBF-SEM) is advanced to enable rapid and efficient acquisition of three-dimensional (3D) ultrastructural information from Langerhans islets of mouse pancreas corresponding to the CLEM images of human. We confirmed the three-dimensional architecture of compact islets (tail) and diffuse islets (head) of the pancreas from normal adult C57BL/6 J mice by SBF-SEM .
2. Langerhans islets have compact and diffuse type islets
A large number of endocrine cells, constituting 1–2% of the total volume of the human pancreas in adults, are distributed in more than 1 million islets of Langerhans, first described by Paul Langerhans in 1869. The pancreatic islets, in turn, are distributed throughout the pancreas at variable densities in different lobules, although the density in the tail portion is usually slightly higher . Pancreatic islet endocrine stem cells differentiated to mature islet endocrine cells produce four major peptide hormones: insulin (β-cell granule), glucagon (α-cell granule), somatostatin (δ-cell granule), and pancreatic polypeptide (PP-cell granule), all of which show specific views by electron microscopy [3, 4, 5]. Human and rodent pancreases are developed from two different embryological origins; the dorsal origin develops the body and tail portions, whereas the ventral origin derives the head portion of the pancreas. The majority of the pancreas is derived from the dorsal anlage [3, 5, 6, 7, 8]. The islets can be classified into two types . “Compact” islets comprise the majority (90%); they are covered by nests of connective tissues. Compact islets are composed of trabeculae of endocrine cells interspersed with clear capsules between adjacent pancreatic exocrine acini . Other islets are “diffuse”; they have no nests separating them from adjacent exocrine acini. However, the ultrastructure supporting “diffuse” pancreatic islets including islet-encapsulating basement membranes, extracellular matrix, and adjacent exocrine acini have not been elucidated in detail [5, 10, 11, 12, 13]. Regenerating islet-derived gene 1 alpha (REG1α) is secreted by the exocrine pancreas or β cells and affects islet cell regeneration [14, 15], thereby regulating the development of Langerhans islet architecture and diabetogenesis [10, 16, 17].
Conventional histochemical methods, such as aldehyde-fuchsin staining, Hellerstrom-Hellman silver staining, and immunohistochemical labelling of peptide hormones, are currently the major approaches used with light microscopy to directly distinguish between types of endocrine cells [18, 19]. Although examination of multiple peptide contents in combination with investigation of the ultrastructural features of individual endocrine cells would provide a detailed analyses of physiological and pathological alterations of pancreatic islets in genetically and epigenetically divergent samples such as human tissues, correlative light and electron microscopy observations combined with double immunostaining using fluorescently labelled secondary antibodies in the same Epon-embedded sample is an improved technique for correlative light-electron microscopy mapping which has been described before [20, 21, 22, 23, 24].
3. Correlative light-electron microscopy (CLEM)
For the last quarter century, correlative microscopy, combining the power and advantages of different imaging systems (light, electron, X-ray, NMR, etc.), such as confocal laser scanning microscopy (CLSM), super-resolution microscopy (SFM), transmission electron microscopy (TEM) and scanning electron microscopy (SEM), atomic force microscopy (AFM), magnetic resonance imaging (MRI), superconducting quantum interference devices (SQUIDs), and in vivo imaging (IVIS@) containing micro/nano CT (computed tomography), has become an important tool for biomedical research (Figure 1) [25, 26, 27, 28, 29, 30, 31]. In particular, the development of a series of hybrid approaches in technological advancements of microscopy techniques, labelling tools, and fixation or preparation procedures allow correlating functional fluorescence microscopy data and ultrastructural information from a singular biological event. A key role in recent advancements of nanotechnology-based biomedical sciences is based on information obtained by light or electron microscopy. As correlative light electron microscopy (CLEM) approaches become increasingly accessible, long-standing questions of biology and clinical medicine regarding structure-function relation are being revisited [26, 31, 32, 33, 34, 35, 36].
