Reduction of Glyoxalase 1 Expression Links Fetal Methylmercury Exposure to Autism Spectrum Disorder Pathogenesis

Abstract

Glyoxalase 1 (Glo1) is an essential enzyme to detoxify methylglyoxal (MGO), a cytotoxic byproduct of glycolysis. Accumulating studies have shown an important role of Glo1 in regulating cortical development and neurogenesis, potentially contributing to the pathogenesis of autism spectrum disorder (ASD) when impaired. We have previously shown that prenatal exposure to non-apoptotic low-dose methylmercury (MeHg), an environmental pollutant, induces premature cortical neurogenesis and ASD-like behaviors in a rodent model. In this study, we aimed to determine the underlying molecular mechanisms that mediate prenatal MeHg-induced premature neuronal differentiation and abnormal neurodevelopment. Using single-cell RNA sequencing (scRNA-seq) and real-time quantitative PCR (RT-qPCR), we found that prenatal MeHg exposure at a non-apoptotic dose significantly reduced Glo1 gene expression in embryonic cultured radial glia precursors (RGPs). In cultured RGPs, the knockdown of Glo1 expression increased neuronal production at the expense of the cultured RGPs population, while overexpression of Glo1 restored MeHg-induced neuronal differentiation back to normal levels. Furthermore, we found that co-treatment with both MeHg and multiple MGO scavengers or a CREB inhibitor (iCREB) mitigated MeHg-induced premature neuronal differentiation, reinforcing the role of Glo1 and CREB in mediating MeHg-induced neuronal differentiation. Our findings demonstrate a direct link between MeHg exposure and expression of an ASD risk gene Glo1 in cortical development, supporting the important role of gene–environment interaction in contributing to the etiology of neural developmental disorders, such as ASD.

1. Introduction

Glyoxalase 1 (Glo1) is a pivotal enzyme that detoxifies methylglyoxal (MGO), a cytotoxic metabolite that can originate as an endogenous byproduct of glycolysis as well as from other sources such as dietary intake and environmental exposure to pollutants. Emerging research discloses the relationship between Glo1 and autism spectrum disorder (ASD). One study reported that post-mortem brain tissue from patients with ASD had reduced Glo1 enzymatic activity and increased MGO levels compared to control patients [1]. Following this report, several studies have identified genetic variants in the Glo1 gene and suggest a link between reduced Glo1 enzymatic activity to the etiology of ASD [2,3]. Moreover, an increasing number of studies have focused on Glo1 function in regulating neurodevelopment and neurogenesis. A recent study revealed that Glo1 knockdown leading to MGO accumulation can induce premature neuronal differentiation from embryonic cultured radial glia precursors (RGPs) during cortical development [4]. Another study shows that Glo1 inhibition/MGO accumulation can activate tyrosine receptor kinase B (TrkB) signaling, which in turn stimulates a kinase cascade: phosphorylation of protein kinase B (Akt) leading to phosphorylation of extracellular signal-regulated kinases (ERKs) to enhance cAMP response element-binding protein (CREB) phosphorylation/activation and the expression of the brain-derived neurotrophic factor (BDNF), an integral pathway in neurogenesis [5]. This suggests the Glo1 and CREB may participate in a communal pathway that affects cultured embryonic RGPs’ neuronal differentiation. While the development of the brain is known to be influenced by the environment it is exposed to, the specific mechanisms through which environmental factors may regulate Glo1 expression remain unclear.

