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胎儿对母体新陈代谢的操纵是印制的Igf2基因的一个关键功能
Jorge Lopez-Tello1, Hannah E J Yong2, Ionel Sandovici3
1Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Cell metabolism
|July 12, 2023
概括
胎儿基因Igf2 (胰岛素样生长因子2) 通过胎盘激素操纵母亲的新陈代谢. 胎盘细胞中的Igf2丧失限制胎儿生长,并影响后代的代谢健康.
科学领域:
- 生殖生物学 生殖生物学
- 发育生物学是发展生物学.
- 内分泌学 在内分泌学.
背景情况:
- 母婴互动涉及合作和冲突.
- 对于母体生理学的胎儿操纵来转移营养是众所周知的,但人们对其了解甚少.
- 印制的Igf2基因在胎盘内分泌细胞中表达.
研究的目的:
- 研究Igf2在胎盘内分泌细胞中的作用.
- 阐明胎儿操纵母亲生理学的机制.
- 了解Igf2对胎儿生长和后代代谢的影响.
主要方法:
- 在小鼠胎盘内分泌细胞中删除Igf2基因.
- 对胎盘内分泌信号,激素产生和母亲胰岛素抵抗的分析.
- 评估胎儿生长,血糖水平和长期后代代谢健康状况.
主要成果:
- 消去Igf2会损害胎盘内分泌信号,但不会改变胎盘形态.
- Igf2控制着胎盘激素的产生 (例如,益生素) 和与怀孕相关的胰岛素抵抗.
- 缺少胎盘Igf2的胎儿表现出生长限制和低血糖症.
- 在胎盘细胞中,Igf2调节蛋白质合成和能量平衡.
- 在成年后代中,Igf2损失导致了长期的代谢效应.
结论:
- 胎盘内分泌细胞中的Igf2是胎儿资源分配的关键媒介.
- 胎儿拥有一个内在的系统,可以操纵母亲的新陈代谢,使其受益.
- 这种Igf2介导系统的破坏对胎儿发育和长期代谢健康有重大影响.
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