3.1 Sample preparation for CLEM
For good observation of a biological sample in CLEM, fixation remains the ultrastructure of cells or tissue as close to the living material as possible, and subsequent dehydration and embedding. For light microscopy, the chemical fixation was originally designed to preserve the molecular structures of cells and tissues as well as the immunolocalization of components during the subsequent steps of preparation, such as alcohol dehydration and paraffin embedding [37, 38, 39]. On the other hand, double fixation with GA and OsSO4 is suitable for EM observation of the ultrastructure of biomaterials. During the whole process of the fixation and embedding, tissue antigens undergo physicochemical modifications which results in masking of the mostly linear epitopes carried by the tissue components. For that reason, the fixative of immunoelectron microscopy (immuno-EM) is routinely limited to low concentration (0.05~0.5%) glutaraldehyde (GA) and formaldehyde (FA) before antigen-antibody reaction because osmium tetroxide (OsO4) markedly reduce antigen-antibody response [40, 41].
3.1.2 Antigen-antibody assay
The quality of correlative image matching critically depends on the ability to maintain the native organisation of cell or tissue during fixation and subsequent sample preparation. Basically, CLEM imaging based on immuno-EM is three different approaches on antigen-antibody assay: (I) serial sectioning, (II) pre-embedding, and (III) post-embedding because TEM imaging is necessary for section-based assay such as ultra-thick sectioning of the embedded samples [26, 35, 42, 43].
I. Serial sectioning
Serial sectioning for CLEM was reported by Baskin D.G et al. (1979), using immunocytochemistry with osmium-fixed tissues, and broadly used for bioscience and clinical medicine embedding in Epoxy resin [20, 21, 22, 23, 24, 45].
In the pre-embedding method, all of the immunostaining is done prior to embedding the tissue. For pre-embedding labelling, all of the immunostaining is done prior to embedding the tissue in resin for ultrathin sectioning on TEM or preparing the samples on SEM. Antigen-antibody reaction is limited by antibody penetration, as usually under 10 μm thickness.
3.1.3 Antigen masking
The chemistry of epitope masking itself has been poorly understood. The molecular mechanisms behind antigen masking was that the formaldehyde easily cross-linked amino residues of soluble and structure molecules , resulting in artificial changes of the molecular structures.
Antigen masking mechanisms are assumed mainly as follows: (I) molecular modifications of the antigen-carrying proteins upon fixation and embedding, (II) intramolecular modifications leading to antigen masking intrinsic to the protein, and (III) intermolecular effects on other proteins located in close contact with the antigen-bearing one.
3.1.4 Antigen retrieval
To obtain antigen-antibody reaction, some antigen retrieval techniques are frequently used such as enzyme treatment, quick freezing and freeze substitution, freeze-thaw technique, and heating by a microwave apparatus or a high-pressure oven [38, 39, 49, 50, 51, 52, 53]. Heat-induced antigen retrieval (HIAR) was developed as a method frequently used for LM and EM samples [49, 51, 53]. The antigen retrieval effect was assumed to be caused by breaks of the cross-linked molecules. Precise mechanisms of (HIAR) is that the extended polypeptides by heating are charged negatively or positively at basic or acidic pH and that an electrostatic repulsion force acts to prevent random entangling of polypeptides caused by hydrophobic attractive force and to expose antigenic determinants, during cooling process of HIAR solution. HIAR is a powerful tool to all types of immuno-EM for antigen-antibody assay [54, 55, 56].
3.2 CLEM using genetically labelled tag
Many biological functions depend critically upon fine details of cell and tissue molecular architecture that developed imaging technique revealing evolutionally. To overcome the limitation of immune assay and capture in vivo imaging and subsequent data acquisition, genetically labelled tag (GFP, mini-SOG, and APEX2) is applied broadly to intact living cells, tissues, and animal models (Drosophila, Caenorhabditis elegans, zebrafish, and rodents) for 3D CLEM imaging. GFP is converted to HRP-DAB reaction products by photoconversion or by immunolabelling with anti-GFP antibody. New generation of genetically labelled tags (mini-SOG and APEX2) are specialised for CLEM imaging [57, 58, 59, 60, 61, 62, 63, 97, 98].
I. Mini singlet oxygen generator (mini-SOG)
Mini-SOG is a small flavoprotein (106 amino acids) derived from Arabidopsis phototropin 2 capable of singlet oxygen production upon blue light irradiation to generate the polymerisation of diaminobenzidine into an osmiophilic reaction product resolvable by EM.
