Abstract 4134622: Hyperglycemia Induces Heterotaxy Syndrome by Lowering Intracellular pH

Background: Pregestational diabetes is an established risk factor for congenital heart disease (CHD), including heterotaxy syndrome, which results from abnormal left-right (L-R) axis. However, the specific mechanism by which hyperglycemia disturbs the L-R axis still remains unsolved. In addition, it is unknown how a variety of heterotaxy is provoked by pregestational diabetes. Methods: We conducted whole-mount in situ hybridization, reporter analysis and RNA-seq in mouse embryos of streptozotocin-induced diabetic dams and Wnt3a –/– embryos. Additionally, the effect of high-glucose conditions on intracellular pH (pH i ) was investigated. We also examined the influence of maternal vitamin A intake on L-R axis formation in embryos of diabetic dams. Results: We observed various patterns of Pitx2 expression in embryos of diabetic dams, indicating disrupted L-R axis. The initial step of L-R axis formation was impaired, with Nodal expression, which induces Nodal - Pitx2 cascade in the lateral plate mesoderm, being regressed in the node. Consistent with the resemblance to the phenotype of Wnt3a –/– embryos, canonical Wnt signaling was downregulated in embryos of diabetic dams. As the RNA-seq analysis suggested dysregulation of glycolysis, we assessed pH i to find that hyperglycemia lowers pH i in the primitive streak, leading to the regression of Nodal expression in the node. Furthermore, maternal vitamin A intake was found to increase the incidence and diversity of L-R axis defects, likely as a result of dysregulation of retinoic acid metabolism apparent in embryos of diabetic dams and Wnt3a –/– embryos. Conclusions: Hyperglycemia downregulates canonical Wnt signaling by lowering pH i , which not only impairs L-R axis formation but also dysregulates retinoid metabolism. Consequently, embryos of diabetic dams become vulnerable to fluctuation of maternal vitamin A intake, resulting in diverse L-R axis defects. These findings provide insights into the etiology of CHD and suggest the importance of diet for prevention of heterotaxy during diabetic pregnancy.

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Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4134622
Primary Topic
Metabolism and Genetic Disorders
Type
article
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article

Abstract 4134622: Hyperglycemia Induces Heterotaxy Syndrome by Lowering Intracellular pH

Chikara Meno, Ryohei Matsuoka, Shouichi Ohga, Keiko Kitajima
Circulation
Metabolism and Genetic Disorders
article

Abstract 4134622: Hyperglycemia Induces Heterotaxy Syndrome by Lowering Intracellular pH

Chikara Meno, Ryohei Matsuoka, Shouichi Ohga, Keiko Kitajima
article en

Abstract

Background: Pregestational diabetes is an established risk factor for congenital heart disease (CHD), including heterotaxy syndrome, which results from abnormal left-right (L-R) axis. However, the specific mechanism by which hyperglycemia disturbs the L-R axis still remains unsolved. In addition, it is unknown how a variety of heterotaxy is provoked by pregestational diabetes. Methods: We conducted whole-mount in situ hybridization, reporter analysis and RNA-seq in mouse embryos of streptozotocin-induced diabetic dams and Wnt3a –/– embryos. Additionally, the effect of high-glucose conditions on intracellular pH (pH i ) was investigated. We also examined the influence of maternal vitamin A intake on L-R axis formation in embryos of diabetic dams. Results: We observed various patterns of Pitx2 expression in embryos of diabetic dams, indicating disrupted L-R axis. The initial step of L-R axis formation was impaired, with Nodal expression, which induces Nodal - Pitx2 cascade in the lateral plate mesoderm, being regressed in the node. Consistent with the resemblance to the phenotype of Wnt3a –/– embryos, canonical Wnt signaling was downregulated in embryos of diabetic dams. As the RNA-seq analysis suggested dysregulation of glycolysis, we assessed pH i to find that hyperglycemia lowers pH i in the primitive streak, leading to the regression of Nodal expression in the node. Furthermore, maternal vitamin A intake was found to increase the incidence and diversity of L-R axis defects, likely as a result of dysregulation of retinoic acid metabolism apparent in embryos of diabetic dams and Wnt3a –/– embryos. Conclusions: Hyperglycemia downregulates canonical Wnt signaling by lowering pH i , which not only impairs L-R axis formation but also dysregulates retinoid metabolism. Consequently, embryos of diabetic dams become vulnerable to fluctuation of maternal vitamin A intake, resulting in diverse L-R axis defects. These findings provide insights into the etiology of CHD and suggest the importance of diet for prevention of heterotaxy during diabetic pregnancy.

CirculationVol. 150(Suppl_1)
Kyushu University (JP)
Good health and well-being
Openalex Percentile: Top 70%
Metabolism and Genetic Disorders
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