Extracellular ducts within the wall of the spermatheca of tsetse flies (Glossina spp.) (Dipt., Glossrnidae)

1972 ◽  
Vol 61 (4) ◽  
pp. 669-672 ◽  
Author(s):  
A. M. Jordan
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Secretory Cells ◽  
Tsetse Flies ◽  
Glossina Austeni ◽  
Transmission Electron ◽  
Cellular Layer

Each spherical spermatheca of Glossina austeni Newst. is composed of a cuticular lining of the lumen which is surrounded by a layer of secretory cells. When the spermatheca is immersed in Amann's lactophenol the cells of the cellular layer lift away from the cuticular intima revealing numerous clubbed processes projecting outwards from the surface of the intima. Sections of spermathecae examined by transmission electron microscopy show that one clubbed process is associated with each cell of the cellular layer. The “porous” head of the process is within a fluidfilled cavity in the cell, lined with microvilli. The stalk of each process is an extracellular duct down which secretions from the cellular layer pass into the lumen of the spermatheca. It is considered that these secretions are the medium, probably containing nutrients, in which spermatozoa are held while in the spermatheca.

Scanning and Transmission Electron Microscopy of Isolated Cells from the Avian Salt Gland

1977 ◽  
Vol 35 ◽  
pp. 488-489
Author(s):  
Ian G. Thompson
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Physiological Stress ◽  
Single Cells ◽  
Salt Gland ◽  
Secretory Cells ◽  
Surface Coat ◽  
Isolated Cells ◽  
Structural Differentiation ◽  
Transmission Electron

With the advent of new techniques for isolating single cells for biochemical and physiological investigation, an important consideration is the morphological integrity of these cells after dissociation from the intact tissue. Do isolated cells retain the degree of structural differentiation that is apparent in vivo? The principal secretory cells of the avian salt gland are an example of cells that are highly differentiated in form under conditions of physiological stress. This report describes the ultrastructure of dissociated salt gland cells as visualized with the scanning and transmission electron microscope.The dissociation procedure employed here was the same as that applied to the exocrine pancreas. For transmission electron microscopy the cell suspension was centrifuged and the resultant pellet prefixed in cacodylate buffered 3% glutaraldehyde- 1% paraformaldehyde, postfixed in unbuffered 1% osmium tetroxide, and embedded in epon-araldite. An assessment of the cell surface coat following enzymatic dissociation was facilitated by the inclusion of ruthenium red (500 ppm) in both the aldehyde and osmium fixation steps.

Characterization of mammary cells from the lactating rat by electron microscopy

1978 ◽  
Vol 36 (2) ◽  
pp. 560-561
Author(s):  
P. Sadhukhan ◽  
J. Chakraborty ◽  
M. S. Soloff ◽  
M. H. Wieder ◽  
D. Senitzer
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Cell Types ◽  
Myoepithelial Cells ◽  
Mammary Tissue ◽  
Secretory Cells ◽  
Isolated Cells ◽  
Transmission Electron ◽  
Cell Processes ◽  
Phosphatase Cytochemistry

The means to identify cells isolated from the mammary gland of the lactating rat as a prerequisite for cell purification have been developed.The cells were isolated from mammary tissue with 0. 1% collagenase, and they were visualized by scanning and transmission electron microscopy and by alkaline phosphatase cytochemistry.The milk-secreting cells have surface microvilli, whereas the surface of the myoepithelial cells is smooth (Fig. 1). The two isolated epithelial cell types are readily distinguishable by transmission electron microscopy (Fig. 2). The secretory cells contain vacuoles and a relatively extensive rough endoplasmic reticulum, whereas the myoepithelial cells contain a more osmiophilic cytoplasm, contractile filaments (Fig. 3) and elongate processes. These features are consistent with the appearance of the two cell types in situ.Incubation of isolated cells with oxytocin prior to glutaraldehyde fixation resulted in the contraction of the myoepithelial cell processes (Figs. 4 & 5). This physiological response to oxytocin shows that the isolated myoepithelial cells were intact. The appearance of isolated secretory cells was unchanged by the presence of oxytocin.

Scanning and transmission electron microscopy of the female reproductive system of Schistosoma margrebowiei Le Roux, 1933

1990 ◽  
Vol 64 (3) ◽  
pp. 181-192 ◽  
Author(s):  
A. H. H. Awad ◽  
A. J. Probert
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Secretory Cell ◽  
Single Type ◽  
Secretory Cells ◽  
Female Reproductive System ◽  
Sense Organs ◽  
Vitelline Duct ◽  
Dense Bodies ◽  
Transmission Electron

ABSTRACTTransmission electron microscopy shows that the uterus of female Schistosoma margrebowiei possesses the same ultrastructure as that of the tegument but lacks spines and sense organs. It does not possess secretory cells and opens at the gonopore which by scanning electron microscopy was seen to be composed of numerous leaf-like protrusions. The morphology of the ovary is comparable with that of other Digenea. Immature and mature ova possess cortically arranged granules and occur within the posterior zone of the ovary. Cilia and lamellae line the luminal surface of the oviduct and ootype, the lamellae running unidirectionally along the duct. Only a single type of secretory cell is seen within Mehlis' gland and this produces dense bodies which are associated with Goldi bodies. Narrow cytoplasmic channels supported by microtubules deliver these secretory bodies to the ootype. The vitelline duct is lined with cilia and lamellae and the vitelline gland contains four types of cells, S1, S2, S3 and S4. Calcareous corpuscles are found within mature S4 cells.

