Vasoactive Intestinal Peptide Induces an Immunosuppressant Microenvironment in the Maternal-Fetal Interface of Non-Obese Diabetic Mice and Improves Early Pregnancy Outcome

Problem: Impaired pregnancy in non-obese diabetic (NOD) mice was related to limited vascular remodeling and autoimmune background. Vasoactive intestinal peptide (VIP) has anti-inflammatory and immunosuppressant effects, so we explored its ability to modulate the immune microenvironment at the early...

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Autor principal: Hauk, V.
Otros Autores: Azzam, S., Calo, G., Gallino, L., Paparini, D., Franchi, A., Ramhorst, R., Leirós, C.P
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2014
Acceso en línea:Registro en Scopus
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Aporte de:Registro referencial: Solicitar el recurso aquí
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024 7 |2 cas  |a vasoactive intestinal polypeptide, 37221-79-7; Cytokines; Forkhead Transcription Factors; FOXP3 protein, human; Nuclear Receptor Subfamily 1, Group F, Member 3; Receptors, Vasoactive Intestinal Peptide, Type II; Vasoactive Intestinal Peptide 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a AAJID 
100 1 |a Hauk, V. 
245 1 0 |a Vasoactive Intestinal Peptide Induces an Immunosuppressant Microenvironment in the Maternal-Fetal Interface of Non-Obese Diabetic Mice and Improves Early Pregnancy Outcome 
260 |c 2014 
270 1 0 |m Leirós, C.P.; Ciudad Universitaria, Pab II. 4th floor, 1428 Buenos Aires, Argentina; email: cpleiros@qb.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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504 |a Roca, V., Calafat, M., Larocca, L., Ramhorst, R., Farina, M., Franchi, A.M., Pérez Leirós, C., Potential immunomodulatory role of VIP in the implantation sites of prediabetic nonobese diabetic mice (2009) Reproduction, 138, pp. 733-742 
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504 |a Couvineau, A., Laburthe, M., VPAC receptors: structure, molecular pharmacology and interaction with accessory proteins (2011) Br J Pharmacol, 166, pp. 42-50 
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504 |a Bjøro, T., Sand, O., Ostberg, B.C., Gordeladze, J.O., Torjesen, P., Gautvik, K.M., Haug, E., The mechanisms by which vasoactive intestinal peptide (VIP) and thyrotropin releasing hormone (TRH) stimulate prolactin release from pituitary cells (1990) Biosci Rep, 10, pp. 189-199 
504 |a Deutsch, P.J.S.Y., Sun, Y., Kroog, G.S., Vasoactive intestinal peptide increases intracellular cAMP and gonadotropin-alpha gene activity in JEG-3 syncytial trophoblasts (1990) J Biol Chem, 265, pp. 10274-10281 
504 |a Marzioni, D., Fiore, G., Giordano, A., Nabissi, M., Florio, P., Verdenelli, F., Petraglia, F., Castellucci, M., Placental expression of substance P and vasoactive intestinal peptide: evidence for a local effect on hormone release (2005) J Clin Endocrinol Metab, 90, pp. 2378-2383 
504 |a Jovanovic, S.G.L., Grbovic, L., Jovanovic, A., Pregnancy does not alter the response of uterine arteries to vasoactive intestinal polypeptide (2000) Mol Hum Reprod, 6, pp. 361-368 
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504 |a Gomariz, R.P., Arranz, A., Juarranz, Y., Gutierrez-Cañas, I., Garcia-Gomez, M., Leceta, J., Martínez, C., Regulation of TLR expression, a new perspective for the role of VIP in immunity (2007) Peptides, 28, pp. 1825-1832 
