Archives of Asthma, Allergy and Immunology

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The effects of early low dose exposures to the Environmental Estrogen Bisphenol A on the Development of Childhood Asthma

Terumi Midoro-Horiuti* and Randall M Goldblum

University of Texas Medical Branch, Department of Pediatrics, 301 University Blvd. Galveston, Galveston, USA

*Address for Correspondence: Terumi Midoro-Horiuti, University of Texas Medical Branch, Department of Pediatrics, 301 University Blvd, Galveston, USA, TX 77555-0366; Email: tmidoro@utmb.edu

Dates: Submitted: 25 May 2017; Approved: 07 July 2017; Published: 07 July 2017

How to cite this article: Horiuti TM, Goldblum RM. The effects of early low dose exposures to the Environmental Estrogen Bisphenol A on the development of Childhood Asthma. Arch Asthma Allergy Immunol. 2017; 1: 015-027

Copyright: © 2017 Horiuti TM, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abbreviations: BALF: Broncho Alveolar Lavage Fluid; BBzP, di-n-butyl phthalate and butylbenzyl phthalate; BPA: Bisphenol A; BW: Body Weight; ER: Estrogen Receptor; IP: Intraperitoneal; FEV1: Forced Expiratory Volume in the first second of expiration; Intraperitoneal; MBzP, Monobenzyl phthalate; NHANES: National Health and Nutrition Examination Survey; OVA: Ovalbumin; PN: Post Natal; PND: Post Natal Day

SUMMARY

Exposure to environmental chemicals is a potential cause for the rapid increase in the prevalence of allergic asthma over the last few decades. The production of the environmental estrogen bisphenol A, the monomer of polycarbonate plastics, has increased rapidly over the last 50 years, such that bisphenol A is one of the most highly produced chemicals. It is detectable in the urine of the vast majority of the human population. While the relationship between the increase of bisphenol A in our environment and the prevalence of asthma does not prove a cause and effect relationship, it provides a strong rationale for experiments that have tested the hypothesis. Because of its small molecular size and hydrophobicity, bisphenol A is easily transferred from the mother to the fetus, via the placenta and in breast milk.

We have reviewed all the publications available on medline on the human epidemiological studies of the early bisphenol A exposure on the development of allergic asthma and experimental studies using mouse model of the effects of early bisphenol A exposure on the development of asthma. There are eight human epidemiological studies and five mouse model studies currently published.

The human studies suggest that bisphenol A exposure in early life enhances the likelihood of developing asthma on at least one of the study groups. The effects of early bisphenol A exposure were observed as an enhanced development of asthma before adolescent in the animal model.

INTRODUCTION

Allergic diseases, including asthma are often considered to be related to our genes and/or environment. However, changes of the genetic code in a population typically take a long period of time, suggesting that the recent, rapid increase in the prevalence of allergic diseases is more likely to be due to the changes in our environment, which may alter gene expression (gene/environment interaction [1]). Further, during the last few decades, campaigns to promote smoking cessation in the US and elsewhere have reduced exposure to direct and second hand smoke in pregnant women and their children. The concentrations of the six other common air pollutants (ozone, carbon monoxide, nitrogen dioxide, particulate matter, sulfur dioxide and lead) have also decreased by 60% during these decades (EPA, http://www.epa.gov/airtrends/aqtrends.html), yet the overall prevalence of asthma has increased during this period. Another important consideration is that the increasing prevalence of allergic rhinitis and asthma is seen predominantly in women after adolescent, while prevalence of allergic rhinitis and asthma in boys and young men decrease during and after adolescent. These observations coupled with an increase in the incidence of new or recurrent asthma in women who took hormone replacement therapy after menopause [2], suggest an effects of female hormones on the development of allergic diseases, including asthma. Other reports show the human and mouse fetuses are T helper type (Th) 2 dominant [3,4] and endogenous (e.g. estradiol, E2) and exogenous (environmental) estrogens induce Th2 development [5-7].

