Suppr超能文献

从卵裂期的小鼠胚胎中去除卵裂球会改变胎盘的功能,这与胎盘的氧化应激和炎症有关。

Blastomere removal from cleavage-stage mouse embryos alters placental function, which is associated with placental oxidative stress and inflammation.

机构信息

Center of Reproductive Medicine, Jinling Hospital, Nanjing University School of Medicine, 305 East Zhongshan Road, Nanjing 210002, PR China.

Anhui Provincial Laboratory for Local Livestock and Poultry, Genetic Resource Conservation and Breeding, College of Animal Sciences and Technology, Anhui Agricultural University, 130 Changjiang West Road, Hefei 230036, PR China.

出版信息

Sci Rep. 2016 Apr 25;6:25023. doi: 10.1038/srep25023.

Abstract

Blastomere biopsy is an essential technique in preimplantation genetic diagnosis (PGD), a screening test that can detect genetic abnormalities of embryos before their transfer into uterus. Our results showed that the weights of fetuses derived from biopsied embryos were lower than that of non-biopsied counterparts at E12.5, E15.5, and E18.5. The ratio of fetal/placental (F/P) weights in the biopsied group was significantly lower than that in the non-biopsied group at E18.5. At E18.5, the mRNAs for selected glucose transporters, system A amino acid transporters, system L amino acid transporters, and imprinted genes were downregulated in the placentae of biopsied group, and the GLUT1 and CAT3 protein levels were decreased too. More apoptotic cells were detected by TUNEL in the placentae of biopsied group. Placentae from biopsied embryos exhibited lower levels of SOD and GSH. Furthermore, the concentration of MDA increased in the placentae from biopsied group. The levels of IL1B, IL6, and TNFA also significantly increased in the placentae of biopsied group. This study suggested that placental function may be sensitive to blastomere biopsy procedures, and placental oxidative stress and inflammation associated with blastomere biopsy may be critical factors of abnormal placental function and further influence the fetal development.

摘要

卵裂球活检是胚胎植入前遗传学诊断(PGD)的一项重要技术,这是一种在胚胎移植入子宫前进行的筛选测试,可以检测胚胎的遗传异常。我们的结果表明,在 E12.5、E15.5 和 E18.5 时,来自活检胚胎的胎儿体重低于未活检胚胎。在 E18.5 时,活检组的胎儿/胎盘(F/P)重量比显著低于未活检组。在 E18.5 时,活检组胎盘内选定的葡萄糖转运体、系统 A 氨基酸转运体、系统 L 氨基酸转运体和印迹基因的 mRNAs 下调,GLUT1 和 CAT3 蛋白水平也降低。TUNEL 检测显示活检组胎盘中有更多的凋亡细胞。来自活检胚胎的胎盘中 SOD 和 GSH 的水平较低。此外,来自活检组的胎盘中 MDA 的浓度增加。IL1B、IL6 和 TNFA 的水平在活检组的胎盘组织中也显著增加。本研究表明,胎盘功能可能对卵裂球活检过程敏感,与卵裂球活检相关的胎盘氧化应激和炎症可能是胎盘功能异常的关键因素,并进一步影响胎儿发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60e5/4842963/b55fdf58778d/srep25023-f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验