P–015 Characterization of ultrastructural morphology of human sperms by field-emission scanning electron microscopy using the NanoSuit method

2021 ◽  
Vol 36 (Supplement_1) ◽  
Author(s):  
S So ◽  
Y Takaku ◽  
I Ohta ◽  
F Tawara ◽  
T Hariyama

Abstract Study question Can the NanoSuit method to observe sperm cells in wet conditions help treat male infertility using a field emission scanning electron microscope (FE-SEM)? Summary answer Compared with the conventional fixation method, the NanoSuit method can easily prepare FE-SEM samples without causing contraction and denaturation of human sperm cells. What is known already Evaluation of sperm morphology by optical microscopy is important for identifying male infertility. FE-SEM observation is useful for a more detailed evaluation of sperm morphology; however, a lot of the morphological information of the cells is lost by chemical fixation, dehydration, and freeze-drying. The NanoSuit method enables FE-SEM observation of unfixed cells under a high vacuum environment by electron beam polymerization of extracellular substances called NanoSuit. It has been reported that a sample prepared by the NanoSuit method retains the morphological information of live cells better than a sample prepared by the conventional fixation method. Study design, size, duration This laboratory study was conducted with informed consent and IRB approval. Semen parameters were within the WHO normal reference range. Participants/materials, setting, methods The conventional fixation method sample was prepared by fixing (glutaraldehyde and osmium), dehydration (ethanol and t-butyl alcohol), and freeze-drying. The NanoSuit method sample was introduced into the FE-SEM directly without conducting the above treatments. For observation, a JSM–7100F (JEOL, Japan) was used at an acceleration voltage of 1.0 kV. The vacuum level of the observation chamber was 10–3 to 10–6 Pa. Main results and the role of chance Sperm head segmentation (acrosome, equatorial segment, and post acrosome), midpiece, and tail including endpiece could be clearly identified in the FE-SEM sample prepared by the NanoSuit method. Transmission electron microscopy revealed the existence of a thin polymerized extra layer, the NanoSuit, on the surface of the sperm. It is suggested that the presence of the NanoSuit layer enables FE-SEM observation of the unfixed sperm. The conventional fixation method causes a statistically significant contraction in the sperm head size compared to that calculated from optical micrographs (13.5 μm2 vs. 11.6 μm2, p < 0.001). Furthermore, wheat germ agglutinin (WGA), a lectin, which is known to have the ability to bind to the sperm surface, did not bind to the fixed FE-SEM samples. This means that the original cell surface properties are lost in the fixed sperm sample. On the other hand, the FE-SEM sample prepared by the NanoSuit method did not show a statistically significant contraction of the sperm head compared to that calculated from optical micrographs (13.2 μm2 vs 12.9 μm2, p = 0.416); it also revealed a detailed binding pattern of gold-labelled WGA to the sperm surface. These results indicate that the NanoSuit method can prepare FE-SEM samples without sperm contraction and denaturation. Limitations, reasons for caution Characteristic sperm morphology in patients with male infertility should be investigated in future studies. Wider implications of the findings: The NanoSuit method does not use chemical carcinogens and can prepare an FE-SEM sample in a shorter time than the conventional fixation method. The evaluation of ultrastructural morphology of unfixed sperms by this method may be useful for the identification of new morphological features and the evaluation of male infertility. Trial registration number Not applicable

Author(s):  
Charles TurnbiLL ◽  
Delbert E. Philpott

The advent of the scanning electron microscope (SCEM) has renewed interest in preparing specimens by avoiding the forces of surface tension. The present method of freeze drying by Boyde and Barger (1969) and Small and Marszalek (1969) does prevent surface tension but ice crystal formation and time required for pumping out the specimen to dryness has discouraged us. We believe an attractive alternative to freeze drying is the critical point method originated by Anderson (1951; for electron microscopy. He avoided surface tension effects during drying by first exchanging the specimen water with alcohol, amy L acetate and then with carbon dioxide. He then selected a specific temperature (36.5°C) and pressure (72 Atm.) at which carbon dioxide would pass from the liquid to the gaseous phase without the effect of surface tension This combination of temperature and, pressure is known as the "critical point" of the Liquid.


