Fine structure of the lumbosacral neural folds in the mouse embryo

Development ◽  
1980 ◽  
Vol 55 (1) ◽  
pp. 279-290
Author(s):  
Doris B. Wilson ◽  
Laurel A. Finta
Keyword(s):  
Electron Microscopy ◽  
Mouse Embryo ◽  
Intercellular Space ◽  
Intercellular Spaces ◽  
Lumbosacral Region ◽  
Transmission Electron ◽  
Junctional Complexes ◽  
Pass Through ◽  
Means Of Transmission ◽  
Gap Junctional

The neural folds in the lumbosacral region of the normal 8-day and 9-day mouse embryo were studied by means of transmission electron microscopy with and without lanthanum treatment. The cells showed an abundance of ribosomes, microtubules arranged parallel to the long axes of the cells, and microfilaments extending across the apices. At the luminal border junctional complexes were common, and an occasional midbody was seen stretching between adjacent cells nearing the end of telophase. In the 8-day embryos, gap junctional vesicles (annular nexuses) bounded by layered membranes and containing cytoplasm with ribosome-like material were commonly observed; at 9 days the vesicles were relatively rare. The lanthanum-treated material demonstrated that the tracer was able to pass through the subluminal junctional complexes and throughout the intercellular spaces. However, the space between the membranes of the gap junctional vesicles lacked lanthanum and thus apparently did not communicate with the intercellular space.

Ultrastructural Analysis of the Salivary Glands of Gromphadorhina Portentosa (Schaum)

1977 ◽  
Vol 35 ◽  
pp. 638-639
Author(s):  
P.J. Dailey
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Salivary Glands ◽  
Secretory Vesicles ◽  
The Past ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
Gromphadorhina Portentosa ◽  
Scanning Electron ◽  
Topographical Relief

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.

Structural Properties of Amorphous Silicon Produced by Electron Irradiation

1999 ◽  
Vol 557 ◽  
Author(s):  
J. Yamasaki ◽  
S. Takeda
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Distribution Function ◽  
Structural Properties ◽  
Electron Irradiation ◽  
Low Temperatures ◽  
Crystalline Silicon ◽  
Transmission Electron ◽  
Amorphous Si ◽  
Means Of Transmission

AbstractThe structural properties of the amorphous Si (a-Si), which was created from crystalline silicon by 2 MeV electron irradiation at low temperatures about 25 K, are examined in detail by means of transmission electron microscopy and transmission electron diffraction. The peak positions in the radial distribution function (RDF) of the a-Si correspond well to those of a-Si fabricated by other techniques. The electron-irradiation-induced a-Si returns to crystalline Si after annealing at 550°C.

The development of the notochord in the chick embryo, studied by scanning and transmission electron microscopy

Development ◽  
1976 ◽  
Vol 35 (2) ◽  
pp. 383-401
Author(s):  
Mary Bancroft ◽  
Ruth Bellairs
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Chick Embryo ◽  
Intercellular Spaces ◽  
Notochordal Cells ◽  
Fibrillar Material ◽  
Transmission Electron ◽  
Phases Of Development ◽  
Scanning Electron

The notochord of the chick embryo between stages 5 and 23 inclusive has been studied by scanning electron microscopy, supplemented by transmission electron microscopy. Three main phases of development are described, and these have been designated: bilaminar; rodlike, unvacuolated; rod-like and vacuolated. The change in shape of the organ from bilaminar to rod-like is accompanied by changes in the shape, orientation and position of the cells, an increase in the complexity of the cell contacts, and the laying down of a basal lamina. The change from the unvacuolated to the vacuolated phase is accompanied by increasing complexity within the cytoplasm. Most of the vacuoles are intracellular and appear empty though some contain a granular material. The notochordal sheath appears to be secreted by the notochordal cells and fine fibrillar material has been seen in the intercellular spaces. By stage 23, most of the notochordal cells have become so highly vacuolated that the cytoplasm has become closely packed around the nucleus.

scholarly journals The Transport System of Nacre Components through the Surface Membrane of Gastropods

2016 ◽  
Vol 672 ◽  
pp. 103-112 ◽  
Author(s):  
Elena Macías-Sánchez ◽  
Antonio G. Checa ◽  
Marc G. Willinger
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Calcium Carbonate ◽  
Lamellar Structure ◽  
Surface Membrane ◽  
Organic Matrix ◽  
X Ray ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
Electron Energy Loss

