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Immune Cells in the Uterine Remodeling: Are They the Target of Endocrine Disrupting Chemicals?

Meyer, Nicole, Zenclussen, Ana Claudia·2020·Frontiers in Immunology
DOI 10.3389/fimmu.2020.00246PMC PMC7043066
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Figure 1 Role of immune cells and endocrine disrupting chemicals (EDCs) for uterine vascular remodeling during pregnancy. In humans and rodents including mice immune cells like uterine natural killer cells, mast cells, dendritic cells, T cells, especially regulatory T cells, B cells, macrophages and their secreted mediators support uterine vascular remodeling at the feto-maternal interface. EDCs are found in herbicides and pesticides as well as in many daily used products like cosmetics, plastic containers and bottles, food cans, and pharmacological drugs like contraceptive pills and many others. EDCs can impair uterine remodeling processes directly or indirectly due to a hormonal imbalance and in turn an altered immune cell number or function.
Figure 1 Role of immune cells and endocrine disrupting chemicals (EDCs) for uterine vascular remodeling during pregnancy. In humans and rodents including mice immune cells like uterine natural killer cells, mast cells, dendritic cells, T cells, especially regulatory T cells, B cells, macrophages and their secreted mediators support uterine vascular remodeling at the feto-maternal interface. EDCs are found in herbicides and pesticides as well as in many daily used products like cosmetics, plastic containers and bottles, food cans, and pharmacological drugs like contraceptive pills and many others. EDCs can impair uterine remodeling processes directly or indirectly due to a hormonal imbalance and in turn an altered immune cell number or function.CC BY · PubMed Central

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Research works printed but not linked: 189

  1. Calkins, 2011, Fetal origins of adult disease, Curr Probl Pediatr Adolesc Health Care, 41, 158, 10.1016/j.cppeds.2011.01.001 · DOI · Paper page
  2. Cartwright, 2010, Remodelling at the maternal-fetal interface: relevance to human pregnancy disorders, Reproduction, 140, 803, 10.1530/REP-10-0294 · DOI
  3. Maybin, 2015, Menstrual physiology: implications for endometrial pathology and beyond, Hum Reprod Update, 21, 748, 10.1093/humupd/dmv038 · DOI
  4. Zenclussen, 2015, Cellular regulation of the uterine microenvironment that enables embryo implantation, Front Immunol., 6, 321, 10.3389/fimmu.2015.00321 · DOI
  5. Grzechocinska, 2017, The role of metalloproteinases in endometrial remodelling during menstrual cycle, Ginekol Pol., 88, 337, 10.5603/GP.a2017.0063 · DOI
  6. Nair, 2017, The Mechanism of Menstruation.
  7. Berbic, 2013, Immunology of normal and abnormal menstruation, 387
  8. Jones, 2004, Identification of chemokines important for leukocyte recruitment to the human endometrium at the times of embryo implantation and menstruation, J Clin Endocrinol Metab., 89, 6155, 10.1210/jc.2004-0507 · DOI
  9. Berbic, 2014, Inflammation and endometrial bleeding, Climacteric, 17, 47, 10.3109/13697137.2014.963964 · DOI
  10. Jabbour, 2006, Endocrine regulation of menstruation, Endocr Rev., 27, 17, 10.1210/er.2004-0021 · DOI · Paper page
  11. Osol, 2009, Maternal uterine vascular remodeling during pregnancy, Physiology., 24, 58, 10.1152/physiol.00033.2008 · DOI
  12. Boss, 2018, Placental formation in early pregnancy: how is the centre of the placenta made?, Hum Reprod Update, 24, 750, 10.1093/humupd/dmy030 · DOI
  13. Burke, 2010, Uterine NK cells, spiral artery modification and the regulation of blood pressure during mouse pregnancy, Am J Reprod Immunol, 63, 472, 10.1111/j.1600-0897.2010.00818.x · DOI
  14. Whitley, 2010, Cellular and molecular regulation of spiral artery remodelling: lessons from the cardiovascular field, Placenta, 31, 465, 10.1016/j.placenta.2010.03.002 · DOI
  15. Cecchettini, 2011, Vascular smooth-muscle-cell activation: proteomics point of view, Int Rev Cell Mol Biol., 288, 43, 10.1016/B978-0-12-386041-5.00002-9 · DOI
  16. Wanjare, 2013, Derivation and maturation of synthetic and contractile vascular smooth muscle cells from human pluripotent stem cells, Cardiovasc Res., 97, 321, 10.1093/cvr/cvs315 · DOI
  17. Lacolley, 2012, The vascular smooth muscle cell in arterial pathology: a cell that can take on multiple roles, Cardiovasc Res., 95, 194, 10.1093/cvr/cvs135 · DOI
  18. Rensen, 2007, Regulation and characteristics of vascular smooth muscle cell phenotypic diversity, Neth Heart J., 15, 100, 10.1007/BF03085963 · DOI
