Christensen Karen E, Faquette Marie-Lou, Keser Vafa, Reagan Alaina M, Gebert Aaron T, Bottiglieri Teodoro, Howell Gareth R, Rozen Rima
Departments of Human Genetics and Pediatrics, McGill University, Montreal, QC H3A 0C7, Canada.
The Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada.
Nutrients. 2025 Aug 1;17(15):2536. doi: 10.3390/nu17152536.
: Low folate intake before and during pregnancy increases the risk of neural tube defects and other adverse outcomes. Gene variants such as 677C>T (rs1801133) may increase risks associated with suboptimal folate intake. Our objective was to use BALB/cJ mice to evaluate the effects of the TT genotype and low folate diets on embryonic development and MTHFR protein expression in pregnant mice. : Female 677CC (mCC) and 677TT (mTT) mice were fed control (2 mg folic acid/kg (2D)), 1 mg folic acid/kg (1D) and 0.3 mg folic acid/kg (0.3D) diets before and during pregnancy. Embryos and maternal tissues were collected at embryonic day 10.5. Embryos were examined for developmental delays and defects. Methyltetrahydrofolate (methylTHF) and total homocysteine (tHcy) were measured in maternal plasma, and MTHFR protein expression was evaluated in maternal liver. : MethylTHF decreased due to the experimental diets and mTT genotype. tHcy increased due to 0.3D and mTT genotype; mTT 0.3D mice had significantly higher tHcy than the other groups. MTHFR expression was lower in mTT liver than mCC. MTHFR protein expression increased due to low folate diets in mCC mice, whereas in mTT mice, MTHFR expression increased only due to 1D. Developmental delays were increased in the litters of mTT mice fed 1D and 0.3D. : The mouse models the effects of the 677TT genotype in humans and provides a folate-responsive model for examination of the effects of folate intake and the 677C>T variant during gestation.
孕期前后叶酸摄入量低会增加神经管缺陷及其他不良后果的风险。诸如677C>T(rs1801133)等基因变异可能会增加与叶酸摄入不足相关的风险。我们的目标是使用BALB/cJ小鼠来评估TT基因型和低叶酸饮食对怀孕小鼠胚胎发育及亚甲基四氢叶酸还原酶(MTHFR)蛋白表达的影响。:雌性677CC(mCC)和677TT(mTT)小鼠在孕期前后分别喂食对照饮食(2毫克叶酸/千克(2D))、1毫克叶酸/千克(1D)和0.3毫克叶酸/千克(0.3D)的饮食。在胚胎第10.5天收集胚胎和母体组织。检查胚胎是否存在发育延迟和缺陷。检测母体血浆中的甲基四氢叶酸(methylTHF)和总同型半胱氨酸(tHcy),并评估母体肝脏中MTHFR蛋白的表达。:实验饮食和mTT基因型导致methylTHF降低。0.3D饮食和mTT基因型导致tHcy升高;mTT 0.3D小鼠的tHcy显著高于其他组。mTT肝脏中的MTHFR表达低于mCC。低叶酸饮食使mCC小鼠的MTHFR蛋白表达增加,而在mTT小鼠中,MTHFR表达仅因1D饮食而增加。喂食1D和0.3D饮食的mTT小鼠的仔鼠发育延迟增加。:该小鼠模型模拟了人类677TT基因型的影响,并提供了一个叶酸反应模型,用于研究孕期叶酸摄入和677C>T变异的影响。