Prenatal exposure to tobacco smoke is a significant risk-factor for airway disease development. Furthermore, the high prevalence of pregnant smoking women requires the establishment of strategies for offspring lung protection. Therefore, we here aimed to understand the molecular mechanism of how prenatal smoke exposure affects fetal lung development. We used a mouse model recapitulating clinical findings of prenatally exposed children, where pregnant mice were exposed to smoke until c-section or spontaneous delivery, and offspring weight development and lung function was monitored. Additionally, we investigated pulmonary transcriptome changes in fetal lungs (GD18.5) by mRNA/miRNA arrays, network analyses and qPCR. The results demonstrated that prenatally exposed mice showed intrauterine and postnatal growth retardation, and impaired lung function. 1340 genes and 133 miRNAs were found to be significantly dysregulated by in utero smoke exposure, and we identified Insulin-like growth factor 1 (Igf1) as a top hierarchical node in a network analysis. Moreover, Igf1 mRNA was increased in female murine offspring and in prenatally exposed children. These findings suggest that prenatal smoking is associated with a dysregulation of several genes, including Igf1 in a sex-specific manner. Thus, our results could represent a novel link between smoke exposure, abberant lung development and impaired lung function.
Smoking during pregnancy is a recognized risk factor for low birth weight1,2 and impaired lung function in offspring3,4,5. In addition, even a sole exposure to maternal nicotine, a component of tobacco smoke, affects the metabolism and the structuaral development of the offspring lung6. Furthermore, there is evidence for increased risk of preschool wheeze7,8,9, asthma8,9 and COPD10,11,12 in the offspring. Despite this knowledge and intensive anti-tobacco campaigns in several countries, the number of women smoking during pregnancy remains high worldwide. These facts prompted demands for research on consequences of prenatal smoke exposure including downstream biological effects13.
Besides adverse health consequences of maternal smoking, it has been proposed that grandmaternal as well as grandpaternal smoking during pregnancy is sufficient to affect weight gain of the grandchildren, even if their mother was not smoking during her pregnancy14,15. Moreover, it was shown that grandmaternal smoking affects asthma susceptibility16,17,18 in grandchildren. These observations were supported by studies in rats where maternal perinatal s.c. nicotine induced airway hyperreactivity until the 3rd generation19. If these transgenerational effects hold true, even highly successful smoking cessation programs would take decades to become fully effective.
Various growth factors play a role during the process of fetal lung development20,21,22,23,24,25,26. As previous studies revealed, one of these factors is insulin-like growth factor (IGF), while it was shown that mice depleted from either Igf1 or its receptor Igf1r demonstrated a failure in lung development27,28. In addition to this, few studies showed sex-specific differences in the IGF-system of the offspring following maternal smoking29,30. Therefore, it is important to develop means to protect the developing fetal lung as well as to understand the mechanisms of how cigarette smoke affects fetal and early postnatal lung development.
Thus, in this study we aimed to investigate the underlying molecular mechanisms of in utero smoke exposure and the resulting predisposition for chronic lung diseases. Along this line, we identified dysregulations of 1340 genes and 133 microRNAs in the fetal lung, while one central hierarchical node was Igf1. In addition, an increase of IGF1 was also observed in school children with prenatal and early-life cigarette smoke-exposure history.
Materials and Methods
For a detailed description of RNA isolation and qPCR please refer to the Supplementary Information.
The study was conducted according to the guidelines for the use and care of laboratory animals according to the Federal Act on the Protection of Animals (Germany). The study was approved by the Government of the District of Upper Bavaria (GZ. 55.2-1-54-2532-91-11). Balb/c mice, obtained from Charles River (Sulzfeld, Germany), were housed in a specific pathogen-free facility with a 12 h day-night cycle at a constant temperature and humidity. The mice were provided with standard rodent chow and water ad libitum. Eight-week old virgin females were mated 1:1 with proven male breeder for 24 h (defined as embryonic day (ED) 0.5). To allow proper implantation of the fertilized oocyte, mice were exposed to smoke or filtered air (see below) only from gestational day (GD) 2.5 until spontaneous delivery or until GD 17.5 followed by caesarean section at GD 18.5. Since the successful fertilization wasn’t possible at the start of exposure, non-pregnant mice were equally exposed to cigarette smoke (CS) until pregnancy could be excluded through maternal weight control. For caesarean section (c-section), pregnant mice were anaesthetized with Ketamine/Xylazine on GD 18.5. Uteri were visually inspected for resorbed fetuses and the uterine position of each fetus was recorded. Fetuses were weighed and sacrificed by i.p. injection of pentobarbital for organ removal. Fetal lungs were carefully removed, weighed (Mettler Toledo, Greifensee, Switzerland), and stored in RNAlater (Ambion, Austin, USA) at 4 °C overnight and then at −80 °C until RNA isolation.
Cigarette smoke exposure protocol
Mainstream CS served as a surrogate for active smoking and was generated as previously described31. Briefly, smoke was generated from 3R4F Research Cigarettes (Tobacco Research Institute, University of Kentucky, Lexington, KY) and drawn into the exposure chamber with a membrane pump. Mice were exposed to 10 cigarettes for 50 min every morning until c-section or spontaneous delivery. Total particulate matter (TPM) concentrations were monitored by drawing an air sample from the exposure chamber through a quartz fiber filter (at 3rd, 6th, and 9th cigarette, each day during the exposure). The TPM mass concentration was obtained by gravimetric analysis of the filters before and after exposure and was then related to the chamber volume.