504 |a Gonzalez-Rey, E., Delgado, M., Vasoactive intestinal peptide and regulatory T-cell induction: a new mechanism and therapeutic potential for immune homeostasis (2007) Trends Mol Med, 13, pp. 241-251 
504 |a Delgado, M., Munoz-Elias, E.J., Martinez, C., Gomariz, R.P., Ganea, D., VIP and PACAP38 modulate cytokine and nitric oxide production in peritoneal macrophages and macrophage cell lines (1999) Ann N Y Acad Sci, 897, pp. 401-414 
504 |a Roca, V., Larocca, L., Calafat, M., Aisemberg, J., Meiss, R., Franchi, A.M., Pérez Leirós, C., Reduced nitric oxide synthase and cyclo-oxygenase activity in the uterus of non-obese diabetic mice (2006) Reproduction (Cambridge, England), 132, pp. 931-938 
504 |a Hauk, V., Calafat, M., Larocca, L., Fraccaroli, L., Grasso, E., Ramhorst, R., Perez Leirós, C., Vasoactive intestinal peptide/vasoactive intestinal peptide receptor relative expression in salivary glands as one endogenous modulator of acinar cell apoptosis in a murine model of Sjögren's syndrome (2011) Clin Exp Immunol, 166, pp. 309-316 
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504 |a Lin, Y., Ren, L., Wang, W., Di, J., Zeng, S., Saito, S., Effect of TLR3 and TLR7 activation in uterine NK cells from non-obese diabetic (NOD) mice (2009) J Reprod Immunol, 82, pp. 12-23 
504 |a Li, C., Wang, W., Wang, H., Zhong, Y., Di, J., Lin, Y., Proteomic analysis of proteins differentially expressed in uterine lymphocytes obtained from wild-type and NOD mice (2009) J Cell Biolchem, 108, pp. 447-457 
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504 |a Spong, C.Y., Lee, S.J., Cune, S.K.M.C., Gibney, G., Abebe, D.T., Alvero, R., Brenneman, D.E., Hill, J.M., Maternal regulation of embryonic growth: the role of vasoactive intestinal peptide (1999) Endocrinology, 140, pp. 917-924 
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504 |a Durant, S., Christeff, N., Coulaud, J., Nunez, E.A., Dardenne, M., Homo-Delarche, F., Basal concentrations of various steroids in the nonobese diabetic (NOD) mouse and effect of immobilization stress (1998) Autoimmunity, 28, pp. 249-258 
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520 3 |a Problem: Impaired pregnancy in non-obese diabetic (NOD) mice was related to limited vascular remodeling and autoimmune background. Vasoactive intestinal peptide (VIP) has anti-inflammatory and immunosuppressant effects, so we explored its ability to modulate the immune microenvironment at the early maternal-placental interface and improve pregnancy in NOD mice. Method of study: Implantation sites were isolated from pregnant NOD mice at gestational day 9.5 and were incubated with VIP for evaluation of cytokine or transcription factor expression by RT-PCR, immunoblotting, and immunohistochemistry. Alternatively, pregnant mice were injected with VIP at day 6.5 and studied at day 9.5. Results: VIP and VPAC receptors were detected in viable implantation sites. VIP immunostaining was found predominantly on trophoblast giant cells. The in vitro treatment of viable implantation sites with VIP increased IL-10, TGF-β, and Foxp3 expression. Sites with resorption processes presented lower VIP expression, reduced suppressant markers, and increased IL-17 and RORγT expression compared with viable sites and VIP reduced RORγT expression. Pregnant mice treated with VIP at day 6.5 presented an even distribution of viable implantation sites with an increased expression of IL-10, TGF- β, and Foxp3. Conclusion: VIP induces an immunosuppressant profile at the early maternal-placental interface of NOD mice and improves pregnancy outcome. © 2013 John Wiley & Sons Ltd.  |l eng 