Based on these clinical observations and the concomitant high production and ubiquitous exposure of humans to BPA, we chose to focus our studies of asthma development on environmental estrogens, and particularly on BPA, as a model for assessing the effects of exposure to estrogenic chemicals on the development of allergic diseases. We review here evidence that early life exposures to BPA may enhance the development of allergic asthma (Figure 1).

Figure 1: The structures of endogenous estrogens and BPA.

BPA was first synthesized by a Russian chemist Alexander Dianin in 1891, and tests were conducted in the 1930s to determine whether BPA could be used for hormone replacement therapy [8,9]. However BPA proved less effective than other synthetic estrogens. In 1952, manufacturing processes for polymerizing BPA monomers to form polycarbonate plastic were developed and the production of BPA has increased exponentially since then (Figure 2, modified from [10]). In addition to polycarbonate plastic containers, BPA is widely used as a coating of metal cans, baby bottles, toys and receipt papers, and to a lesser extent in other household plastics. Thus, BPA is now ubiquitous, not only in our environment, but also in human tissues and secretions [11]. Its small molecular weight (228.29 g/mol) and hydrophobicity also allow BPA to be rapidly transferred to fetus through placenta and also into the breast milk [12], providing pathways into the next generation.

Figure 2: Temporal relationships between the increases of asthma prevalence and BPA production.

BPA exposure and metabolism in humans

We identified eight English language manuscripts concerning the relationship between human exposure to BPA and the subsequent development of asthma. These exposures are mainly via consumption of food and drinks [13], and also non-oral exposures such as dermal exposure is reported [14,15]. BPA is absorbed through gastrointestinal tract and enters the hepatic portal vein to the liver, and then to the systemic circulation. Most of the absorbed BPA is conjugated to glucuronide by predominantly by UDP-glucuronosyltransferases in the intestinal epithelium and in liver. This makes BPA more hydrophilic and allows it to be excreted into urine [16]. However, the biologically active form is predominantly residual unconjugated BPA, which can bind to estrogen receptors (ERs) in various tissues and alters biological processes [17]. Thus, it is the small amount of unconjugated BPA in the blood and tissues, termed the “internal dosage”-as assessed from blood measures-that is likely to have the most important effects in human toxicology [18]. However, BPA concentrations/excretion into the urine “exposure assessment from urinary measures of BPA” is most commonly used in epidemiological studies.

Effects of BPA exposure on allergic diseases-human epidemiological studies

There are eight epidemiological studies of the effects of BPA exposure on the development of allergic asthma published accessible in Medline: Vaidya et al. [19] Spanier et al. [20,21], Donohue et al. [22], Kim et al. [23], Whyatt et al. [24], Gascon et al. [25] and Wang et al. [26] (Table 1). Each of these eight human epidemiological studies identified at least one indicator of an association between BPA exposure and asthma, which was significantly increased with prenatal or self (direct) BPA exposure of children.

Table 1: Human epidemiological data of early BPA exposure on the development of allergic asthma.
Author
year
Recruitment
N            year
BPA
measure
Outcome
wheezing
asthma diagnosis¯
Vaidya
2012
10,348   2005-2006 6yr- 6yr- 6yr-         asthma in females
allergen specific IgE antibodies
asthma episode in past 12mo in females
Spanier
2012
365      2003-2006 G16,
G26w
every 6mo to 3yr               wheeze at age 6mo w uBPA at 16 w
~wheeze at age yr w uBPA
Donohue
2013
568       1998-2006 3rd
Trimester3, 5, 7yr
5, 6, 7yr 5-12yr       ↓wheeze at age 5yr w prenatal uBPA
wheeze at age 5&6yr w uBPA at age 3 yr
wheeze at age 7yr w uBPA at age 7yr
Spanier
2014
208       2003-2006 G16,
G26w
every 6mo to 5yr 4, 5yr          ↓FEV1 at age 4yr w maternal uBPA  
wheezing w 16w uBPA
~FEV1 or wheeze w child uBPA
Kim
2014
127 7-8yr 9-10, 11-12yr 9-12yr         wheeze at 11-12yr w uBPA at 7-8yr in girls
asthma at 11-12yr w uBPA at 7-8yr in girls
Whyatt
2014
292       1998-2006 3, 5, 7yr 5, 6, 7, 9, 11yr 5yr               asthma, persistent wheeze, exsecise-induced
wheeze among prenatal MBzP only  
Gascon
2015
462        2004-2008 G12,
G32w
6mo, 14mo, 4yr,
7yr
7yr                  wheeze at any age chest infection at any age
bronchitis
Wang
2016
453 3, 6yr 3, 6yr 3,6yr               asthma at 3, 6yr