Methylmercury (MeHg) is a well-known environmental toxicant that can pass through the blood–brain barrier and placenta and affect fetal neurodevelopment, causing cognitive deficits and motor dysfunction in children [6,7,8]. MeHg affects millions of people worldwide and is considered one of the top 10 chemicals of major public health concern by the World Health Organization [9]. Our recent study investigated the effect of prenatal non-apoptotic low-dose MeHg exposure during gestation on neurobehavioral outcomes. In this study, we treated pregnant mice with 0 or 0.2 ppm MeHg drinking water from embryonic day 0 (E0) until postnatal day 0 (P0). We found that low-dose MeHg could lead to ASD-like behaviors in adult rodents. This was characterized by impaired communication, sociability, and repetitive behaviors. Moreover, we found that prenatal low-dose MeHg exposure resulted in premature neuronal differentiation during the development of the cerebral cortex [10]. These findings suggest that MeHg, when given at a non-apoptotic dose in vivo, perturbs cortical neurogenesis in the fetal period, leading to long-lasting impacts on neuro-performance. On the other hand, the epidemiological evidence for the relationship between MeHg exposure and ASD remains inconclusive [11,12,13,14,15], and the underlying mechanism between prenatal MeHg exposure and postnatal ASD onset is unknown. Therefore, deciphering the underlying cellular and molecular mechanisms that mediate MeHg-induced abnormal neurodevelopment (premature neuronal differentiation) will provide new insights into how non-genetic factors such as environmental chemical exposure contribute to ASD etiology.

The goal of this study is to understand the environment–gene interaction in relation to ASD, inspiring the possible biomarkers for the early detection of ASD at high risk and potential targeted therapeutic strategies. We hypothesized that prenatal exposure to MeHg at the non-apoptotic dosage induces neuronal differentiation by reducing the expression of Glo1. Here, we show that the knockdown of Glo1 expression in cultured embryonic RGPs leads to premature neuronal differentiation, and phenocopying MeHg exposure. In contrast, Glo1 overexpression reverses MeHg-induced premature neuronal differentiation back to normal levels. Moreover, the co-treatment of MeHg with either MGO scavengers or a CREB inhibitor in cultured embryonic cortical RGPs could restore MeHg-induced neuronal differentiation. Our study reveals a novel mechanistic link between Glo1 regulation and MeHg-induced adverse effects on brain development.

2. Materials and Methods

2.1. Single-Cell RNA Sequencing (scRNA-seq)

All scRNA-seq pre-processing was previously described in iScience, by Loan et al., 2023 [10].

2.2. Differential Gene Expression

Differentially expressed genes between control (0 ppm) radial glial precursors (RGPs) (including RGP1 and RGP2 clusters), and MeHg (0.2 ppm) RGPs were identified via the “FindMarkers” function in Seurat v5.0.1 with default settings. Volcano plots were generated using the EnhancedVolcano function from genes identified via “FindMarkers”. Discriminated genes were based on p-value adjusted and Log2 fold-change. Log2 fold-change > 0.5 and p-value adjusted < 10e⁻¹⁴. These differentially expressed genes were used in iRegulon (Cytoscape) to identify gene regulatory networks that connect transcription factors to their predicted target genes as described previously [16].

2.3. Primary Cultured RGPs

Primary cultured RGPs were obtained from E11–12 pooled cortices dissected from CD-1 mice (Charles River Laboratories) as previously described [17]. Briefly, embryos were transferred to ice-cold Hanks’ balanced salt solution (HBSS) (cat#14175103, Thermo Fisher Scientific, Waltham, MA, USA), and the cerebral cortices were isolated from the brain after the meninges were removed. The cortical tissue was mechanically triturated with a plastic pipette and seeded on coverslips in a 24-well plate or directly into a 6-well plate (Thermo Fisher Scientific), both pre-coated with 15% poly-L-ornithine (PLO) (cat#72302, Sigma-Aldrich, Burlington, MA, USA) and 5% laminin (cat#CB40232, Thermo Fisher Scientific).

For immunocytochemical experiments, cells were plated in a 24-well plate at a density of 200,000 cells/mL. For RT-qPCR experiments, 1,000,000 cells were seeded in each well of a 6-well plate. The cultured RGPs were cultured in a Neurobasal Medium (cat#21103049, Thermo Fisher Scientific, containing 4500 mg/L glucose) containing 1X GlutaMAX supplement (cat#35050061, Thermo Fisher Scientific), 2% B27 supplement (cat#17504044, Thermo Fisher Scientific), 1% penicillin-streptomycin (cat#15140122, Thermo Fisher Scientific), and 40 ng/mL fibroblast growth factor 2 (FGF2) (cat#10018B, PeproTech, Cranbury, NJ, USA).