  19. Louis, 2010, Vascular smooth muscle cell motility: from migration to invasion, Exp Clin Cardiol., 15, e75
  20. Bulmer, 2012, The role of vascular smooth muscle cell apoptosis and migration during uterine spiral artery remodeling in normal human pregnancy, FASEB J., 26, 2975, 10.1096/fj.12-203679 · DOI
  21. Liu, 2017, dNK derived IFN-gamma mediates VSMC migration and apoptosis via the induction of LncRNA MEG3: a role in utero-vascular transformation, Placenta, 50, 32, 10.1016/j.placenta.2016.12.023 · DOI
  22. Kaufmann, 2003, Endovascular trophoblast invasion: implications for the pathogenesis of intrauterine growth retardation and preeclampsia, Biol Reprod., 69, 1, 10.1095/biolreprod.102.014977 · DOI
  23. Whitley, 2009, Trophoblast-mediated spiral artery remodelling: a role for apoptosis, J Anat., 215, 21, 10.1111/j.1469-7580.2008.01039.x · DOI
  24. Gellersen, 2014, Cyclic decidualization of the human endometrium in reproductive health and failure, Endocr Rev., 35, 851, 10.1210/er.2014-1045 · DOI
  25. Vinketova, 2016, Human decidual stromal cells as a component of the implantation niche and a modulator of maternal immunity, J Pregnancy., 2016, 8689436, 10.1155/2016/8689436 · DOI
  26. Pollard, 1998, Complexity in uterine macrophage responses to cytokines in mice, Biol Reprod., 58, 1469, 10.1095/biolreprod58.6.1469 · DOI
  27. Huang, 2006, Regulation of chemokine production in response to pro-inflammatory cytokines in first trimester decidual cells, J Reprod Immunol., 72, 60, 10.1016/j.jri.2006.03.002 · DOI
  28. Sentman, 2004, Recruitment of uterine NK cells: induction of CXC chemokine ligands 10 and 11 in human endometrium by estradiol and progesterone, J Immunol., 173, 6760, 10.4049/jimmunol.173.11.6760 · DOI
  29. Kitaya, 2005, Central role of interleukin-15 in postovulatory recruitment of peripheral blood CD16(-) natural killer cells into human endometrium, J Clin Endocrinol Metab., 90, 2932, 10.1210/jc.2004-2447 · DOI
  30. Carlino, 2008, Recruitment of circulating NK cells through decidual tissues: a possible mechanism controlling NK cell accumulation in the uterus during early pregnancy, Blood, 111, 3108, 10.1182/blood-2007-08-105965 · DOI
  31. Magatti, 2019, Perinatal mesenchymal stromal cells and their possible contribution to fetal-maternal tolerance, Cells, 8, 1401, 10.3390/cells8111401 · DOI
  32. Klemmt, 2006, Stromal cells from endometriotic lesions and endometrium from women with endometriosis have reduced decidualization capacity, Fertil Steril., 85, 564, 10.1016/j.fertnstert.2005.08.046 · DOI
  33. Giuliani, 2014, Characterization of uterine NK cells in women with infertility or recurrent pregnancy loss and associated endometriosis, Am J Reprod Immunol, 72, 262, 10.1111/aji.12259 · DOI
  34. Salker, 2010, Natural selection of human embryos: impaired decidualization of endometrium disables embryo-maternal interactions and causes recurrent pregnancy loss, PLoS ONE., 5, e10287, 10.1371/journal.pone.0010287 · DOI
  35. Kuo, 2019, Trophoblast-endothelium signaling involves angiogenesis and apoptosis in a dynamic bioprinted placenta model, Biotechnol Bioeng., 116, 181, 10.1002/bit.26850 · DOI
  36. Harris, 2010, Review: trophoblast-vascular cell interactions in early pregnancy: how to remodel a vessel, Placenta, 31, S93, 10.1016/j.placenta.2009.12.012 · DOI
  37. Harris, 2006, Invasive trophoblasts stimulate vascular smooth muscle cell apoptosis by a fas ligand-dependent mechanism, Am J Pathol., 169, 1863, 10.2353/ajpath.2006.060265 · DOI · Paper page
  38. Ashton, 2005, Uterine spiral artery remodeling involves endothelial apoptosis induced by extravillous trophoblasts through Fas/FasL interactions, Arterioscler Thromb Vasc Biol., 25, 102, 10.1161/01.ATV.0000148547.70187.89 · DOI
  39. James, 2010, Pre-eclampsia: fitting together the placental, immune and cardiovascular pieces, J Pathol., 221, 363, 10.1002/path.2719 · DOI
  40. Khong, 1986, Inadequate maternal vascular response to placentation in pregnancies complicated by pre-eclampsia and by small-for-gestational age infants, Br J Obstet Gynaecol., 93, 1049, 10.1111/j.1471-0528.1986.tb07830.x · DOI · Paper page
  41. van der Heijden, 2005, Uterine artery remodeling in pseudopregnancy is comparable to that in early pregnancy, Biol Reprod., 73, 1289, 10.1095/biolreprod.105.044438 · DOI
  42. Stieglitz, 2019, The microstructure in the placenta is influenced by the functional diversity of HLA-G allelic variants, Immunogenetics, 71, 455, 10.1007/s00251-019-01121-0 · DOI
  43. Fu, 2017, Natural Killer cells promote fetal development through the secretion of growth-promoting factors, Immunity, 47, 1100, 10.1016/j.immuni.2017.11.018 · DOI
