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Query: UMLS:C0276640 (TEM)
 20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Ring-X-bearing Drosophila males were irradiated with 0, 1000, 2000 or 3000 R of X-rays and mated to females that had been injected with saline or 10(-4) M TEM. The mortality and the fertility of the treated females were recorded. The rate of dominant lethals, of entire sex chromosome loss and partial loss of the Y chromosome, the sex ratio, and the rate of mosaics were determined on the progency. TEM slightly increased the rate of mortality of the females. But it did not influence the yield of mutations recovered from the irradiated spermatozoa.
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PMID:Effects of treating drosophila females with TEM on their mortality, and the yields of mutation recovered from x-irradiated sperm. 40 79

Samples of human semen frozen in liquid nitrogen ( - 196 degrees C) with no glycerol, 5 and 10% glycerol were compared with samples that were untreated, with 10% glycerol but not frozen, and spermatozoa frozen at -20 degrees C. SEM and TEM of the samples indicates that 10% glycerol caused fewer surface changes of the spermatozoa than other treatments. Motility counts after the various freezing treatments were also highest when 10% glycerol was used as the cryoprotectant. Nonetheless, cryopreservation is detrimental to spermatozoa and often causes considerable damage to the acrosome with a leakage of the acrosomal contents.
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PMID:Surface structure of spermatozoa frozen for artificial insemination. 88 75

In order to suggest a valid experimental model for correlated studies regarding the complex phenomena of reproductive biology in humans, light (LM), transmission (TEM) and scanning electron microscopic (SEM) observations were carried out on vaginae of sexually mature New-Zealand albino rabbits, both in estrus and at 5 h after mating. To avoid artifacts depending upon the operative times for specimen removal and, in particular, to well visualize the inner surface of this organ, vaginal irrigation with fixative was performed prior to the surgical removal. Our data demonstrate that the upper 2/3 of the vaginal duct form a kind of 'cervico-vaginal canal' which shares many histological features with the human endocervix. In fact, this portion is lined within by a monostratified epithelium provided with tall microvillous and ciliated cells and often invaginated in crypts. After mating, the microvillous cells showed evidence of secretory activity, exhibiting dome-like luminal surfaces. Secretory droplets often contacted cilia and spermatozoa present in the mucosal furrows and crypts. Because of these singular features and the morphofunctional interactions between vaginal epithelium and male gametes, we believe the rabbit to be a helpful model for comparative biology in humans, concerning sperm capacitation and the general reactivity of the female genital tract during the reproductive cycle.
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PMID:The mucosa of the rabbit vagina: a proposed experimental model for correlated morphofunctional studies in humans. 160 62

The endometrium of an infertile patient with Kartagener's syndrome showed initial secretory phase characteristics at SEM, whereas TEM analysis demonstrated several alterations in the central and peripheral microtubular distribution in 87% of the cilia examined. Such aspects seemed appropriate for a normal implantation, but the ciliary immotility or dyskinesia could cause an altered flow of the endometrial secretions and compromise the upstream movement of the spermatozoa.
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PMID:Ultrastructural aspects of endometrial surface in Kartagener's syndrome. 173 4

The distribution of filamentous actin around the maturing sperm head and in spermatozoa of four species of Australian conilurine rodents was investigated at the light and electron microscopic levels. Similar results were obtained for all the species studied. Mechanically isolated spermatids had NBD-phallacidin-positive longitudinal bands of fluorescence over the dorsolateral surface and, in late spermatids, bands of bright fluorescence passed perpendicularly from the dorsal convex to ventral concave surface. TEM observations indicated that these regions corresponded to filaments of ectoplasmic specializations and granular filamentous material around the tubulobulbar complexes, respectively. In testicular and cauda spermatozoa NBD-phallacidin fluorescent material was present in the two ventral processes that extended from the upper concave surface of the sperm head; also fainter material occurred along the concave border and as a dorsocaudal spur. Its distribution was identical for testicular and cauda spermatozoa. TEM of late spermatids showed that in the ventral process closest to the apical hook there were between 170 and 245 filaments, which attached to the inner surface of the postacrosomal dense lamina; in the more caudal ventral process about 70 filaments occurred. No filaments were, however, visible in the mature spermatozoon but, after immunocytochemical labelling for actin, deposition of gold particles was evident over ventral processes of both late spermatids and cauda spermatozoa. Within the female tract these ventral processes made contact with the zona matrix and were taken into the egg cytoplasm unchanged in morphology. The possible functional significance of the filamentous actin in these structures is discussed.
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PMID:Distribution of filamentous actin in and around spermatids and in spermatozoa of Australian conilurine rodents. 175 Oct 42