For the shRNA experiment (Glo1 knockdown), cultured RGPs were cultured in Neurobasal Medium (cat#A2477501, Thermo Fisher Scientific) with a reduced glucose (cat#G7021, Sigma-Aldrich) concentration (2250 mg/L). Since Glo1 plays an important role in detoxifying the toxic MGO, knocked down Glo1 can lead to an increase in MGO concentration, resulting in oxidative stress and cell death [18]. To minimize the toxic effect of MGO, we limited the supply of glucose in the medium to reduce the MGO accumulation. We found that a medium with a glucose concentration of 2250 mg/L is optimal for the shRNA knockdown experiment.

2.4. Pharmacological Treatments

2.4.1. 250 nM MeHg

Primary E11–12 cultured RGPs were exposed to 0 nM or 250 nM MeHg [17] for 24 h or 48 h. A concentration of 250 nM MeHg was achieved by a 1:250 dilution of 62.5 µM MeHg that was freshly prepared from a stock solution of 4 mM MeHg(II)Cl (cat#33553, Alfa Aesar, Ward Hill, MA, USA) through serial dilution with the culture medium.

2.4.2. Aminoguanidine (AG)

Cultured RGPs were exposed to 0 nM or 100 µM AG (cat#396494, Sigma-Aldrich) for 48 h. A concentration of 100 µM AG was prepared by initially diluting it in 100% DMSO to a concentration of 100 mM and then further diluting it in a culture medium 1000 times to achieve the final concentration of 100 µM AG, with a final DMSO concentration of 0.1%. For the MeHg + AG co-treatment experiment, experimental conditions were (i) Control (0 nM MeHg + DMSO), (ii) 250 nM MeHg + DMSO, (iii) 100 µM AG, (iv) 250 nM MeHg + 100 µM AG.

2.4.3. N-acetyl-l-cysteine (NAC)

Primary cultured cells were exposed to 0 nM or 600 µM NAC (cat#A9165, Sigma-Aldrich) for 48 h. A concentration of 600 µM NAC was achieved by diluting it in 100% DMSO to 600 mM and then further diluting the solution 1000 times in a culture medium. This resulted in a final concentration of 600 µM NAC, with a DMSO concentration of 0.1%. For the MeHg + NAC co-treatment experiment, the experimental conditions were (i) control (0 nM MeHg + DMSO), (ii) 250 nM MeHg + DMSO, (iii) 600 µM NAC, (iv) 250 nM MeHg + 600 µM NAC.

2.4.4. CREB Inhibitor (iCREB)

Primary cultured cells were exposed to 0 nM or 80 nM iCREB, 666-15 (cat#30780, Cayman Chemical Company, Ann Arbor, MI, USA) for 48 h. A concentration of 80 nM iCREB was achieved by diluting it in 100% DMSO to 80 µM and then further diluting it in a culture medium 1000 times. This resulted in a final concentration of 80 nM iCREB, with a DMSO concentration of 0.1%. A concentration of 80 nM iCREB was achieved by diluting iCREB in DMSO. For MeHg + iCREB co-treatment experiment conditions were (i) control (0 nM MeHg + DMSO), (ii) 250 nM MeHg + DMSO, (iii) 80 nM iCREB, (iv) 250 nM MeHg + 80 nM iCREB.

2.4.5. Plasmid Transfections

For the cultured RGPs transfections, 0.9 μg DNA (1:2 ratio of PB-CAG-eGFP versus the pSUPER-Glo1 shRNA or an empty vector (EV); 1:2 ratio of PB-CAG-eGFP versus pcDNA3-Flag-Glo1 or EV) and 1 μL Lipofectamine™ Stem Transfection Reagent (Thermo Scientific STEM00003) were mixed with 50 μL Opti-MEM medium, incubated for 30 min and added to cultured RGPs 24 h after plating. The knockdown efficiency of Glo1-shRNA has been validated in a previous publication both in culture and in vivo [4]. The expression efficiency of the Flag-Glo1 plasmid has been validated in a previous publication as well [4].

