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囊胚形成及滋养外胚层紧密连接相关蛋白的正常组装需要钠钾ATP酶β1亚基的表达。

Na/K-ATPase beta1 subunit expression is required for blastocyst formation and normal assembly of trophectoderm tight junction-associated proteins.

作者信息

Madan Pavneesh, Rose Keeley, Watson Andrew J

机构信息

Department of Obstetrics and Gynaecology, University of Western Ontario, Children's Health Research Institute-Victoria Research Laboratories, London, Ontario N6A 4G5, Canada.

出版信息

J Biol Chem. 2007 Apr 20;282(16):12127-34. doi: 10.1074/jbc.M700696200. Epub 2007 Feb 22.

Abstract

Na/K-ATPase plays an important role in mediating blastocyst formation. Despite the expression of multiple Na/K-ATPase alpha and beta isoforms during mouse preimplantation development, only the alpha1 and beta1 isoforms have been localized to the basolateral membrane regions of the trophectoderm. The aim of the present study was to selectively down-regulate the Na/K-ATPase beta1 subunit employing microinjection of mouse 1 cell zygotes with small interfering RNA (siRNA) oligos. Experiments comprised of non-injected controls and two groups microinjected with either Stealthtrade mark Na/K-ATPase beta1 subunit oligos or nonspecific Stealthtrade mark siRNA as control. Development to the 2-, 4-, 8-, and 16-cell and morula stages did not vary between the three groups. However, only 2.3% of the embryos microinjected with Na/K-ATPase beta1 subunit siRNA oligos developed to the blastocyst stage as compared with 73% for control-injected and 91% for non-injected controls. Na/K-ATPase beta1 subunit down-regulation was validated by employing reverse transcription-PCR and whole-mount immunofluorescence methods to demonstrate that Na/K-ATPase beta1 subunit mRNAs and protein were not detectable in beta1 subunit siRNA-microinjected embryos. Aggregation chimera experiments between beta1 subunit siRNA-microinjected embryos and controls demonstrated that blockade of blastocyst formation was reversible. The distribution of Na/K-ATPase alpha1 and tight junction-associated proteins occludin and ZO-1 were compared among the three treatment groups. No differences in protein distribution were observed between control groups; however, all three polypeptides displayed an aberrant distribution in Na/K-ATPase beta1 subunit siRNA-microinjected embryos. Our results demonstrate that the beta1 subunit of the Na/K-ATPase is required for blastocyst formation and that this subunit is also required to maintain a normal Na/K-ATPase distribution and localization of tight junction-associated polypeptides during preimplantation development.

摘要

钠钾ATP酶在介导囊胚形成过程中发挥着重要作用。尽管在小鼠植入前发育过程中多种钠钾ATP酶α和β亚型均有表达,但只有α1和β1亚型定位于滋养外胚层的基底外侧膜区域。本研究的目的是通过向小鼠单细胞受精卵显微注射小干扰RNA(siRNA)寡核苷酸,选择性下调钠钾ATP酶β1亚基。实验包括未注射的对照组以及两组分别显微注射Stealth™钠钾ATP酶β1亚基寡核苷酸或非特异性Stealth™ siRNA作为对照的组。三组在发育至2细胞、4细胞、8细胞、16细胞和桑椹胚阶段方面没有差异。然而,与注射对照的胚胎73%以及未注射对照的胚胎91%相比,显微注射钠钾ATP酶β1亚基siRNA寡核苷酸的胚胎只有2.3%发育至囊胚阶段。通过逆转录聚合酶链反应和全胚胎免疫荧光方法验证了钠钾ATP酶β1亚基的下调,结果表明在显微注射β1亚基siRNA的胚胎中检测不到钠钾ATP酶β1亚基的mRNA和蛋白质。β1亚基siRNA显微注射胚胎与对照之间的聚集嵌合体实验表明,囊胚形成的阻断是可逆的。比较了三个处理组中钠钾ATP酶α1以及紧密连接相关蛋白闭合蛋白和ZO-1的分布。对照组之间未观察到蛋白质分布的差异;然而,在显微注射钠钾ATP酶β1亚基siRNA的胚胎中,所有这三种多肽均呈现异常分布。我们的结果表明,钠钾ATP酶的β1亚基是囊胚形成所必需的,并且该亚基在植入前发育过程中对于维持正常的钠钾ATP酶分布以及紧密连接相关多肽的定位也是必需的。

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