Alcohol consumption during pregnancy induces Fetal Alcohol Spectrum Disorder (FASD), which has been proposed to arise from competitive inhibition of retinoic acid (RA) biosynthesis. We provide biochemical and developmental evidence identifying acetaldehyde as responsible for this inhibition. In the embryo, RA production by RALDH2 (ALDH1A2), the main retinaldehyde dehydrogenase expressed at that stage, is inhibited by ethanol exposure. Pharmacological inhibition of the embryonic alcohol dehydrogenase activity, prevents the oxidation of ethanol to acetaldehyde that in turn functions as a RALDH2 inhibitor. Acetaldehyde-mediated reduction of RA can be rescued by RALDH2 or retinaldehyde supplementation. Enzymatic kinetic analysis of human RALDH2 shows a preference for acetaldehyde as a substrate over retinaldehyde. RA production by hRALDH2 is efficiently inhibited by acetaldehyde but not by ethanol itself. We conclude that acetaldehyde is the teratogenic derivative of ethanol responsible for the reduction in RA signaling and induction of the developmental malformations characteristic of FASD. This competitive mechanism will affect tissues requiring RA signaling when exposed to ethanol throughout life.
Alcohol (ethanol; EtOH) exposure of human embryos results in a complex set of anatomical, mental and behavioral abnormalities collectively known as Fetal Alcohol Spectrum Disorder (FASD)1,2. Children with FASD can exhibit facial dysmorphology, microcephaly, short stature, central nervous system and neurodevelopmental abnormalities including intellectual disabilities and behavioral and psychological problems. The incidence of FASD can reach 2–5% of school children3,4,5,6. Oxidation of EtOH to acetaldehyde (AcAL) is the first step in the alcohol detoxification process7. This reaction is performed mainly by members of the alcohol dehydrogenase (ADH) enzyme family, peroxisomal catalase and the cytochrome P450 CYP2E18. Efficient oxidation of AcAL to acetate is of great importance for its elimination due to its high toxicity. In adults, this oxidation reaction is mainly performed by members of the aldehyde dehydrogenase family, like; ALDH2, ALDH1B1, and ALDH1A18.
One of the models to explain the etiology of FASD, proposed an inhibitory effect on retinoic acid (RA) biosynthesis9,10,11. RA is produced from vitamin A (retinol, ROL) first by alcohol dehydrogenase (ADH), or short-chain dehydrogenase/reductase (SDR)-mediated oxidation to produce retinaldehyde (RAL). A subsequent oxidation step from RAL to RA is performed by aldehyde dehydrogenases12,13. The EtOH/RA competition model suggested that the enzymatic overlap between EtOH detoxification and RA biosynthesis results in competitive inhibition. RA performs numerous regulatory functions during embryogenesis and adult tissue homeostasis, including tumor suppression. Therefore, its levels and localization are continuously regulated, and deviation from normal physiological levels results in multiple, and sometimes severe developmental malformations14,15,16.
Developmental biochemical characterization of the competition model during early embryogenesis, showed that EtOH exposure reduced RA signaling, affected known RA-regulated genes, and induced phenotypes recapitulating the malformations characteristic of FASD17. Of particular importance was the demonstration that ROL or RAL supplementation of EtOH-treated embryos18 or increasing the retinaldehyde dehydrogenase activity19 can rescue the abnormally low RA signaling levels, restore normal gene expression and prevent the characteristic developmental malformations. In agreement, retinaldehyde dehydrogenase 2 (RALDH2; ALDH1A2) knockdown resulted in enhanced sensitivity to alcohol19. As AcAL is oxidized to acetic acid by an ALDH enzyme, and RALDH2 is the earliest zygotic RALDH (ALDH) expressed in the embryo20, these results suggested that RALDH2 is probably the earliest enzymatic activity competed by EtOH, resulting in the inhibition of RA biosynthesis.
In this study, we elucidated the etiology of ethanol in FASD during early embryogenesis, as an inhibitor of RA biosynthesis. We demonstrate that in early embryogenesis, both EtOH and its oxidation product, AcAL, similarly repress RA signaling. Importantly, during early development, the RA-inhibitory effect of EtOH is dependent on its oxidation to AcAL by ADH. Furthermore, we show that EtOH and AcAL inhibit the activity of human RALDH2 (hRALDH2) in vivo. Surprisingly, the kinetic analysis revealed AcAL to be a preferred substrate of hRALDH2 over RAL, while EtOH is not an inhibitor of this enzyme. Our study elucidates the mechanism of RA inhibition during early embryogenesis and suggests possible roles for EtOH in some types of tumors.
