Thirdhand smoke (THS), the persistent residue of tobacco smoke that remains after a cigarette is extinguished, materialized as a threat for human health over the last decade. These toxic residues end up depositing on surfaces and objects where tobacco has been used (e.g., homes) and persist for weeks/months after the last smoking.1 THS toxicants undergo chemical reactions and changes over time potentially making them more toxic.2 Given that the routes of exposure to THS involve skin absorption, inhalation and ingestion,3 it is thought to be more toxic by producing more toxicants in the blood of the exposed person.4 Indeed, there is a growing body of evidence documenting THS-induced health risks,5 including cardiovascular disease (CVD). For example, we previously showed that THS exposure modulates platelet function and enhances thrombogenesis in adult exposed mice.6 However, it has not yet been established whether prenatal/in utero THS exposure impacts platelet function and related disorders, which is paramount since the developing embryo is especially sensitive to environmental toxicants, including cigarette smoke.7 Therefore, this study was designed to address this issue, utilizing the offspring of exposed females. In addition, we also examined whether sex differences exist in THS-induced effects.
We employed our innovative THS exposure approach which has been peer-reviewed4,6 and accepted as one that provides exposure conditions that mimic those in multiple real-life human situations.4 According to our experimental design, the female breeders were exposed to THS smoke or clean air starting 1 week before mating and throughout the whole pregnancy period by placing them in cages that are furnished with either THS or clean-air exposed materials. After delivery (post-natal day 4), the offspring were moved to clean air cages and housed until 8-10 weeks of age, before experimentation. All animal experimental protocols were approved by the Institutional Animal Care and Use Committee.
We first sought to investigate the in vivo effect of in utero THS exposure on hemostasis and thrombosis. Thus, the tail bleeding time assay revealed that the THSexposed males and females exhibit substantially shortened bleeding time compared to clean air exposed controls (Figure 1A). In fact, the average bleeding time in males was 395 ± 65.14 seconds (sec) in clean air group versus 68.80 ± 14.87 sec in the THS group; whereas in females it was 449.40 ± 45.07 seconds and 44.50 ± 12.56 sec for clean air and THS groups, respectively. As the time needed for cessation of bleeding was significantly reduced in the in utero THS–exposed mice, we therefore hypothesized that these mice are more vulnerable to thrombosis. This was tested by employing the FeCl3 carotid artery injury–induced thrombosis model. As depicted in Figure 1B, in utero THS mice of both sexes displayed a significant reduction in the occlusion time, with the average in males being 1,080 ± 60.00 sec in clean air group versus 210.80 ± 79.37 sec in THS group; whereas the females recorded 1,150 ± 114.30 sec and 281 ± 116.50 sec for the control and experimental groups, respectively. Taken together, these results show that in utero THS exposure enhances hemostasis and renders mice at higher risk of developing thrombosis. However, when males are compared with females, the results did not show any sex-based differences for either hemostasis or thrombus formation.
Notably, the platelet and other blood cells count was measured in both in utero THS- and clean air-exposed mice, as changes in platelet number may contribute to the hemostasis and thrombosis phenotype observed. The in utero THS exposure did not affect the platelet count or other hematological parameters (Table 1).
In light of the bleeding time and thrombosis data, another set of experiments evaluated the manifestation of the potential prothrombotic phonotype at the level of platelet physiology by studying platelet functional parameters in vitro. Hence, we first determined the effect of in utero THS exposure on agonist-induced platelet aggregation, which was found (Figure 2A) to be substantially increased, in response to either thrombin (0.1 U/mL) or ADP (1 μmol/L) in male and female mice exposed to THS in utero. However, when comparing platelet aggregation of both sexes, our analysis did not reveal a statistical significance, with either of the agonists.
Given that platelet granule secretion is known to contribute significantly to platelet activity,8 we investigated agonist-induced ATP release and P-selectin surface expression as markers for dense and a-granules release, respectively. Dense granules as well as a-granules secretion were increased in platelets obtained from in utero THS exposed mice, in response to either ADP or thrombin (Figure 2B; Online Supplementary Figure S1i and ii). These data revealed that platelet secretion contributes to the THS prothrombotic phenotype. In terms of sexdependent differences, the in utero THS-exposed males showed much higher ADP-induced dense granule secretion compared to females, but no statistical difference was observed in the clean air-exposed mice (Figure 2B). Moreover, no differences between the two sexes were observed with thrombin regardless of exposure type (Figure 2B). In contrast, a-granules secretion was significantly elevated in THS exposed females compared to males following stimulation by thrombin; but this was not the case with ADP (Online Supplementary Figure S1i and ii).
