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首页> 外文期刊>Placenta >Placental expression of 2,3 bisphosphoglycerate mutase in IGF-II knock out mouse: correlation of circulating maternal 2,3 bisphosphoglycerate and fetal growth.
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Placental expression of 2,3 bisphosphoglycerate mutase in IGF-II knock out mouse: correlation of circulating maternal 2,3 bisphosphoglycerate and fetal growth.

机译:在IGF-II基因敲除小鼠中胎盘2,3双磷酸甘油酸突变酶的表达:循环中的母体2,3双磷酸甘油酸与胎儿生长的相关性。

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Bisphosphoglycerate mutase (BPGM) catalyses the formation of 2,3 bisphosphoglycerate (BPG) a ligand of haemoglobin. BPG facilitates liberation of oxygen from haemoglobin at low oxygen tension enabling efficient delivery of oxygen to tissues. We describe expression of BPGM in mouse labyrinthine trophoblasts, located at the maternal-placental interface. Expression is lower in placentae of igf2(+/-) knockout mice, a widely used model of growth restriction, compared to wild type placentae. Circulating maternal BPG increased throughout gestation but this increase was less in wt mothers carrying igf2(+/-) pups than in those carrying exclusively wt pups. This reduction was observed well before term and may contribute to the low birth weight of igf2(+/-) pups. Strikingly, we also measured reductions of fetal and placental weight in wt littermates of igf2(+/-) pups compared to pups developing in an exclusively wt environment. These data suggest that placental expression of BPGM can influence maternal BPG concentrations and supports a hypothesis under which BPG synthesized in the placenta may act on maternal haemoglobin to enhance delivery of oxygen to the developing fetus.
机译:双磷酸甘油酸突变酶(BPGM)催化血红蛋白配体2,3双磷酸甘油酯(BPG)的形成。 BPG有助于在低氧张力下从血红蛋白释放氧气,从而将氧气有效地输送到组织。我们描述了位于母体-胎盘界面的小鼠迷宫滋养细胞中BPGM的表达。与野生型胎盘相比,igf2(+/-)敲除小鼠的胎盘中的表达较低,igf2(+/-)敲除小鼠是一种广泛使用的生长限制模型。循环孕产妇的BPG在整个妊娠期均增加,但与仅携带wt幼仔的母亲相比,携带igf2(+/-)幼仔的wt母亲的这种增加较少。这种减少是在足月前很早就观察到的,并且可能有助于降低igf2(+/-)幼仔的出生体重。令人惊讶的是,与仅在wt环境中发育的幼崽相比,我们还测量了igf2(+/-)幼崽的wt同窝仔中胎儿和胎盘重量的减少。这些数据表明,BPGM的胎盘表达可以影响母体的BPG浓度,并支持一种假设,即胎盘中合成的BPG可能作用于母体的血红蛋白,从而增强了向发育中的胎儿的氧气输送。

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