ADH activity is required to convert EtOH to its teratogenic derivative
To analyze the competition of EtOH for the ADH enzymes available as proposed by the RA biosynthesis inhibition model, we established the conditions for their inhibition using 4-methylpyrazole (4MP)21. Late blastula (st. 8.5) Xenopus embryos were treated with increasing concentrations of 4MP (1 µM–1 mM) and the effect on RA levels was studied during early/mid-gastrula (st. 10.5). We monitored the expression of the RA target genes, HoxA1 and HoxB1 22 by quantitative real-time PCR (qPCR). Inhibition of the ADH activity only had a very mild repressive effect on Hox expression (Supplementary Fig. S1a,b) suggesting that 4MP at these concentrations does not affect the production of RA. Taking advantage of 4MP, we investigated whether EtOH hampers RA biosynthesis, or it has to be oxidized to AcAL to achieve its teratogenic effect (Fig. 1a,b and Supplementary Fig. S2a,b). EtOH alone (0.5% v/v; 86 mM) induced a strong reduction (about 50% inhibition) in HoxA1, HoxB1, Dhrs3 and Cyp26A1 expression. This expression repressive effect of EtOH was blocked by 4MP (1 mM) supporting the requirement to oxidize EtOH to AcAL by members of the ADH family.
Oxidation of ROL to RAL during gastrula stages has been attributed to retinol dehydrogenases (RDH) of the SDR family23,24. To study the role of SDRs in EtOH teratogenesis, we employed chloral hydrate (CH)25 and carbenoxolone (CBX)26 as RDH inhibitors. Late blastula embryos were treated with 5–30 mM CH or 10 µM to 1 mM CBX exhibited a reduction in Hox expression (Supplementary Fig. S1c–f). Inhibition of the RDH activity with 10 mM CH or 1 mM CBX repressed HoxA1, HoxB1, Dhrs3 and Cyp26A1 expression by over 50% (Fig. 1c,d and Supplementary Fig. S2c,d). EtOH treatment (86 mM), had a similar repressive effect which was not affected by RDH inhibition and they behaved additively reaching about 90% inhibition of gene expression (Fig. 1c,d and Supplementary Fig. S2c,d). Also, 1 mM CBX did not inhibit the Hox repressive effect of EtOH (Fig. 1e,f). We conclude that, while the RDH is central for the oxidation of ROL to RAL in early embryos, enzymes of the ADH family are required for the oxidation of EtOH to its RA-repressive metabolite, acetaldehyde.
Acetaldehyde recapitulates the teratogenic effects of ethanol
To determine the effect of AcAL exposure on RA-regulated genes, embryos were treated with various acetaldehyde concentrations in the physiological range27,28,29,30,31. Embryos were exposed to AcAL (1–10 µM) from late blastula (st. 8.5), and the expression levels of several RA-regulated genes was analyzed by qPCR during early/mid-gastrula (st. 10.5). The expression of HoxA1, HoxB1, HoxB4, Dhrs3, Cyp26A1, and Rdh10 was affected by the AcAL treatment such that Hox gene expression was reduced in a concentration-dependent fashion, while Cyp26A1 and Dhrs3 showed repression and Rdh10 was up-regulated (Supplementary Fig. S3).
To further link acetaldehyde to the EtOH-induced reduction of RA levels, the expression of the RA-regulated genes was studied in embryos treated in parallel with AcAL (5 µM), EtOH (0.5%), the RALDH inhibitor, 4-diethylaminobenzaldehyde (DEAB, 100 µM)32 and RA (1 µM). Acetaldehyde treatment induced a 30% to 60% reduction or increase in expression depending on the gene in question and in accordance with its normal response to RA signaling (Fig. 2). The EtOH and DEAB treatments resulted in very similar effects on gene expression, consistent with AcAL inducing a reduction in RA signaling. In contrast, RA exposure induced the expected opposite effect (Fig. 2).
