BPA Alters Estrogen Receptor Expression in the Heart After Viral Infection Activating Cardiac Mast Cells and T Cells Leading to Perimyocarditis and Fibrosis

Myocarditis is an inflammatory heart disease that leads to dilated cardiomyopathy (DCM) and heart failure. Sex hormones play an important role in the development of myocarditis with testosterone driving disease in males and estrogen being cardioprotective in females. The human population is widely exposed to the endocrine disruptor bisphenol A (BPA) from plastics such as water bottles, plastic food containers, copy paper, and receipts. Several clinical and numerous animal studies have found an association between elevated BPA levels and cardiovascular disease. A recent report found elevated levels of BPA in the serum of patients with DCM compared to healthy controls. In this study we examined whether exposure to BPA for 2 weeks prior to viral infection and leading up to myocarditis at day 10 altered inflammation in female BALB/c mice housed in standard plastic cages/water bottles with soy-free food and bedding. We found that a human relevant dose of BPA (25 μg/L) in drinking water, with an estimated exposure of 5 μg BPA/kg BW, significantly increased myocarditis and pericarditis compared to control water without altering viral genome levels in the heart. BPA exposure activated ERα and ERβ in the spleen 24 h after infection and phosphorylated ERα and ERβ during myocarditis, but decreased ERα and increased ERβ mRNA in the heart as measured by qRT-PCR. Exposure to BPA significantly increased CD4+ T cells, IFNγ, IL-17A, TLR4, caspase-1, and IL-1β in the heart. BPA exposure also increased cardiac fibrosis compared to controls. Mast cells, which are associated with cardiac remodeling, were found to increase in number and degranulation, particularly along the pericardium. Interestingly, plastic caging/water bottle exposure alone led to increased mast cell numbers, pericardial degranulation and fibrosis in female BALB/c mice compared to animals housed in glass cages/water bottles with soy-free food and bedding. These data suggest that BPA exposure may increase the risk of developing myocarditis after a viral infection in women.

[1]  E. Jabłońska,et al.  Immunomodulatory effects of synthetic endocrine disrupting chemicals on the development and functions of human immune cells. , 2019, Environment international.

[2]  P. Hunt,et al.  Chemical Contaminants from Plastics in the Animal Environment. , 2019, Journal of the American Association for Laboratory Animal Science : JAALAS.

[3]  L. Cooper,et al.  Elevated Sera sST2 Is Associated With Heart Failure in Men ≤50 Years Old With Myocarditis , 2019, Journal of the American Heart Association.

[4]  H. Yokota,et al.  Biotransformation of Bisphenol A and Its Adverse Effects on the Next Generation , 2018, Endocrine Disruptors.

[5]  V. Regitz-Zagrosek,et al.  Sex-specific regulation of collagen I and III expression by 17&bgr;-Estradiol in cardiac fibroblasts: role of estrogen receptors , 2018, Cardiovascular research.

[6]  S. Huber,et al.  Age-Associated Changes in Estrogen Receptor Ratios Correlate with Increased Female Susceptibility to Coxsackievirus B3-Induced Myocarditis , 2017, Front. Immunol..

[7]  T. Yun,et al.  From the Cover: Lifelong Exposure of C57bl/6n Male Mice to Bisphenol A or Bisphenol S Reduces Recovery From a Myocardial Infarction , 2017, Toxicological sciences : an official journal of the Society of Toxicology.

[8]  H. Brenhouse,et al.  Effects of Water Bottle Materials and Filtration on Bisphenol A Content in Laboratory Animal Drinking Water. , 2017, Journal of the American Association for Laboratory Animal Science : JAALAS.

[9]  M. Marino,et al.  Sex Differences in Estrogen Receptor α and β Levels and Activation Status in LPS‐Stimulated Human Macrophages , 2017, Journal of cellular physiology.

[10]  L. Cooper,et al.  Cardiac myosin-Th17 responses promote heart failure in human myocarditis. , 2016, JCI insight.

[11]  Chaoqian Xu,et al.  Bisphenol A, an environmental estrogen-like toxic chemical, induces cardiac fibrosis by activating the ERK1/2 pathway. , 2016, Toxicology letters.

[12]  K. Kabashima,et al.  Roles of basophils and mast cells in cutaneous inflammation , 2016, Seminars in Immunopathology.

[13]  T. Kawakami,et al.  Signal transduction and chemotaxis in mast cells. , 2016, European journal of pharmacology.