Vaidya et al. performed a secondary analysis of urinary BPA data from the National Health and Nutrition Examination Survey (NHANES) 2005-2006 (http://www.cdc.gov/nchs/nhanes.htm). Using the data from 10,348 subjects older than 6 years, they examined the urinary BPA concentrations/excretion (BPA/Cr) ratio from 2,548 (24.6% of the total subjects: 1,270 males and 1,278 females). They then related the urinary BPA excretion to the blood concentration of total IgE, specific IgE antibodies against 19 allergens, and other urinary environmental estrogens (Benzophenone-3, 4-tert-Octylphenol, Triclosan, Methyl paraben, Ethyl paraben, Propyl paraben and Butyl paraben). The diagnosis of asthma was based on the history of wheezing, the number of eosinophil in peripheral blood, total IgE concentration and history of other atopic diseases. Urinary BPA concentration had a significant positive association with increased concentrations of IgE antibodies to various specific allergens and with the history of asthma episodes in the previous 12 months among women, but not with those in men.

Spanier et al. collected samples of urine from 365 women at 16±2 weeks of pregnancies, in their birth cohort study from 2003 to 2006 in Cincinnati, Ohio, and measured the urinary BPA concentration and BPA/creatinine ratios in samples from women older than 18 years and paired these with their children. They followed the mother-infant pairs for five years and reported the follow-up data collected from phone interviews when each child was 6, 18 and 30 months old and home visits at child’s age of 12, 24 and 36 month, and 3 and 5 years of age [20,21]. They used a questionnaire from National Health and Nutrition Examination Survey (NHANES) to identify those with wheezing, “Has [child’s name] had wheezing or whistling in his/her chest in the last 6 months?” They also conducted a trajectory analysis to identify distinct groups of wheeze trajectories and phenotypes. This study identified a significant correlation between maternal urinary BPA concentration at 16 (but not 26) weeks of pregnancy with child’s wheezing by postnatal age 6 months. Spanier et al. continued this study using phone interviews and tests of lung function on 4 and 5 year olds. They identified a significant association between maternal urinary BPA concentrations at 16 and 26 weeks of pregnancy with decreased forced expiratory volume in the first second of expiration (FEV1) of 4 years old children, but not with FEV1 at 5 years.

Donohue et al. recruited 568 mothers of African American or Dominican origin and their child pairs, who had lived in Northern Manhattan or South Bronx for at least 1 year, from 1998 to 2006. They analyzed their urinary BPA data from late in pregnancy, when the children were 3, 5 and 7 years old. Wheezing history was elicited for the previous 12 months and at 5, 6 and 7 years old, and one clinic visit between the ages of 5-12 years old. They identified an inverse association between maternal urinary BPA concentration during late pregnancy and child’s wheezing at age 5 and 6 years. However, they also noted a significant correlation between the child’s own urinary BPA concentration and wheezing at age 7 years. There was also a significant correlation between the child’s urinary concentration of BPA and the prevalence of asthma at 3, 5 and 7 years of age [22].