  44. Hauk, 2019, Trophoblast VIP deficiency entails immune homeostasis loss and adverse pregnancy outcome in mice, FASEB J., 33, 1801, 10.1096/fj.201800592RR · DOI
  45. Gohner, 2017, Immune-modulatory effects of syncytiotrophoblast extracellular vesicles in pregnancy and preeclampsia, Placenta., 60, S41, 10.1016/j.placenta.2017.06.004 · DOI
  46. Croy, 2006, Uterine natural killer cells: a specialized differentiation regulated by ovarian hormones, Immunol Rev., 214, 161, 10.1111/j.1600-065X.2006.00447.x · DOI
  47. Vacca, 2011, Origin, phenotype and function of human natural killer cells in pregnancy, Trends Immunol., 32, 517, 10.1016/j.it.2011.06.013 · DOI
  48. Beagley, 2003, Regulation of innate and adaptive immunity by the female sex hormones oestradiol and progesterone, FEMS Immunol Med Microbiol., 38, 13, 10.1016/S0928-8244(03)00202-5 · DOI
  49. Gibson, 2015, Estrogen-dependent regulation of human uterine natural killer cells promotes vascular remodelling via secretion of CCL2, Hum Reprod., 30, 1290, 10.1093/humrep/dev067 · DOI · Paper page
  50. Ledee-Bataille, 2005, Role of the endometrial tripod interleukin-18,−15, and−12 in inadequate uterine receptivity in patients with a history of repeated in vitro fertilization-embryo transfer failure, Fertil Steril., 83, 598, 10.1016/j.fertnstert.2004.11.021 · DOI
  51. Cooper, 2002, In vivo evidence for a dependence on interleukin 15 for survival of natural killer cells, Blood, 100, 3633, 10.1182/blood-2001-12-0293 · DOI
  52. Beuneu, 2009, Dynamic behavior of NK cells during activation in lymph nodes, Blood, 114, 3227, 10.1182/blood-2009-06-228759 · DOI
  53. Croy, 2003, Uterine natural killer cells: insights into their cellular and molecular biology from mouse modelling, Reproduction, 126, 149, 10.1530/rep.0.1260149 · DOI
  54. Croy, 2012, Imaging of vascular development in early mouse decidua and its association with leukocytes and trophoblasts, Biol Reprod., 87, 125, 10.1095/biolreprod.112.102830 · DOI
  55. Ratsep, 2015, BA. Uterine natural killer cells: supervisors of vasculature construction in early decidua basalis, Reproduction., 149, R91, 10.1530/REP-14-0271 · DOI
  56. King, 2000, Recognition of trophoblast HLA class I molecules by decidual NK cell receptors–a review, Placenta, 21, S81, 10.1053/plac.1999.0520 · DOI
  57. Sojka, 2019, Uterine natural killer cells, Front Immunol., 10, 960, 10.3389/fimmu.2019.00960 · DOI
  58. Vacca, 2019, Heterogeneity of NK cells and other innate lymphoid cells in human and murine decidua, Front Immunol., 10, 170, 10.3389/fimmu.2019.00170 · DOI
  59. Ashkar, 2003, Assessment of requirements for IL-15 and IFN regulatory factors in uterine NK cell differentiation and function during pregnancy, J Immunol., 171, 2937, 10.4049/jimmunol.171.6.2937 · DOI
  60. Meyer, 2017, Safeguarding of fetal growth by mast cells and natural killer cells: deficiency of one is counterbalanced by the other, Front Immunol., 8, 711, 10.3389/fimmu.2017.00711 · DOI · Paper page
  61. Greenwood, 2000, Ultrastructural studies of implantation sites from mice deficient in uterine natural killer cells, Placenta, 21, 693, 10.1053/plac.2000.0556 · DOI
  62. Guimond, 1998, Engraftment of bone marrow from severe combined immunodeficient (SCID) mice reverses the reproductive deficits in natural killer cell-deficient tg epsilon 26 mice, J Exp Med., 187, 217, 10.1084/jem.187.2.217 · DOI
  63. Meyer, 2017, Chymase-producing cells of the innate immune system are required for decidual vascular remodeling and fetal growth, Sci Rep., 7, 45106, 10.1038/srep45106 · DOI · Paper page
  64. Renaud, 2017, Natural Killer-cell deficiency alters placental development in rats, Biol Reprod., 96, 145, 10.1095/biolreprod.116.142752 · DOI
  65. Ashkar, 2000, Interferon gamma contributes to initiation of uterine vascular modification, decidual integrity, and uterine natural killer cell maturation during normal murine pregnancy, J Exp Med., 192, 259, 10.1084/jem.192.2.259 · DOI
  66. Chen, 2015, Expression of interferon gamma by decidual cells and natural killer cells at the human implantation site: implications for preeclampsia, spontaneous abortion, and intrauterine growth restriction, Reprod Sci., 22, 1461, 10.1177/1933719115585148 · DOI
  67. Lockwood, 2013, Decidual cell regulation of natural killer cell-recruiting chemokines: implications for the pathogenesis and prediction of preeclampsia, Am J Pathol., 183, 841, 10.1016/j.ajpath.2013.05.029 · DOI
  68. Lockwood, 2014, Interferon-gamma protects first-trimester decidual cells against aberrant matrix metalloproteinases 1. 3, and 9 expression in preeclampsia, Am J Pathol, 184, 2549, 10.1016/j.ajpath.2014.05.025 · DOI