APEX is an engineered peroxidase that functions as an electron microscopy tag and a promiscuous labelling enzyme for live-cell proteomics. APEX2 (enhanced ascorbate peroxidase) is an engineered peroxidase that catalyses DAB reaction to render target structures electron-dense.
3.3 CLEM using formalin-fixed paraffin-embedded sample (FFPE) for clinical medicine
Using haematoxylin and eosin staining or fluorescence immunostaining of paraffin sections of formalin-fixed paraffin-embedded sample (FFPE) for clinical medicine and simple low-vacuum scanning electron microscopy revealed a three-dimensional survey method for assessing cell/tissue architectures. The CLEM methods are applied widely to human biomaterial resources for clinical medicine [64, 65].
3.4 CLEM using glutaraldehyde and osmium tetroxide-fixed Epon-embedded samples for human Langerhans islets
This study is a developing method of correlative light and electron microscopy imaging of the tissue specimens. The method utilises serial sections obtained from Epon-embedded specimens fixed with glutaraldehyde and osmium tetroxide .
3.4.1 Tissue preparation
Small pieces of human and mouse pancreatic tissue were prefixed with 2.5% glutaraldehyde in 0.1 M phosphate buffer (PB; pH 7.4) for 1 h and postfixed with 1% osmium tetroxide in 0.1 M PB for 1 h. The specimens were routinely dehydrated by passing the tissue through a series of solutions with increasing ethanol concentrations and then embedded in Epon 812 epoxy resin. To examine the specimens, thick Epon sections were first cut at 0.5-μm thickness and routinely stained with toluidine blue (TB). These sections were checked and trimmed to visualise Langerhans islets during the next step.
To identify compact and diffuse Langerhans islets, Epon sections of the human pancreas were prepared, routinely fixed with glutaraldehyde and OsO4, stained with TB, and observed with a light microscope (Figure 3). The compact islets were revealed as large collections of endocrine cells having round to oval shapes (Figure 3A, black arrowheads). Their nuclei have homogeneous chromatin patterns with nucleoli, and the cells have moderately light cytoplasm. In contrast, diffuse islets were composed of trabeculae of endocrine cells interspersed between adjacent acini (Figure 2B, red arrowheads).
3.4.2 Improved serial sectioning techniques
Then, ultrathin sections were cut at 70–80-nm thickness with a diamond knife on an ultramicrotome and mounted on Φ1 × 2 mm single-slit copper grids with a Formvar film covered by evaporated carbon (Figure 2A). Then, serial 0.5-μm thick sections were cut and put on MAS-coated glass slides (Matsunami Adhesive Slides, Matsunami Glass, Osaka, Japan) for subsequent immunohistochemical staining (Figure 2B). The ultrathin sections of the human pancreas tissues on copper grids were double-stained with uranyl acetate and lead citrate and, finally, observed under a H-7500 transmission electron microscope (Hitachi, Tokyo, Japan) at an accelerating voltage of 80 kV. Electron microscopy images and montages of Langerhans islets were edited by Photoshop imaging software (Adobe Systems Incorporated, San Jose, CA, USA).
3.4.3 Immunohistochemistry in Epoxy thick sections
Immunohistochemistry in serial thick sections of Epon blocks. The 0.5-μm thick Epon sections on MAS-coated glass slides were placed on a heating plate and heated to 60–80°C for 15 min. During immunohistochemical staining of the peptide hormones (insulin and glucagon) and REG1α, we noted that two pretreatments after the removal of Epoxy resin, including antigen retrieval by autoclaving and extraction of osmium tetroxide with hydrogen peroxide (Figure 3).
I. Removal of Epoxy resin
Epoxy resin was then removed from the sections by treatment with a mixture of ethoxide and absolute ethanol (1,2, v/v) for 30 min, washed in pure ethanol, and rehydrated in phosphate-buffered saline (PBS, pH 7.4). Prior to using the ethoxide/absolute ethanol mixture, saturated sodium ethoxide was aged for approximately 2 weeks until it turned dark brown .
II. Antigen retrieval by autoclaving
The specimens underwent two optional pretreatments. For antigen retrieval pretreatment, the specimens were autoclaved in 10 mM sodium citrate buffer (pH 6.0) at 120°C for 10 min and rinsed in PBS.