Characterization of pregnant mice
After mating, maternal weight was monitored daily until delivery. Urine was collected four hours after the last smoke exposure and cotinine was quantified by ELISA (Calbiotech, Spring Valley, US). For an independent confirmation of smoke exposure, carbon monoxide hemoglobin (CO-Hb) was determined in venous blood obtained from the retrobulbar venous plexus in anesthetized animals 30 min after the last cigarette (Hemoxymeter (OSM3, Radiometer, Copenhagen).
Characterization of murine offspring
Body weight was recorded daily in spontaneously delivered offspring until postnatal day (PND) 56. Lung function was performed at PND21. A total of 303 offspring were analyzed (Supplementary Table S1). Since body weight was confounded by litter size, only pups from litters above the median (>6) were included in the final molecular analyses. To further avoid ill-defined seasonal effects, animals obtained from different experimental batches at different seasons were included in the molecular analyses.
Lung function analyses
Following intraperitoneal anesthesia (ketamine 140 mg/kg; xylazine 7 mg/kg), mice were tracheostomized, intubated (19 G tube) and placed on a warming plate. Pancuronium (1 mg/kg, i.p.) was added to avoid spontaneous breathing during examination. For baseline lung function measurements, mice were ventilated with a tidal volume of 11 ml/kg at a frequency of 150 breaths/minute with a positive end-expiratory pressure of 2 cm H2O on a computer controlled ventilator (FlexiVent®, SCIREQ©, Montreal, QC, Canada). The following perturbations were performed: Maximal Vital Capacity (MVC) maneuver, single compartment (snapshot), constant phase model (Primewave-8), and pressure-volume loops with constantly increasing pressure (PVr-P). All perturbations were performed one-by-one until three acceptable measurements (coefficient of determination > 0.95) were recorded in each individual subject, of which an average was calculated. Due to a body weight difference in male and female mice, the inspiratory capacity was calculated in relation to the body weight. After lung function testing at baseline level, mice were transferred to a Buxco R/C system (Troy, NY) to assess airway reactivity. Metacholine (MCh) was applied to the intubated mice via an in-line nebulizer and administered at increasing concentrations (0, 12.5, 25, 37.5 mg/ml) for 20 sec. Resistance (R) and Compliance (C) were measured continuously for 3 min. The average was calculated and plotted against the MCh concentration.
Peripheral blood mononuclear cells (PBMCs) were isolated from a subsample of 23 healthy children (age 4–15 years) with a history of early-life smoke exposure and compared to age-matched controls participating in the Munich Clinical Asthma Research Association (CLARA) study32. Early-life smoke exposure was defined as smoking of the mother during pregnancy and smoking of one or two parents at home at the time of inclusion into the study. ‘Non-smoking’ was defined as no smoking of either parent as well as no smoking at home throughout the pregnancy. According to this definition, six children were exposed (during pregnancy and currently at home), and 17 children had non-smoking parents. PBMC, isolated within 24 hours after blood withdrawal, were cultured (X-Vivo (Lonza, Basel, Switzerland) with plate-bound anti-CD3 (3 mg/mL) and soluble anti-CD28 (1 mg/mL) at 37 °C for 48 h. RNA was isolated with the RNeasy Mini-Kit and processed (1 mg) with reverse transcriptase (Qiagen, Hilden, Germany). Gene-specific PCR products of IGF1 and IGFBP3 were amplified with the CFX96 Touch Real-time-PCR Detection System (Bio-Rad, Munich, Germany) for 40 cycles.
The study has been approved by the local ethics committee of LMU Munich (project nr 379-08). All methods were carried out in accordance with relevant guidelines and regulations. Parents have agreed to participation in the study, and informed consent was obtained from all families.
Gene expression analysis in murine lungs at embryonic day 18.5
Selection criteria of samples for RNA profiling
Both androgens and estrogens can influence lung development and physiology in prenatal life33. To limit undefined effects from interactions between neighboring siblings of different sexes, we selected fetuses which had two neighbors of identical sex or were positioned at the end of the uterus having a neighbor of the same sex (Supplementary Fig. S1). We further took one male and one female offspring per litter. In order to avoid detecting acute but transient effects, the mRNA and miRNA profiling were performed 24 h after the last cigarette smoke exposure (ED 18.5).
Total RNA (n = 12/group; each six males and females) was isolated using the miRNeasy Mini (QIAGEN) kit. The Agilent 2100 Bioanalyzer was used to assess RNA quality where only high quality RNA, (RIN ≥ 8.7, 260/280 ratio > 1.8, no degradation as detected by RNA agarose gel), was used for microarray analysis. For mRNA profiling, 30 ng of total RNA was amplified using the Ovation PicoSL WTA System V2 in combination with the Encore Biotin Module (Nugen). Amplified cDNA was hybridized on an Affymetrix Mouse Gene ST 2.1 array plate. Staining and scanning were done according to the Affymetrix expression protocol including minor modifications as suggested in the Encore Biotin protocol. For microRNA profiling, 800 ng of total RNA was labeled with the FlashTag Biotin HSR kit (Genisphere) and hybridized on Affymetrix miRNA 3.0 arrays. Staining and scanning were done according to the Affymetrix expression protocol (Fluidics FS450_0002). Array data has been submitted to the GEO database at NCBI (GSE67888).
