Foteva Vladimira, Fisher Joshua J, Qiao Yixue, Smith Roger
Mothers and Babies Research Program, Hunter Medical Research Institute, Newcastle, NSW 2305, Australia.
School of Medicine and Public Health, University of Newcastle, Newcastle, NSW 2308, Australia.
J Dev Biol. 2025 Mar 5;13(1):8. doi: 10.3390/jdb13010008.
Molybdenum is an essential trace element sourced during pregnancy from the maternal diet. Studies regarding molybdenum have primarily focused on overexposure in animal and cell culture studies. The effects of molybdenum supplementation on placental function are unknown. An immortalised trophoblast cell line was used to examine the placental cellular response to molybdenum in its bioavailable form as molybdate. Cells of the extravillous trophoblast first-trimester cell line HTR8-SVneo were cultured in complete cell media in the presence of 10 nM to 1 mM of ammonium molybdate or sodium molybdate. Following the addition of the molybdate salts, cell growth, viability, and several gene pathways were monitored. Sodium molybdate salt in doses from 10 nM to 1 mM did not affect cell growth or viability. Exposure to ammonium molybdate at a 1 mM concentration significantly decreased cell growth and viability ( < 0.05). Gene pathways involving molybdoenzyme expression, molybdenum cofactor synthesis, antioxidant response, and angiogenesis were affected following supplementation, although these effects differed depending on the dose and molybdate salt utilised. Molybdoenzyme activity was not affected by supplementation in a dose-dependent manner. The results indicate sodium molybdate is a more appropriate salt to use in vitro, as ammonium molybdate exposure reduced cell viability and growth and downregulated the expression of antioxidant genes ( < 0.01), ( < 0.001) and ( < 0.001), suggestive of an inflammatory response. Sodium molybdate affected gene, protein, and activity levels of molybdoenzyme, antioxidant, and angiogenic molecules in vitro. This work demonstrates that sodium molybdate supplementation has pleiotropic effects in vitro and is well tolerated by placental cells at a range of nanomolar and micromolar concentrations.
钼是孕期从母体饮食中获取的一种必需微量元素。关于钼的研究主要集中在动物和细胞培养研究中的过度暴露情况。钼补充剂对胎盘功能的影响尚不清楚。使用一种永生化滋养层细胞系来研究胎盘细胞对生物可利用形式的钼(即钼酸盐)的反应。将早孕期绒毛外滋养层细胞系HTR8-SVneo的细胞在含有10 nM至1 mM钼酸铵或钼酸钠的完全细胞培养基中培养。添加钼酸盐后,监测细胞生长、活力以及几条基因通路。10 nM至1 mM剂量的钼酸钠对细胞生长或活力没有影响。暴露于1 mM浓度的钼酸铵会显著降低细胞生长和活力(<0.05)。补充钼后,涉及钼酶表达、钼辅因子合成、抗氧化反应和血管生成的基因通路受到影响,尽管这些影响因所用剂量和钼酸盐种类而异。钼酶活性不受补充剂剂量依赖性影响。结果表明,钼酸钠是体外实验中更合适的盐,因为暴露于钼酸铵会降低细胞活力和生长,并下调抗氧化基因(<0.01)、(<0.001)和(<0.001)的表达,提示存在炎症反应。钼酸钠在体外影响钼酶、抗氧化剂和血管生成分子的基因、蛋白质和活性水平。这项工作表明,补充钼酸钠在体外具有多效性,并且在一系列纳摩尔和微摩尔浓度下能被胎盘细胞良好耐受。