III. Extraction of osmium tetroxide
To extract osmium tetroxide, the specimens were placed in 0.3% hydrogen peroxide for 10 min and rinsed in PBS.
184.108.40.206 Immunoperoxidase-3,3'-diaminobenzidine (DAB) staining
For immunoperoxidase-3,3′-diaminobenzidine (DAB) staining, the specimens were treated with 3% fish gelatin (Sigma-Aldrich, St. Louis, MO, USA) in PBS for 10 min, followed by incubation with each primary antibody (insulin, glucagon, and REG1α) in PBS at 4°C overnight. Immunocontrols were performed using the same procedure with the exception that incubation with the primary antibody was omitted. The specimens were then incubated with a horseradish peroxidase (HRP)-conjugated secondary antibody in PBS for 1 h and visualised by exposure to metal-enhanced DAB (Pierce, Rockford, IL, USA) for 5 min. Finally, the specimens were incubated in 0.04% osmium tetroxide in 0.1 M PB for 30 sec to enhance contrast of the DAB reaction products.
The immunoreactivity of the HRP-DAB reaction was dramatically enhanced by autoclave treatment, and the effect was more prominent in insulin immunostaining (Figure 4D and E, insets; arrows) than in glucagon immunostaining (Figure 4F and G, insets; arrows). Immunocontrols not incubated with primary antibodies have reduced backgrounds caused by secondary antibody conjugated-HRP-DAB reaction products and osmification (Figure 4B and C).
220.127.116.11 Double-fluorescence immunostaining
For single- or double-fluorescence immunostaining experiments, de-osmified thick sections were treated with 3% fish gelatin in PBS for 10 min, followed by primary antibodies in PBS at 4°C overnight. Immunocontrols were performed using the same procedure with the exception that incubation with the primary antibody was omitted. As secondary fluorescently labelled antibodies, we used Alexa Fluor® 594 and Alexa Fluor 488-conjugated secondary antibodies. Immunostained sections were sealed with VECTASHIELD mounting medium (Vector Laboratories). Fluorescence signals for Alexa Fluor 488 or Alexa Fluor 594 were observed with a BX-61 fluorescence microscope (Olympus, Tokyo, Japan). After obtaining fluorescence images, some thick sections were additionally stained with TB for re-examination of morphology (Figure 2B).
Combined analyses using immunohistochemical localisation of hormones and ultrastructure of endocrine cells in animal pituitary glands have been previously reported (Baskin et al., 1979). In those studies, to achieve simultaneous examination, Epon thick sections were prepared from tissues fixed with glutaraldehyde and OsO4 and peroxidase-DAB immunostaining was used for light microscopy, while electron microscopic observations were carried out in serial ultrathin sections . Conventional double fixation was useful because lipid membranes, such as the plasma membrane of cells and vesicles, are well preserved. Epon-embedded sections are frequently used for ultrastructural analyses by electron microscopy because they exhibit well-preserved tissue morphology. However, the weak tissue antigenicity of Epon-embedded sections poses a problem for immunoassays. There have been attempts to improve immunolabelling of epoxy sections by etching hydrophobic Epoxy resin with different alkali solutions , retrieving antigenicity by sodium metaperiodate [21, 67], protease treatments , or heating (autoclaving or microwaving) thick or ultrathin sections for immunoelectron microscopy with various salt solutions [45, 56, 69, 70, 71]. In the present study, in addition to etching the hydrophobic Epon, we utilised autoclaving and pretreatment with hydrogen peroxide to enhance endocrine peptide immunoreactivity. It is believed that heating treatment retrieves immunoreactivity of masked antigens by exposing epitopes hidden because of cross-linking with aldehyde fixatives, whereas hydrogen peroxide treatment may increase immunoreactivity by reducing osmification of the target molecules [56, 69]. These pretreatments of Epon section are broadly applied to antibodies of immunohistochemistry not only for peptide hormones but also for several organelle markers: mitochondria, lysosome and peroxisome, or membrane proteins (aquaporin-1, aquaporin-2 and megalin) or soluble proteins—immunoglobulins (IgA and Ig kappa light chain), J chain, and albumin [45, 68, 71]. Overall, we demonstrated that a combination of double fixation, embedding in Epon, and immunohistochemistry with effective pretreatments was a very useful and robust approach for the simultaneous examination of cellular ultrastructure and antigen distribution in individual cells of the human pancreas. Points to be aware of regarding to pitfall or the limitations of this method: (I) carefully select for combination of first antibodies in double-fluorescence immunostaining, matching for the pretreatment conditions (heating or de-osmification) and (II) weaker DAPI staining for nucleus fluorescence staining after autoclaving .