The surface membrane is a lamellar structure exclusive of gastropods that is formed during the shell secretion. It protects the surface of the growing nacre and it is located between the mantle epithelium and the mineralization compartment. At the mantle side of the surface membrane numerous vesicles provide material, and at the nacre side, the interlamellar membranes detach from the whole structure. Components of nacre (glycoproteins, polysaccharides and calcium carbonate) cross the structure to reach the mineralization compartment, but the mechanism by which this occurs is still unknown. In this paper we have investigated the ultrastructure of the surface membrane and the associated vesicle layer by means of Transmission Electron Microscopy. Electron Energy Loss Spectroscopy and Energy-dispersive X-ray Spectroscopy were used for elemental analysis. The analyses revealed the concentration of calcium in the studied structures: vesicles, surface membrane, and interlamellar membranes. We discuss the possible linkage of calcium to the organic matrix.

scholarly journals EM∩IM: software for relating ion mobility mass spectrometry and electron microscopy data

The Analyst ◽  
2016 ◽  
Vol 141 (1) ◽  
pp. 70-75 ◽  
Author(s):  
Matteo T. Degiacomi ◽  
Justin L. P. Benesch
Keyword(s):  
Electron Microscopy ◽  
Mass Spectrometry ◽  
Structural Biology ◽  
Cross Sections ◽  
Ion Mobility ◽  
Ion Mobility Mass Spectrometry ◽  
Density Maps ◽  
Transmission Electron ◽  
Microscopy Data ◽  
Means Of Transmission

EM∩IM enables the calculation of collision cross-sections from electron density maps obtained, for example, by means of transmission electron microscopy. This capability will further aid the integration of ion mobility mass spectrometry with modern structural biology.

Mechanisms of misfit strain relaxation in epitaxially grown BLT (Bi4-xLaxTi3O12, x = 0.75) thin films

2003 ◽  
Vol 779 ◽  
Author(s):  
Hyung Seok Kim ◽  
Sang Ho Oh ◽  
Ju Hyung Suh ◽  
Chan Gyung Park
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Transmission Electron Microscopy ◽  
Strain Relaxation ◽  
Lattice Misfit ◽  
Misfit Strain ◽  
Misfit Dislocations ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
20 Nm

AbstractMechanisms of misfit strain relaxation in epitaxially grown Bi4-xLaxTi3O12 (BLT) thin films deposited on SrTiO3 (STO) and LaAlO3 (LAO) substrates have been investigated by means of transmission electron microscopy (TEM). The misfit strain of 20 nm thick BLT films grown on STO substrate was relaxed by forming misfit dislocations at the interface. However, cracks were observed in 100 nm thick BLT films grown on the same STO. It was confirmed that cracks were formed because of high misfit strain accumulated with increasing the thickness of BLT, that was not sufficiently relaxed by misfit dislocations. In the case of the BLT film grown on LAO substrate, the magnitude of lattice misfit between BLT and LAO was very small (~1/10) in comparison with the case of the BLT grown on STO. The relatively small misfit strain formed in layered structure of the BLT films on LAO, therefore, was easily relaxed by distorting the film, rather than forming misfit dislocations or cracks, resulting in misorientation regions in the BLT film.

scholarly journals Bisphosphonate’s Effect on Tongue Mucosa: An Experimental Electron Microscopy Study

Medicina ◽  
2020 ◽  
Vol 56 (2) ◽  
pp. 51
Author(s):  
Theodora Papamitsou ◽  
Antonios Morsi-Yeroyannis ◽  
Anastasios Papanastasiou ◽  
Nikolaos Bakalopoulos ◽  
Eva-Maria Dietrich ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Intercellular Space ◽  
Wistar Rats ◽  
Middle Layer ◽  
Microscopy Study ◽  
Electron Microscopy Study ◽  
Control Group ◽  
The Past ◽  
Transmission Electron ◽  
Experimental Group

Background and objectives: Bisphosphonates (BPs) are selective inhibitors of osteoclasts, used for the treatment of bone disorders. The objective of this study is to investigate the possible effects of BPs on the tongue’s mucosa. Materials and Methods: Specimens of the tongue of 20 female 12-month old Wistar rats were taken. Ten were used as control group, while in the remaining alendronate (Fosamax, Merck) was administered per os from 13 weeks. Observation of the harvested samples was made by Transmission Electron Microscopy (TEM). Results: In the experimental group, focal alterations were observed to various extent in all specimens. The basement membrane was intact. Furthermore, an increase at the intercellular space was observed, predominantly at the middle layer, and the desmosomes were disorganized. In the lamina propria focal edema was observed. Conclusions: Investigation on the effect of BPs on the tongue’s mucosa through TEM hasn’t been documented in the past. According to our results, BPs seem to cause mild mucosal lesions on the tongue.

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