To show that acetaldehyde recapitulates the developmental malformations induced by ethanol33, we analyzed the developmental defects resulting from these treatments (Fig. 3). Embryos were treated with AcAL (5 µM), EtOH (0.5%), or DEAB (60 µM) and allowed to develop to st. 34 (Fig. 3a–d). All three treatments affected the formation of the head, the eye, the trunk, and the tailbud (Fig. 3a–d). The length of the embryos was determined for all samples and it was found that there is a significant shortening in the treated embryos compared to controls (Fig. 3a–d). A more detailed and quantitative comparison between these treatments, was performed on a second set of treated embryos allowed to develop to stage 45. The distance between eyes (W3,) head width (W5), and head length (L1) were measured according to Nakatsuji32. All head parameters were significantly reduced in AcAL-treated embryos (Fig. 3f,j,l,n) and the effects were similar to those induced by EtOH treatment or down-regulation of RA biosynthesis (DEAB; Fig. 3h,i,k,m,o). These results show that AcAL, as the intermediate in EtOH detoxification, induces the same set of molecular and developmental defects as the actual alcohol exposure.
One striking effect of EtOH exposure is a reduction in brain size34. To characterize the brain malformations resulting from AcAL-exposure, embryos were treated with AcAL (5 µM) or EtOH (0.5%), and the relative position of rhombomere 5 (R5) and the midbrain-hindbrain boundary (MHB) were determined using HoxB3 and en2 as markers, respectively (Supplementary Fig. S4). Measurement of distance from the rostral end of the neural plate (RNP) to the MHB or from the MHB to R5 revealed a statistically significant reduction of about 15% in brain size (Supplementary Fig. S4).
Acetaldehyde competes with retinaldehyde for the available RALDH2 activity
We previously showed that the embryonic, RALDH2-dependent RA production is sensitive to EtOH19. To determine whether EtOH also inhibits the human RALDH2 enzyme, embryos injected with a hRaldh2 expression plasmid were exposed to EtOH from the midblastula transition and analyzed during early/mid-gastrula (st. 10.5). hRaldh2 overexpression resulted in the expected gene-dependent up-regulation (HoxB1, HoxA1, HoxB4, Dhrs3, and Cyp26A1) and down-regulation (Rdh10) in expression supporting the conclusion that this enzyme increases the endogenous RA (Fig. 4a–d and Supplementary Fig. S5a,b). EtOH treatment induced the opposite effect on gene expression consistent with a reduction in RA levels, while a combination of both treatments had a rescuing effect (Fig. 4a–d and Supplementary Fig. S5a,b). We conclude that hRALDH2 can produce RA and this activity is susceptible to EtOH-promoted inhibition.
To show that this conclusion also holds true for acetaldehyde, embryos were injected with the hRaldh2 expression plasmid and treated with AcAL. Acetaldehyde treatment alone induced the expected abnormal expression of RA-regulated genes (HoxB1, HoxA1, HoxB4, Dhrs3, Cyp26A1, and Rdh10) like EtOH exposure consistent with a reduction in RA signaling (Fig. 4e–h and Supplementary Fig. S5c,d). Increasing the amount of RALDH2 activity had a rescuing effect and partially restored normal expression levels. These results further support the effect of AcAL on RA signaling through the competition for the available RALDH activity in vivo.
These results and the use of 4MP inhibition support the conclusion that EtOH is converted to AcAL by enzymes of the ADH family and AcAL in turn competes for the RALDH activity. Previously we have shown that during early gastrula, organizer-specific genes like gsc and chordin are affected by EtOH and RA18. To further support the necessity to oxidize EtOH to AcAL to induce the detrimental effects on gene expression, embryos were treated with the ADH inhibitor 4MP. Both, EtOH and AcAL at physiological concentrations reduced the expression of gsc and chordin (Fig. 5b,c,g). The inclusion of 4MP in these treatments rescued the detrimental effects of EtOH (Fig. 5e,g) but had no influence on the gene expression effect of the AcAL treatment (Fig. 5f,g) further supporting the teratogenic role of AcAL.
To provide in vivo evidence of the acetaldehyde/retinaldehyde competition, embryos were treated with AcAL (5 µM), RAL (1 µM) or a combination of both, and the expression of known RA-regulated genes was determined. This type of analysis shows that RAL supplementation results in effects consistent with increased RA, while AcAL treatment induces the opposite response in agreement with a reduction in RA levels (Fig. 4i–l and Supplementary Fig. S5e,f). Moreover, combined treatment has a rescuing effect on RA target gene expression. These results suggest that increased RAL levels can rescue the teratogenic effects of acetaldehyde.
