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Query: UNIPROT:P56851 (epididymal)
11,273 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Six specific agglutinins were used to identify the terminal sugar residues in the surface oligosaccharides of rabbit and hamster spermatozoa by specific agglutination. Species differences in epididymal sperm were found in the terminal residues, resembling alpha-D-mannose, D-galactose, N-acetyl-D-glucosamine, and N-acetyl-D-galactosamine. Species similarities were found in terminal residues, resembling L-fucose and N-acetylneuraminic acid. When ejaculated rabbit sperm were compared to epididyimal sperm, the latter were more agglutinable with a specific agglutinin recognizing N-acetyl-D-glucosamine.
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PMID:Terminal saccharides on sperm plasma membranes: identification by specific agglutinins. 504 Oct 26

Previous results demonstrated that androgen-dependent rat specific epididymal proteins (SEP) were bound to spermatozoa during their maturation in the epididymis. This paper describes the purification of glycoprotein DE, which constitutes 40% of SEP, and the identification and semiquantitative determination of the sugars forming its oligosaccharide chain. Affinity chromatography on Sepharose-Concanavalin A produced a sample of D-E 95% pure in which 10.5 g of sugar were present per 100 g protein. The percentual composition of the oligosaccharide was D-mannose 19%; D-galactose 3%; N-acetyl-D-glucosamine 33%; N-acetyl-neuraminic acid 31% and D-glucose 13%.
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PMID:Carbohydrate composition of specific rat epididymal protein. 716 Sep 23

The qualitative nature and distribution of glycoproteins in the mouse epididymis during postnatal development was examined by using lectin cytochemical procedures on paraffin sections and lectin blots on electrophoretically separated luminal fluid polypeptides transferred onto nitrocellulose. Histochemical results revealed the presence of glycoproteins with terminal alpha-D-mannose, N-acetyl-D-glucosamine and neuraminic acid in the principal cells along the epididymis during early stages of development (1st week), and glycoproteins containing terminal alpha-L-fucose, N-acetyl-D-galactosamine and alpha-D-galactose in specific regions of the duct during the differentiation state (2nd-3rd week). Lectin staining localized in the Golgi region and at the apical surface increased during development. Specific changes occurred with age and between cell types. Examination of the epididymal luminal fluid glycopeptides by lectin blot analysis revealed the presence of a large number of glycoproteins with various saccharide moieties at 7 days of age. Epididymal differentiation was accompanied either by the disappearance of some glycoproteins (apparent molecular mass: 16, 17.5, 22, 28, 30 and 74 kDa) or the appearance of new glycoproteins in the proximal (23, 13 kDa) and distal regions (29, 20.5, 19 and 14.4 kDa), or along the entire epididymal duct (26 kDa). The main changes occurred in the epididymis of 21-day-old mice and were completed before spermatozoa reached the epididymal lumen.
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PMID:Characterization of glycoconjugates in the epididymal epithelium and luminal fluid during postnatal development of the mouse. 909 Dec 48

The metabolism, rate of intracellular accumulation of sugars, motility and ultrastructure of ejaculated tammar sperm were impaired by swim-up into artificial media, particularly when the cells were subsequently exposed to N-acetyl-D-glucosamine (NAG). The inclusion of hyaluronate, serum albumin, catalase or Desferal in swim-up media helped prevent deterioration of sperm motility, but failed to prevent detrimental NAG-induced metabolic and ultrastructural changes. However, the sperm were unavoidably diluted during swim-up into artificial media and their behavioural properties were modified by dilution. Thus, sperm collected from the cauda epididymidis were immotile and their rate of oxygen uptake was low in undiluted caudal epididymal semen (CES). Nevertheless, these sperm were viable, and vigorous motility was induced by 5- to 50-fold dilution in Krebs-Ringer phosphate (KRP). Sperm respiration also dramatically increased with moderate dilution (5- or 15-fold) in KRP, but decreased again at higher rates (50-fold). This suggested that motility and the metabolic properties of tammar sperm are modified both by dilution and on leaving the suppressing conditions of the epididymis. Diluted tammar epididymal sperm also displayed a Pasteur effect, but rapidly lost capacity for motility in an oxygen-depleted atmosphere. It was concluded that swim-up procedures compromise ejaculated tammar sperm by promoting dilution-induced changes. This may alter the permeability of the membrane with loss of the enzymes that process the ammonia generated during the metabolism of NAG in seminal plasma. Subsequent exposure to NAG further promotes ultrastructural damage culminating in loss of viability.
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PMID:The ultrastructure and metabolism of ejaculated tammar wallaby sperm are impaired by swim-up procedures when compared with sperm from the cauda epididymidis. 1089 91

To understand the cytochemical properties of epididymal epithelial cells, the characteristics of glycoconjugates in the mouse epididymis were examined using the technique of lectin histochemistry combined with immunohistochemistry. Characteristic staining patterns depending on the type of lectins were observed in the epididymal epithelium. Principal cells expressed N-acetyl-D-galactosamine (GalNAc), N-acetyl-D-glucosamine (GlcNAc), and Fucose in the proximal region of the epididymis and Mannose, Glucose, and Galactose in the distal region of the epididymis. Basal cells expressed Mannose, Glucose, Galactose, and GlcNAc in the proximal region and Galactose in the distal region. On the other hand, clear cells expressed various sugar residues and differences among regions were not observed. Interestingly, principal cells, clear cells, and basal cells specifically reacted with Ulex Europaeus-Agglutinin I (UEA-I lectin), Maackia Amurensis-Lectin I (MAL-I lectin), and Griffonia simplicifolia Lectin I-B4 (GS-I B lectin), respectively. These findings indicate that the selectivity in lectin reactivity for distinct cell types and segment-dependent staining in the epididymis may be related to cellular and regional differences in function. Furthermore, because some lectins stain particular cells or cellular compartments selectively, these lectins could be useful markers for histopathological evaluation of diseases or diagnosis of male infertility.
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PMID:Cell- and region-specific expression of sugar chains in the mouse epididymal epithelium using lectin histochemistry combined with immunohistochemistry. 2264 5