A pivotal role for galectin-1 in fetomaternal tolerance

A successful pregnancy requires synchronized adaptation of maternal immune-endocrine mechanisms to the fetus. Here we show that galectin-1 (Gal-1), an immunoregulatory glycan-binding protein, has a pivotal role in conferring fetomaternal tolerance. Consistently with a marked decrease in Gal-1 expres...

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Autor principal: Blois, S.M
Otros Autores: Ilarregui, J.M, Tometten, M., Garcia, M., Orsal, A.S, Cordo-Russo, R., Toscano, M.A, Bianco, G.A, Kobelt, P., Handjiski, B., Tirado, I., Markert, U.R, Klapp, B.F, Poirier, F., Szekeres-Bartho, J., Rabinovich, G.A, Arck, P.C
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2007
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a galectin 1, 258495-34-0; Galectin 1; Interleukin-2 Receptor alpha Subunit; Polysaccharides 
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100 1 |a Blois, S.M. 
245 1 2 |a A pivotal role for galectin-1 in fetomaternal tolerance 
260 |c 2007 
270 1 0 |m Blois, S.M.; University Medicine Berlin, Biomedical Research Building, Campus Virchow, Augustenburger Platz 1, Berlin 13353, Germany; email: sandra.blois@charite.de 
506 |2 openaire  |e Política editorial 
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504 |a Toscano, M.A., Differential glycosylation of TH1, TH2 and TH17 effector cells selectively regulates susceptibility to cell death (2007) Nat. Immunol, 8, pp. 825-834 
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504 |a Jeschke, U., Binding of galectin-1 (Gal-1) on trophoblast cells and inhibition of hormone production of trophoblast tumor cells in vitro by Gal-1 (2004) Histochem. Cell Biol, 121, pp. 501-508 
504 |a Erlebacher, A., Zhang, D., Parlow, A.F., Glimcher, L.H., Ovarian insufficiency and early pregnancy loss induced by activation of the innate immune system (2004) J. Clin. Invest, 114, pp. 39-48 
504 |a Blois, S.M., Lineage, maturity, and phenotype of uterine murine dendritic cells throughout gestation indicate a protective role in maintaining pregnancy (2004) Biol. Reprod, 70, pp. 1018-1023 
504 |a Fulcher, J.A., Galectin-1-matured human monocyte-derived dendritic cells have enhanced migration through extracellular matrix (2006) J. Immunol, 177, pp. 216-226 
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520 3 |a A successful pregnancy requires synchronized adaptation of maternal immune-endocrine mechanisms to the fetus. Here we show that galectin-1 (Gal-1), an immunoregulatory glycan-binding protein, has a pivotal role in conferring fetomaternal tolerance. Consistently with a marked decrease in Gal-1 expression during failing pregnancies, Gal-1-deficient (Lgals1-/-) mice showed higher rates of fetal loss compared to wild-type mice in allogeneic matings, whereas fetal survival was unaffected in syngeneic matings. Treatment with recombinant Gal-1 prevented fetal loss and restored tolerance through multiple mechanisms, including the induction of tolerogenic dendritic cells, which in turn promoted the expansion of interleukin-10 (IL-10)-secreting regulatory T cells in vivo. Accordingly, Gal-1's protective effects were abrogated in mice depleted of regulatory T cells or deficient in IL-10. In addition, we provide evidence for synergy between Gal-1 and progesterone in the maintenance of pregnancy. Thus, Gal-1 is a pivotal regulator of fetomaternal tolerance that has potential therapeutic implications in threatened pregnancies. © 2007 Nature Publishing Group.  |l eng 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: National Science and Technology Development Agency, PICT 2003–05–13787 
536 |a Detalles de la financiación: Universidad de Buenos Aires, M091 
536 |a Detalles de la financiación: German Academic Exchange Service London 
536 |a Detalles de la financiación: Council for Higher Education 
536 |a Detalles de la financiación: John Simon Guggenheim Memorial Foundation 
536 |a Detalles de la financiación: European Commission 
536 |a Detalles de la financiación: Cancer Research Institute 
536 |a Detalles de la financiación: Ligue Contre le Cancer 
536 |a Detalles de la financiación: Mizutani Foundation for Glycoscience 
536 |a Detalles de la financiación: Sixth Framework Programme 
536 |a Detalles de la financiación: Deutsche Forschungsgemeinschaft, AR232/8–1 
536 |a Detalles de la financiación: 1Charité, University Medicine Berlin, Biomedical Research Building, Campus Virchow, Augustenburger Platz 1, Berlin 13353, Germany. 2Laboratorio de Inmunopatología, Instituto de Biología y Medicina Experimental (IBYME), Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET), Vuelta de Obligado 2490, Buenos Aires C1428, Argentina. 3Department of Medicine, Division of Hepatology, Gastroenterology, and Endocrinology, Charité, University Medicine Berlin, Berlin 13353, Germany. 4Unidad de Inmunología, Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Universidad de Granada, Granada 18012, Spain. 5Placenta-Labor, Department of Obstetrics, Friedrich-Schiller-University Jena, 07740 Jena, Germany. 6Departement de Biologie du Developpement, Institut Jacques Monod, Unités Mixtes de Recherche Centre National de la Recherche 7592, Univ. Paris 6 and Paris 7, Paris 75251 Paris, France. 7Department of Medical Microbiology and Immunology, Reproductive and Tumor Immunology Research Group of the Hungarian Academy of Sciences, Pecs University Medical School, Pecs 7643, Hungary. 8Departmento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires C1428, Argentina. 9J.M.I. and M.T. contributed equally to this work. Correspondence should be addressed to P.C.A. (petra.arck@charite.de), S.M.B. (sandra.blois@charite.de) or G.A.R. (gabyrabi@ciudad.com.ar). 