Kim et al. collected 127 urine samples from 7-8 year old elementary school children in Seoul, Korea in 2005, who agreed to a baseline survey and a methacholine challenge test. They then identified their “wheezing outcomes” at age 9-10 and 11-12 years old. Children were considered to have asthma when they met either of the following criteria: 1) “wheezing or the use of asthma medication in the previous 12 months” or 2) the same history combined with an asthma diagnosis or a history of wheezing”. They identified a significant correlation between urinary BPA concentration at 7-8 years old and wheezing and asthma at 11-12 years old among girls, but not in boys [27]. The Whyatt et al., group also analyzed the association of asthma and exposure combination of BPA, di-n-butyl phthalate and butylbenzyl phthalate (BBzP) among 229, inner-city women and their children at age 5-11 years [22]. They measured phthalates in spot urine collected from the mother during pregnancy at 33.9±3.1 week’s gestation and BPA in child urine at 3, 5 and/or 7 years old. They found significant association between the children’s urinary BPA concentration and respiratory outcomes, in those from women whose maternal prenatal urinary monobenzyl phthalate (MBzP) were above median, but not in those children from women whose values below the median.

In 2015, Gascon at al. reported a correlation between prenatal BPA exposure and respiratory tract infection and allergy, among subjects recruited in Catalonia, Spain, from 2004 to 2008 [25]. They analyzed the maternal urinary concentration of BPA at 12 and 32 weeks of gestation in 391 women and related these to symptoms of allergy, atopy and respiratory infections in the children at 6 and 14 months, and 4 and 7 years old. They found the relative risks of wheeze, chest infections and bronchiolitis, at any age, increased with each doubling in the concentration of the mother’s prenatal urinary BPA [25].

Wang et al. [26] recruited 453 children age 3 and 6 years old from Taiwan and analyzed their own urinary BPA concentration, serum total IgE and diagnosis of asthma using the questionnaire from International Study of Asthma and Allergies in Childhood (ISAAC). They found an association between their urinary BPA concentration and asthma, as well as serum total IgE concentration.

One of the major differences between these studies was the timing/ages at which the subjects were tested for BPA exposure, particularly between pre and postnatal exposures. Interestingly, two recent reports from a consortium of European states showed a strong correlation between the mother’s urinary BPA concentration and those of their child (p=0.001 and <0.001) at various postnatal ages [28,29]. This finding may suggest that a dietary lifestyle of the household is a major determinant of the extent of exposure to BPA for all of the family members.

Effects of BPA on the development of asthma-studies from mouse models

We identified six reports, two from our group [30,16] and one each from Bauer et al. [31], Petzold et al. [32], O’Brien et al. [33] and Nygaard et al. [34], concerning the effects of maternal BPA exposure on the development of asthma in mouse models (Table 2). Only mouse were used on the asthma model study for the effects of BPA, most likely because of the availability for lung function testing devices, whole body plethysmography and direct measurement of airway resistance.

