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钙向人类胎儿胎盘转运的分子生物学

The Molecular Biology of Placental Transport of Calcium to the Human Foetus.

作者信息

Walker Valerie

机构信息

Department of Clinical Biochemistry, University Hospital Southampton NHS Foundation Trust, Southampton General Hospital, Southampton SO16 6YD, UK.

出版信息

Int J Mol Sci. 2025 Jan 4;26(1):383. doi: 10.3390/ijms26010383.

DOI:10.3390/ijms26010383
PMID:39796238
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11720126/
Abstract

From fertilisation to delivery, calcium must be transported into and within the foetoplacental unit for intracellular signalling. This requires very rapid, precisely located Ca transfers. In addition, from around the eighth week of gestation, increasing amounts of calcium must be routed directly from maternal blood to the foetus for bone mineralisation through a flow-through system, which does not impact the intracellular Ca concentration. These different processes are mediated by numerous membrane-sited Ca channels, transporters, and exchangers. Understanding the mechanisms is essential to direct interventions to optimise foetal development and postnatal bone health and to protect the mother and foetus from pre-eclampsia. Ethical issues limit the availability of human foetal tissue for study. Our insight into the processes of placental Ca handling is advancing rapidly, enabled by developing genetic, analytical, and computer technology. Because of their diverse sources, the reports of new findings are scattered. This review aims to pull the data together and to highlight areas of uncertainty. Areas needing clarification include trafficking, membrane expression, and recycling of channels and transporters in the placental microvilli; placental metabolism of vitamin D in gestational diabetes and pre-eclampsia; and the vascular effects of increased endothelial Orai expression by pregnancy-specific beta-1-glycoproteins PSG1 and PSG9.

摘要

从受精到分娩,钙必须转运至胎儿-胎盘单位内部并在其中进行细胞内信号传导。这需要非常快速且定位精确的钙转运。此外,从妊娠约第8周起,越来越多的钙必须通过一个不影响细胞内钙浓度的流通系统,直接从母体血液输送至胎儿用于骨骼矿化。这些不同的过程由众多位于细胞膜的钙通道、转运体和交换体介导。了解这些机制对于指导干预措施以优化胎儿发育和出生后骨骼健康,并保护母亲和胎儿免受先兆子痫影响至关重要。伦理问题限制了用于研究的人类胎儿组织的可获得性。借助不断发展的基因、分析和计算机技术,我们对胎盘钙处理过程的认识正在迅速推进。由于来源多样,新发现的报告较为分散。本综述旨在整合数据并突出存在不确定性的领域。需要阐明的领域包括胎盘微绒毛中通道和转运体的运输、膜表达及循环利用;妊娠糖尿病和先兆子痫中胎盘维生素D的代谢;以及妊娠特异性β-1-糖蛋白PSG1和PSG9增加内皮Orai表达的血管效应。

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