Further support for the involvement of a RALDH enzyme, probably RALDH2 at these stages, in the AcAL-induced reduction in RA levels was obtained using DEAB. According to our previous observations18, embryos simultaneously treated with DEAB and AcAL should exhibit a stronger reduction in RA signaling levels due to a double inhibition of the RALDH enzymatic activity Analysis of the expression of RA-regulated genes (HoxB1, HoxB4, Cyp26A1 and Dhrs3) revealed lower expression levels in the combined treatment than in each of the individual treatments (Fig. 4m–p).
Acetaldehyde is an efficient substrate of RALDH2
The results obtained by analyzing RA-dependent gene expression in vivo supported the conclusions: i) AcAL recapitulates all the molecular and developmental effects originally attributed to EtOH, ii) the effect of AcAL is mainly mediated through the inhibition of RA biosynthesis, and finally, iii) AcAL is produced through ADH-mediated oxidation of EtOH. To biochemically demonstrate the competition between RAL and AcAL for the RALDH activity, we established in vitro enzyme assays with a recombinant hRALDH2 enzyme35. To test whether acetaldehyde might function as a competing substrate of hRALDH2, we studied the oxidation of AcAL. Using the previously described reaction conditions35 we tested increasing concentrations of AcAL (Fig. 6a,b). At low concentrations (1–80 µM), the reactions reached substrate depletion after 30 min (Fig. 6a) but, during the first 5 minutes, all reactions behaved linearly and showed a clear concentration dependence (Fig. 6b). Michaelis-Menten analysis of the reaction kinetics gave a Km of 8.47 ± 1.6 µM and a Vmax of 1.03 ± 0.06 nmol/min/mg hRALDH2 for acetaldehyde (Fig. 6c). The Km for AcAL is about half of that for RAL, with very similar Vmax for both substrates35, suggesting a hRALDH2 preference for AcAL.
To clearly demonstrate the competition between RAL and AcAL for hRALDH2, we analyzed the reaction progression by HPLC to directly determine the oxidation of RAL to RA in the presence of AcAL. Oxidation reactions of RAL by hRALDH2 were performed with increasing concentrations of AcAL (1–100 µM). At different times points, samples were collected, and the production of RA was quantitated. The addition of AcAL to the reaction mixture resulted in a concentration-dependent inhibition of the oxidation of RAL to RA (Fig. 6d) demonstrating the competition between RAL and AcAL for the available hRALDH2.
To rule out an inhibitory effect of EtOH on the activity of hRALDH2, the oxidation of all-trans retinaldehyde (RAL) was performed in the presence of increasing concentrations of EtOH. EtOH was increased for up to three times the maximal concentration in human blood. At all EtOH concentrations, the oxidation of RAL was not affected by the presence of EtOH (up to 257 mM) showing that it has no effect on the activity of hRALDH2 (Fig. 5e). Similarly, acetic acid (25 µM-1 mM), the oxidation product of AcAL did not affect the hRALDH2 activity (Fig. 6f).
RALDH2 is the most abundant ALDH expressed during early gastrula
The identification of acetaldehyde as the teratogenic metabolite of ethanol exposure prompted us to understand the ability of the early embryo to oxidize AcAL, a reaction efficiently performed by mitochondrial ALDH2 in the adult liver36,37. To determine whether ALDH2 is available in the embryo, the temporal pattern of Aldh2 expression was studied by qPCR. The results show that Aldh2 transcripts are maternally deposited in the oocyte, but their level decreases steeply, over 90% reduction, towards the onset of gastrulation becoming almost absent (Fig. 7a). These results show that during the high EtOH sensitivity window, from MBT until mid-gastrulation18, Aldh2 expression is very low. As our results support a competition between AcAL and RAL, we also determined the temporal expression pattern of the three known Raldh genes: Raldh1 (Aldh1A1), Raldh2 (Aldh1A2) and Raldh3 (Aldh1A3). Although all three genes are expressed zygotically, Raldh2 is the earliest transcribed from midblastula (st. 8.5), while Raldh1 and Raldh3 expression only starts with the onset of gastrulation (Fig. 7a).
