Lectin-based analysis of fucose and sialic acid expressions on human amniotic IgA during normal pregnancy
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  • 作者:Magdalena Orczyk-Pawi?owicz (1)
    Daria Augustyniak (2)
    Lidia Hirnle (3)
    Iwona K?tnik-Prastowska (1)
  • 关键词:Amniotic fluid ; Fucosylation ; Glycovariant ; Glycotope ; Immunoglobulin A ; Lectin ; Pregnancy ; Sialylation
  • 刊名:Glycoconjugate Journal
  • 出版年:2013
  • 出版时间:August 2013
  • 年:2013
  • 卷:30
  • 期:6
  • 页码:599-608
  • 全文大小:436KB
  • 参考文献:1. Haltiwanger, R.S., Lowe, J.B.: Role of glycosylation in development. Annu. Rev. Biochem. 73, 491-73 (2004) CrossRef
    2. Becker, D.J., Lowe, J.B.: Fucose: biosynthesis and biological function in mammals. Glycobiology 13, 41-3 (2003) CrossRef
    3. Schauer, R.: Sialic acids as regulators of molecular and cellular interactions. Curr. Opin. Struct. Biol. 19, 507-14 (2009) CrossRef
    4. Orczyk-Pawi?owicz, M., K?tnik-Prastowska, I.: Terminal monosaccharide expression on amniotic glycoproteins as biomarkers of fetus maturity. Biochem. Soc. Trans. 39, 344-48 (2011) CrossRef
    5. Jeschke, U., Toth, B., Scholz, C., Friese, K., Makrigiannakis, A.: Glycoprotein and carbohydrate binding protein expression in the placenta in early pregnancy loss. J. Reprod. Immunol. 85, 99-05 (2010) CrossRef
    6. Uszyński, W., Uszyński, M., Zekanowska, E., Kuczyński, J., Szymański, M.: Selectins in human amniotic fluid and cord blood plasma. A preliminary report. Thromb. Res. 127, 60-1 (2011) CrossRef
    7. Carson, D.D., Farrar, J.D., Laidlaw, J., Wright, D.A.: Selective activation of the N-glycosylation apparatus in uteri by estrogen. J. Biol. Chem. 265, 2947-955 (1990)
    8. Kobata, A.: The N-linked sugar chain of human immunoglobulin G: their unique pattern, and their functional roles. Biochim. Biophys. Acta 1780, 472-78 (2008) CrossRef
    9. Brinkman-Van der Linden, E.C.M., Havenaar, E.C., Van Ommen, E.C.R., Van Kamp, G.J., Gooren, L.J.G., Van Dijk, W.: Oral estrogen treatment induces a decrease in expression of sialyl Lewis x on alpha1-acid glycoprotein in females and male-to-female transsexuals. Glycobiology 6, 407-12 (1996)
    10. Jeschke, U., Xiaoyu, W., Volker, B., Friese, K., Stahn, R.: Glycodelin and amniotic fluid transferrin as inhibitors of E-selectin-mediated cell adhesion. Histochem. Cell Biol. 119, 345-54 (2003)
    11. Jeschke, U., Stahn, R., Goletz, C., Wang, X.Y., Briese, V., Friese, K.: HCG in trophoblast tumour cells of the cell line Jeg3 and hCG isolated from amniotic fluid and serum of pregnant women carry oligosaccharides of the sialyl Lewis x and sialyl Lewis a type. Anticancer. Res. 23, 1087-092 (2003)
    12. Orczyk-Pawi?owicz, M., Hirnle, L., K?tnik-Prastowska, I.: The expression of fucose isoforms of amniotic and plasma alpha-1-acid glycoprotein derived from 2nd and 3rd trimester normal pregnancies. Clin. Biochem. 42, 1517-523 (2009) CrossRef
    13. Hirnle, L., K?tnik-Prastowska, I.: Amniotic fibronectin fragmentation and expression of its domains, sialyl and fucosyl glycotopes associated with pregnancy complicated by intrauterine infection. Clin. Chem. Lab. Med. 45, 208-14 (2007) CrossRef
    14. Orczyk-Pawi?owicz, M., Augustyniak, D., Hirnle, L., K?tnik-Prastowska, I.: Degree of sialylation and fucosylation of plasma and amniotic immunoglobulin G changes progressively during normal pregnancy. Prenat. Diagn. 35, 432-39 (2012) CrossRef
    15. Briese, V., Kunkel, S., Plath, C., Wutzke, K.D., Plesse, R.: Sialic acid, steroids and proteohormones in maternal, cord and retroplacental blood. Z. Geburtshilfe Neonatol. 203, 63-8 (1999)
    16. Bowen, J.M., Chamley, L., Keelan, J.A., Mitchell, M.D.: Cytokines of the placenta and extra-placental membranes: roles and regulation during human pregnancy and parturition. Placenta 23, 257-73 (2002) CrossRef