[14]  S. Ndaw,et al.  Occupational exposure of cashiers to Bisphenol A via thermal paper: urinary biomonitoring study , 2016, International Archives of Occupational and Environmental Health.

[15]  P. Hunt,et al.  Direct measurement of Bisphenol A (BPA), BPA glucuronide and BPA sulfate in a diverse and low-income population of pregnant women reveals high exposure, with potential implications for previous exposure estimates: a cross-sectional study , 2016, Environmental Health.

[16]  S. Liao,et al.  Prenatal exposure to bisphenol-A is associated with Toll-like receptor–induced cytokine suppression in neonates , 2016, Pediatric Research.

[17]  Yun-Chul Hong,et al.  Bisphenol A, Hypertension, and Cardiovascular Diseases: Epidemiological, Laboratory, and Clinical Trial Evidence , 2016, Current Hypertension Reports.

[18]  S. Othman,et al.  Tualang Honey Protects against BPA-Induced Morphological Abnormalities and Disruption of ERα, ERβ, and C3 mRNA and Protein Expressions in the Uterus of Rats , 2015, Evidence-based complementary and alternative medicine : eCAM.

[19]  S. Huber ERβ and ERα Differentially Regulate NKT and Vγ4+ T-cell Activation and T-regulatory Cell Response in Coxsackievirus B3 Infected Mice. , 2015, Journal of clinical & cellular immunology.

[20]  D. Choubey,et al.  Bisphenol A (BPA) stimulates the interferon signaling and activates the inflammasome activity in myeloid cells , 2015, Molecular and Cellular Endocrinology.

[21]  M. Marino,et al.  Molecular Mechanisms of Action of BPA , 2015, Dose-response : a publication of International Hormesis Society.

[22]  R. Budinsky,et al.  Extensive metabolism and route-dependent pharmacokinetics of bisphenol A (BPA) in neonatal mice following oral or subcutaneous administration. , 2015, Toxicology.

[23]  Jone Corrales,et al.  Global Assessment of Bisphenol A in the Environment , 2015, Dose-response : a publication of International Hormesis Society.

[24]  William H. Bisson,et al.  Environmental immune disruptors, inflammation and cancer risk. , 2015, Carcinogenesis.

[25]  S. Jozan,et al.  Influence of A Continuous Very Low Dose of Gamma-Rays on Cell Proliferation, Apoptosis and Oxidative Stress , 2015, Dose-response : a publication of International Hormesis Society.

[26]  Xiaoshu Cheng,et al.  Elevated Serum Bisphenol A Level in Patients with Dilated Cardiomyopathy , 2015, International journal of environmental research and public health.

[27]  A. Schecter,et al.  Exposure assessment of adult intake of bisphenol A (BPA) with emphasis on canned food dietary exposures. , 2015, Environment international.

[28]  Lorna M. Lopez,et al.  Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans , 2015, PloS one.

[29]  Huanxiang Liu,et al.  The Molecular Mechanism of Bisphenol A (BPA) as an Endocrine Disruptor by Interacting with Nuclear Receptors: Insights from Molecular Dynamics (MD) Simulations , 2015, PloS one.

[30]  S. Belcher,et al.  Bisphenol A alters autonomic tone and extracellular matrix structure and induces sex-specific effects on cardiovascular function in male and female CD-1 mice. , 2015, Endocrinology.

[31]  V. Regitz-Zagrosek,et al.  Comparative proteomic analysis reveals sex and estrogen receptor β effects in the pressure overloaded heart. , 2014, Journal of proteome research.

[32]  Jianglin Fan,et al.  Bisphenol A Exposure Enhances Atherosclerosis in WHHL Rabbits , 2014, PloS one.

[33]  Hongsheng Wang,et al.  Modulation of cytokine expression in human macrophages by endocrine-disrupting chemical Bisphenol-A. , 2014, Biochemical and biophysical research communications.

[34]  Hong-Sheng Wang,et al.  Impact of Bisphenol A on the Cardiovascular System — Epidemiological and Experimental Evidence and Molecular Mechanisms , 2014, International journal of environmental research and public health.

[35]  Wei Duan,et al.  Improved Efficacy and Reduced Toxicity of Doxorubicin Encapsulated in Sulfatide-Containing Nanoliposome in a Glioma Model , 2014, PloS one.

[36]  D. Dolinoy,et al.  Perinatal bisphenol A exposures increase production of pro-inflammatory mediators in bone marrow-derived mast cells of adult mice , 2014, Journal of immunotoxicology.