Table 2: Mouse model studies of early BPA exposure on the development of asthma phenotype.
Author Strain BPA exp BPA dose Allergen (OVA) sensitization analyses
Year Star end μg/KgBW/d route Systemic Airway day
(PND) (μg) dose age dose age (PN)
(PN) (PN)
Midoro BALB/c -28 17 2,000 drinking 5 μg x 1 i.p. 4d 3% aerosol 10min 13-15d 17d ↑ AHR in BPA/OVA
2010 water x3d ↑ Eos in BALF in BPA/OVA
↑serum IgE anti-OVA in BPA/OVA
Nakajima BALB/c -28 21 2,000 drinking 5 μg x 1 i.p. 4d 3% aerosol 10min 18-20d 22d ↑AHR in BPA/BPPA/OVA and BPA/no BPA/OVA
2012 -28 0 water x3d ↑Eos in BALF in BPA/BPA/OVA and BPA/no BPA/OVA
0 21
Bauer C57BL/6 -21 21 0.5,5,50,500 gavage 100 μg x 2 i.t. 6w 1% aerosol 1hr 8w 8w ↓Nt in BALF in male BPA50/OVA woLPS
2012 w/wo 100 ng LPS 1d ~Eos in BALF in male/femle BPA/OVA
mucosal sensitization ↑lung histology in female high BPA/OVA wo LPS and female BPA/OVA w LPS
↑lung histology in male BPA/OVA wo LPS
Bauer C57BL/6 -21 21 0.5,5,50,500 gavage 100 μg x 2 i.p. 6w 1% aerosol 1hr 7-11w 7-11w ↓Eos in BALF in female BPA0.5, 5, 50/OVA
2013 1d ~Eos in BALF in female BPA500/OVA
peritoneal sensitization ↓serum IgE anti-OVA in female BPA/OVA
~AHR in female BPA/OVA
Petzold BALB/c -28 21 1,000 drinking 20 μg x 2 i.p. 6&8w 20 μg/40 μL i.n. 8&9w 9 w ~AHR
2014 6d ~Eos in BALF
~serum IgE anti-OVA
~IL-4, IL-5, IL-13, IFNᵞfrom splenocytes
O'Brien BALB/c -35 21 0.008, 8, 8,400 chow 20 μg x 1 i.p. 12w 3% aerosol 20min 13w 13w ↑serum IgE anti-OVA in low BPA
2014 x2d ↑↑serum IgE anti-OVA in moderate and high BPA
↑IL-13 from splenocyte from moderate & high BPA/OVA
↑↑↑IFNᵞ from splenocyte from BPA/OVA
~IL-4, IL-5, TNFa from splenocytes from BPA/OVA
↑total Leu in BALF in female high BPA/OVA
↓total Leu in BALF in male low & high BPA/OVA
↓Eos female high BPA/OVA
~Mp, PMN, Ly in females BPA/OVA
↓Mp, PMN, Eos in male low BPA/OVA
↓PMN, Ly in male high BPA/OVA
↓PMN in male moderate BPA/OVA
↓IL-4, IL-13, TNFa in BALF from female low and high BPA/OVA
~IL-4, IL-13, TNFa in BALF from male low and high BPA/OVA
↓IL-17 in BALF from BPA/OVA
↓CysLTs in BALF from high BPA/OVA
~Eotaxin-1 in BALF from BPA/OVA
↑RANTES in lung homogenate in low BPA/OVA
no change in female lung histology
↓inflammatory score in male high BPA/OVA
Nygaard BAL B/c 0 21 1,400-4,500 drinking 10 μg x 2 i.p. 4&18d 10 μg i.n. 25d 30d ↑Eos in BALF in 100μg/ml
2015 OlaHsd & 14,000-44,000 wo adjuvant ↑trend serum IgE anti-OVA in 100μg/ml
~serum IgG1, IgG2 anti-OVA
non detectable IL-5, IL-10, IL-17, IFNᵞ in BALF
~IL-4, IL-13, IL-10, IL-2, IL-17, IFNᵞ from splenocytes

To our knowledge, we were the first to report an effect of maternal BPA exposure on the development of asthma in their offspring. In our studies, we added 10 µg/ml of BPA to the drinking water of 8-10 weeks old female BALB/c mice (F0, about 2 mg BPA/KgBW/day), starting seven days before mating and continued throughout their pregnancy and nursing period. This protocol produced a similar range of BPA concentrations in the sera of the offspring (F1) to that described in human studies [18]. Some of the pups were sensitized to ovalbumin (OVA), using a “suboptimal” protocol, [35] in order to avoid overwhelming effects of OVA sensitization. The mice received a single intraperitoneal (i.p.) injection of 5 µg OVA on post natal day (PND) 4 and they were exposed to 3% OVA aerosol on PND 14-16. Airway hyperresponsiveness (AHR) was analyzed 48 hours after the last aerosol exposure. Serum OVA-specific IgE antibodies were assessed by ELISA, and eosinophilic airway inflammation were assessed by enumerating each cell type in the bronchoalveolar lavage fluid (BALF). Only the OVA sensitized pups from BPA exposed mothers (BPA/OVA) had significant increases in their serum IgE anti-OVA antibody concentration, and enhanced eosinophil numbers in BALF and AHR, relative to all three control groups (no BPA/no OVA, no BPA/OVA and BPA/no-OVA) [36]. Interestingly, these same indicators of allergic asthma were also observed in the F2 and F3 generation of females, despite the absence of additional exposures to BPA (non-published data).