These expression patterns raise the possibility that any RALDH could be a target for AcAL competition. For this reason, we determined the RALDH relative abundance during early gastrula (st. 10.5). We found that the transcript levels of Aldh2, Raldh1, and Raldh3 are 0.06, 0.01, and 0.01-fold lower respectively relative to the expression of Raldh2 (Fig. 7b). This result places Raldh2 as the major RA-producing enzyme at this developmental stage, but also as the primary target for acetaldehyde due to low quantities of ALDH2 in the early embryo.
One of the models proposed to explain the teratogenic effects of EtOH was based on biochemical knowledge, and it suggested that the ethanol detoxification competes with ROL for the available alcohol-oxidizing enzymatic activities also necessary for RA biosynthesis9,10,11. This competition between substrates ultimately would result in the reduction of RA levels to teratogenic levels (Fig. 8). Biosynthesis of RA requires two oxidation steps, the first from ROL to RAL is rate limiting based on enzymatic considerations9,38, while the second oxidation of RAL to RA is limited by enzyme availability39. In recent years, it has become evident that during early embryogenesis, the oxidation of ROL is performed mainly by members of the SDR family like, RDH10 and RDH223,24,40,41. On the other hand, EtOH is oxidized by middle-chain ADH enzymes7,42,43. Taking advantage of enzyme family specific inhibitors, we obtained additional evidence of channeling of the EtOH and ROL to different enzyme families for oxidation. Inhibition of the SDR activity did not prevent EtOH from affecting the expression of RA-regulated genes. In contrast, inhibition of enzymes of the ADH family efficiently prevented the RA-antagonizing activity of EtOH. These results show that EtOH requires ADH-mediated oxidation to achieve its RA-reducing activity and, it does not compete for the SDR enzymes during early embryogenesis (Fig. 8).
AcAL, a highly toxic organic compound, induces a wide range of pharmacological, behavioral, and carcinogenic responses in humans44,45. AcAL can form adducts with DNA, proteins, and lipids and promote the formation of reactive oxygen species7,46,47. The requirement for an ADH activity to trigger the RA-inhibiting effect of EtOH places the focus on AcAL as the mediator of this effect. Further support was obtained by treating embryos with AcAL or EtOH at physiological concentrations. The set of developmental malformations obtained from both treatments were indistinguishable, suggesting that both compounds affect the same set of developmental processes, and EtOH is being oxidized to AcAL for the teratogenic effect to be induced. Together, all these observations shift the focus from EtOH to AcAL as the main teratogenic compound from alcohol exposure competing for the second oxidation step in RA biosynthesis (Fig. 8).
For the competition model to take place, AcAL should function under physiological conditions, as an efficient substrate for enzymes with RALDH activity. In previous studies, we provided evidence showing that in Xenopus embryos the onset of gastrulation is the most alcohol sensitive developmental stage when the most severe FAS-like malformations are induced18. Interestingly, RA signaling in vertebrate embryos has been shown, to begin with the onset of gastrulation, in the region of the embryonic organizer18,48,49. At these stages, most components of the RA biosynthetic and signaling network are apparently present and await the RALDH-mediated oxidation of RAL to RA to complete and activate the pathway48,50,51,52. The biosynthesis of RA and the onset of signaling correlate with the start of expression of the Raldh2 gene in vertebrate embryos20,53,54,55,56. In agreement, mutation of the Raldh2 gene results in the earliest embryonic lethality among mutations in members of the RA metabolic network57. This observation suggests that the enzyme encoded by this gene is crucial for gastrulation and early neurulation20,53,55,56. All these observations place the focus on the RALDH2 enzyme as one of the earliest targets of the alcohol exposure. For this reason, we characterized in more detail the RALDH2 enzyme and in particular the human ortholog to try and understand its role in the induction of FASD35.
Focusing on hRALDH2, we could show that the effects of EtOH on RA-regulated genes can be rescued by increasing the level of RALDH2 activity in the embryo. In the original model, EtOH would inhibit RAL formation9. Then, according to the model, the addition of RALDH2 would have no effect as no substrate would be available. The restricted availability of RALDH2 or RAL-oxidizing activity was experimentally demonstrated50, supporting the labile condition of RA biosynthesis at the onset of gastrulation. At these stages, Raldh2 transcript accumulation is just beginning, and enzyme availability is low. In agreement, our results show that the increase in RALDH2 activity compensates for the competition by AcAL and allows sufficient oxidation of RAL to RA, supplementing the limiting availability of this enzyme.
