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Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy

The sugar moiety of IgA is known to provide a link between the innate and adaptive immune systems. Terminally located glycotopes on IgA are potential ligands engaged in the interactions which may modulate the biological activities of IgA. In the present work the expressions of Maackia amurensis (MAA...

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Autores principales: Orczyk-Pawiłowicz, Magdalena, Augustyniak, Daria, Hirnle, Lidia, Kątnik-Prastowska, Iwona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717160/
https://www.ncbi.nlm.nih.gov/pubmed/23250795
http://dx.doi.org/10.1007/s10719-012-9460-8
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author Orczyk-Pawiłowicz, Magdalena
Augustyniak, Daria
Hirnle, Lidia
Kątnik-Prastowska, Iwona
author_facet Orczyk-Pawiłowicz, Magdalena
Augustyniak, Daria
Hirnle, Lidia
Kątnik-Prastowska, Iwona
author_sort Orczyk-Pawiłowicz, Magdalena
collection PubMed
description The sugar moiety of IgA is known to provide a link between the innate and adaptive immune systems. Terminally located glycotopes on IgA are potential ligands engaged in the interactions which may modulate the biological activities of IgA. In the present work the expressions of Maackia amurensis (MAA), Sambucus nigra (SNA), Lens culinaris (LCA), Tetragonolobus purpureus (LTA), and Ulex europaeus (UEA) reactive glycotopes on maternal plasma and amniotic IgA were evaluated in relation to the progression of a normal human pregnancy, from the 2nd trimester, throughout the 3rd trimester, perinatal period, post-date pregnancy and delivery, by lectin-IgA-ELISA, using specific biotinylated lectins. The amniotic and maternal plasma IgA concentrations and a degree of SNA and LCA reactivity of maternal plasma IgA were almost unaltered during the normal pregnancy. The amniotic IgA from the 2nd trimester was decorated by MAA-, SNA-reactive and LCA-, LTA-, and UEA-reactive glycotopes. At the turn of the 2nd and 3rd trimesters the expression of MAA-, SNA-, LTA-, and UEA-reactive glycotopes, except for LCA-reactive, increased and remained almost at unaltered levels throughout the perinatal period and delivery. However, in the post-date pregnancy the expression of LCA-, LTA-, and UEA-reactive and SNA-reactive glycotopes were significantly higher. The unique fucosylated and sialylated glycovariants of amniotic IgA associated with the progression of the normal pregnancy may illustrate a general importance of carbohydrate-lectin receptor interactions in the control and modulation of biological events to ensuring homeostasis during pregnancy, protection and well-being of fetus.
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spelling pubmed-37171602013-07-23 Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy Orczyk-Pawiłowicz, Magdalena Augustyniak, Daria Hirnle, Lidia Kątnik-Prastowska, Iwona Glycoconj J Article The sugar moiety of IgA is known to provide a link between the innate and adaptive immune systems. Terminally located glycotopes on IgA are potential ligands engaged in the interactions which may modulate the biological activities of IgA. In the present work the expressions of Maackia amurensis (MAA), Sambucus nigra (SNA), Lens culinaris (LCA), Tetragonolobus purpureus (LTA), and Ulex europaeus (UEA) reactive glycotopes on maternal plasma and amniotic IgA were evaluated in relation to the progression of a normal human pregnancy, from the 2nd trimester, throughout the 3rd trimester, perinatal period, post-date pregnancy and delivery, by lectin-IgA-ELISA, using specific biotinylated lectins. The amniotic and maternal plasma IgA concentrations and a degree of SNA and LCA reactivity of maternal plasma IgA were almost unaltered during the normal pregnancy. The amniotic IgA from the 2nd trimester was decorated by MAA-, SNA-reactive and LCA-, LTA-, and UEA-reactive glycotopes. At the turn of the 2nd and 3rd trimesters the expression of MAA-, SNA-, LTA-, and UEA-reactive glycotopes, except for LCA-reactive, increased and remained almost at unaltered levels throughout the perinatal period and delivery. However, in the post-date pregnancy the expression of LCA-, LTA-, and UEA-reactive and SNA-reactive glycotopes were significantly higher. The unique fucosylated and sialylated glycovariants of amniotic IgA associated with the progression of the normal pregnancy may illustrate a general importance of carbohydrate-lectin receptor interactions in the control and modulation of biological events to ensuring homeostasis during pregnancy, protection and well-being of fetus. Springer US 2012-12-19 2013 /pmc/articles/PMC3717160/ /pubmed/23250795 http://dx.doi.org/10.1007/s10719-012-9460-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Orczyk-Pawiłowicz, Magdalena
Augustyniak, Daria
Hirnle, Lidia
Kątnik-Prastowska, Iwona
Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy
title Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy
title_full Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy
title_fullStr Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy
title_full_unstemmed Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy
title_short Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy
title_sort lectin-based analysis of fucose and sialic acid expressions on human amniotic iga during normal pregnancy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717160/
https://www.ncbi.nlm.nih.gov/pubmed/23250795
http://dx.doi.org/10.1007/s10719-012-9460-8
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