High Maternal Glycine Levels Increase the Risk of Developing Atrial Septal Defect in the Offspring

IF 8.4 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Ya-Nan Qiao PhD , Wei-Cheng Chen PhD , Yu-Ling Chen MD , Jie Xiang BS , Yu-Fan Ke BS , Li Cao PhD , Lei Li PhD , Jing Cao PhD , Rui Zhao PhD , Jian-Yuan Zhao PhD
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引用次数: 0

Abstract

Amino acid imbalance is linked to increased congenital heart disease risk. Here, we found women carrying rs2545801 C/C genotypes exhibited increased glycine levels and increased risk for atrial septal defects (ASDs) in their offspring. Elevated maternal glycine levels during the first trimester were correlated with a higher ASD risk in the offspring. Additionally, feeding pregnant mice with high-glycine chow increased ASD risk in their offspring. Mechanistically, elevated maternal glycine led to increased lysine-glycylation of lysine-688 within the TEK receptor tyrosine kinase and inhibited TEK-PI3K-AKT/FOXO1 signaling in cardiac endothelial cells. These findings indicate that lysine-glycylation exerts teratogenic effects and may be a target for ASD intervention.
母体甘氨酸水平高会增加子代房间隔缺损的风险
氨基酸失衡与先天性心脏病风险增加有关。在这里,我们发现携带rs2545801 C/C基因型的女性在其后代中表现出更高的甘氨酸水平和更高的房间隔缺陷(asd)风险。妊娠前三个月母体甘氨酸水平升高与后代患ASD的风险升高相关。此外,给怀孕的老鼠喂食高甘氨酸的食物会增加其后代患自闭症的风险。机制上,母体甘氨酸升高导致TEK受体酪氨酸激酶中赖氨酸-688的赖氨酸-甘氨酸化增加,并抑制心脏内皮细胞中TEK- pi3k - akt /FOXO1信号传导。这些发现表明赖氨酸-甘氨酸化具有致畸作用,可能是ASD干预的靶点。
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来源期刊
JACC: Basic to Translational Science
JACC: Basic to Translational Science CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
14.20
自引率
1.00%
发文量
161
审稿时长
16 weeks
期刊介绍: JACC: Basic to Translational Science is an open access journal that is part of the renowned Journal of the American College of Cardiology (JACC). It focuses on advancing the field of Translational Cardiovascular Medicine and aims to accelerate the translation of new scientific discoveries into therapies that improve outcomes for patients with or at risk for Cardiovascular Disease. The journal covers thematic areas such as pre-clinical research, clinical trials, personalized medicine, novel drugs, devices, and biologics, proteomics, genomics, and metabolomics, as well as early phase clinical trial methodology.
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