Statistical transcriptome analysis for mRNA and microRNA profiling from mice
The expression console (v.126.96.36.199, Affymetrix) was used for quality control and to obtain annotated normalized RMA gene-level data and DABG (standard settings including median polish and sketch-quantile normalization). Three samples from the filtered-air group (one male, two females) haven’t fulfilled the quality criteria and were therefore excluded from further analysis. Redundant probe sets with identical expression values in all samples were removed from the dataset. Statistical analyses were performed using the statistical programming environment34 implemented in CARMAweb35. Gene wise testing for differential expression was done employing the (limma) t-test and Benjamini-Hochberg multiple testing correction (FDR < 10%). Sets of significantly regulated miRNAs were filtered for present calls in at least 60% of the samples in at least one group.
Upstream regulator and functional network analysis
The upstream regulator, network and functional analyses were generated through the use of IPA® (Ingenuity Pathway Analysis (QIAGEN)). First, the core analysis module of IPA® was applied to a set of 1340 CS-regulated (|FC| > 1.2, unadj. p < 0.05) mRNAs using default settings including direct and indirect relationships as well as endogenous metabolites. The Mouse Gene 2.1 ST Array was chosen as reference set. Molecules identified as upstream regulators of the dataset were filtered to those transcription regulators, which were regulated in the initial dataset. These molecules were displayed as a network together with their downstream targets. The “grow” function of IPA® was applied to the transcription regulators to identify CS-regulated microRNAs targeting these transcription regulators. Targeting microRNAs with non-inverse regulation were filtered out. An additional core analysis of the molecules in the upstream regulator network was used to identify the functional role of the top networks of these molecules.
The weight gain of mothers and offspring was analyzed using SAS PROCs GLM and MIXED for repeated measure analyses (SAS Institute Inc. 2011. SAS® 9.3 System Options: Reference, Second Edition. Cary, NC: SAS Institute Inc.). Analyzing the weight gain of animals over time requires consideration in between-group effects as well as within subject effects. Typically, control and exposed groups started off with approximately equal weights but ended up being different in their average weight by the end of the study period. In general, the trend parameters, i.e. the shapes of the weight gain curves, differ between groups. This is accounted for by appropriately tested and chosen study group specific trend parameter interactions with time, e.g. by forward or backward selection. Weight gain and group* time interaction parameters were quantified by the natural measure milligram per day (mg/d) with 95%-confidence intervals (CI) and p-values. The corresponding synoptic graphical display of growth curves for control and exposure groups was obtained employing SAS PROC GPLOT. The remaining molecular data obtained in mice were tested for normal distribution using D’Agostino and Pearson omnibus normality test (GraphPAD Prism, GraphPad Software Inc. 2007). Mann-Whitney U test or t-test was applied where appropriate. Differences in mRNA expression levels of children with smoking and non-smoking parents were tested on log ∆CT scale using tobit regression analysis36.
Data availability statement
The microarray data has been submitted to the GEO database at NCBI (GSE67888) and will be available for all readers upon publication.
Effects of CS exposure on maternal characteristics of successful pregnancy
Exposure to CS was monitored by assessing levels of urinary cotinine and peripheral blood CO-Hb, which were both significantly increased in CS-exposed female mice (Table 1). The average TPM exposure was 321 + 89 mg/m³. Eight-week old animals, as used in this study, still gain weight with the age. Age-related weight gain was clearly compromised in CS-exposed non-pregnant mice (mean −80 mg/d; CI 75–84 mg/d; p < 0.0001 Supplementary Fig. S2). This was also true for pregnant mice: CS-exposed dams lagged behind in weight gain by −157 mg/d (95%-CI: 145–168), p < 0.0001 (Fig. 1). This difference remained significant even after the maternal weight was corrected for the size of the litter. Despite the effect of CS on maternal weight gain, the pregnancy rate, duration and number of viable pups or visibly resorbed fetuses did not differ significantly between the groups. Similarly, the number of female and male offspring were equal in both groups indicating that the parameters of successful pregnancy per se were not affected by the CS protocol applied (Table 1).
Reduced intrauterine and postnatal growth of exposed offspring
Smoke-exposed fetuses (ED18.5) had significantly lower body and lung weights as compared to the air-exposed animals. Pulmonary hypotrophy, as indicated by lower lung/body weight ratio, was more pronounced in female offspring resulting in lower lung/body weight ratios in females but not in males (Fig. 2A–C). As expected, postnatal weight gain was lower in females independent of prenatal CS-exposure. Furthermore, the offspring from litters with less than six animals had a stronger weight gain as compared to animals from larger litters (>6) possibly due to the different breast milk availability per animal. Prenatal CS-exposure retarded weight gain in offspring as investigated until PND 56 (Fig. 3A,B). When we corrected our analyses for sex and litter size, the reduced postnatal weight gain of prenatally CS-exposed animals remained highly significant (mean −6.7 mg/d, 95%-CI [4.0, 9.4]).
Reduced lung function in offspring
Next, we investigated whether smoke-induced intrauterine and postnatal growth retardation was associated with lung function deficits. We found that the inspiratory capacity was significantly reduced in three-week old animals after intrauterine CS-exposure. When we stratified for sex, this decrease was present in both males and females (Fig. 4A). In contrast, airway hyperreactivity was only seen in female offspring, even in the absence of any experimental allergen challenge (Fig. 4B,C).