4. CLEM revealed various types of secretory granules in individual endocrine cells of compact and diffuse Langerhans islets of the human pancreas
Correlative light and electron microscopy observations revealed various types of secretory granules in individual endocrine cells of compact and diffuse islets from specimens of the human pancreas (Figures 5 and 7).
4.1 Compact type of Langerhans islet
The use of our modified immunostaining protocol allowed clear observations of the ultrastructure of endocrine cells immunopositive for insulin, glucagon, and REG1α in serial thick and ultrathin sections in compact Langerhans islets of human pancreatic tissue (Figure 5). Immunostaining signals for insulin in β-cell granules and for glucagon in α-cell granules did not colocalize in the islet cells (Figure 5A,D–F), while patterns of immunostaining for insulin and REG1α overlapped in large parts of double-immunopositive endocrine cells (Figure 5G–I). Immunopositive staining for insulin and glucagon was positive for most islet areas whose ultrastructures were determined in serial ultrathin sections of the same islet (Figure 5A,D–F,J, and K). The compact islet illustrated in Figure 4 had a higher ratio of cells positive for glucagon or insulin compared to cells from the compact islets shown in Figure 3. Areas of α or β cells on electron microscopy images were almost completely identical to the areas immunopositive for insulin and glucagon (Figure 5A,D–F,J, and K). These correlative observations revealed that islet cells with low and high immunoreactivity for glucagon included round-shaped granules with low and high electron density (Figure 5P–R; blue arrows), whereas insulin-positive cells with β-cell granules (Figure 5O; red arrows) and condensing vacuoles (Figure 5O, white arrows). Immunocontrols that were not incubated with primary antibodies have less background related to the Alexia 488- and Alexia 594-conjugated secondary antibodies and, in particular, because of secondary antibody cross-reactivity to native human immunoglobulins trapped in pancreatic tissues around the blood vessels and fixative autofluorescence.
Some endocrine cells of compact islets exhibited weak immunostaining for glucagon, and two types of round granules—with high and low electron densities—were observed in the same glucagon-positive cells identified in the corresponding areas of serial sections (Figure 5). During development and diabetogenesis, α cells may transdifferentiate into β cells for islet regeneration [21, 72]. Granules with a low electron density contain glucagon, glucagon-like peptide (GLP)-1, intervening peptide 2, GLP-2, and preproglucagon which is considered to be undergoing post-translational processing because preproglucagon-containing granules are typically revealed as large α-cell granules with a lower electron intensity [3, 73, 74, 75]. In addition, some of the round granules with a low electron density may correspond to δ-cell granules, whose sizes are smaller than those of α-cell granules . We consider that these δ-cell-like granules, which contain somatostatin, would potentially inhibit insulin and glucose secretion, express autocrine or paracrine to somatostatin receptors (SSTRs), and interact with the architecture of the islet [3, 77].