The central aspect of the RALDH2 study was to demonstrate that AcAL is an efficient substrate for this enzyme and as such competes with RAL. Characterization of hRALDH2 for several RAL isomers known to be present in vivo, all-trans, 9-cis, and 13-cis, revealed similar enzymatic efficiencies35. Taking advantage of the same in vitro conditions, we determined the enzymatic parameters of hRALDH2 when acetaldehyde was provided as the substrate. Our results show that the Km measured for acetaldehyde (8.47 µM) is about 2-fold lower than the Km when all-trans RAL is the substrate while the Vmax for both substrates is similar. These results show that hRALDH2 can efficiently use AcAL as a substrate and it has a preference for it over RAL under our experimental conditions. The demonstration that acetaldehyde is a substrate of hRALDH2 strongly supports the competition model between AcAL and RAL for the available RALDH as an important component of the etiology of FASD. Then detoxification of the EtOH ingested can induce a teratogenic reduction in RA levels through the competition for the available RALDH activity. For a direct demonstration of the competition between acetaldehyde and retinaldehyde and the resulting inhibition of RA production, the in vitro reaction products were analyzed by HPLC. This type of analysis demonstrated a concentration-dependent inhibitory effect of AcAL on the production of RA from RAL when both substrates are present together. This result further supports the competition for hRALDH2 and the resulting reduction in RA production.
Acetaldehyde has been studied as a substrate for several vertebrate RALDH enzymes. This substrate has been studied with RALDH1 from human, rat and Xenopus and the RALDH2 from rat. For those enzymes, the Km values reported range from 15 µM to 2500 µM36,58,59,60,61. Kinetic analysis of the human RALDH1 revealed a lower Km when acetaldehyde was used in the 0 to 50 µM range, and it increased dramatically when higher AcAL concentrations were used. These results led to the proposal that the RALDH enzymes bind their substrates cooperatively62. For hRALDH2, we measured the Km with AcAL concentrations in the 0 to 50 µM range, which includes the physiological range in human blood (up to 20 µM)27,28,29,30,31. The range of Km values measured for AcAL for the different RALDH enzymes could reflect real enzymatic differences, or it could be a result of the cooperative behavior and the reaction conditions.
Other acetaldehyde-oxidizing enzymes could be performing the removal of this toxic compound. Analysis of the expression of Alhd2 during early embryogenesis identified maternal transcripts whose levels decrease markedly towards the onset of gastrulation. All other genes studied, Raldh1 (Aldh1A1), Raldh2 (Aldh1A2), Raldh3 (Aldh1A3), were expressed at late blastula by zygotic transcription, while Aldh1B1 transcripts were undetectable at these stages. By early/mid-gastrula, Raldh2 is the most abundant gene expressed among those studied, while the Aldh2 transcripts represent less than 10% of the Aldh transcripts detected. These observations suggest that RALDH2 is placed to perform most of the RA biosynthesis in the embryo. In the case of EtOH exposure, RALDH2 is the most abundant enzyme capable of efficient AcAL oxidation at the expense of RA.
The inhibition of the hRALDH2 activity by AcAL is the biochemical mechanism of the competition model by diverting the early embryonic RALDH activity from RAL oxidation and RA production. The competition of acetaldehyde for the available RALDH2 activity was previously suggested from EtOH rescue experiments using ROL and RAL supplementations18. Also, increasing hRALDH2 enzyme levels, lowered the competition between acetaldehyde and the endogenous substrate, retinaldehyde, and restored RA signaling by supporting its production in the presence AcAL. Alternatively, increasing the available RAL also rescues the effects of AcAL. Then, biochemically, the competition mechanism is explained by the demonstration that AcAL, is a substrate of RALDH2 in vivo and in vitro, and the Km for this substrate is lower than that of RAL, making a preferred substrate.