2.5. Reverse Transcription-Quantitative Real-Time Polymerase Chain Reaction (RT-qPCR)

Cultured RGPs were cultured as previously described. RNA was extracted from cultured RGPs using the PureLink RNA Mini Kit (cat#12183020, Thermo Fisher). Complementary DNA (cDNA) was synthesized using a QuantiTect Reverse Transcription Kit (cat#205311, Qiagen, Hilden, Germany). The RT-qPCR was performed with a SensiFAST SYBR Lo-ROX Kit (cat# BIO-94005, Bioline, Alvinston, Ontario, Canada) on an Mx3000P qPCR System (Agilent, Santa Clara, CA, USA). All qPCRs were performed using the same protocol (95 °C for 2 min for 1 cycle; 95 °C for 10 s, 58 °C, 15 s; 72 °C, 20 s for 40 cycles). All qPCR samples were performed in technical duplicates and then averaged. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as a loading control and the fold expression normalized to GAPDH was used as a readout. PCR primer sequences: Glo1-forward: 5′-GATTTGGTCACATTGGGATTGC-3′, Glo1-reverse: 5′-TCCTTTCATTTTCCCGTCATCAG-3′, GAPDH-forward: 5′-AGGTCGGTGTAACGGATT-3′, GAPDH-reverse: 5′-TGTAGACCATGTAGTTGAG-3′. Primers were validated by running gel electrophoresis and experimental conditions were optimized. Data were analyzed using AriaMX (Agilent, Santa Clara, CA, USA).

2.6. Immunocytochemistry

Cultured RGPs were cultured as previously described. Cells were fixed in 4% paraformaldehyde for 10 min after 48 h in culture and then blocked with 10% normal goat serum (NGS) (cat#16050122, Thermo Fisher Scientific) diluted in 1× PBS with 0.3% Triton X-100 (PBST). The cells were incubated with primary antibodies diluted in 10% NGS in PBS with 0.3% Triton X-100 and then incubated in a humid chamber at 4 °C overnight. Following this, cells were incubated with secondary antibodies diluted in PBST for 1 h at room temperature. After rinsing with PBS, the coverslips were mounted in a Lab Vision PermaFluor Aqueous Mounting Medium (cat#TA-030-FM, Thermo Fisher Scientific). The culture was washed three times for 5 min/time with 1× PBS between each step.

The primary antibodies used for immunocytochemistry were mouse anti-βIII-tubulin (cat#801201, BioLegend, San Diego, California, USA, 1:1000), rabbit anti-Pax6 (cat#901301, BioLegend, 1:1000), rabbit anti-Sox2 (cat#AB5603MI, Sigma-Aldrich, 1:500), and mouse anti-Ki67 (cat#ab15580, Abcam, Cambridge, UK, 1:500). The secondary antibodies used were donkey anti-rabbit Alexa Fluor 555 (cat#A31572, Thermo Fisher Scientific, 1:500) and goat anti-mouse Alexa Fluor 488 (cat#A32723, Thermo Fisher Scientific, 1:500). Nuclear counterstaining was performed with Hoechst 33342 (cat#4082, Cell Signalling Technology, Danvers, MA, USA, 1:1000).

Digital image acquisition was performed using Zeiss Imager M.1 fluorescent microscopy with Zeiss Axiovision software containing z-axis capability (Carl Zeiss Microscopy, Thornwood, NY, USA). For Glo1 overexpression and knockdown experiments, at least 200 successfully transfected cells (GFP⁺), chosen from random microscopic fields, were examined. The percentage of GFP⁺ cells expressing the markers of interest was studied. In the remaining experiments, five random images (20× magnification) per condition were captured for quantitative analysis. At least three independent experiments from three pregnant mice were conducted for all conditions. Quantification was performed using Image J.

3. Results

Glo1 expression is reduced in radial glial precursors (RGPs) following prenatal low-dose MeHg treatment.