593 |a Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina 
593 |a Facultad de Medicina, Universidad de Buenos Aires, CEFYBO-CONICET, Buenos Aires, Argentina 
690 1 0 |a EARLY PREGNANCY 
690 1 0 |a FOXP3 
690 1 0 |a IL-10 
690 1 0 |a NON-OBESE DIABETIC MICE 
690 1 0 |a TGF-Β 
690 1 0 |a VASOACTIVE INTESTINAL PEPTIDE 
690 1 0 |a INTERLEUKIN 10 
690 1 0 |a INTERLEUKIN 17 
690 1 0 |a RETINOID RELATED ORPHAN RECEPTOR GAMMA 
690 1 0 |a TRANSCRIPTION FACTOR FOXP3 
690 1 0 |a TRANSFORMING GROWTH FACTOR BETA 
690 1 0 |a VASOACTIVE INTESTINAL POLYPEPTIDE 
690 1 0 |a VASOACTIVE INTESTINAL POLYPEPTIDE RECEPTOR 1 
690 1 0 |a VASOACTIVE INTESTINAL POLYPEPTIDE RECEPTOR 2 
690 1 0 |a CYTOKINE 
690 1 0 |a FORKHEAD TRANSCRIPTION FACTOR 
690 1 0 |a FOXP3 PROTEIN, HUMAN 
690 1 0 |a VASOACTIVE INTESTINAL POLYPEPTIDE 
690 1 0 |a VASOACTIVE INTESTINAL POLYPEPTIDE RECEPTOR 2 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL MODEL 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a FEMALE 
690 1 0 |a FIRST TRIMESTER PREGNANCY 
690 1 0 |a GESTATIONAL AGE 
690 1 0 |a GIANT CELL 
690 1 0 |a IMMUNOBLOTTING 
690 1 0 |a IMMUNOHISTOCHEMISTRY 
690 1 0 |a IMMUNOMODULATION 
690 1 0 |a IN VITRO STUDY 
690 1 0 |a INSULIN DEPENDENT DIABETES MELLITUS 
690 1 0 |a MICROENVIRONMENT 
690 1 0 |a MOTHER FETUS RELATIONSHIP 
690 1 0 |a MOUSE 
690 1 0 |a NIDATION 
690 1 0 |a NONHUMAN 
690 1 0 |a NONOBESE DIABETIC MOUSE 
690 1 0 |a PREGNANCY OUTCOME 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROTEIN EXPRESSION 
690 1 0 |a REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION 
690 1 0 |a TROPHOBLAST 
690 1 0 |a ANIMAL 
690 1 0 |a CELL CULTURE 
690 1 0 |a DIABETES MELLITUS 
690 1 0 |a DISEASE MODEL 
690 1 0 |a FETOMATERNAL TRANSFUSION 
690 1 0 |a GENETICS 
690 1 0 |a HUMAN 
690 1 0 |a IMMUNOLOGICAL TOLERANCE 
690 1 0 |a IMMUNOLOGY 
690 1 0 |a METABOLISM 
690 1 0 |a ORGAN CULTURE TECHNIQUE 
690 1 0 |a PATHOLOGY 
690 1 0 |a PREGNANCY 
690 1 0 |a PREGNANCY COMPLICATION 
690 1 0 |a PREGNANCY OUTCOME 
690 1 0 |a TUMOR MICROENVIRONMENT 
690 1 0 |a UTERUS 
690 1 0 |a ANIMALS 
690 1 0 |a CELLS, CULTURED 
690 1 0 |a CELLULAR MICROENVIRONMENT 
690 1 0 |a CYTOKINES 
690 1 0 |a DIABETES MELLITUS 
690 1 0 |a DISEASE MODELS, ANIMAL 
690 1 0 |a FEMALE 
690 1 0 |a FORKHEAD TRANSCRIPTION FACTORS 
690 1 0 |a GESTATIONAL AGE 
690 1 0 |a HUMANS 
690 1 0 |a IMMUNE TOLERANCE 
690 1 0 |a MATERNAL-FETAL EXCHANGE 
690 1 0 |a MICE 
690 1 0 |a MICE, INBRED NOD 
690 1 0 |a NUCLEAR RECEPTOR SUBFAMILY 1, GROUP F, MEMBER 3 
690 1 0 |a ORGAN CULTURE TECHNIQUES 
690 1 0 |a PREGNANCY 
690 1 0 |a PREGNANCY COMPLICATIONS 
690 1 0 |a PREGNANCY OUTCOME 
690 1 0 |a RECEPTORS, VASOACTIVE INTESTINAL PEPTIDE, TYPE II 
690 1 0 |a UTERUS 
690 1 0 |a VASOACTIVE INTESTINAL PEPTIDE 
700 1 |a Azzam, S. 
700 1 |a Calo, G. 
700 1 |a Gallino, L. 
700 1 |a Paparini, D. 
700 1 |a Franchi, A. 
700 1 |a Ramhorst, R. 
700 1 |a Leirós, C.P. 
773 0 |d 2014  |g v. 71  |h pp. 120-130  |k n. 2  |p Am. J. Reprod. Immunol.  |x 10467408  |w (AR-BaUEN)CENRE-3647  |t American Journal of Reproductive Immunology 
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