We next examined the effect of prenatal and postnatal BPA exposure, separately [16]. Using the same exposure protocol as described above, we transferred half of the litters between BPA exposed and normal water control dams, within 48 hours of their birth, and used the same protocol to sensitize both groups, creating eight perinatal exposure/postnatal exposure/and sensitization groups. These experiments indicated that prenatal BPA exposure is necessary to produce the asthma phenotype in pups sensitized, using our “suboptimal” OVA protocol.

Bauer et al. [31] and Petzold et al. [32], also examined the effects of maternal (prenatal) BPA exposure on their mouse pups, but did not evaluate the offspring for asthma manifestations until they were in their adolescent and adults. Bauer et al. gave 0.5, 5, 50 or 500 µg/Kg BW/day of BPA by gavage to C57BL/6 mice while Petzold gave 1,000 µg/Kg BW/day of BPA in their drinking water in BALB/c (F0) mice during their pregnancy and until the pups were 3 weeks old. They then (at 3 weeks) sensitized these pups with 100 µg of endotoxin-depleted OVA with or without.

E. coli lipopolysaccharide (LPS) intratracheally (i.t.) three times, followed two weeks later by aerosol OVA challenge twice daily for three days (mucosal sensitization model), or with two injections of 100 µg OVA by i.p., when the adult offspring were 6-8 weeks old and then 1% OVA aerosol at 7-11 postnatal weeks of age (peritoneal sensitization model), and analyzed AHR, eosinophils in BALF and lung histology. Since BALB/c mice are sexually mature around 28-49 days (average 35 days) [37], these are considered adult asthma models. They found that adult female offspring demonstrated enhanced whole-lung inflammation, compared with vehicle treated controls in this mucosal sensitization model. No effect was seen in males. The CD4+, CD8+ and CD4+CD25+FoxP3+ lymphocyte numbers were not significantly changed, compared to the vehicle controls in neither females nor males. Both groups did find a decrease in the number of eosinophil in BALF in the females that had received with 0.5, 5, 50 µg/Kg BW/day BPA exposures, but not in the males. The results of AHR measurements by invasive plethysmography were not different between the groups in the peritoneal sensitization model. When they examined lung histology, only adult female offspring consistently demonstrated enhanced whole-lung inflammation when compared with the controls.

Petzold et al. gave 5 µg/ml of BPA in the drinking water of their pregnant BALB/c females (F0) and continued this until 3 weeks after they delivered their pups. Their adult offspring were sensitized with 20 µg OVA by i.p. injection at 6 and 20 weeks of age, and 40 µg of nasal OVA at 8 and 9 weeks old. At 9 weeks of age their AHR, eosinophil number in BALF, OVA-specific IgE and cytokine production from splenocytes were assessed. They did not find any effects of these maternal BPA exposures on the development of asthma in these adult offspring. No histological data are described for the mice with pre- and perinatal exposure to BPA.