536 |a Detalles de la financiación: We thank E. Hagen, P. Moschansky and P. Busse for excellent technical assistance in generating this work. Pgr–/– mice were provided by J. Lydon (University of Texas). S.M.B., M.T., U.R.M., J.S.-B. and P.C.A. are part of the Embryo Implantation Control Network of Excellence, co-financed by the European Commission throughout the FP6 framework program Life Science, Genomics and Biotechnology for Health. S.M.B is a fellow of the Habilitation program at the Charité, University Medicine Berlin. J.M.I., M.A.T. and G.A.B. are fellows of the CONICET. A.S.O. is supported by the Turkish Higher Education Council. M.G. was supported by the German Academic Exchange Program. This work was supported by research grants from the German Research Foundation (AR232/8–1, P.C.A.), the Drs. Graute and Graute-Oppermann Foundation (P.C.A.), the Charité (P.C.A.), the Sales Foundation/CONICET Program (G.A.R.), the Mizutani Foundation for Glycoscience (G.A.R.), the Cancer Research Institute (E. Shephard Investigator; G.A.R.), the John Simon Guggenheim Memorial Foundation (G.A.R.), the Argentina National Agency for Promotion of Science and Technology (PICT 2003–05–13787; G.A.R.), the University of Buenos Aires (M091; G.A.R.) and the Association pour la Recherche contre le Cancer and Ligue contre le cancer, comité de Paris (F.P.). We are indebted to S. Cookson, B. Huppertz, D.A. Clark, H.F. Rosenberg and several anonymous reviewers for helpful feedback and constructive comments on this article. 
593 |a University Medicine Berlin, Biomedical Research Building, Campus Virchow, Augustenburger Platz 1, Berlin 13353, Germany 
593 |a Laboratorio de Inmunopatología, Instituto de Biología Y Medicina Experimental (IBYME), Consejo Nacional de Investigaciones Cientificas Y Tecnicas (CONICET), Vuelta de Obligado 2490, Buenos Aires C1428, Argentina 
593 |a Department of Medicine, Division of Hepatology, Gastroenterology, and Endocrinology, University Medicine Berlin, Berlin 13353, Germany 
593 |a Departamento de Bioquímica Y Biología Molecular, Facultad de Medicina, Universidad de Granada, Granada 18012, Spain 
593 |a Placenta-Labor, Department of Obstetrics, Friedrich-Schiller-University Jena, 07740 Jena, Germany 
593 |a Departement de Biologie du Developpement, Institut Jacques Monod, Univ. Paris 6 and Paris 7, Paris 75251 Paris, France 
593 |a Department of Medical Microbiology and Immunology, Hungarian Academy of Sciences, Pecs University Medical School, Pecs 7643, Hungary 
593 |a Departmento de Química Biológica, Facultad de Ciencias Exactas Y Naturales, Universidad de Buenos Aires, Buenos Aires C1428, Argentina 
690 1 0 |a GALECTIN 1 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CYTOKINE RELEASE 
690 1 0 |a DENDRITIC CELL 
690 1 0 |a FETOPLACENTAL UNIT 
690 1 0 |a FETUS WASTAGE 
690 1 0 |a IMMUNOREGULATION 
690 1 0 |a IN VIVO CULTURE 
690 1 0 |a MOUSE 
690 1 0 |a NONHUMAN 
690 1 0 |a PREGNANCY DISORDER 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROTEIN BINDING 
690 1 0 |a PROTEIN EXPRESSION 
690 1 0 |a REGULATORY T LYMPHOCYTE 
690 1 0 |a ANIMALS 
690 1 0 |a CD4-POSITIVE T-LYMPHOCYTES 
690 1 0 |a FEMALE 
690 1 0 |a GALECTIN 1 
690 1 0 |a GENE EXPRESSION REGULATION, DEVELOPMENTAL 
690 1 0 |a HISTOCOMPATIBILITY, MATERNAL-FETAL 
690 1 0 |a IMMUNE TOLERANCE 
690 1 0 |a INTERLEUKIN-2 RECEPTOR ALPHA SUBUNIT 
690 1 0 |a MICE 
690 1 0 |a MICE, TRANSGENIC 
690 1 0 |a POLYSACCHARIDES 
690 1 0 |a PREGNANCY 
690 1 0 |a PREGNANCY, ANIMAL 
690 1 0 |a T-LYMPHOCYTES, REGULATORY 
690 1 0 |a TRANSPLANTATION, HOMOLOGOUS 
690 1 0 |a MUS 
700 1 |a Ilarregui, J.M. 
700 1 |a Tometten, M. 
700 1 |a Garcia, M. 
700 1 |a Orsal, A.S. 
700 1 |a Cordo-Russo, R. 
700 1 |a Toscano, M.A. 
700 1 |a Bianco, G.A. 
700 1 |a Kobelt, P. 
700 1 |a Handjiski, B. 
700 1 |a Tirado, I. 
700 1 |a Markert, U.R. 
700 1 |a Klapp, B.F. 
700 1 |a Poirier, F. 
700 1 |a Szekeres-Bartho, J. 
700 1 |a Rabinovich, G.A. 
700 1 |a Arck, P.C. 
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