Using single-cell RNA sequencing (scRNA-seq) analysis in our recently published work [10], we found that prenatal non-apoptotic low-dose 0.2 ppm MeHg exposure favors embryonic radial glial precursor 1 (RGP1) to directly differentiate into cortical neurons, omitting the intermediate progenitor stage (Ref. [10], Figure 1A). Following this, we performed downstream analysis to probe differentially expressed genes (DEGs), specifically in the RGP1 and RGP2 populations using the same scRNA-seq dataset (

Table 1. Differentially expressed genes between 0 ppm and 0.2 ppm MeHg-treated RGPs were identified via the FindMarkers function.

Gene	p-Value	Average log2FC	Regulation (Relative to 0 ppm RGPs)
Glo1	3.08 × 10−164	−0.9240032	Downregulated
Rpl26	2.85 × 10−150	−0.5132826	Downregulated
Cwc22	1.48 × 10−105	−0.7570934	Downregulated
Gm47283	2.01 × 10−90	−0.7192588	Downregulated
Tpm3−rs7	1.08 × 10−86	−0.5086832	Downregulated
Ddx3y	7.17 × 10−59	−0.4261163	Downregulated
Eif2s3y	6.14 × 10−58	−0.4087932	Downregulated
Rsrp1	7.15 × 10−57	−0.5629889	Downregulated
1810026B05Rik	8.95 × 10−52	−0.4919984	Downregulated
Actg1	1.06 × 10−36	−0.2934132	Downregulated
Btbd9	1.43 × 10−33	−0.348239	Downregulated
1110038B12Rik	1.04 × 10−30	−0.3580768	Downregulated
Gm21887	3.84 × 10−29	−0.3112397	Downregulated
Nr2f1	2.92 × 10−24	−0.4025072	Downregulated
Eif4a2	2.04 × 10−23	−0.3295204	Downregulated
Pop4	7.24 × 10−23	−0.3122949	Downregulated
Snhg15	1.97 × 10−19	−0.3127317	Downregulated
Mt1	2.23 × 10−19	−0.3604426	Downregulated
Gadd45g	5.24 × 10−11	−0.2945627	Downregulated
Lix1	4.93 × 10−10	−0.2608959	Downregulated
Ier2	3.09 × 10−08	−0.2509708	Downregulated
Sparc	2.02 × 10−07	−0.258431	Downregulated
Rmst	0.00454018	−0.2614077	Downregulated
Xist	5.78 × 10−163	1.09666796	Upregulated
Rpl21	6.13 × 10−93	1.10845559	Upregulated
Ubc	4.95 × 10−67	0.56325077	Upregulated
Tsix	1.08 × 10−39	0.39728863	Upregulated
Ubb	6.08 × 10−38	0.30566344	Upregulated
Tmem14c	2.16 × 10−29	0.37480296	Upregulated
Hist1h3c	3.85 × 10−26	0.36725854	Upregulated
Jund	3.74 × 10−17	0.25385254	Upregulated
Polr2k	4.83 × 10−15	0.25872311	Upregulated
Tmem108	8.33 × 10−15	0.26318465	Upregulated
Dct	1.67 × 10−14	0.31588436	Upregulated
Hist1h4i	3.47 × 10−13	0.29253036	Upregulated
Hopx	7.64 × 10−12	0.29434801	Upregulated

). This analysis revealed a constant reduction in the expression of the Glo1 gene across different cell clusters (Figure 1B). Consistently, Glo1 was identified as the most statistically significant downregulated gene in the volcano plot (Figure 1C). Further analysis using iRegulon [16] identified CREB1 as a top candidate transcription factor in RGPs to directly regulate the expression of the 14 DEGs, but Glo1 was not the direct target gene (Figure 1D). This suggests that Glo1-controlled CREB activity, supported by the previous work [5], may mediate MeHg-induced embryonic RGP neuronal differentiation.

To assess the role of Glo1 in MeHg-induced neuronal differentiation, we used a monolayer embryonic RGPs culture model (Figure 1E) and exposed precursor cells to low-dose MeHg (Figure 1F). In line with our in vivo model, reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) analysis showed a reduction in Glo1 expression in RGP cultures in response to MeHg exposure.