[37]  Datis Kharrazian The Potential Roles of Bisphenol A (BPA) Pathogenesis in Autoimmunity , 2014, Autoimmune diseases.

[38]  Murugesan V. S. Rajaram,et al.  Estrogen modulation of endosome-associated toll-like receptor 8: an IFNα-independent mechanism of sex-bias in systemic lupus erythematosus. , 2014, Clinical immunology.

[39]  K. Hong,et al.  Cellular Mechanism of the Nonmonotonic Dose Response of Bisphenol A in Rat Cardiac Myocytes , 2014, Environmental health perspectives.

[40]  G. Gilkeson,et al.  Estrogen Receptor Alpha Binding to ERE is Required for Full Tlr7- and Tlr9-Induced Inflammation. , 2014, SOJ immunology.

[41]  C. O'Mahony,et al.  Estimates of Dietary Exposure to Bisphenol A (BPA) from Light Metal Packaging using Food Consumption and Packaging usage Data: A Refined Deterministic Approach and a Fully Probabilistic (FACET) Approach , 2013, Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment.

[42]  Mariana F. Fernández,et al.  In vitro study on the agonistic and antagonistic activities of bisphenol-S and other bisphenol-A congeners and derivatives via nuclear receptors. , 2013, Toxicology and applied pharmacology.

[43]  Ruili Huang,et al.  Bisphenol A affects androgen receptor function via multiple mechanisms. , 2013, Chemico-biological interactions.

[44]  S. Huber,et al.  Autoimmune Myocarditis, Valvulitis, and Cardiomyopathy , 2013, Current protocols in immunology.

[45]  K. Tomer,et al.  The estrogenic content of rodent diets, bedding, cages, and water bottles and its effect on bisphenol A studies. , 2013, Journal of the American Association for Laboratory Animal Science : JAALAS.

[46]  D. Kirchhofer,et al.  PAR-1 contributes to the innate immune response during viral infection. , 2013, The Journal of clinical investigation.

[47]  L. Cooper,et al.  Management of myopericarditis , 2013, Expert review of cardiovascular therapy.

[48]  D. Eastmond,et al.  Dose‐response analysis of bromate‐induced DNA damage and mutagenicity is consistent with low‐dose linear, nonthreshold processes , 2013, Environmental and molecular mutagenesis.

[49]  Y. Lim,et al.  Associations of Bisphenol A Exposure With Heart Rate Variability and Blood Pressure , 2012, Hypertension.

[50]  D. Fairweather,et al.  Update on coxsackievirus B3 myocarditis , 2012, Current opinion in rheumatology.

[51]  W. Mitzner,et al.  Testosterone and interleukin-1β increase cardiac remodeling during coxsackievirus B3 myocarditis via serpin A 3n. , 2012, American journal of physiology. Heart and circulatory physiology.

[52]  Carla J. Berg,et al.  Results of a Feasibility and Acceptability Trial of an Online Smoking Cessation Program Targeting Young Adult Nondaily Smokers , 2012, Journal of environmental and public health.

[53]  Laura N. Vandenberg,et al.  Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses. , 2012, Endocrine reviews.

[54]  M. Petri,et al.  Autoimmune heart disease: role of sex hormones and autoantibodies in disease pathogenesis , 2012, Expert review of clinical immunology.

[55]  S. Belcher,et al.  Rapid estrogen receptor-mediated mechanisms determine the sexually dimorphic sensitivity of ventricular myocytes to 17β-estradiol and the environmental endocrine disruptor bisphenol A. , 2012, Endocrinology.

[56]  A. Shankar,et al.  Urinary Bisphenol A and Hypertension in a Multiethnic Sample of US Adults , 2012, Journal of environmental and public health.

[57]  J. Arnal,et al.  The TLR-mediated response of plasmacytoid dendritic cells is positively regulated by estradiol in vivo through cell-intrinsic estrogen receptor α signaling. , 2012, Blood.

[58]  Jun Wang,et al.  Chronic Oral Exposure to Bisphenol A Results in a Nonmonotonic Dose Response in Mammary Carcinogenesis and Metastasis in MMTV-erbB2 Mice , 2011, Environmental health perspectives.

[59]  L. Cooper,et al.  Clinical and demographic predictors of outcomes in recent onset dilated cardiomyopathy: results of the IMAC (Intervention in Myocarditis and Acute Cardiomyopathy)-2 study. , 2011, Journal of the American College of Cardiology.