Gene expression networks in fetal lungs
With the establishment of our model that mimics findings of prenatally smoke exposed children, we next aimed to shed more light on the molecular mechanisms preceding impaired lung function of CS-exposed offspring. Therefore, we performed mRNA and microRNA arrays in fetal lungs, which revealed 1340 differentially regulated mRNAs (|FC| > 1.2, unadj. p-value < 0.05) and 133 microRNAs (unadj. p-value < 0.05) (Supplementary Fig. S3). The array data is also available at the GEO database at NCBI (GSE67888).
To identify top biological functions associated with changes in global mRNA expression patterns, the core analysis module of the Ingenuity® software was used. Besides other functions (Supplementary Table S2), those associated with embryonic and organismal development were strongly affected by in utero smoking (Supplementary Table S3). To investigate which key developmental molecules could be responsible for these changes, we identified upstream regulators within the dataset and filtered those to transcription regulators which showed mRNA dysregulation. These molecules were displayed as a network together with their downstream targets (Fig. 5). Three transcription factors involved in transcriptional repression such as E2F transcription factors 7 and 8 (E2f7, E2f837), Myb-related protein B (Mybl2)38 responsible for control of cellular proliferation and senescence and histone-lysine N-methyltransferase (Suv39h2) which is highly specific for H3K9 trimethylation39, were up-regulated. In contrast, two transcription factors related to lipid metabolism (CCAAT/enhancer binding protein (C/EBP) alpha (Cebpa) and Sterol regulatory element binding transcription factor 1 (Srebf1)) were down-regulated. In a next step, we included counter-regulated miRNAs targeting the transcription factors to the network, as miRNAs are an additional important level of regulation. Most down-regulated functions involved lipid metabolism and survival, whereas the top up-regulated functions were related to inflammatory and respiratory diseases (Supplementary Table S4). To gain insight into the interactions of these molecules, we performed a network analysis and found Insulin-like growth factor 1 (Igf1) as top hierarchical node in the subnetwork associated with embryonic and organ development (Fig. 6). The in silico analysis of this Igf1-driven subnetwork revealed organismal survival, organismal injury and abnormalities and, most importantly, respiratory disease as its major function (Table 2).
Pulmonary Igf1 and Igf-binding protein (Igfbp3) expressions in mice and exposed children
Since the in silico analyses suggested Igf1 as a main driver of reduced lung weight and function, we further focused on this growth hormone. Igf1 is almost completely bound to one of the six binding proteins (Igfbp). Igfbp3 is the most abundant protein that accounts for the majority of all IGF binding. As it is also downregulated in our array (Fig. 5) we additionally included this hormone in the analysis. Igf1 mRNA expression was significantly increased in female prenatally smoke-exposed lungs at day E18.5, whereas Igfbp3 expression was decreased. This effect was no longer found in offspring of three weeks of age (Fig. 7). To determine whether our model more or less reflects the human situation, we investigated anti-CD3/CD28-stimulated PBMCs of healthy school-aged children with early-life smoke exposure. Interestingly, mRNA expression of IGF1 was significantly higher in PBMCs from children with smoking parents as compared to children from non-smoking parents, whereas mRNA expression of IGFBP3 was not affected (Fig. 8, p = 0.008; p = 0.16).
In this study, we aimed to investigate underlying molecular mechanisms for lung development deficits due to in utero cigarette smoke exposure by using an animal model of maternal smoking during pregnancy. Prenatally exposed mice showed intrauterine and postnatal growth retardation and several alterations on the pulmonary transcriptomic and miRNA levels at E18.5. In addition to this, a reduction of lung function in adolescence was detected, which is of interest as it is a recognized smoking-induced pathology in children3,4,40,41,42,43. Extensive mRNA/miRNA profiling of fetal lungs revealed a dysregulation of 1340 mRNAs and 133 miRNAs of CS-exposed offspring compared to controls. A subsequent in silico construction of networks of transcriptional regulators, revealed, beyond others, Igf1 as major hub in fetal smoke exposed lungs. Deregulation of pulmonary Igf1 together with its main binding partner Igfbp3 was also confirmed by qRT-PCR in murine offspring and further corroborated in school-aged children by showing reduced IGF1 expression in PBMC after prenatal and early-life smoke exposure.
As our goal was to investigate the consequences that are purely related to prenatal smoke-exposure and not to a compromised pregnancy by maternal stress, we designed the exposure in a way that the basic parameters of successful pregnancy remained unaltered. As smoking is linked to reduced fertility and increased rates of abortion44, mice were subjected to smoke after fertilization but prior to the formation of the lung bud. In order to compare the severity of our smoke exposure to other studies and human data, we assessed cotinine, a nicotine metabolite in urine, and carboxyhemoglobin (Co-Hb) levels in the blood.
We observed an 5.12-fold increase of urine cotinine levels, and a 4.84-fold increase in Co-Hb in our model in smoke exposed mothers compared to air controls. However, it has to be noted that in this study samples were drawn 4 h after the last smoke exposure, and the half-time of cotinine in C57BL/6 mice is only 38 min45. Thus, we assume the fold-increase in urine cotinine levels are reflecting light smoking when compared to data from a large cohort of pregnant women46. Nonetheless, intrauterine growth retardation was pronounced and – more importantly - sustained into adulthood, while smoking was stopped at birth. Surprisingly, the offspring did not show catch-up weight gain after weaning, even after the adjustment for sex, litter size and consideration of seasonal effect; thus it is intriguing to speculate that intrauterine smoke-exposure causes a persistent developmental disadvantage.