In the context of FASD, acetaldehyde levels can reach 2–20 µM in the mother’s blood as a result of alcohol intake27,28,29,30,31. During pregnancy, the mother performs the main alcohol detoxification. Among the enzymes involved, ALDH2 is considered a central player in the liver, although additional enzymes are involved63. The remaining AcAL then crosses the placenta64,65, and once it reaches the embryo, it competes and hampers RAL oxidation resulting in reduced RA signaling with teratogenic outcomes. Multiple maternal alleles encoding alcohol and aldehyde dehydrogenases have been identified as risk-increasing or protective for FASD42. These observations support a genetic component for FASD, as genetic polymorphisms might affect enzymatic activity levels and impact on the efficiency of ethanol detoxification.
According to the proposed mechanism, the competition for the RALDH activity by AcAL results in a reduction in RA levels. This teratogenic mechanism is also the basis of the Vitamin A Deficiency Syndrome, and in agreement, the developmental malformations in both diseases are similar66. A similar RA signaling reduction has also been proposed for the Matthew-Wood, Smith-Magenis, and DiGeorge/VeloCardioFacial syndromes and they exhibit reminiscent developmental malformations67,68,69. Alcohol is also recognized as a risk-factor for several different types of tumors70. It has been shown that acetaldehyde is the active carcinogenic metabolite of EtOH among alcoholics45. The tumor-promoting mechanism of EtOH could involve the same biochemical effect on RA levels as this signaling pathway performs numerous regulatory roles beyond embryonic development. RA signaling is involved in tissue homeostasis with anti-proliferative, tumor suppressor roles extending to multiple tissues like prostate, breast, and colon. In some types of cancer, the analysis of RA mediators or target genes are used as biomarkers of tumor prognosis70. Also in these cases, the contribution of EtOH to the disease progression could involve a reduction in RA signaling with its tumor-promoting effect. Therefore, our study suggests new aspects of alcohol as a detrimental compound where RA is crucial for developmental processes or tissue homeostasis.
Embryo staging and treatments
For Xenopus laevis microinjection of plasmids, 2- to 4-cell embryos were injected radially (4 times) in 1X modified Barth’s saline with HEPES (MBSH) and incubated in 0.1X MBSH. For treatment, embryos were incubated until st.8.5 and then treated as indicated. Embryos were staged based on morphological landmarks according to Nieuwkoop and Faber71.
Retinoids and HPLC grade solvents were purchased from Sigma-Aldrich (St. Louis, Missouri): all-trans Retinal (RAL), all-trans Retinoic acid (RA), Dimethyl sulfoxide (DMSO), Acetaldehyde, 4-Diethylaminobenzaldehyde (DEAB), Chloral Hydrate (CH), carbenoxolone (CBX), 4-methylpyrazole (4MP), acetonitrile, hexane and methanol. Stock solutions of RAL, RA, and DEAB, were prepared in DMSO. Experiments were performed in accordance with the relevant guidelines and regulations of the Institutional Ethics Committee of The Hebrew University after their approval and under their supervision.
RALDH2 enzyme assays
Expression and purification of the human RALDH2 protein were according to Shabtai et al.35. hRALDH2 enzymatic activity was monitored either by spectrophotometer or by high-pressure liquid chromatography (HPLC). The RALDH2 enzymatic reaction was performed as previously described35. Standard reactions were performed at 37 °C in 50 mM Hepes/K+ pH 8.5 buffer containing 2 mM MgCl2, 2 mM DTT, 150 mM KCl and 1 mM EDTA (final volume 200 µl). Protein content in the reaction mixtures was 1 µg. Reactions were initiated by addition of the substrate: retinoids or acetaldehyde (1 to 100 µM) in DMSO and a constant NAD+ 1 mM concentration.
For spectrophotometric determination of the hRALDH2 activity, the reaction was monitored at 340 nm for the overall increase in absorbance of produced NADH. A global extinction coefficient of 2,820 M−1s−1 was experimentally determined by measuring the increase in absorbance of increasing NADH under our reaction conditions. Initial rate measurements were carried out at 37 °C on a TECAN Infinite F200Pro spectrophotometer sampling the OD every 10 sec for a total of 30 min. The kinetic constants of RALDH2 were obtained by plotting saturation curves under conditions in which enzyme activity was linear with respect to protein concentration and reaction time, and fitting data from the saturation curve to Michaelis–Menten with the Prism software (Graph Pad Software Inc., San Diego, CA).