[60]  L. Lind,et al.  Circulating levels of bisphenol A and phthalates are related to carotid atherosclerosis in the elderly. , 2011, Atherosclerosis.

[61]  Y. Iwakura,et al.  Interleukin-17A Is Dispensable for Myocarditis but Essential for the Progression to Dilated Cardiomyopathy , 2010, Circulation research.

[62]  M. Friedrich,et al.  Age and gender effects on the extent of myocardial involvement in acute myocarditis: a cardiovascular magnetic resonance study , 2009, Heart.

[63]  G. Rosano,et al.  Gender differences in the cardiovascular effect of sex hormones , 2009, Nature Reviews Cardiology.

[64]  V. Regitz-Zagrosek,et al.  Sex Steroid Hormones , 2009 .

[65]  Laura N. Vandenberg,et al.  Bisphenol-A and the great divide: a review of controversies in the field of endocrine disruption. , 2009, Endocrine reviews.

[66]  M. Mattson Hormesis defined , 2008, Ageing Research Reviews.

[67]  M. Kimura,et al.  Structural evidence for endocrine disruptor bisphenol A binding to human nuclear receptor ERR gamma. , 2007, Journal of biochemistry.

[68]  N. Rose,et al.  Cutting Edge: Cross-Regulation by TLR4 and T cell Ig Mucin-3 Determines Sex Differences in Inflammatory Heart Disease1 , 2007, The Journal of Immunology.

[69]  Ziya Kaya,et al.  Complement Receptor 1 and 2 Deficiency Increases Coxsackievirus B3-Induced Myocarditis, Dilated Cardiomyopathy, and Heart Failure by Increasing Macrophages, IL-1β, and Immune Complex Deposition in the Heart1 , 2006, The Journal of Immunology.

[70]  H. Schultheiss,et al.  Viral Persistence in the Myocardium Is Associated With Progressive Cardiac Dysfunction , 2005, Circulation.

[71]  H. Takano,et al.  Prenatal exposure to bisphenol A up‐regulates immune responses, including T helper 1 and T helper 2 responses, in mice , 2004, Immunology.

[72]  N. Rose,et al.  Mast Cells and Innate Cytokines are Associated with Susceptibility to Autoimmune Heart Disease Following Coxsackievirus B3 Infection , 2004, Autoimmunity.

[73]  Wade V Welshons,et al.  Bisphenol A is released from used polycarbonate animal cages into water at room temperature. , 2003, Environmental health perspectives.

[74]  Wolfgang Völkel,et al.  Metabolism and kinetics of bisphenol a in humans at low doses following oral administration. , 2002, Chemical research in toxicology.

[75]  T. Zacharewski,et al.  In Vitro and in Vivo Interactions of Bisphenol A and Its Metabolite, Bisphenol A Glucuronide, with Estrogen Receptors α and β , 2001 .

[76]  L. R. Harris,et al.  Normal reproductive organ development in Wistar rats exposed to bisphenol A in the drinking water. , 1999, Regulatory toxicology and pharmacology : RTP.

[77]  R. Kandolf,et al.  Enteroviral RNA replication in the myocardium of patients with left ventricular dysfunction and clinically suspected myocarditis. , 1999, Circulation.

[78]  L. Schwartz,et al.  Two types of human mast cells that have distinct neutral protease compositions. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[79]  A. Mantovani,et al.  Evaluation of the interaction of mononuclear phagocytes with ovarian carcinoma cells in a colony assay. , 1986, British Journal of Cancer.

[80]  J. Little,et al.  Evidence for linear response for the induction of mutations in human cells by x-ray exposures below 10 rads. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[81]  L. Rittié Method for Picrosirius Red-Polarization Detection of Collagen Fibers in Tissue Sections. , 2017, Methods in molecular biology.

[82]  S. Huber,et al.  Sex Hormone Receptor Expression in the Immune System , 2016 .

[83]  N. Rose,et al.  Interferon- Protects against Chronic Viral Myocarditis by Reducing Mast Cell Degranulation, Fibrosis, and the Profibrotic Cytokines Transforming Growth Factor- 1, Interleukin-1 , and Interleukin-4 in the Heart , 2004 .

[84]  D. McDonnell,et al.  The estrogen receptor beta-isoform (ERbeta) of the human estrogen receptor modulates ERalpha transcriptional activity and is a key regulator of the cellular response to estrogens and antiestrogens. , 1999, Endocrinology.

[85]  FRCP W. J. MacLennan MD,et al.  The Elderly , 1984, Treatment in Clinical Medicine.