We observed lung function deficits in CS-exposed offspring at the age of three weeks. Of note, female offspring exhibited spontaneous airway hyperreactivity (AHR), even in the absence of allergen challenge, and showed a significant higher expression of Igf1 at E18.5, thus indicating a possible link between Igf1 and lung function. It is intriguing to speculate that the observed lung function differences are due to increased airway remodeling, which has been previously reported in similar models of prenatal smoke exposure47, which we however could not investigate in this study.
Sexual dimorphism is well known in physiological and non-physiological lung responses48 including developmental, hormonal, airway structural and functional differences. For example, female fetuses start mouth movements49, surfactant synthesis and maturation earlier than male fetuses50. In early childhood, girls have larger airways in relation to lung size, and lower specific airway resistance than boys (reviewed in51). Thus, it is conceivable that environmental insults act differently on females and males during development. Nonetheless, the assessment of sex differences has so far been neglected in most inter- or trans- generational animal models.
Fetal smoke-exposed lungs showed regulation of signaling molecules at multiple levels from transcription regulators to their down-stream targets. To avoid seeing acute and transient effects, arrays were performed one day after the last smoke exposure on pups delivered by c-section (E18.5). Thus, even though the fold–changes of gene expression were low, they might indicate the onset of pathology and hence be more relevant than stronger events occurring at the end of molecular cascades.
Lung development is a precisely controlled process of parallel proliferation, differentiation and apoptosis. Transcriptional regulator network showed dysregulation of the genes that are relevant for development and the onset of respiratory diseases. The transcription factors E2f7 and E2f8 protect cooperatively against excessive apoptosis via repression of E2f1 and are strictly required for embryonic development37,52. Mybl2, which controls cell cycle progression and cell fate in embryonic stem cells2, was equally upregulated implying disturbed early developmental processes. On the other hand, Cebpa and Srbf1 which are considered to be critical for lung maturation and respiratory epithelial differentiation (Cebpa), were decreased53,54,55.
IGF1 is an important regulator of somatic growth and cell differentiation56 where the absence of its signaling results in severe growth failure57,58. A specific role of IGF1 for lung development is indicated by strong IGF1 upregulation in lung structural cells in bronchopulmonary dysplasia59 or severe pulmonary hypoplasia resulting from diaphragmatic hernia60. Igf1 deficient mice were shown to exhibit growth failure which was more pronounced in lungs as compared to body weight61,62.
So far, data relating prenatal smoke exposure to changes of pulmonary IGF-1 are limited. One study in adult male smokers reported reduced serum IGF-1 and IGFBP-3 levels that returned to normal levels after smoking cessation63. Two mouse studies have previously implicated the Igf1 axis with prenatal smoke exposure, and of note both found sex-specific effects as we did in this study. The first one used Balb/c mice that were nose-only exposed during the entire pregnancy, and was in contrast to our findings showing lower Igf1 mRNA expression in 30-day old female offspring in comparison to control29. This was related to sex-dependent differences in promoter methylation of Igf1r. This was recently confirmed in a second study using a prenatal smoke model in C57Bl/6 mice, which also showed that Igfr1 CpG methylation was organ- and sex-specific64. The difference to our study could be due to the different time point of analysis as the observed increase in Igf1 levels in our study was only found at E18.5, but not at PND 21 and we did not investigate d30. Along this line, it has been found that Igf1 levels decrease postnatally65. Concerning the Igf1 levels in male offspring, our results were in accordance to the abovementioned study by Meyer et al. showing no significant change in Igf1 expression. However, other investigators did not reveal such a relationship66.
In humans, maternal smoking in pregnancy has been associated with lower placental GH and human cord blood IGF-1 protein concentrations67. Another study, as well, showed a lower cord blood IGF-1 in infants from mothers who smoked during early pregnancy, with the strongest decline in girls as compared to boys68. Similar to our findings in mice, the growth hormone deregulation was more pronounced in females. In this study, we partly validated our findings from the mouse model by the observation that IGF-1 levels are increased in PBMCs from in utero CS-exposed, healthy children at school age. However, the number of human samples used in the present study did not allow stratifying for sex. Further, these children were healthy; thus we do not have any further information on whether they had subtle deficits in lung function and as lung development is vastly different between mice and humans69 they do not reflect the same developmental stages as in our murine model. Nonetheless, this is a first hint that IGF-1 dysregulation might be an important effector of in utero CS-exposure and might indicate a certain ‘molecular defect’ in smoke-exposed children, which could for example result in a changed susceptibility to develop chronic lung diseases such as asthma in later life. Thus, this needs to be further investigated in future studies.
We acknowledge several potential limitations of our study. First, similar to human studies2, murine models do not allow to clearly separate the effects of intrauterine growth retardation from smoke exposure on the developing lung. Second, despite the apparently normal course of pregnancy, placental functions could be affected. Prenatal smoking, albeit at higher doses, has been shown to influence decidua immune responses in mice and humans70. Nicotine exposure has further been linked to altered placental development and function in rats71. In humans, maternal smoking has been related to global72 and gene-specific73 placental DNA-methylation thus indicating an abnormal placental function. Third, although air and smoke test animals were handled in the same way, smoking, is an additional – although unavoidable -, stress factor itself. Moreover, maternal stress during pregnancy can induce low-level maternal corticosterone74 and increase responsiveness to allergen challenge in offspring74,75. Thus, it is possible that besides smoking, elevated maternal stress hormones might have contributed to our findings.