For HPLC analysis of RA production, the enzymatic reaction was stopped by adding 400 µl of acetonitrile. Methanol was added after sample evaporation and subjected to HPLC analysis. HPLC was performed based on Frolik et al.72. Shortly, run protocol: 50 µl/sample were injected and run at 700 psi, 1.1 ml/min, acetonitrile:1% ammonium acetate 80:20 was used as the developing solvent. Instruments: Waters 717 autosampler, Waters 996 Photodiode Array Detector, Waters 600 pump, Waters 600 controller. Column: Spherisorb ODS2 Column, 80 Å, 5 µm, 4.6 mm × 250 mm. Total RA production was measured after 25 min, n = 4 in duplicate.
Whole mount in situ hybridization
The whole mount in situ hybridization was performed as described previously73. Probe information: HoxB374, En275, Gsc18. Comparisons of distances of anatomical markers and structures were analyzed with the ImageJ software package.
Quantitative real-time RT-PCR (qPCR)
Total RNA from embryos was extracted with Aurum™ Total RNA Mini Kit with DNase (Bio-Rad). Each experiment was repeated at least 3 times and involved at least 5-embryos/samples. cDNA was synthesized using iScript cDNA Synthesis kit (Bio-Rad). qPCR was done on an CFX384 Touch™ Real-Time PCR Detection System (Bio-Rad) using the iTaq™ Universal SYBR Green Kit (Bio-Rad). Results were calculated with the ∆∆CT method76, and the primers used were:
Gapdh: 5′GCTCCTCTCGCAAAGGTCAT, 5′GGGCCATCCACTGTCTTCTG;
HoxB1: 5′TCCCCCTCCAACAACAAACC, 5′TTGCCCCAGTGCCAATGAC;
HoxA1 5′CATCGCCTCGTCTGTGGT, 5′GTCAGGTCCGTATGAATGGTG;
HoxB4: 5′CCAAGGATCTGTGCGTCAA, 5′GCAGGATGGAGGCGAACT;
Cyp26A1: 5′CGATTCCTCAAGGTTTGGCTTCA, 5′ATTTAGCGGGTAGGTTGTCCACA;
Rdh10: 5′TTTGAAGCTGTGGTCTGCAT, 5′GCCTGTTTCCTTTGAGCAAT;
Dhrs3: 5′CAGGCGCAAGAAATCCTAAG, 5′CAAAGGCCACGTTACAGGAT;
Raldh1: 5′GAACTTTCCGTTGTTGATGT, 5′GATAGCAGTCAGTGGAGTTTG;
Raldh2: 5′ATGTTTGCCTGGAAGATTGC, 5′GAGAGCAGTGAGCGGAGTCT;
Raldh3: 5′TAAAGCCCTGTCTGTTTCT, 5′CATACTCTCCAAGTTCCCTT;
Aldh2: 5′AGGCTGGGCTGACAAATG, 5′ CACACACTCCGACAGGTTCA;
Aldh1B1: 5′GCAATCCCTTTGACCTGGA, 5′GCACCTTCTGTTTTACCGCTTT;
Chordin: 5′ACTGCCAGGACTGGATGGT, 5′ GGCAGGATTTAGAGTTGCTTC
All statistical comparisons were carried out using Prism software (Graph Pad Software Inc., San Diego, CA). Results are given as the mean ± standard error of the mean (SEM). Tests used were the Two-sample t-test for proportions or nonlinear regression plotting Michaelis–Menten constants, as appropriate. Differences between means were considered significant at a significance level of p < 0.05.
All data generated or analyzed during this study are included in this published article (and its Supplementary Information files).
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We wish to thank Oded Meyuhas for discussions and critically reading the manuscript and Ilana Caspi for experimental advice. This work was supported in part by grants from the Canadian Institutes for Health Research (No. 315426–340200–2000), the Canada-Israel International Fetal Alcohol Consortium (NA), the Manitoba Liquor & Lotteries Corporation (RG-003–14), the Chief Scientist of the Israel Ministry of Health (No. 3–10068) and the Wolfson Family Chair in Genetics to A.F.
The authors declare that they have no competing interests.
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Journal of Biological Chemistry (2019)
Insights into retinoic acid deficiency and the induction of craniofacial malformations and microcephaly in fetal alcohol spectrum disorder
Alcoholism: Clinical and Experimental Research (2019)