A preliminary study on the glycosylation of the reproductive tract in the Ostrich (Struthio camelus camelus).
Struthioniformes
glycans
lectins
oviduct
uterus
vagina
Journal
Reproduction in domestic animals = Zuchthygiene
ISSN: 1439-0531
Titre abrégé: Reprod Domest Anim
Pays: Germany
ID NLM: 9015668
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
06
10
2020
accepted:
07
11
2020
pubmed:
12
11
2020
medline:
23
7
2021
entrez:
11
11
2020
Statut:
ppublish
Résumé
Glycosylation of the reproductive tract of an adult female red-necked ostrich (Struthio camelus camelus) carrying a fully formed calcified egg in her uterus when accidently killed by a blow to the head was examined using lectin histochemistry on samples from the infundibulum, magnum, uterus and vagina. Glycans in the luminal epithelium and underlying glands were described after staining with 23 lectins after neuraminidase pre-treatment in some cases. Ciliated and non-ciliated cells were evident at all levels in the luminal epithelium, the latter full of richly glycosylated secretory granules. The ciliated cells also showed glycosylation and, in the magnum, these cells often stained more intensely than the non-ciliated cells. High mannose and complex N-glycans, α1,6-linked fucosyl and sialic acid residues were present throughout the tract and there was a complete absence of GalNAcα1,3(LFucα1,2)Galß1,3/4GlcNAcß1- and rare terminal GalNAcα1- residues. Fucose in α1,2-linkage as H2 antigen and Le
Substances chimiques
Polysaccharides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
130-141Informations de copyright
© 2020 Wiley-VCH GmbH.
Références
Aitken, R. N. C., & Johnston, H. S. (1963). Observations on the fine structure of the infundibulum of the avian oviduct. Journal of Anatomy, 97, 87-99.
Bakst, M. R., & Bauchan, G. (2016). Lectin staining of the uterovaginal junction and sperm-storage tubule epithelia in broiler hens. Poultry Science, 95, 948-955. https://doi.org/10.3382/ps/pev440
Fernández-López, J., Martínez, A., Fernández-Ginés, J. M., Sayas-Barberá, E., Sendra, E., & Pérez-Alvarez, J. A. (2006). Gelling and color properties of ostrich (Struthio camelus) egg white. Journal of Food Quality, 29, 171-183. https://doi.org/10.1111/j.1745-4557.2006.00065
Johnston, H. S., Aitken, R. N. C., & Wyburn, G. M. (1963). The fine structure of the uterus of the domestic fowl. Journal of Anatomy, 97, 333-344.
Jones, C. J. P., Aplin, J. D., & Burton, G. J. (2010). First trimester histiotrophe shows altered sialylation compared with secretory phase glycoconjugates in human endometrium. Placenta, 31, 576-580. https://doi.org/10.1016/j.placenta.2010.04.011
Jones, C. J. P., Carter, A. M., Aplin, J. D., & Enders, A. C. (2007). Glycosylation at the fetomaternal interface in hemomonochorial placentae from five widely separated species of mammal: Is there evidence for convergent evolution? Cells Tissues Organs, 185, 269-284. https://doi.org/10.1159/000102175
Jones, C. J. P., Morrison, C. A., & Stoddart, R. W. (1992). Histochemical analysis of rat testicular glycoconjugates. 2. Beta-galactosyl residues in O-and N-linked glycans in seminiferous tubules. Histochemical Journal, 24, 327-336. https://doi.org/10.1007/BF01046164
Jung, J. G., Lim, W., Park, T. S., Kim, J. N., Han, B. K., Song, G., & Han, J. Y. (2011). Structural and histological characterization of oviductal magnum and lectin-binding patterns in Gallusdomesticus. Reproductive Biology and Endocrinology, 9, 62. https://doi.org/10.1186/1477-7827-9-62
Madekurozwa, M.-C. (2008). A gross anatomical and histo-morphological study of the vagina of the emu (Dromaius novaehollandiae) and ostrich (Struthio camelus). Australian Journal of Experimental Agriculture, 48, 1332-1337. https://doi.org/10.1071/EA08129
Madekurozwa, M.-C., & Mpango, M. M. (2020). The shell gland in laying and natural moulting commercial egg-type chickens: A histomorphological and ultrastructural study. Anatomia Histologia Embryologia, 49, 521-531. https://doi.org/10.1111/ahe.12556
Mann, K. (1999). Isolation of a glycosylated form of the chicken eggshell protein ovocleidin and determination of the glycosylation site. Alternative glycosylation/phosphorylation at an N-glycosylation sequon. FEBS Letters, 463, 12-14. https://doi.org/10.1016/s0014-5793(99)01586-0
Muwazi, R. T., Baranga, J., Kayanja, F. I. B., & Schliemann, H. (1982). The oviduct of the ostrich Struthio camelus massaicus. Journal Für Ornithologie, 123, 425-433. https://doi.org/10.1007/BF01643275
Parizzi, R. C., Santos, J. M., Oliveira, M. F., Maia, M. O., Sousa, J. A., Miglino, M. A., & Santos, T. C. (2008). Macroscopic and microscopic anatomy of the oviduct in the sexually mature Rhea (Rheaamericana). Anatomia Histologia Embryologia, 37, 169-176. https://doi.org/10.1111/j.1439-0264.2007.00822.x
Richardson, K. C. (1935). The secretory phenomena in the oviduct of the fowl, including the process of shell formation examined by microincineration technique. Philosophical Transactions of the Royal Society of London Series B-biological Sciences, 225, 149-156.