Acrosome reactions were induced in seminal spermatozoa of the megachiropteran Pteropus poliocephalus, the grey-headed flying fox, using the ionophore A23187 (10 microM in Tyrodes solution with 1% w/v BSA). Samples were taken at 0, 10, and 120 minutes and fixed for electron microscopy. Initial motility of approximately 70% decreased to approximately 10% over 2 hours. The first motile spermatozoa without acrosomal caps were seen after 6 minutes, and by 90 minutes approximately 60% of motile spermatozoa had completed the acrosome reaction. The first sign of the reaction (by TEM) appears to be swelling and cavitation of the acrosomal matrix within the apical and principal segments, followed or possibly accompanied by fusion and fenestration of the outer acrosomal and plasma membranes and dispersion of the matrix except from the equatorial segment. The end-product of the reaction thus conforms to that seen in other eutherian mammals. However, the reaction exposes a uniquely moulded organization of subacrosomal material ("pseudoperforatorium"), shaped like an anvil over the rostral rim of the flattened nucleus and encased by the remaining inner acrosomal membrane. This has two "lateral" spikes on each side that extend approximately to the same width as the head in the region of the equatorial segment. While these barbs could serve to stabilize or anchor the apical segment of the acrosome, their exposure following the acrosome reaction suggests some specific mechanical role in penetration of the zona pellucida or in protecting more caudal structures from abrasive damage.
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PMID:The acrosome reaction in spermatozoa of the grey-headed flying fox (Pteropus poliocephalus: Chiroptera) exposes barbed subacrosomal material. 322 19

In this study we have examined the behaviour and the localization of the fucose-binding protein (FBP) in boar spermatozoa during ionophore induced acrosome reaction (AR) by means of normal TEM and specimen preparation in toto. During early stages of AR the FBP is first localized at the border between equatorial segment and anterior acrosome. With the propagation of the AR the FBP is dramatically expressed and visible over the entire surface of the acrosome and equatorial segment. TEM pictures of this stages show that the FBP is associated with the OAM. At later stages of AR, when acrosomal ghost formation occur, the FBP is associated with the acrosomal ghost, and equatorial segment and to a very low degree also with the IAM. It is concluded from this data that the FBP is responsible for the specific binding of the ghost-sperm unit to the zona pellucida.
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PMID:Electron microscopic localization of a fucose-binding protein in acrosome reacted boar spermatozoa by the fucosyl-peroxidase-gold method. 355 1

The present SEM and TEM study clearly indicated that the epithelial cells of the ampulla vasis deferentis of the dog are capable of performing phagocytosis of degraded spermatozoa and even inert latex beads as in other animals described previously and further supported our working hypothesis that epithelial phagocytosis may be a common event in the vas deferens of mammals, though its precise significance remains to be clarified.
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PMID:Scanning and transmission electron microscopic study of the ampullary region of the dog vas deferens, with special reference to epithelial phagocytosis of spermatozoa and latex beads. 381 43

The adult cat oviduct was viewed by SEM and TEM as spermatozoa of the same species and inert latex beads were injected into its lumen. The present study demonstrates that nonciliated epithelial cells in extensive areas of the oviduct as well as luminal macrophages are capable of actively taking up both the spermatozoa and the latex beads in the manner of phagocytosis. The epithelial cells are thus able to eliminate foreign bodies including degenerating spermatozoa in order to scavenge the lumen, though the cellular mechanisms involved in their phagocytosic activity remain to be elucidated.
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PMID:Phagocytosis of spermatozoa and latex beads by the epithelial cell of the cat oviduct: combined SEM and TEM study. 383 15

A fucose binding protein was detected in boar spermatozoa by means of a specifically developed modified enzyme-linked-lectin-assay using glycosylated peroxidase derivatives. The distribution of the fucose binding protein was assessed by means of fluorescence microscopy with fluoresceinyl-glycosylated peroxidase. Fucose binding was particularly prominent at the apical region of the sperm head. In order to gain more insight into the precise localization of the carbohydrate binding protein electron microscopical studies were performed using fucosyl peroxidase coupled to colloidal gold. In ultrathin sections as well as in specimens prepared in toto for TEM an intensive binding of fucosylperoxidase-colloidal gold was predominantly found at the apical part of the acrosome appearing as a crescent-like area. In some cases this binding pattern was replaced by a triangle-like intensive labelling at the equatorial segment as revealed clearly by specimens prepared in toto. By SDS-PAGE of the SDS-extractable sperm-proteins, followed by transblotting to nitrocellulose and visualization with the fucosylperoxidase by enzymatic amplification with 4-chloro-1-naphthol mainly one protein with the reduced molecular weight of approximately 53 kdal and some small proteins with apparent molecular weights less than 20 kdal was found to be responsible for the fucose-binding ability of porcine spermatozoa.
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PMID:Evidence for a fucose-binding protein in boar spermatozoa. 390 13


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