Next, we investigated the impact of in utero THS on aIIbb3 activation; which was more pronounced in the THS exposed mice, in response to 5 μmol/L ADP and 0.1 U/mL thrombin (Online Supplementary Figure S1iii and iv); which is in accordance with the enhanced aggregation response and was demonstrated in both sexes. Interestingly, our analysis revealed a significant sexbased difference (higher in males) with both agonists.
As platelets are activated, phosphatidylserine (PS) becomes exposed at their outer surface, for the assembly of coagulation factor complexes.9 Subsequently, we determined the impact of in utero THS exposure on PS expression. We found PS expression to be markedly enhanced upon stimulation with thrombin or ADP following THS in utero exposure (Online Supplementary Figure S1v and vi), which was documented in males and females. However, when both sexes were compared, it was found that the ADP effects were more pronounced in THS-exposed females compared to males. In contrast, when thrombin was analyzed, the effects in males were found to be higher than females. This discrepancy between the release of dense granules versus a-granules in males and females might be attributed to the fact that the former was performed using platelet-rich plasma whereas the latter using washed platelets; given that the presence of other plasma factors makes it difficult to assess whether the sex difference is inherent to platelets or related to plasma.10 As for PS exposure, female platelets showed more significant elevation in comparison to those from males with ADP. However, this trend is completely reversed when thrombin-stimulated platelets were utilized with a significant elevation in PS in males compared to females. This could be explained by the variation in dose-response between males and female platelets.11 It also should be noted that these are different platelet functional responses. In addition, analogy could be inferred from the race disparity of thrombin PAR4 receptor that triggers enhanced platelet aggregation as well as calcium mobilization when activated in African lineage compared to Caucasian.12 Similarly, a sex disparity in the receptors of different agonists or their downstream signaling pathways could explain the aforementioned discrepancies.
Collectively, our functional assays provide evidence that in utero exposure to THS triggers a state of platelet hyperactivity and contributes to the prothrombotic phenotype in the offspring mice.
In summary, these data provide evidence that the negative health effects of maternal THS exposure extend to the “non-exposed” offspring. Thus, our findings document for the first time that in utero THS exposure drives platelets into a state of hyperactivity, that manifests in a host of enhanced functional responses (e.g., aggregation). Together, these effects ultimately lead to a prothrombotic phenotype. It is noteworthy that this danger, according to our current and published data, does not only affect “directly” THS-exposed mice as we have shown before6 but expands to the offspring of the exposed pregnant mice as well. Interestingly and importantly, this prothrombotic phenotype endured despite the fact that offspring mice were not exposed to THS as they were moved to clean-air exposed cages until they reached 8-10 weeks of age. These data also highlight the underestimated risk of exposure to THS toxicants that persist up to several months after the last smoking has taken place.1,13 It is also important to note that this phenotype is consistent with the state of hyperactive platelets we reported previously as a result of exposure to other forms of tobacco that are perceived as safe, namely e-cigarettes14 and hookah/waterpipe.15
As for the comparisons between males and females, although no sex differences could be demonstrated in bleeding time, thrombosis or platelet aggregation, we did observe significant differences in dense and a-granule secretion, aIIbb3 activation as well as PS exposure when compared sex-wise.
In conclusion, our data clearly demonstrates for the first time that in utero THS exposure modulates the platelet biology in the non-exposed offspring, making them more susceptible to cardiovascular diseases.
- Received June 7, 2021
- Accepted September 8, 2021
Disclosure: no conflicts of interest to disclose.
Contributions: FK conceived studies, revised the manuscript, analyzed data; FA conceived studies, revised the manuscript, analyzed data; HA wrote the manuscript, performed research and data analysis; AA, ZK, PL, KH, VR and ME performed research and data analysis.
research reported in this publication was supported by the National Institute of Environmental Health Sciences and the National Heart, Lung, And Blood Institute of the National Institutes of Health under Awards Number R21ES029345 and R01HL145053. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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