  69. Choudhury, 2017, Extravillous trophoblast and endothelial cell crosstalk mediates leukocyte infiltration to the early remodeling decidual spiral arteriole wall, J Immunol., 198, 4115, 10.4049/jimmunol.1601175 · DOI
  70. Xu, 2016, An M1-like macrophage polarization in decidual tissue during spontaneous preterm labor that is attenuated by rosiglitazone treatment, J Immunol., 196, 2476, 10.4049/jimmunol.1502055 · DOI
  71. Zhao, 2018, Hypoxia regulates placental angiogenesis via alternatively activated macrophages, Am J Reprod Immunol, 80, e12989, 10.1111/aji.12989 · DOI
  72. Jetten, 2014, Anti-inflammatory M2, but not pro-inflammatory M1 macrophages promote angiogenesis in vivo, Angiogenesis, 17, 109, 10.1007/s10456-013-9381-6 · DOI
  73. Gustafsson, 2008, Gene expression profiling of human decidual macrophages: evidence for immunosuppressive phenotype, PLoS ONE., 3, e2078, 10.1371/journal.pone.0002078 · DOI
  74. Heikkinen, 2003, Phenotypic characterization of human decidual macrophages, Clin Exp Immunol., 131, 498, 10.1046/j.1365-2249.2003.02092.x · DOI
  75. Svensson, 2011, Macrophages at the fetal-maternal interface express markers of alternative activation and are induced by M-CSF and IL-10, J Immunol., 187, 3671, 10.4049/jimmunol.1100130 · DOI
  76. Lash, 2016, Decidual macrophages: key regulators of vascular remodeling in human pregnancy, J Leukoc Biol., 100, 315, 10.1189/jlb.1A0815-351R · DOI
  77. Helige, 2014, Distribution of decidual natural killer cells and macrophages in the neighbourhood of the trophoblast invasion front: a quantitative evaluation, Hum Reprod., 29, 8, 10.1093/humrep/det353 · DOI
  78. Abrahams, 2004, Macrophages and apoptotic cell clearance during pregnancy, Am J Reprod Immunol, 51, 275, 10.1111/j.1600-0897.2004.00156.x · DOI
  79. Sonora, 2014, Anti-tissue transglutaminase antibody inhibits apoptotic cell clearance by macrophages in pregnant NOD mice, J Reprod Immunol., 103, 59, 10.1016/j.jri.2013.11.001 · DOI
  80. Madazli, 2003, Maternal plasma levels of cytokines in normal and preeclamptic pregnancies and their relationship with diastolic blood pressure and fibronectin levels, Acta Obstet Gynecol Scand., 82, 797, 10.1034/j.1600-0412.2003.00206.x · DOI
  81. Schonkeren, 2011, Differential distribution and phenotype of decidual macrophages in preeclamptic versus control pregnancies, Am J Pathol., 178, 709, 10.1016/j.ajpath.2010.10.011 · DOI
  82. Sharma, 2007, Leptin, IL-10 and inflammatory markers (TNF-α, IL-6, and IL-8) in pre-eclamptic, normotensive pregnant and healthy non-pregnant women, Am J Reprod Immunol, 58, 21, 10.1111/j.1600-0897.2007.00486.x · DOI
  83. Zak, 2019, Correlation of tumor necrosis factor alpha, interleukin 6 and interleukin 10 with blood pressure, risk of preeclampsia and low birth weight in gestational diabetes, Physiol Res., 68, 395, 10.33549/physiolres.934002 · DOI
  84. Hennessy, 1999, A deficiency of placental IL-10 in preeclampsia, J Immunol., 163, 3491, 10.4049/jimmunol.163.6.3491 · DOI
  85. Zenclussen, 2005, Abnormal T-Cell reactivity against paternal antigens in spontaneous abortion, Am J Pathol., 166, 811, 10.1016/S0002-9440(10)62302-4 · DOI
  86. Svensson, 2004, Stromal cells direct local differentation of regulatory dendritic cells, Immunity., 21, 805, 10.1016/j.immuni.2004.10.012 · DOI
  87. Schumacher, 2014, Regulatory T cells: regulators of life, Am J Reprod Immunol, 72, 158, 10.1111/aji.12238 · DOI
  88. Svensson-Arvelund, 2015, The human fetal placenta promotes tolerance against the semiallogeneic fetus by inducing regulatory T cells and homeostatic M2 macrophages, J Immunol., 194, 1534, 10.4049/jimmunol.1401536 · DOI
  89. Boij, 2015, Regulatory T-cell subpopulations in severe or early-onset preeclampsia, Am J Reprod Immunol, 74, 368, 10.1111/aji.12410 · DOI
  90. Sasaki, 2004, Decidual and peripheral blood CD4+CD25+ regulatory T cells in early pregnancy subjects and spontaneous abortion cases, Mol Hum Reprod., 10, 347, 10.1093/molehr/gah044 · DOI
  91. Zare, 2019, Analysis of the frequencies and functions of CD4(+)CD25(+)CD127(low/neg), CD4(+)HLA-G(+), and CD8(+)HLA-G(+) regulatory T cells in pre-eclampsia, J Reprod Immunol., 133, 43, 10.1016/j.jri.2019.06.002 · DOI
  92. Hafeez, 2014, The role of regulatory T cells in preeclampsia, Egypt J Immunol., 21, 45
  93. Care, 2018, Reduction in regulatory T cells in early pregnancy causes uterine artery dysfunction in mice, Hypertension, 72, 177, 10.1161/HYPERTENSIONAHA.118.10858 · DOI