Virus-Like and Membrane-Bound Particles in the Venom Apparatus of a Parasitoid Wasp (Hymenoptera:Braconidae)

1981 ◽  
Vol 39 ◽  
pp. 610-611
Author(s):  
Karthryn M. Edson
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Reproductive System ◽  
Inner Core ◽  
Parasitoid Wasp ◽  
Accessory Gland ◽  
Secretory Cells ◽  
Transmission Electron ◽  
Membrane Bound ◽  
Secretory Apparatus

Successful parasitism of a host by a parasitoid wasp may be aided by secretions from the venom apparatus, an accessory gland of the female parasitoid's reproductive system. In the present study, transmission electron microscopy of the venom apparatus of Meteorus leviventris reveals virus-like and membrane-bound particles which may influence successful parasitism of the host. This is the first evidence of such particles within the venom apparatus of a parasitoid.The venom apparatus of M. leviventris consists of a venom reservoir with two highly ramified gland filaments attached to it by a common duct.TEM of the secretory cells of the gland filaments reveals particles approximately 50 nm in diameter contained within a cytoplasmic stroma (Fig. 1). These virus-like particles (VLP) have a dense inner core and a hexagonal congifuration. Similar particles are found free within the cytoplasm or associated with vacuoles (Fig. 2).Secretory cells of the gland filaments contain a secretory apparatus which consists of an array of microvilli converging on a central lumen (Fig. 3).

Techniques for Transmission Electron Microscopy of Fiber-Matrix Interfaces in Aluminum Alloy-Boron Composites by Ion Erosio

1971 ◽  
Vol 29 ◽  
pp. 204-205
Author(s):  
G. G. Shaw
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Aluminum Alloy ◽  
Electron Beam ◽  
Pure Aluminum ◽  
Ion Milling ◽  
Transmission Electron ◽  
Fiber Matrix ◽  
Ion Erosion ◽  
Row Of Fibers

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.

Direct Observation of Heat Exchanger Deposits by Cross Sectioning

1967 ◽  
Vol 25 ◽  
pp. 364-365
Author(s):  
R. W. Anderson ◽  
D. L. Senecal
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Heat Exchanger ◽  
Direct Observation ◽  
Cross Sections ◽  
Preparation Method ◽  
Specimen Preparation ◽  
Flowing Water ◽  
Transmission Electron ◽  
Deposit Layer

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.

Phase Transformations in Ti-7w/oMo-3w/oMe Alloy

1974 ◽  
Vol 32 ◽  
pp. 514-515
Author(s):  
S. Fujishiro
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Transmission Electron Microscopy ◽  
Tensile Strength ◽  
Mechanical Processing ◽  
Ray Method ◽  
X Ray ◽  
Transmission Electron ◽  
Water Quench ◽  
Alpha Beta

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.

Two- or three-way observations of the identical cell elements within the same sections by LM, TEM and/or SEM

1978 ◽  
Vol 36 (2) ◽  
pp. 82-83 ◽  
Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Light Microscopy ◽  
Thin Sections ◽  
Transmission Electron ◽  
Identical Cell ◽  
Electron Microscopes ◽  
Scanning Electron

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).

Comparative Microstructures of Ion Milled and Electrochemically Thinned Composite Materials

1974 ◽  
Vol 32 ◽  
pp. 546-547
Author(s):  
R.R. Russell
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Composite Materials ◽  
Great Difficulty ◽  
Ion Milling ◽  
Transmission Electron ◽  
Ion Damage ◽  
Intermetallic Composite

Transmission electron microscopy of metallic/intermetallic composite materials is most challenging since the microscopist typically has great difficulty preparing specimens with uniform electron thin areas in adjacent phases. The application of ion milling for thinning foils from such materials has been quite effective. Although composite specimens prepared by ion milling have yielded much microstructural information, this technique has some inherent drawbacks such as the possible generation of ion damage near sample surfaces.

Maytansine-Induced Mitotic Arrest in Human Lymphoblasts

1977 ◽  
Vol 35 ◽  
pp. 460-461
Author(s):  
Tai-Te Chao ◽  
John Sullivan ◽  
Awtar Krishan
Keyword(s):  
Electron Microscopy ◽  
Cell Cycle ◽  
Transmission Electron Microscopy ◽  
Tubulin Polymerization ◽  
Vinca Alkaloids ◽  
Antimitotic Activity ◽  
Transmission Electron ◽  
Flow Microfluorometry ◽  
Brain Tubulin

Maytansine, a novel ansa macrolide (1), has potent anti-tumor and antimitotic activity (2, 3). It blocks cell cycle traverse in mitosis with resultant accumulation of metaphase cells (4). Inhibition of brain tubulin polymerization in vitro by maytansine has also been reported (3). The C-mitotic effect of this drug is similar to that of the well known Vinca- alkaloids, vinblastine and vincristine. This study was carried out to examine the effects of maytansine on the cell cycle traverse and the fine struc- I ture of human lymphoblasts.Log-phase cultures of CCRF-CEM human lymphoblasts were exposed to maytansine concentrations from 10-6 M to 10-10 M for 18 hrs. Aliquots of cells were removed for cell cycle analysis by flow microfluorometry (FMF) (5) and also processed for transmission electron microscopy (TEM). FMF analysis of cells treated with 10-8 M maytansine showed a reduction in the number of G1 cells and a corresponding build-up of cells with G2/M DNA content.

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