O’Brien et al., gave 50 ng, 50 µg or 50 mg/Kg (low, moderate and high) doses of BPA in rodent chow to BALB/c mice, starting from 2 weeks before mating, until the weaning of the offspring [33]. These BPA doses translate into about 8 ng, 8 µg and 8 mg BPA/Kg BW/day, based on the chow consumption data from Bachmanov [38]. They then analyzed the effects of these three different doses of BPA on the serum IgE anti-OVA antibodies, cytokine and chemokine production, differential cell numbers and lung histology, in their male and female offspring. They detected modest increases in serum IgE anti-OVA in low BPA exposure group and 2-fold increase in moderate and high BPA exposed groups. IL-13 was increase in the moderate BPA exposure group and IFNᵞ production from splenocytes from all the BPA exposure groups was increased. Total leukocyte number in the BALF from female in their high BPA exposure group, and RANTES in lung homogenate in low BPA exposure groups were increased.

Nygaard et al., fed 0, 10, or 100 µg/ml BPA in the maternal drinking water to BALB/c OlaHsd mice (about 0, 2 or 20 mg BPA/KgBW/day). Their drinking water consumption was about 3 ml/day during gestation and 12 ml/day during lactation. They used these data to calculate BPA intakes: 1.4 (during gestation) and 14 (during lactation) mg/Kg BW/day for those who received 10 µg/ml BPA in their drinking water and 14 during (gestation) and 44 (lactation) for those receiving 100 µg/ml BPA. The offspring were sensitized with 10 µg OVA by i.p. injection, without any adjuvant, on PND 4 and 18, and on PND 25, 10 µg OVA i.n. The pups were analyzed for the number of eosinophil in their BALF, serum IgE, IgG1, IgG2 anti-OVA antibodies, and cytokine concentrations in BALF and cytokine production from splenocytes on PND 30. They detected significant increases of eosinophil numbers in BALF and a trend of high serum IgE anti-OVA in the 100 µg/ml exposure group.

Potential mechanism of effects of early BPA exposure

Fetal/newborn cells are skewed toward a Th2 pattern, partially due to low production of IL12 and the propensity of Th1 cells to undergo apoptosis after antigen exposure [39,40]. “Immune-maturing” infections promote a subsequent shift toward Th1 responses in most children, while an increasing proportion remain prone to develop pathological Th2 responses [41]. Most cases of asthma develop in early childhood [42] and often continue into adulthood, with a very large impact on public health and health care delivery. Thus a better understanding of the roles of genetics and environmental exposures during early life is very important [43].

Studies have shown the effects of BPA on the epigenetic alterations on several body systems in humans and rodent. These are focused mainly on endocrine/reproductive/metabolic system, [44-53] developmental cells, [51,54-57] cancer, neuro/behaviour [58,59] and cardiac [60]. Genome-wide CpG methylation analyses of “saliva DNA” from 60 Egyptian girls aged 10-13 and urinary BPA in spot samples shows general association of higher urinary BPA concentration with less genomic methylation [61]. The pathway analyses shows reduced methylation involvement in immune function with increasing urinary BPA in this study.

Non-genomic signaling is a potentially important mechanism of the effects of environmental estrogen exposure, which induces epigenetic modifications [62,63]. This response is initiated by ligand binding to receptors, ERα, ERβ or G protein coupled receptor (GPR)30, and activating signaling cascades that eventually alter kinase activities [62]. These kinases, phospho AKT, protein kinase A (PKA), protein kinase C (PKC) and extracellular signal-regulated kinase (ERK) phosphorylate one of the polycomb proteins, a histone methyltransferase (HMT) termed EZH2, [62,64] enhancer of zeste homolog 2 (EZH2) preferentially methylates histone H3K27, thus generating a binding site for the polycomb repressive complex (PRC)1 [65-68]. EZH2 also recruits DNA methyltransferase (DNMT) [68] and is a member of PRC2. Our group detected ERα on T-cells, mast cells and basophils [69,70]. The role of the PRC2 components in T-cell differentiation is somewhat controversial with observations indicating that they can have either activating [71,72] or repressive activities [73-76]. If these alterations persist, they can produce permanent epigenetic consequences (DNA methylation) within those sequences, therefore causing the development of asthma.