  94. Samstein, 2012, Extrathymic generation of regulatory T cells in placental mammals mitigates maternal-fetal conflict, Cell, 150, 29, 10.1016/j.cell.2012.05.031 · DOI
  95. Cornelius, 2015, An increased population of regulatory T cells improves the pathophysiology of placental ischemia in a rat model of preeclampsia, Am J Physiol Regul Integr Comp Physiol., 309, R884, 10.1152/ajpregu.00154.2015 · DOI
  96. Woidacki, 2015, Transfer of regulatory T cells into abortion-prone mice promotes the expansion of uterine mast cells and normalizes early pregnancy angiogenesis, Sci Rep., 5, 13938, 10.1038/srep13938 · DOI
  97. Bonney, 2017, Impact of immune deficiency on remodeling of maternal resistance vasculature 4 weeks postpartum in mice, Reprod Sci., 24, 514, 10.1177/1933719116678691 · DOI
  98. Drudy, 1991, The ultrastructure of mast cells in the uterus throughout the normal menstrual cycle and the postmenopause, J Anat., 175, 51, 10.1016/0378-5122(91)90169-Q · DOI
  99. Bytautiene, 2008, IgE-independent mast cell activation augments contractility of non-pregnant and pregnant guinea pig myometrium, Int Arch Allergy Immunol., 147, 140, 10.1159/000135701 · DOI
  100. Schmerse, 2014, In vivo visualization of uterine mast cells by two-photon microscopy, Reproduction, 147, 781, 10.1530/REP-13-0570 · DOI · Paper page
  101. Woidacki, 2013, Mast cells rescue implantation defects caused by c-kit deficiency, Cell Death Dis., 4, e462, 10.1038/cddis.2012.214 · DOI · Paper page
  102. Rudolph, 1992, Mast cells mediators evoke contractility and potentiate each other in mouse uterine horns, Gen Pharmacol., 23, 833, 10.1016/0306-3623(92)90233-A · DOI
  103. Rudolph, 1997, On the mechanism of action of ethodin in inducing myometrium contractions, Gen Pharmacol., 28, 381, 10.1016/S0306-3623(96)00288-1 · DOI
  104. Meyer, 2017, Simultaneous ablation of uterine natural killer cells and uterine mast cells in mice leads to poor vascularization and abnormal doppler measurements that compromise fetal well-being, Front Immunol., 8, 1913, 10.3389/fimmu.2017.01913 · DOI
  105. Meyer, 2018, High frequency ultrasound for the analysis of fetal and placental development in vivo, J Vis Exp, 8, 141, 10.3791/58616 · DOI
  106. De Filippo, 2013, Mast cell and macrophage chemokines CXCL1/CXCL2 control the early stage of neutrophil recruitment during tissue inflammation, Blood, 121, 4930, 10.1182/blood-2013-02-486217 · DOI
  107. Dudeck, 2015, Mast-cell-derived TNF amplifies CD8(+) dendritic cell functionality and CD8(+) T cell priming, Cell Rep., 13, 399, 10.1016/j.celrep.2015.08.078 · DOI
  108. Galli, 2008, Immunomodulatory mast cells: negative, as well as positive, regulators of immunity, Nat Rev Immunol., 8, 478, 10.1038/nri2327 · DOI
  109. Bloxham, 1976, From ovulation to blastocyst attachment. A review of early embryonic life in the mouse, Folia Vet Lat., 6, 319
  110. Mezouar, 2018, Isolation of human placental mast cells, Curr Protoc Cell Biol., 80, e52, 10.1002/cpcb.52 · DOI
  111. Tchougounova, 2003, The chymase, mouse mast cell protease 4, constitutes the major chymotrypsin-like activity in peritoneum and ear tissue. a role for mouse mast cell protease 4 in thrombin regulation and fibronectin turnover, J Exp Med, 198, 423, 10.1084/jem.20030671 · DOI
  112. Leskinen, 2003, Mast cell chymase induces smooth muscle cell apoptosis by a mechanism involving fibronectin degradation and disruption of focal adhesions, Arterioscler Thromb Vasc Biol., 23, 238, 10.1161/01.ATV.0000051405.68811.4D · DOI
  113. Wang, 2001, Mast cell chymase inhibits smooth muscle cell growth and collagen expression in vitro: transforming growth factor-beta1-dependent and -independent effects, Arterioscler Thromb Vasc Biol., 21, 1928, 10.1161/hq1201.100227 · DOI
  114. den Dekker, 2012, Mast cells induce vascular smooth muscle cell apoptosis via a toll-like receptor 4 activation pathway, Arterioscler Thromb Vasc Biol., 32, 1960, 10.1161/ATVBAHA.112.250605 · DOI
  115. Urata, 1990, Identification of a highly specific chymase as the major angiotensin II-forming enzyme in the human heart, J Biol Chem., 265, 22348, 10.1016/S0021-9258(18)45712-2 · DOI
  116. Hering, 2010, Effects of circulating and local utero-placental angiotensin II in rat pregnancy, Hypertension, 56, 311, 10.1161/HYPERTENSIONAHA.110.150961 · DOI
  117. Yaghini, 2010, Angiotensin II-induced vascular smooth muscle cell migration and growth are mediated by cytochrome P450 1B1-dependent superoxide generation, Hypertension, 55, 1461, 10.1161/HYPERTENSIONAHA.110.150029 · DOI
  118. Meng, 2017, Angiotensin II regulates dendritic cells through activation of NF-κB /p65, ERK1/2, and STAT1 Pathways, Cell Physiol Biochem., 42, 1550, 10.1159/000479272 · DOI