Glo1 reduction facilitates premature neuronal differentiation in culture.

To assess the effect of Glo1 downregulation on cultured embryonic RGPs, we transfected E11-E12 embryonic RGPs with a GFP reporter construct, together with a validated Glo1-shRNA [4]. After 2 days in culture following transfections, immunocytochemical analysis revealed that knockdown of Glo1 increased the percentage of βIII tubulin⁺ neurons (Figure 2B,C) but reduced the number of Ki-67⁺ proliferating precursors (Figure 2D,E) and the number of Sox2⁺ RGPs (Figure 2F,G), phenocopying MeHg-induced neuronal differentiation in culture [17].

Glo1 overexpression reduces MeHg-induce premature neuronal differentiation.

To investigate if overexpression of Glo1 can block premature neuronal differentiation caused by 250 nM MeHg exposure, we used our embryonic RGP cultures treated with either (i) control (0 nM MeHg + GFP construct with empty vector (EV) plasmids), (ii) 250 nM MeHg + GFP construct with EV plasmids, (iii) 250 nM MeHg + GFP construct with Flag-Glo1 plasmids, and (iv) 250 nM MeHg + GFP construct with Flag-Glo1 plasmids for 2 days in culture (Figure 3A). Immunocytochemical analysis showed that overexpression of Glo1 can reverse the increased number of βIII tubulin⁺ neurons (Figure 3B,C) and reduced number of Sox2⁺ RGPs (Figure 3D,E) caused by 250 nM MeHg back to the normal level.

MGO-regulated CREB pathway mediates MeHg-induced neuronal differentiation.

To test whether the accumulated MGO due to reduced Glo1 expression is responsible for MeHg-induced premature neuronal differentiation, we cultured embryonic RGPs in the presence of MeHg (250 nM) and MGO scavengers, N-acetyl-l-cysteine (NAC) or aminoguanidine (AG). First, E11–12 RGPs were treated with either (i) control (0 nM MeHg + 0 nM NAC), (ii) 250 nM MeHg, (iii) 600 µM NAC, or (iv) 250 nM MeHg + 600 µM NAC for 2 days in culture (Figure 4A). Immunocytochemical analysis revealed that NAC co-treatment with MeHg prevented MeHg-induced premature neuronal differentiation by recovering the increased number of β-III tubulin⁺ neurons and reducing the number of Pax6⁺ RGPs back to the normal level (Figure 4B–D). Subsequently, we used a second MGO scavenger, 100 µM AG, and repeated the aforementioned experiment (Figure 4E). Immunocytochemical analysis revealed that co-treatment of AG with MeHg can also prevent MeHg-induced premature neuronal differentiation as NAC did (Figure 4F–H). However, AG treatment alone increased the number of β III tubulin⁺ neurons and reduced the number of Pax6⁺ RGPs. Interestingly, AG is similar in structure to metformin [19], an FDA-approved drug we have previously shown to cause premature neuronal differentiation in cultured E11–12 RGPs [20].

Since our previous work showed that MeHg promoted CREB phosphorylation at Ser133, to induce premature neuronal differentiation, we employed CREB inhibitor (666-15), in the cultured embryonic RGPs: (i) control (0 nM MeHg + 0 nM iCREB), (ii) 250 nM MeHg + 0 nM iCREB, (iii) 0 nM MeHg + 80 nM iCREB, or (iv) 250 nM MeHg + 80 nM iCREB for 2 days in culture (Figure 4I). We showed that 80 nM iCREB can recover MeHg-induced premature neuronal differentiation as MGO scavengers did (Figure 4J–L). Since previous work reported that accumulated MGO can stimulate CREB activity by promoting CREB phosphorylation at Ser133 [5], our work, here, suggests that the MGO-regulated CREB pathway mediates MeHg-induced neuronal differentiation.

