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溶质载体家族38成员4(SLC38A4)及A系统与胎儿出生体重异常的关联

Association of SLC38A4 and system A with abnormal fetal birth weight.

作者信息

Li Zhen, Lai Guangrui, Deng Lijun, Han Yue, Zheng Danfeng, Song Weiwei

机构信息

Departments of Gynaecology and Obstetrics, and.

出版信息

Exp Ther Med. 2012 Feb;3(2):309-313. doi: 10.3892/etm.2011.392. Epub 2011 Nov 28.

Abstract

In this study, we aimed to explore the correlation between solute carrier family 38 member 4 (SLC38A4) and system A activity in human placentas from pregnancies with abnormal fetal birth weight. We collected placentas from consenting women immediately after their full-term babies were born, with normal, low birth weight or macrosomia, and used real-time PCR and Western blot analysis to detect the levels of SLC38A4 mRNA and protein [also known as sodium-coupled neutral amino acid transport protein 4 (SNAT4)]. Isotope incorporation assay was applied to measure system A activity in the placentas. Compared to the normal birth weight (NBW) group, placentas from the fetal macrosomia (FM) group had significantly increased levels of SLC38A4 mRNA and SNAT4 (both were increased by almost 2-fold; P<0.05), while no significant changes were detected in the placentas from the low birth weight (LBW) group. In addition, system A activity in the placentas from the FM and LBW groups was significantly different from that in the NBW group (1.2±0.20, 0.6±0.14 vs. 1.0±0.18, P<0.05). The data suggest that SNAT4 and system A have a strong association with abnormal fetal birth weight and that they may play a crucial role in fetal growth and development.

摘要

在本研究中,我们旨在探讨溶质载体家族38成员4(SLC38A4)与出生体重异常的妊娠中人类胎盘系统A活性之间的相关性。我们在足月婴儿出生后立即从同意参与的女性中收集胎盘,这些婴儿出生体重正常、低体重或巨大儿,并使用实时PCR和蛋白质印迹分析来检测SLC38A4 mRNA和蛋白质[也称为钠偶联中性氨基酸转运蛋白4(SNAT4)]的水平。采用同位素掺入法测定胎盘中系统A的活性。与正常出生体重(NBW)组相比,巨大儿(FM)组胎盘的SLC38A4 mRNA和SNAT4水平显著升高(两者均增加近2倍;P<0.05),而低出生体重(LBW)组胎盘未检测到显著变化。此外,FM组和LBW组胎盘的系统A活性与NBW组显著不同(分别为1.2±0.20、0.6±0.14和1.0±0.18,P<0.05)。数据表明,SNAT4和系统A与胎儿出生体重异常密切相关,并且它们可能在胎儿生长发育中起关键作用。

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