  119. Derbala, 2019, Mast cell-induced immunopathology in recurrent pregnancy losses, Am J Reprod Immunol, 82, e13128, 10.1111/aji.13128 · DOI
  120. Purcell, 1992, Human placental mast cells: a role in pre-eclampsia?, Med Hypotheses, 39, 281, 10.1016/0306-9877(92)90123-T · DOI
  121. Szewczyk, 2012, Mast cells and histamine: do they influence placental vascular network and development in preeclampsia?, Mediators Inflamm., 2012, 307189, 10.1155/2012/307189 · DOI
  122. Lyall, 2013, Spiral artery remodeling and trophoblast invasion in preeclampsia and fetal growth restriction: relationship to clinical outcome, Hypertension, 62, 1046, 10.1161/HYPERTENSIONAHA.113.01892 · DOI
  123. Ball, 2006, Late sporadic miscarriage is associated with abnormalities in spiral artery transformation and trophoblast invasion, J Pathol., 208, 535, 10.1002/path.1927 · DOI
  124. Duley, 2009, The global impact of pre-eclampsia and eclampsia, Semin Perinatol., 33, 130, 10.1053/j.semperi.2009.02.010 · DOI · Paper page
  125. Garovic, 2013, Preeclampsia and the future risk of hypertension: the pregnant evidence, Curr Hypertens Rep., 15, 114, 10.1007/s11906-013-0329-4 · DOI
  126. Brosens, 1972, The role of the spiral arteries in the pathogenesis of preeclampsia, Obstet Gynecol Annu., 1, 177
  127. Pijnenborg, 1991, Placental bed spiral arteries in the hypertensive disorders of pregnancy, Br J Obstet Gynaecol., 98, 648, 10.1111/j.1471-0528.1991.tb13450.x · DOI
  128. Jafri, 2017, Immune regulation of systemic hypertension, pulmonary arterial hypertension, and preeclampsia: shared disease mechanisms and translational opportunities, Am J Physiol Regul Integr Comp Physiol., 313, R693, 10.1152/ajpregu.00259.2017 · DOI
  129. Huang, 2018, Identification of placental nutrient transporters associated with intrauterine growth restriction and pre-eclampsia, BMC Genomics, 19, 173, 10.1186/s12864-018-4518-z · DOI
  130. Chen, 2018, Down-regulation of placental folate transporters in intrauterine growth restriction, J Nutr Biochem., 59, 136, 10.1016/j.jnutbio.2018.06.003 · DOI
  131. Godfrey, 2000, Fetal nutrition and adult disease, Am J Clin Nutr., 71, 1344, 10.1093/ajcn/71.5.1344s · DOI
  132. Pluchino, 2014, Hormonal causes of recurrent pregnancy loss (RPL), Hormones., 13, 314, 10.14310/horm.2002.1505 · DOI
  133. Berkane, 2017, From pregnancy to preeclampsia: a key role for estrogens, Endocr Rev., 38, 123, 10.1210/er.2016-1065 · DOI · Paper page
  134. Cantonwine, 2019, Estrogen metabolism pathways in preeclampsia and normal pregnancy, Steroids, 144, 8, 10.1016/j.steroids.2019.01.005 · DOI
  135. Baud, 2019, Hormonal changes associated with intra-uterine growth restriction: impact on the developing brain and future neurodevelopment, Front Endocrinol., 10, 179, 10.3389/fendo.2019.00179 · DOI
  136. Balaguer, 2017, Structural and functional evidences for the interactions between nuclear hormone receptors and endocrine disruptors at low doses, C R Biol., 340, 414, 10.1016/j.crvi.2017.08.002 · DOI
  137. Feng, 2016, Endocrine disrupting effects of triclosan on the placenta in pregnant rats, PLoS ONE., 11, e0154758, 10.1371/journal.pone.0154758 · DOI
  138. Diamanti-Kandarakis, 2009, Endocrine-disrupting chemicals: an Endocrine Society scientific statement, Endocr Rev., 30, 293, 10.1210/er.2009-0002 · DOI · Paper page
  139. Petrakis, 2017, Endocrine disruptors leading to obesity and related diseases, Int J Environ Res Public Health., 14, e1282, 10.3390/ijerph14101282 · DOI
  140. Heindel, 2017, Metabolism disrupting chemicals and metabolic disorders, Reprod Toxicol., 68, 3, 10.1016/j.reprotox.2016.10.001 · DOI · Paper page
  141. Papalou, 2019, Endocrine disrupting chemicals: an occult mediator of metabolic disease, Front Endocrinol., 10, 112, 10.3389/fendo.2019.00112 · DOI
  142. Rasier, 2006, Female sexual maturation and reproduction after prepubertal exposure to estrogens and endocrine disrupting chemicals: a review of rodent and human data, Mol Cell Endocrinol., 187, 10.1016/j.mce.2006.04.002 · DOI
  143. Adeel, 2017, Environmental impact of estrogens on human, animal and plant life: a critical review, Environ Int., 99, 107, 10.1016/j.envint.2016.12.010 · DOI
  144. Kadokawa, 2018, Reconsidering the roles of endogenous estrogens and xenoestrogens: the membrane estradiol receptor G protein-coupled receptor 30 (GPR30) mediates the effects of various estrogens, J Reprod Dev., 64, 203, 10.1262/jrd.2017-153 · DOI
  145. La Rosa, 2014, Xenoestrogens alter estrogen receptor (ER) α intracellular levels, PLoS ONE., 9, e88961, 10.1371/journal.pone.0088961 · DOI