    17. Goldblum, R.M., Hilton, S.: Amniotic fluid and the fetal mucosal immune system. In: Ogra, P.L., Mestecky, J., Lamm, M.E., Strober, W., Bienenstock, J., McGhee, J.R. (eds.) Mucosal immunology, 2nd edn, pp. 1555-564. Academic, London (1999)
    18. Quan, C.P., Forestier, F., Bouvet, J.-P.: Immunoglobulins of the human amniotic fluid. Am. J. Reprod. Immunol. 42, 219-25 (1999) CrossRef
    19. Jauniaux, E., Jurkovic, D., Gulbis, B., Liesnard, C., Lees, C., Campbell, S.: Materno-fetal immunoglobulin transfer and passive immunity during the first trimester of human pregnancy. Hum. Reprod. 10, 3297-300 (1995) CrossRef
    20. Quan, C.P., Berneman, A., Pirts, R., Avrameas, S., Bouvet, J.P.: Natural polyreactive secretory immunoglobulin A autoantibodies as a possible barrier to infection in humans. Infect. Immun. 65, 3997-004 (1997)
    21. Quan, C.P., Watanabe, S., Forestier, F., Bouvet, J.P.: Human amniotic IgA inhibits natural IgG autoantibodies of maternal or unrelated origin. Eur. J. Immunol. 28, 4001-009 (1998) CrossRef
    22. Arnold, J.N., Dwek, R.A., Rudd, P.M., Sim, R.B.: Mannan binding lectin and its interaction with immunoglobulins in health and in disease. Immunol. Lett. 106, 103-10 (2006) CrossRef
    23. Kerr, M.A.: The structure and function of human IgA. Biochem. J. 271, 285-96 (1990)
    24. Monteiro, R.C.: Role of IgA and IgA Fc receptors in inflammation. J. Clin. Immunol. 30, 1- (2010) CrossRef
    25. Royle, L., Roos, A., Harvey, D.J., Wormald, M.R., van Gijlswijk-Janssen, D., Redwan, el-R.M., Wilson, I.A., Daha, M.R., Dwek, R.A., Rudd, P.M.: Secretory IgA N- and O-glycans provide a link between the innate and adaptive immune systems. J. Biol. Chem. 278, 20140-0153 (2003)
    26. Arnold, J.N., Royle, L., Dwek, R.A., Rudd, P.M., Sim, R.B.: Human immunoglobulin glycosylation and the lectin pathway of complement activation. John S. Axford (ed), Glycobiology and Medicine, pp 27-3. Springer, Printed in the Netherlands (2005)
    27. Mattu, T.S., Pleass, R.J., Willis, A.C., Kilian, M., Wormald, M.R., Lellouch, A.C., Rudd, P.M., Woof, J.M., Dwek, R.A.: The glycosylation and structure of human serum IgA1, Fab, and Fc regions and the role of N-glycosylation on Fc alpha receptor interactions. J. Biol. Chem. 273, 2260-272 (1998) CrossRef
    28. Knibbs, R., Goldstein, I.J., Ratcliff, R.M., Shibuya, N.: Characterization of the carbohydrate binding specificity of the leukoagglutinating lectin from / Maackia amurensis. Comparison with other sialic acid-specific lectins. J. Biol. Chem. 266, 83-8 (1991)
    29. Shibuya, N., Goldstein, I.J., Broekaert, W.F., Nsimba-Lubaki, M., Peeters, B., Peumans, W.J.: The elderberry ( / Sambucus nigra L.) bark lectin recognizes the Neu5Ac(α2,6)Gal/GalNAc sequence. J. Biol. Chem. 262, 1596-601 (1987)
    30. Kornfeld, K., Reitman, M.L., Kornfeld, R.: The carbohydrate-binding specificity of pea and lentil lectins. Fucose is an important determinant. J. Biol. Chem. 256, 6633-640 (1981)
    31. Yan, L., Wilkins, P.P., Alvarez-Manilla, G., Do, S.I., Smith, D.F., Cummings, R.D.: Immobilized / Lotus tetragonolobus agglutinin binds oligosaccharides containing the Le x determinant. Glycoconj. J. 14, 45-5 (1997) CrossRef
    32. Audette, G.F., Vandonselaar, M., Delbaere, L.T.J.: The 2.2?? resolution structure of the O(H) blood-group-specific Lectin I from / Ulex europaeus. J. Mol. Biol. 304, 423-33 (2000) CrossRef
    33. Orczyk-Pawi?owicz, M., Hirnle, L., K?tnik-Prastowska, I.: High expression of α1,2- and α1,6-linked fucoses on amniotic AGP as a biomarker of fetal postmaturity risk. J. Immunoassay Immunochem. 32, 103-13 (2011) CrossRef