In summary, we here show that prenatal smoke exposure is associated with deregulated pulmonary transcriptomes, miRNA levels and Igf1 in a sex-specific manner. To our knowledge we are the first to report a change in pulmonary transcriptomes and miRNA levels at day E18.5, which Ingenuity Pathway Analysis (IPA) predicted to be involved in respiratory disease as one of the top hits. These findings, taken together with the previously reported Igf1 dysregulation might not only indicate an aberrant lung development, but might also alter the offsprings’ response to environmental insults, such as allergens or cigarette smoke and therewith predispose for the development of chronic lung diseases.
Benjamin-Garner, R. & Stotts, A. Impact of smoking exposure change on infant birth weight among a cohort of women in a prenatal smoking cessation study. Nicotine Tob Res 15, 685–692 (2013).
Bjerg, A., Hedman, L., Perzanowski, M., Lundback, B. & Ronmark, E. A strong synergism of low birth weight and prenatal smoking on asthma in schoolchildren. Pediatrics 127, e905–912 (2011).
Moshammer, H. et al. Parental smoking and lung function in children: an international study. Am J Respir Crit Care Med 173, 1255–1263 (2006).
Hollams, E. M., de Klerk, N. H., Holt, P. G. & Sly, P. D. Persistent effects of maternal smoking during pregnancy on lung function and asthma in adolescents. Am J Respir Crit Care Med 189, 401–407 (2014).
Gilliland, F. D., Berhane, K., Li, Y. F., Rappaport, E. B. & Peters, J. M. Effects of early onset asthma and in utero exposure to maternal smoking on childhood lung function. Am J Respir Crit Care Med 167, 917–924 (2003).
Maritz, G. S. & Harding, R. Life-long programming implications of exposure to tobacco smoking and nicotine before and soon after birth: evidence for altered lung development. Int J Environ Res Public Health 8, 875–898 (2011).
Duijts, L. et al. Fetal exposure to maternal and paternal smoking and the risks of wheezing in preschool children: the Generation R Study. Chest 141, 876–885 (2012).
Burke, H. et al. Prenatal and passive smoke exposure and incidence of asthma and wheeze: systematic review and meta-analysis. Pediatrics 129, 735–744 (2012).
den Dekker, H. T. et al. Tobacco Smoke Exposure, Airway Resistance, and Asthma in School-age Children: The Generation R Study. Chest 148, 607–617 (2015).
Beyer, D., Mitfessel, H. & Gillissen, A. Maternal smoking promotes chronic obstructive lung disease in the offspring as adults. Eur J Med Res 14(Suppl 4), 27–31 (2009).
Svanes, C. et al. Early life origins of chronic obstructive pulmonary disease. Thorax 65, 14–20 (2010).
Duijts, L., Reiss, I. K., Brusselle, G. & de Jongste, J. C. Early origins of chronic obstructive lung diseases across the life course. Eur J Epidemiol 29, 871–885 (2014).
Leone, F. T. et al. An Official American Thoracic Society Research Statement: Current Understanding and Future Research Needs in Tobacco Control and Treatment. Am J Respir Crit Care Med 192, e22–41 (2015).
Golding, J., Northstone, K., Gregory, S., Miller, L. L. & Pembrey, M. The anthropometry of children and adolescents may be influenced by the prenatal smoking habits of their grandmothers: a longitudinal cohort study. Am J Hum Biol 26, 731–739 (2014).
Miller, L. L., Pembrey, M., Davey Smith, G., Northstone, K. & Golding, J. Is the growth of the fetus of a non-smoking mother influenced by the smoking of either grandmother while pregnant? PLoS One 9, e86781 (2014).
Li, Y. F., Langholz, B., Salam, M. T. & Gilliland, F. D. Maternal and grandmaternal smoking patterns are associated with early childhood asthma. Chest 127, 1232–1241 (2005).
Magnus, M. C. et al. Grandmother’s smoking when pregnant with the mother and asthma in the grandchild: the Norwegian Mother and Child Cohort Study. Thorax 70, 237–243 (2015).
Miller, L. L., Henderson, J., Northstone, K., Pembrey, M. & Golding, J. Do grandmaternal smoking patterns influence the etiology of childhood asthma? Chest 145, 1213–1218 (2014).
Rehan, V. K., Liu, J., Sakurai, R. & Torday, J. S. Perinatal nicotine-induced transgenerational asthma. Am J Physiol Lung Cell Mol Physiol 305, L501–507 (2013).
Raaberg, L. et al. Epidermal growth factor transcription, translation, and signal transduction by rat type II pneumocytes in culture. Am J Respir Cell Mol Biol 6, 44–49 (1992).
Raaberg, L., Nexo, E., Poulsen, S. S. & Jorgensen, P. E. An immunologic approach to induction of epidermal growth factor deficiency: induction and characterization of autoantibodies to epidermal growth factor in rats. Pediatr Res 37, 169–174 (1995).
Raaberg, L., Nexo, E., Jorgensen, P. E., Poulsen, S. S. & Jakab, M. Fetal effects of epidermal growth factor deficiency induced in rats by autoantibodies against epidermal growth factor. Pediatr Res 37, 175–181 (1995).
Warburton, D. et al. Epigenetic role of epidermal growth factor expression and signalling in embryonic mouse lung morphogenesis. Dev Biol 149, 123–133 (1992).
Minoo, P. & King, R. J. Epithelial-mesenchymal interactions in lung development. Annu Rev Physiol 56, 13–45 (1994).
Peters, K. et al. Targeted expression of a dominant negative FGF receptor blocks branching morphogenesis and epithelial differentiation of the mouse lung. EMBO J 13, 3296–3301 (1994).