  146. Pennie, 1998, Differential activation by xenoestrogens of ER alpha and ER beta when linked to different response elements, J Endocrinol., 158, R11, 10.1677/joe.0.158r011 · DOI
  147. Kovats, 2015, Estrogen receptors regulate innate immune cells and signaling pathways, Cell Immunol., 294, 63, 10.1016/j.cellimm.2015.01.018 · DOI
  148. Yoshino, 2004, Prenatal exposure to bisphenol A up-regulates immune responses, including T helper 1 and T helper 2 responses, in mice, Immunology, 112, 489, 10.1111/j.1365-2567.2004.01900.x · DOI
  149. Liu, 2017, Bisphenol A metabolites and Bisphenol S in paired maternal and cord serum, Environ Sci Technol., 51, 2456, 10.1021/acs.est.6b05718 · DOI
  150. Mu, 2018, Developmental effects and estrogenicity of Bisphenol A alternatives in a zebrafish embryo model, Environ Sci Technol., 52, 3222, 10.1021/acs.est.7b06255 · DOI
  151. Lehmler, 2018, Exposure to Bisphenol A, Bisphenol F, and Bisphenol S in adults, U. S., and children: The National Health and Nutrition Examination Survey 2013–2014, ACS Omega, 3, 6523, 10.1021/acsomega.8b00824 · DOI
  152. Yang, 2019, A mechanism for the effect of endocrine disrupting chemicals on placentation, Chemosphere, 231, 326, 10.1016/j.chemosphere.2019.05.133 · DOI
  153. Li, 2013, Exposure levels of environmental endocrine disruptors in mother-newborn pairs in China and their placental transfer characteristics, PLoS ONE, 8, e62526, 10.1371/journal.pone.0062526 · DOI
  154. Covaci, 2002, Distribution of PCBs and organochlorine pesticides in umbilical cord and maternal serum, Sci Total Environ., 298, 45, 10.1016/S0048-9697(02)00167-5 · DOI
  155. Rogers, 2013, Review: endocrine disrupting chemicals and immune responses: a focus on bisphenol-A and its potential mechanisms, Mol Immunol., 53, 421, 10.1016/j.molimm.2012.09.013 · DOI
  156. Kim, 2003, Down-regulation of inducible nitric oxide synthase and tumor necrosis factor-alpha expression by Bisphenol A via nuclear factor-kappaB inactivation in macrophages, Cancer Lett., 196, 69, 10.1016/S0304-3835(03)00219-2 · DOI
  157. Yoshitake, 2008, Suppression of NO production and 8-nitroguanosine formation by phenol-containing endocrine-disrupting chemicals in LPS-stimulated macrophages: involvement of estrogen receptor-dependent or -independent pathways, Nitric Oxide, 18, 223, 10.1016/j.niox.2008.01.003 · DOI
  158. Byun, 2005, Bisphenol A-induced downregulation of murine macrophage activities in vitro and ex vivo, Environ Toxicol Pharmacol., 19, 19, 10.1016/j.etap.2004.02.006 · DOI
  159. Segura, 1999, In vitro effect of the resin component Bisphenol A on substrate adherence capacity of macrophages, J Endod, 25, 341, 10.1016/S0099-2399(06)81168-4 · DOI
  160. Youn, 2002, Evaluation of the immune response following exposure of mice to Bisphenol A: induction of Th1 cytokine and prolactin by BPA exposure in the mouse spleen cells, Arch Pharm Res., 25, 946, 10.1007/BF02977018 · DOI
  161. Lee, 2003, Enhanced interleukin-4 production in CD4+ T cells and elevated immunoglobulin E levels in antigen-primed mice by bisphenol A and nonylphenol, endocrine disruptors: involvement of nuclear factor-AT and Ca2+, Immunology, 109, 76, 10.1046/j.1365-2567.2003.01631.x · DOI
  162. Yan, 2008, Exposure to Bisphenol A prenatally or in adulthood promotes T(H)2 cytokine production associated with reduction of CD4CD25 regulatory T cells, Environ Health Perspect., 116, 514, 10.1289/ehp.10829 · DOI
  163. Ohshima, 2007, Transmaternal exposure to bisphenol a modulates the development of oral tolerance, Pediatr Res., 62, 60, 10.1203/PDR.0b013e3180674dae · DOI
  164. Pisapia, 2012, Effects of some endocrine disruptors on cell cycle progression and murine dendritic cell differentiation, Gen Comp Endocrinol., 178, 54, 10.1016/j.ygcen.2012.04.005 · DOI
  165. Goto, 2007, Orally administered bisphenol A disturbed antigen specific immunoresponses in the naive condition, Biosci Biotechnol Biochem., 71, 2136, 10.1271/bbb.70004 · DOI
  166. Yurino, 2004, Endocrine disruptors (environmental estrogens) enhance autoantibody production by B1 cells, Toxicol Sci., 81, 139, 10.1093/toxsci/kfh179 · DOI
  167. O'Brien, 2014, Bisphenol A at concentrations relevant to human exposure enhances histamine and cysteinyl leukotriene release from bone marrow-derived mast cells, J Immunotoxicol., 11, 84, 10.3109/1547691X.2013.800925 · DOI
  168. Uramaru, 2014, Structure-activity relationship of a series of 17 parabens and related compounds for histamine release in rat peritoneal mast cells and skin allergic reaction in guinea pigs, J Toxicol Sci., 39, 83, 10.2131/jts.39.83 · DOI