4. Discussion

Our previous publication found that exposure to the environmental contaminant MeHg during gestation could lead to ASD-like behaviors in adult rodents and premature neuronal differentiation of the cerebral cortex [10]. The present study demonstrates how MeHg interacts with gene expression to impact neural developmental processes, potentially contributing to the onset of previously observed ASD symptoms. Specifically, our study reports four major findings. First, we reveal that prenatal exposure to non-apoptotic MeHg significantly reduces Glo1 gene expression in embryonic RGPs both in vivo and in culture. Second, the knockdown of Glo1 expression in embryonic RGPs can cause premature neuronal differentiation, phenocopying low-dose MeHg exposure. Third, Glo1 overexpression in embryonic RGPs prevents MeHg-induced premature neuronal differentiation. Finally, co-treatment of MeHg with either MGO scavengers or iCREB in embryonic RGPs reverses MeHg-induced neuronal differentiation back to normal.

An increasing number of studies have shown that reduced Glo1 enzyme activity due to Glo1 polymorphisms and increased MGO levels are found in post-mortem brain tissues from patients with ASD, potentially contributing to the etiology of ASD [2,3]. Intriguingly, gestational diabetes often causes an overproduction of MGO, a circulating toxic intermediate metabolite that can pass through the placenta barrier to enter the fetal circulation [4,21,22]. At the same time, gestational diabetes has been associated with neurodevelopmental disorders, including ASD [23,24,25]. In this regard, the Glo1-regulated MGO pathway seems to be a pivotal node that can connect environmental factors to neural developmental disorders, such as ASD. In this study, we show that fetal exposure to non-apoptotic MeHg causes a reduction in Glo1 expression, leading to an accumulation of MGO, which may underlie MeHg-induced premature neuronal differentiation of embryonic RGPs. Our recently published work also shows that the same dosage of MeHg in embryos can lead to ASD-like behaviors in adult rodents [10]. This suggests that the gene–environment interaction between MeHg and Glo1 gene expression may contribute to ASD pathogenesis by perturbing the embryonic neural precursor development. Aligning with our findings, recent work has shown that the Glo1-regulated MGO pathway is important to regulating embryonic neural precursor maintenance, and perturbations in this pathway in vivo can lead to premature neuronal differentiation during the embryonic stage and long-lasting alterations in adult neural precursor pools [4]. It is important to note that a recent publication studied the effect of prenatal exposure to valproic acid (VPA) on Glo1 levels in postnatal mice. Here, the researchers found that VPA exposure during gestation results in increased Glo1 levels starting at 8 weeks postnatally which are accompanied by ASD-like behaviors [26]. It is interesting to observe that two different environmental factors can cause different outcomes of Glo1 expression, in relation to ASD progression. Our work shows that prenatal MeHg treatment causes an immediate reduction in Glo1 to impact the cortical development, potentially leading to ASD behavior later in life. On the other hand, prenatal VPA exposure leads to delayed Glo1 accumulation postnatally to alter the neuronal circuitry, contributing to ASD etiology. Together, these findings suggest that Glo1 is an important player contributing to non-genetic ASD.

Previous work from our lab put forward the theory that CREB phosphorylation is essential for low-dose MeHg to promote neuronal differentiation. Our current results suggest that CREB activation may act as downstream signaling of reduced Glo1 caused by MeHg exposure. This postulation is supported by a recent discovery that MGO accumulation due to reduced Glo1 levels can act on tyrosine kinase receptors to stimulate the Akt signaling pathway to enhance CREB phosphorylation/activity [5]. Moreover, the same concentration of MeHg treatment (250 nM) in other cell lines is capable of stimulating Akt signaling to promote CREB phosphorylation/activation [27].

Overall, our study shows that reduced Glo1 expression is essential for prenatal non-apoptotic low-dose MeHg exposure to induce premature neuronal differentiation in fetal cortical development. Our findings demonstrate a direct link between MeHg exposure and expression of an ASD risk gene Glo1 in cortical development, supporting the important role of gene–environment interaction in contributing to the etiology of neural developmental disorders, such as ASD. Future studies could investigate whether Glo1 can serve as a biomarker to identify a group of infants exposed to MeHg with a high risk of developing an ASD-like phenotype.