    34. Wu, A.M., Lisowska, E., Duk, M., Yang, Z.: Lectins as tools in glycoconjugate research. Glycoconj. J. 26, 899-13 (2009) CrossRef
    35. K?tnik, I., Jadach, J., Krotkiewski, H., Gerber, J.: Investigating the glycosylation of normal and ovarian cancer haptoglobins using digoxigenin-labeled lectins. Glycosyl. Dis. 1, 97-04 (1994)
    36. Cederquist, L.L., Ewool, L.C., Bonsnes, R.W., Litwin, S.D.: Detectability and pattern of immunoglobulins in normal amniotic-fluid throughout gestation. Am. J. Obstet. Gynecol. 130, 220-24 (1978)
    37. Hampel, D.J., K?ttgen, B., Dudenhausen, J.W., K?ttgen, E.: Fetal fibronectin as a marker for an imminent preterm delivery. A new technique using the glycoprotein lectin immunosorbent assay. J. Immunol. Methods 224, 31-2 (1999)
    38. Maenuma, K., Yim, M., Komatsu, K., Hoshino, M., Takahashi, Y., Bovin, N., Irimura, T.: Use of a library of mutated / Maackia amurensis hemagglutinin for profiling the cell lineage and differentiation. Proteomics 8, 3274-283 (2008) CrossRef
    39. Novak, J., Julian, B.A., Mestecky, J., Renfrow, M.B.: Glycosylation of IgA1 and pathogenesis of IgA nephropathy. Semin. Immunopathol. 34, 365-82 (2012) CrossRef
    40. Mor, G., Cardenas, I., Abrahams, V., Guller, S.: Inflammation and pregnancy: the role of the immune system at the implantation site. Ann. N. Y. Acad. Sci. 1221, 80-7 (2011) CrossRef
    41. Denison, F.C., Roberts, K.A., Barr, S.M., Norman, J.E.: Obesity, pregnancy, inflammation, and vascular function. Reproduction 140, 373-85 (2010) CrossRef
    42. Orczyk-Pawi?owicz, M., Florjański, J., Zalewski, J., K?tnik-Prastowska, I.: Relative amounts of sialic acid and fucose of amniotic fluid glycoconjugates in relation to pregnancy age. Glycoconj. J. 22, 433-42 (2005) CrossRef
    43. Hirnle, L.: Analysis of fibronectin molecular forms in amniotic fluid and plasma of pregnant women during normal and complicated by intrauterine infection pregnancies. Habilitation Thesis, Wroc?aw Medical University, Wroc?aw, Poland (2006)
    44. Van Dijk, W., Poland, D.C.: Anti-inflammatory properties of specific glycoforms of human alpha1-acid glycoprotein. Adv. Exp. Med. Biol. 535, 251-56 (2003) CrossRef
    45. Kreisman, L.S., Cobb, B.A.: Infection, inflammation and host carbohydrates: a glyco-evasion hypothesis. Glycobiology 22, 1019-030 (2012) CrossRef
    46. Chaturvedi, P., Warren, C.D., Altaye, M., Morrow, A.L., Ruiz-Palacios, G., Pickering, L.K., Newburg, D.S.: Fucosylated human milk oligosaccharides vary between individuals and over the course of lactation. Glycobiology 11, 365-72 (2001) CrossRef
    47. Romero, R., Espinoza, J., Goncalves, L.F., Kusanovic, J.P., Friel, L.A., Nien, J.K.: Inflammation in preterm and term labour and delivery. Semin. Fetal Neonatal. Med. 11, 317-26 (2006) CrossRef
    48. Hilder, L., Costeloe, K., Thilaganathan, B.: Prolonged pregnancy: evaluating gestation-specific risks of fetal and infant mortality. Br. J. Obstet. Gynaecol. 105, 169-73 (1998) CrossRef
    49. Mor, G., Cardenas, I.: The immune system in pregnancy: a unique complexity. Am. J. Reprod. Immunol. 63, 425-33 (2010) CrossRef
  • 作者单位:Magdalena Orczyk-Pawi?owicz (1)
    Daria Augustyniak (2)
    Lidia Hirnle (3)
    Iwona K?tnik-Prastowska (1)

    1. Department of Chemistry and Immunochemistry, Wroc?aw Medical University, Bujwida 44a, 50-345, Wroc?aw, Poland
    2. Department of Pathogen Biology and Immunology, Institute of Genetics and Microbiology, University of Wroc?aw, Wroc?aw, Poland
    3. Department of Obstetrics and Gynaecology, Clinic of Reproduction and Obstetrics, Wroc?aw Medical University, Wroc?aw, Poland
文摘
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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