4.2 Diffuse type of Langerhans islet
Immunoreactive staining for insulin and glucagon was also clearly observed in endocrine cells of diffuse islets, while exocrine cells of adjacent glandular acini were not immunostained (Figures 6 and 7). The immunoreactivities for REG1α and insulin showed different distributions in the same endocrine cells in serial thin sections of diffuse islets (Figure 5B and C). Fluorescently immunostained sections were subsequently stained with TB, and islet structures were found to be well preserved following double-fluorescence immunostaining (Figure 7G and H). Electron microscopy observations of serial ultrathin sections were performed to reveal structural details of diffuse islets in addition to identifying the hormones produced by the respective cells (Figure 7). It was found that β cells double-positive for REG1α and insulin were also the cells that exhibited zymogen-like condensing vacuoles (200–500 nm in size) and many organelles, such as mitochondria, Golgi apparatus, endoplasmic reticulum (ER), and lipofuscin granules (Figure 7J and L, white arrows) . In addition, these endocrine cell granules in contact with exocrine acinar-like cell clusters have electron-dense cores and clear halos. However, insulin and REG1α double-positive endocrine cells consisted of several granular morphologies of human islet endocrine cells. We classified the granules of human islets into four types (α-, β-, δ-, and PP-cell granules) as described previously [3, 5, 74, 76] where (I) α-cell type (glucagon secretory), electron-dense without a clear halo occasionally presenting with a grey halo (Figure 6K, red arrowheads); (II) β-cell type (insulin secretory), granules of this type have electron-dense cores with a crystalline shape (Figure 7K–N, blue arrowheads); (III) δ-cell type (somatostatin secretary), larger and electron-opaque (Figure 7K,L, and N, cyan arrowheads); and (IV) PP-secretory cell type, spherical and smaller granules with a small halo (Figure 7L, green arrowheads). Interestingly, islet endocrine cells in contact with adjacent exocrine acinar-like cell clusters (ATLANTIS) contained zymogen-like granules (Figure 7M, yellow arrow), and cell-to-cell contacts were also detected (Figure 7N, white arrows).
Correlative light and electron microscopy analyses of serial thick and ultrathin sections showed intracellular organelles and membrane interdigitations near cell-to-cell contact areas as well as typical α- or β-cell granules in individual insulin- and glucagon-positive endocrine cells located in both compact and diffuse islets (Figures 5 and 7). Human Langerhans islets contain polygonal endocrine cells that are demarcated by intercellular structures, such as tight junctions, gap junctions, and membrane structures, including interdigitations and invaginations . In diffuse Langerhans islets, we found that some endocrine cells appear to have direct cell-to-cell contacts with adjacent endocrine and exocrine acinar-like cells (Figure 7). These results indicate that electric or metabolic coupling exists not only between adjacent endocrine cells but also between endocrine cells and the surrounding pancreatic exocrine acinar-like cell clusters [10, 44]. We also identified insulin and REG1α double-positive cells that contained zymogen-like condensing granules in the endocrine islet cells, with several types of granules morphologically classified as β-, δ-, and PP-cell like granules (Figure 6).
5. Three-dimensional scanning electron microscopy (3D SEM) with volume imaging
Scanning electron microscopy (SEM) is a powerful technique for three dimensional CLEM imaging. SEM is traditionally used for imaging detecting the surface of cells, tissues, and the whole multicellular organisms by secondary electron beam. Recently, the critical advancement includes serial ultrastructural observation with scanning electron microscopy (SEM) using backscattered electron with specific tissue preparation methods to increase heavy metal deposition for efficient SEM imaging. In brief, three volume SEM methods: serial block-face electron microscopy (SBF-SEM), focused ion beam SEM (FIB-SEM), and array tomography using serial sectioning are illustrated in Figure 8 [79, 80, 81, 82, 83, 84, 85, 96].
6. Serial block-face scanning electron microscopy (SBF-SEM) revealed novel architecture of Langerhans islets
Serial block-face imaging using scanning electron microscopy (SBF-SEM) is advanced to enable rapid and efficient acquisition of three-dimensional (3D) ultrastructural information of large field of 3D volume imaging such as Langerhans islet over 100 μm size, providing a highly spatial resolution of the ultrastructure of diffuse islets from the head portion of mouse pancreas, which has a ventral origin [8, 86, 87].