Kaartinen, V. et al. Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction. Nat Genet 11, 415–421 (1995).
Epaud, R. et al. Knockout of insulin-like growth factor-1 receptor impairs distal lung morphogenesis. PLoS One 7, e48071 (2012).
Liu, J. P., Baker, J., Perkins, A. S., Robertson, E. J. & Efstratiadis, A. Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGFreceptor (Igf1r). Cell 75, 59–72 (1993).
Meyer, K. F. et al. Prenatal exposure to tobacco smoke sex dependently influences methylation and mRNA levels of the Igf axis in lungs of mouse offspring. Am J Physiol Lung Cell Mol Physiol 312, L542–L555 (2017).
Clifton, V. L. et al. Effect of maternal asthma, inhaled glucocorticoids and cigarette use during pregnancy on the newborn insulin-like growth factor axis. Growth Horm IGF Res 20, 39–48 (2010).
John, G. et al. The composition of cigarette smoke determines inflammatory cell recruitment to the lung in COPD mouse models. Clin Sci (Lond) 126, 207–221 (2014).
Raedler, D. et al. Identification of novel immune phenotypes for allergic and nonallergic childhood asthma. J Allergy Clin Immunol 135, 81–91 (2015).
Melgert, B. N., Ray, A., Hylkema, M. N., Timens, W. & Postma, D. S. Are there reasons why adult asthma is more common in females? Curr Allergy Asthma Rep 7, 143–150 (2007).
R Development Core Team. R: A language and environment for statistical computing. (R Foundation for Statistical Computing Vienna, Austria. http://www.R-project.org/), 2011.
Rainer, J., Sanchez-Cabo, F., Stocker, G., Sturn, A. & Trajanoski, Z. CARMAweb: comprehensive R- and bioconductor-based web service for microarray data analysis. Nucleic Acids Res 34, W498–503 (2006).
Ballenberger, N., Lluis, A., von Mutius, E., Illi, S. & Schaub, B. Novel statistical approaches for non-normal censored immunological data: analysis of cytokine and gene expression data. PLoS One 7, e46423 (2012).
Li, J. et al. Synergistic function of E2F7 and E2F8 is essential for cell survival and embryonic development. Dev Cell 14, 62–75 (2008).
Mowla, S. N., Lam, E. W. & Jat, P. S. Cellular senescence and aging: the role of B-MYB. Aging Cell 13, 773–779 (2014).
Schuhmacher, M. K., Kudithipudi, S., Kusevic, D., Weirich, S. & Jeltsch, A. Activity and specificity of the human SUV39H2 protein lysine methyltransferase. Biochim Biophys Acta 1849, 55–63 (2015).
Martinez-Mesa, J. et al. Life course association of maternal smoking during pregnancy and offspring’s height: data from the 1993 Pelotas (Brazil) birth cohort. J Adolesc Health 51, S53–57 (2012).
Iniguez, C. et al. Maternal smoking during pregnancy and fetal biometry: the INMA Mother and Child Cohort Study. Am J Epidemiol 178, 1067–1075 (2013).
Delpisheh, A., Brabin, L., Drummond, S. & Brabin, B. J. Prenatal smoking exposure and asymmetric fetal growth restriction. Ann Hum Biol 35, 573–583 (2008).
Horta, B. L., Victora, C. G., Menezes, A. M., Halpern, R. & Barros, F. C. Low birthweight, preterm births and intrauterine growth retardation in relation to maternal smoking. Paediatr Perinat Epidemiol 11, 140–151 (1997).
Castles, A., Adams, E. K., Melvin, C. L., Kelsch, C. & Boulton, M. L. Effects of smoking during pregnancy. Five meta-analyses. Am J Prev Med 16, 208–215 (1999).
Siu, E. C. & Tyndale, R. F. Characterization and comparison of nicotine and cotinine metabolism in vitro and in vivo in DBA/2 and C57BL/6 mice. Mol Pharmacol 71, 826–834 (2007).
Pickett, K. E., Rathouz, P. J., Kasza, K., Wakschlag, L. S. & Wright, R. Self-reported smoking, cotinine levels, and patterns of smoking in pregnancy. Paediatr Perinat Epidemiol 19, 368–376 (2005).
Blacquiere, M. J. et al. Maternal smoking during pregnancy induces airway remodelling in mice offspring. Eur Respir J 33, 1133–1140 (2009).
Bjerg, A. et al. Higher risk of wheeze in female than male smokers. Results from the Swedish GA 2 LEN study. PLoS One 8, e54137 (2013).
Hepper, P. G., Shannon, E. A. & Dornan, J. C. Sex differences in fetal mouth movements. Lancet 350, 1820 (1997).
Torday, J. S. & Nielsen, H. C. The sex difference in fetal lung surfactant production. Exp Lung Res 12, 1–19 (1987).
Becklake, M. R. & Kauffmann, F. Gender differences in airway behaviour over the human life span. Thorax 54, 1119–1138 (1999).
Ouseph, M. M. et al. Atypical E2F repressors and activators coordinate placental development. Dev Cell 22, 849–862 (2013).
Xu, Y., Ikegami, M., Wang, Y., Matsuzaki, Y. & Whitsett, J. A. Gene expression and biological processes influenced by deletion of Stat3 in pulmonary type II epithelial cells. BMC Genomics 8, 455 (2007).