Robinson, D. S., King, R., & Bowen, D. J. (1968). The occurrence of neutral and acidic mucins in the reproductive tract of the laying hen. Histochemie, 13, 97-104.
Saber, A. S., Emara, S. A. M., & AboSaeda, O. M. M. (2009). Light, scanning and transmission electron microscopical study on the oviduct of the ostrich (Struthio camelus). Journal of Veterinary Anatomy, 2, 79-89. https://doi.org/10.21608/JVA.2009.42315
Schauer, R. (1985). Sialic acids and their role as biological masks. Trends in Biochemical Sciences, 10, 357-360. https://doi.org/10.1016/0968-0004(85)90112-4
Shanawany, M. M., & Dingle, J. (1999) Ostrich Production Systems, Part 1-2. Food & Agriculture Organization of the United Nations, Rome. ISSN 0254-6019.
Sharaf, A. M. (2011). Chemical characteristics of whole eggs from avian species: A comparative study. Journal of Food and Dairy Sciences, 2, 225-235. https://doi.org/10.21608/jfds.2011.81948
Sharaf, A., Eid, W., & Abuel-Atta, A. A. (2012). Morphological aspects of the ostrich infundibulum and magnum. Bulgarian Journal of Veterinary Medicine, 15, 145-159.
Sharaf, A., Eid, W., & Abuel-Atta, A. A. (2013). Age-related morphology of the ostrich oviduct (isthmus, uterus and vagina). Bulgarian Journal of Veterinary Medicine, 16, 145-158.
Solomon, S. E. (1971). The characterisation and distribution of acidic mucopolysaccharides in the oviduct of the domestic fowl. Research in Veterinary Science, 12, 225-227. https://doi.org/10.1016/S0034-5288(18)34183-3
Sugino, H., Nitoda, T., & Juneja, L. R. (1996). General composition of hen eggs. pp 13-24. In T. Yamamoto, L.R. Juneja, H. Hatta & M. Kim (Eds). Hen Eggs: Basic and Applied Science (pp 13-24). CRC Press.
Wani, H., Darzi, M. M., Kamil, S. A., Wani, S. A., Munshi, Z. H., Shakoor, A., Raja, T. A., Shoukat, S., Kashani, B., & Shah, A. (2017). Histological and histochemical studies on the reproductive tract of Kashmir Faverolla chicken. Journal of Entomology and Zoology Studies, 2017(5), 2256-2262.
Wyburn, G. M., Johnston, H. S., Draper, M. H., & Davidson, M. F. (1970). The Fine Structure of the Infundibulum and Magnum of the Oviduct of Gallus Domesticus. Quarterly Journal of Experimental Physiology and Cognate Medical Sciences, 55, 213-232. https://doi.org/10.1113/expphysiol.1970.sp002071
Wyburn, G. M., Johnston, H. S., Draper, M. H., & Davidson, M. F. (1973). The ultrastructure of the shell forming region of the oviduct and the development of the shell of Gallus domesticus. Quarterly journal of experimental physiology and cognate medical sciences, 58, 143-151.