Author(s):  
Linda M. Sicko ◽  
Thomas E. Jensen

The use of critical point drying is rapidly becoming a popular method of preparing biological samples for scanning electron microscopy. The procedure is rapid, and produces consistent results with a variety of samples. The preservation of surface details is much greater than that of air drying, and the procedure is less complicated than that of freeze drying. This paper will present results comparing conventional air-drying of plant specimens to critical point drying, both of fixed and unfixed material. The preservation of delicate structures which are easily damaged in processing and the use of filter paper as a vehicle for drying will be discussed.


Author(s):  
P. A. Madden ◽  
W. R. Anderson

The intestinal roundworm of swine is pinkish in color and about the diameter of a lead pencil. Adult worms, taken from parasitized swine, frequently were observed with macroscopic lesions on their cuticule. Those possessing such lesions were rinsed in distilled water, and cylindrical segments of the affected areas were removed. Some of the segments were fixed in buffered formalin before freeze-drying; others were freeze-dried immediately. Initially, specimens were quenched in liquid freon followed by immersion in liquid nitrogen. They were then placed in ampuoles in a freezer at −45C and sublimated by vacuum until dry. After the specimens appeared dry, the freezer was allowed to come to room temperature slowly while the vacuum was maintained. The dried specimens were attached to metal pegs with conductive silver paint and placed in a vacuum evaporator on a rotating tilting stage. They were then coated by evaporating an alloy of 20% palladium and 80% gold to a thickness of approximately 300 A°. The specimens were examined by secondary electron emmission in a scanning electron microscope.


2001 ◽  
Vol 22 (3) ◽  
pp. 303-308 ◽  
Author(s):  
Hareesh Joshy ◽  
Mitsuru Kuramoto

AbstractThe shape and size of spermatozoa of 11 frog species from India and Sri Lanka were examined by scanning electron microscopy. The spermatozoa of the genera Limnonectes and Euphlyctis were of the generalized type with a thick sperm head and a thin tail, whereas Indirana semipalmata had peculiar spermatozoa with a densely coiled sperm head and a thick tail. Rhacophorus microtympanum is likely to belong to the genus Philautus from sperm morphology. The spermatozoa of Microhyla ornata and Ramanella obscura were very similar, with a cone-shaped sperm head and a thin tail.


2013 ◽  
Vol 9 ◽  
pp. 2877-2885 ◽  
Author(s):  
Jun Hu ◽  
Jindan Wu ◽  
Qian Wang ◽  
Yong Ju

We describe herein the two-component charge-transfer (CT) interaction induced organogel formation with 18β-glycyrrhetinic acid appended pyrene (GA-pyrene, 3) as the donor, and 2,4,7-trinitrofluorenone (TNF, 4) as the acceptor. The use of TNF (4) as a versatile electron acceptor in the formation of CT gels is demonstrated through the formation of gels in a variety of solvents. Thermal stability, stoichiometry, scanning electron microscopy (SEM), optical micrographs, and circular dichroism (CD) are performed on these CT gels to investigate their thermal and assembly properties. UV–vis, fluorescence, mass spectrometric as well as variable-temperature 1H NMR experiments on these gels suggest that the CT interaction is one of the major driving forces for the formation of these organogels.


Author(s):  
Mark E. Gettner ◽  
Myron C. Ledbetter ◽  
Philip S. Woods

Our objective is to take advantage of the resolving power of the scanning electron microscope (SEM) to study details of karyotype morphology for which the light microscope is limited. To the best of our knowledge the SEM has not been used to study karyotypes. To demonstrate the feasibility of this, we chose initially to examine a standard method used in light microscopy, namely the Carnoy-fixed peripheral lymphocyte chromosome technique that has found such universal favor (1), and to modify it for SEM observation. Methods were devised to permit observation and indexing by light microscopy prior to SEM observation. We report here our preliminary results using cells smeared on subbed slides then osmium ligated, and cells smeared on aluminum coated glass without metal staining. Both types of preparations were Giemsa stained and were observed uncoated.


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