6.1 Sample preparation using conductive Epon with carbon (ketjenblack)
Samples for SBF-SEM observations were postfixed with osmium and stained en bloc, as described previously. Briefly, mouse pancreatic tissues were prefixed with 2.5% glutaraldehyde in 0.1 M phosphate buffer (PB; pH 7.4) overnight, and tissues were washed with cacodylate buffer (pH 7.4). Notice that perfusion-fixation is easy to open the vessels and cell-to-cell contacts due to pressure artefacts. Tissues were then treated with 2% OsO4 (Nisshin EM, Tokyo, Japan) in 0.1 M cacodylate buffer containing 0.15% K4[Fe(CN)6] (Nacalai Tesque, Kyoto, Japan) for 1 h on ice and 0.1% thiocarbohydrazide (Sigma-Aldrich) for 20 min and 2% OsO4 for 30 min at room temperature. Thereafter, the tissues were treated with 2% uranyl acetate at 37°C for 3 h. Tissues were then treated with lead aspartate solution at 60°C for 30 min. The specimens were routinely dehydrated by passing the tissue through a series of solutions with increasing ethanol concentrations; infiltrated with acetone dehydrated with a molecular sieve, a 1:1 mixture of resin and acetone, and 100% resin; and then embedded in Epon 812 epoxy resin with carbon (ketjenblack) at 60°C for 3 days/overnight. Epon 812 epoxy resin with/without carbon (ketjenblack) enables for three-dimensional (3D) ultrastructural information of a large field of 3D volume imaging such as Langerhans islet over 100 μm size. Following trimming of islets from mouse pancreas, samples were imaged with a Sigma™VP (Carl Zeiss, Munich, Germany) equipped with 3View (Gatan Inc., Pleasanton, CA, USA). The serial images of SBF-SEM were handled with Fiji/ImageJ and segmented and reconstructed to 3D images using MIB (
Samples for SBF-SEM observations were postfixed with osmium and stained en bloc and embedded in conductive resins with ketjenblack significantly reduced the charging of samples during SBF-SEM imaging. Conductive resins were produced by adding the carbon black filler, ketjenblack, to resins commonly used for electron microscopic observations of biological specimens. Carbon black mostly localised around tissues and did not penetrate cells, whereas the conductive resins significantly reduced the charging of samples during SBF-SEM imaging. When serial images were acquired, embedding into the conductive resins improved the resolution of images by facilitating the successful cutting of samples in SBF-SEM [1, 88].
6.2 ATLANTIS in diffuse type of Langerhans islet
Endocrine cells from diffuse islets were also in contact with adjacent exocrine acinar-like cell clusters (ATLANTIS) without a clear capsule (Figure 8D–I). The morphologies of granules in endocrine cells of diffuse islets (Figure 8F) mainly consisted of three types: (I) granules with a spherical dense core and a small halo similar to PP-cell granules (Figure 9F, green arrowheads), (II) granules with a low electron-dense core without halo similar to δ-cell granules (Figure 8F, cyan arrowheads), and (III) granules with a spherical or crystal-shaped dense core with a clear halo similar to β-cell granules .
Serial SBF-SEM images revealed that zymogen-like granules are broadly distributed in these endocrine islet cells in contact with acinar-like cells. The zymogen-like granules have an isotropic distribution from ATLANTIS to the islet cells through direct contact with lamellar ERs in diffuse islets of the pancreatic head portion in adult normal mice derived from ventral origins (Figure 9G–I). Electron microscopic observations showed the same architecture in human diffuse islets in contact with acinar-like cells without a clear capsule. The typical diffuse endocrine islet in contact with acinar-like cells showed typical features of being rich in PP with a paucity of glucagon [3, 8]. Further, endocrine islet cells colocalised most of the PP-cell-like granules and zymogen-like granules directly through cell-to-cell contact sites with lamellar ERs, even if zymogen-like granules were excreted from the ATLANTIS. Using the correlative light and electron microscopy imaging described in the present study, additional basic and clinical studies for the precise identification of the observed granules in glucagon- and insulin-positive cells as well as the immunohistochemical detection of peptide components in human Langerhans islets for detailed clinical analyses of diabetes mellitus and chronic kidney or intestinal diseases closely related to metabolic disorders warrant further investigation [4, 5, 10, 16, 71, 78, 79, 89, 90, 91, 92, 93].
Interestingly, recently developed super-resolution microscopy (SFM) enables a detailed analysis distribution of biological molecules at an even higher resolution (e.g. a lateral resolution of 20–50 nm) by stochastic optical reconstruction microscopy when it is combined with new light microscopy technologies for nano-level analyses, an approach which may be applied to chemically fixed and Epon-embedded specimens [30, 33, 94, 95]. In combination with immunohistochemistry and in situ hybridization in Epon sections, the correlative microscopy observation method would be a more powerful approach capable of revealing human islet regeneration under genomic and transcriptome control such as SSTR expression in β cells from human islets [3, 70, 77].
This work was supported by the JSPS KAKENHI Grant Number 16 K08439 and by the EM facility in the National Institute for Physiological Sciences in Japan.
Competing interest statement
The authors declare that there are no conflicts of interest.