Sato, A., Xu, Y., Whitsett, J. A. & Ikegami, M. CCAAT/enhancer binding protein-alpha regulates the protease/antiprotease balance required for bronchiolar epithelium regeneration. Am J Respir Cell Mol Biol 47, 454–463 (2012).
Xu, Y. et al. Transcriptional programs controlling perinatal lung maturation. PLoS One 7, e37046 (2012).
Lopez, I. P. et al. Differential organ phenotypes after postnatal Igf1r gene conditional deletion induced by tamoxifen in UBC-CreERT2; Igf1r fl/fl double transgenic mice. Transgenic Res 24, 279–294 (2015).
Guevara-Aguirre, J. et al. Growth hormone receptor deficiency is associated with a major reduction in pro-aging signaling, cancer, and diabetes in humans. Sci Transl Med 3, 70ra13 (2011).
Kruis, T. et al. Heterozygous mutation within a kinase-conserved motif of the insulin-like growth factor I receptor causes intrauterine and postnatal growth retardation. J Clin Endocrinol Metab 95, 1137–1142 (2010).
Chetty, A., Andersson, S., Lassus, P. & Nielsen, H. C. Insulin-like growth factor-1 (IGF-1) and IGF-1 receptor (IGF-1R) expression in human lung in RDS and BPD. Pediatr Pulmonol 37, 128–136 (2004).
Miyazaki, E., Ohshiro, K., Taira, Y. & Puri, P. Altered insulin-like growth factor I mRNA expression in human hypoplastic lung in congenital diaphragmatic hernia. J Pediatr Surg 33, 1476–1479 (1998).
Wang, J., Zhou, J., Powell-Braxton, L. & Bondy, C. Effects of Igf1 gene deletion on postnatal growth patterns. Endocrinology 140, 3391–3394 (1999).
Pais, R. S. et al. Transcriptome analysis in prenatal IGF1-deficient mice identifies molecular pathways and target genes involved in distal lung differentiation. PLoS One 8, e83028 (2013).
Renehan, A. G., Atkin, W. S., O’Dwyer, S. T. & Shalet, S. M. The effect of cigarette smoking use and cessation on serum insulin-like growth factors. Br J Cancer 91, 1525–1531 (2004).
Meyer, K. F. et al. The fetal programming effect of prenatal smoking on Igf1r and Igf1 methylation is organ- and sex-specific. Epigenetics 12, 1076–1091 (2017).
Copeland, K. C., Colletti, R. B., Devlin, J. T. & McAuliffe, T. L. The relationship between insulin-like growth factor-I, adiposity, and aging. Metabolism 39, 584–587 (1990).
Palmer, R. M., Wilson, R. F., Coward, P. Y. & Scott, D. A. Analysis of circulating insulin-like growth factor-1 (IGF-1) and IGF binding protein-3 (IGFBP-3) in tobacco smokers and non-smokers. Tob Induc Dis 1, 157–170 (2002).
Coutant, R. et al. Relationships between placental GH concentration and maternal smoking, newborn gender, and maternal leptin: possible implications for birth weight. J Clin Endocrinol Metab 86, 4854–4859 (2001).
Fleisch, A. F. et al. Associations of maternal prenatal smoking with umbilical cord blood hormones: the Project Viva cohort. Metabolism 72, 18–26 (2017).
Metzger, R. J., Klein, O. D., Martin, G. R. & Krasnow, M. A. The branching programme of mouse lung development. Nature 453, 745–750 (2008).
Prins, J. R. et al. Smoking during pregnancy influences the maternal immune response in mice and humans. Am J Obstet Gynecol 207, 76 e71–14 (2012).
Zhang, H. et al. The interplay of DNA methylation over time with Th2 pathway genetic variants on asthma risk and temporal asthma transition. Clin Epigenetics 6, 8 (2014).
Suter, M. et al. Maternal tobacco use modestly alters correlated epigenome-wide placental DNA methylation and gene expression. Epigenetics 6, 1284–1294 (2011).
Suter, M. et al. In utero tobacco exposure epigenetically modifies placental CYP1A1 expression. Metabolism 59, 1481–1490 (2010).
Lim, R., Fedulov, A. V. & Kobzik, L. Maternal stress during pregnancy increases neonatal allergy susceptibility: role of glucocorticoids. Am J Physiol Lung Cell Mol Physiol 307, L141–148 (2014).
Pincus-Knackstedt, M. K. et al. Prenatal stress enhances susceptibility of murine adult offspring toward airway inflammation. J Immunol 177, 8484–8492 (2006).
We thank Rabea Imker and Anke Bettenbrock for excellent technical assistance. This work was supported from the Helmholtz Alliance ‘Aging and Metabolic Programming, AMPro’ (J.B.).
The authors declare no competing interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
About this article
Cite this article
Dehmel, S., Nathan, P., Bartel, S. et al. Intrauterine smoke exposure deregulates lung function, pulmonary transcriptomes, and in particular insulin-like growth factor (IGF)-1 in a sex-specific manner. Sci Rep 8, 7547 (2018). https://doi.org/10.1038/s41598-018-25762-5
Prenatal smoke exposure induces persistent Cyp2a5 methylation and increases nicotine metabolism in the liver of neonatal and adult male offspring
Current Pathobiology Reports (2020)
Journal of Allergy and Clinical Immunology (2020)
Frontiers in Pediatrics (2019)
Recent advances in our understanding of the mechanisms of lung alveolarization and bronchopulmonary dysplasia
American Journal of Physiology-Lung Cellular and Molecular Physiology (2019)