DISCUSSION

We have summarized here the results from eight human epidemiological studies and six experimental mouse models, all of which are related to the effect of early life BPA exposure on the development of allergic asthma. The reason for summarizing these together was our recognition that both experimental approaches have strengths and weaknesses in understanding the effects of BPA, and potentially other environmental estrogens, on the development of asthma in humans. For instance, direct human studies are the most important for understanding the relationship between exposures to chemicals like BPA at various phases of life, and the development and timing and manifestations of asthma. However, human studies have the drawback that their measurements of urinary BPA in the children may only be a biomarker for exposure to other chemicals that co-exist with BPA in certain environments. Further, while urinary measurements and excretion rates of chemicals like BPA are convenient, they only represent the conjugated (water soluble) BPA, which our group and others have shown are not active in cellular assays, most likely because they cannot bind to ERs [17,77]. Carefully controlled and performed animal studies should overcome some of these shortcomings, since the major difference between the experimental and control groups should be the extent of their exposure to purified BPA. While we and others have tried to carefully design the studies to closely imitate the human exposure, by delivering appropriate amounts of BPA through the oral route to achieve burdens of free BPA in blood and tissues of genetically susceptible mice, it is also important to consider the appropriate time for testing for the asthma phenotype. Further, the choice of the strain of mice to be used in these studies should match the genetic susceptibility to allergic disease of humans at the same stage of development. Thus, it is not surprising that results from the more sensitive strain of mice might be more likely to recapitulate findings in human infants that are known to be susceptible to allergic sensitization.

Thus, one of the reasons for reviewing mouse experiments and comparing their findings with human epidemiological studies was to begin to confirm the relevance of the human studies well enough to consider hypothetical mechanisms for these common disease features and plan experiment to test these. For instance, this may be the case when we compare the results of our and Nygaard’s mouse studies with those of the human studies of Spanier et al. [21]. It may also be useful to look at the effect of postnatal BPA exposure of humans (e.g. Vaidya) in the context of current mouse studies that assessed the effect of BPA on asthma outcomes in childhood, adolescences and adults life. Clearly more thought and the development of new study designs may improve our understanding of this important process.

Yet another approach that we and others are embarking on is to define the mechanistic steps between pre and postnatal BPA exposures and the development of asthma. We anticipate that this approach may also define biomarkers of BPA’s effects, which will be consistent between humans and mice. Preliminary results from these approaches suggest that exposure to BPA, especially during the prenatal period, may cause epigenetic alterations that could last throughout the lifetime of the mice and perhaps humans and even be passed to subsequent generations. Such studies may also help to explain some to the age and gender difference that are so prominent in human asthma, which starts as a male dominant disease in childhood, but are overtaken by women around the time of their menarche. This pattern may explain some of the gender effects in several of the human studies of pre and postnatal BPA exposures [19,23].

CONCLUSION

We have reviewed here the effects of early BPA exposure on allergic asthma development in mouse models and human epidemiological studies. The effects of early BPA exposure were observed as an enhanced development of asthma before adolescent in the animal model. All of the human studies suggest that BPA exposure in early life enhances the likelihood of developing asthma on at least one of the study groups. In contrast, maternally derived BPA exposures in the various mouse systems seem to manifest themselves only during infancy. Comparing the age of wheezing illness in humans, suggest that BPA exposure might be an important component in bronchiolitis, a wheezing illness associated with concurrent viral infections, as well a risk factor the later development of asthma. Further studies on the timing of the onset of asthma as well as the molecular mechanisms of BPA’s effect may help in planning approaches for preventing these very common human diseases.

FUNDING

This work was supported by grants R21ES02540601 from National Institute of Environmental Health Science and Allergic Respiratory Disease Award from American Lung Association/American Academy of Allergy, Asthma and Immunol to T.M.H.

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