  169. Jin, 2010, Effect of endocrine disrupting chemicals on the transcription of genes related to the innate immune system in the early developmental stage of zebrafish (Danio rerio), Fish Shellfish Immunol., 28, 854, 10.1016/j.fsi.2010.02.009 · DOI
  170. Nowak, 2019, Immunomodulatory effects of synthetic endocrine disrupting chemicals on the development and functions of human immune cells, Environ Int., 125, 350, 10.1016/j.envint.2019.01.078 · DOI
  171. Camarca, 2016, Human peripheral blood mononuclear cell function and dendritic cell differentiation are affected by bisphenol-A exposure, PLoS ONE., 11, e0161122, 10.1371/journal.pone.0161122 · DOI
  172. Svajger, 2016, In vitro impact of bisphenols BPA, BPF, BPAF, and 17β-estradiol (E2) on human monocyte-derived dendritic cell generation, maturation and function, Int Immunopharmacol., 34, 146, 10.1016/j.intimp.2016.02.030 · DOI
  173. Hung, 2010, Modulation of cytokine expression in human myeloid dendritic cells by environmental endocrine-disrupting chemicals involves epigenetic regulation, Environ. Health Perspect., 118, 67, 10.1289/ehp.0901011 · DOI
  174. Couleau, 2015, Effects of endocrine disruptor compounds, alone or in combination, on human macrophage-like THP-1 cell response, PLoS ONE., 10, e0131428, 10.1371/journal.pone.0131428 · DOI
  175. Ustyugova, 2007, 3,4-dichloropropionaniline suppresses normal macrophage function, Toxicol Sci., 97, 364, 10.1093/toxsci/kfm048 · DOI
  176. Pottenger, 2000, The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration, Toxicol Sci., 54, 3, 10.1093/toxsci/54.1.3 · DOI
  177. Richter, 2007, In vivo effects of bisphenol A in laboratory rodent studies, Reprod Toxicol., 24, 199, 10.1016/j.reprotox.2007.06.004 · DOI · Paper page
  178. Ehrlich, 2012, Urinary bisphenol A concentrations and early reproductive health outcomes among women undergoing IVF, Hum Reprod., 27, 3583, 10.1093/humrep/des328 · DOI
  179. Mok-Lin, 2010, Urinary bisphenol A concentrations and ovarian response among women undergoing IVF, Int J Androl., 33, 385, 10.1111/j.1365-2605.2009.01014.x · DOI
  180. Minguez-Alarcon, 2019, Urinary concentrations of bisphenol A, parabens and phthalate metabolite mixtures in relation to reproductive success among women undergoing in vitro fertilization, Environ Int., 126, 355, 10.1016/j.envint.2019.02.025 · DOI
  181. Grindler, 2018, Exposure to phthalate, an endocrine disrupting chemical, alters the first trimester placental methylome and transcriptome in women, Sci Rep., 8, 6086, 10.1038/s41598-018-24505-w · DOI
  182. Adibi, 2010, Transcriptional biomarkers of steroidogenesis and trophoblast differentiation in the placenta in relation to prenatal phthalate exposure, Environ Health Perspect., 118, 291, 10.1289/ehp.0900788 · DOI
  183. Zhao, 2014, Disruption of the hormonal network and the enantioselectivity of bifenthrin in trophoblast: maternal-fetal health risk of chiral pesticides, Environ Sci Technol., 48, 8109, 10.1021/es501903b · DOI
  184. Muller, 2018, Bisphenol A exposure during early pregnancy impairs uterine spiral artery remodeling and provokes intrauterine growth restriction in mice, Sci Rep., 8, 9196, 10.1038/s41598-018-27575-y · DOI
  185. Ye, 2019, Bisphenol A exposure alters placentation and causes preeclampsia-like features in pregnant mice involved in reprogramming of DNA methylation of WNT2, FASEB J., 33, 2732, 10.1096/fj.201800934RRR · DOI
  186. Tachibana, 2007, Effects of bisphenol A (BPA) on placentation and survival of the neonates in mice, J Reprod Dev., 53, 509, 10.1262/jrd.18171 · DOI
  187. Backlin, 1998, Polychlorinated biphenyl (PCB) exposure produces placental vascular and trophoblastic lesions in the mink (Mustela vison): a light and electron microscopic study, APMIS, 106, 785, 10.1111/j.1699-0463.1998.tb00225.x · DOI
  188. Meyer, 2019, Exposure to 17α-ethinyl estradiol during early pregnancy affects fetal growth and survival in mice, Environ Pollut., 251, 493, 10.1016/j.envpol.2019.04.144 · DOI · Paper page
  189. Bansal, 2017, Sex- and dose-specific effects of maternal bisphenol A exposure on pancreatic islets of first- and second-generation adult mice offspring, Environ Health Perspect., 125, 097022, 10.1289/EHP1674 · DOI

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Metadata

Authors
Meyer, N., & Zenclussen, A. C.
Venue
Frontiers in Immunology
Publisher
Frontiers Media SA
Published
2020-02-19
Volume
11
ISSN
1664-3224
DOI
10.3389/fimmu.2020.00246
PMC
PMC7043066
Cited by
39
References
7
Licence
creativecommons.org/licenses/by/4.0/ (vor)
Funders
Deutsche Forschungsgemeinschaft

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